• P

    Inspection Analyst  

    - 00907
    Job DescriptionJob DescriptionEn este rol serás responsable de adminis... Read More
    Job DescriptionJob Description

    En este rol serás responsable de administrar las funciones de recepción y atención presencial, asegurando una experiencia de servicio organizada, ágil y alineada a los estándares de Premier. Este rol apoya el flujo adecuado de visitas, la canalización de gestiones y distintas funciones administrativas y operacionales relacionadas a servicio y reclamaciones.

    RESPONSABILIDADES PRINCIPALES

    Administrar el área de recepción asegurando una atención ágil, organizada y alineada a los estándares de servicio establecidos.Brindar atención presencial a clientes, visitantes y colaboradores, manteniendo una experiencia cordial y profesional.Gestionar el flujo de visitas y solicitudes presenciales, asegurando tiempos de espera mínimos y la correcta canalización de cada gestión.Atender y canalizar consultas recibidas de forma presencial y mediante correo electrónico u otras plataformas establecidas por la compañía, cumpliendo con los tiempos de respuesta establecidos.Apoyar en la gestión de reclamaciones de accidente, incluyendo orientación al cliente, coordinación de gestiones y seguimiento a solicitudes.Manejar la correspondencia y mensajería, asegurando su correcta recepción, distribución y control.Apoyar en gestiones administrativas y operacionales del área, según sea requerido.Mantener el área de recepción organizada y libre de acumulación de clientes o gestiones pendientes.Cumplir con los protocolos, políticas y procedimientos internos, asegurando consistencia en la ejecución del servicio.

    Dependiendo de las necesidades operacionales del área, la persona podrá apoyar en tareas relacionadas a Claims, incluyendo:

    Impresión de documentos requeridos para envío por correo o entrega en oficina.

    Notificar a clientes y/o talleres sobre cheques listos para recogido.

    Dar seguimiento a documentación necesaria para la resolución de reclamaciones.

    Asistir en solicitudes, reservaciones y extensiones de alquiler de autos.

    Gestionar facturas relacionadas al proceso.

    Orientar a clientes y reclamantes sobre procesos y documentación relacionada a reclamaciones.

    Manejar correos electrónicos relacionados a reclamaciones, incluyendo documentación para indexación y notificación correspondiente al ajustador.

    REQUISITOS, CONOCIMIENTOS, DESTREZAS Y HABILIDADES

    Bachillerato en Administración de Empresas o área relacionada.

    Experiencia previa en funciones administrativas, servicio al cliente o áreas relacionadas, preferiblemente en entornos dinámicos y de alto volumen de atención.

    Dominio de herramientas tecnológicas y colaborativas, incluyendo Google Workspace y sistemas administrativos.

    Capacidad para adaptarse a nuevas tecnologías, sistemas y cambios en entornos dinámicos.

    Habilidad para manejar múltiples tareas, establecer prioridades y administrar el tiempo manteniendo altos estándares de calidad.

    Atención al detalle en el manejo de información y procesos.

    Alto enfoque en servicio al cliente, con actitud proactiva y orientada a la solución.

    Excelentes destrezas interpersonales y de comunicación.

    Capacidad para mantener la organización y el profesionalismo en ambientes dinámicos.

    Dominio de español y capacidad de comunicarse en inglés en contextos profesionales.

    ¿QUÉ OFRECEMOS?

    Un entorno dinámico donde podrás desarrollarte, aportar ideas y crecer profesionalmente, siendo parte de un equipo que trabaja con pasión y compromiso.

    ¡Únete a Premier y sé parte de la experiencia que nos distingue!

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  • B

    Tecnico de Farmacia  

    - 00909
    Job DescriptionJob DescriptionDISPONIBILIDAD DEL ROLDisponibilidad par... Read More
    Job DescriptionJob Description


    DISPONIBILIDAD DEL ROLDisponibilidad para trabajar de martes a sábado

    RESPONSABILIDADES ESPECÍFICAS

    Remueve aquellos medicamentos que estén próximos a expirar y los coloca en el área asignada.Da prioridad al uso de medicamentos que estén próximos a expirar para utilizar estos antes de que llegue la fecha de expiración.Dispensa los medicamentos en las cantidades apropiadas de acuerdo con la dosis y frecuencia que se prescribe.Inspecciona y guarda siempre los medicamentos devueltos por el personal de enfermería para reutilizarlos.Anota las temperaturas diariamente de las neveras, el cuarto limpio y temperatura ambiente de acuerdo con el programa establecido.Anota las presiones del cuarto limpio diariamente.Sirve los medicamentos en un período de tiempo razonable, tomando en cuenta la cantidad de pacientes a ser despachados.Despacha las requisiciones de material médico quirúrgico y manejo de la piel correctamente y en un tiempo adecuado.Asigna correctamente los tamaños de apósitos y cantidades en las requisiciones de úlceras de forma electrónica.Despacha correctamente los Foley de acuerdo con la autorización del plan.Entrega adecuadamente a Island Wide los medicamentos despachados, identificando las cajas correctamente y con el sello de envío indicado.Entrega adecuadamente al carrero de la compañía los medicamentos despachados y suplido, identificando las cajas correctamente con el nombre de la enfermera(o).Da seguimiento a aquellos medicamentos que están pendiente a ser dispensados.Anota continuamente, antes que se terminen, aquellos medicamentos cuya cantidad en la farmacia es insuficiente para suplir los medicamentos a los pacientes.Informa al farmacéutico sobre cualquier error cometido o situación que ocurra inmediatamente.Acomoda la mercancía que se recibe en la farmacia en las áreas asignadas para cada categoría de medicamento.Organiza periódicamente las góndolas para reacomodar aquellos medicamentos que estén fuera del sitio que tiene asignado.Organiza periódicamente los medicamentos que están en las neveras.Procura que los medicamentos que requieren refrigeración no estén fuera de la nevera por más tiempo del necesario.Hace entrada de data correcta y rápida en BOATS y Rx-30.Hace nota en el sistema BOATS cuando realiza alguna intervención con médico, paciente, manejador de caso o personal de enfermería.Sigue las reglas establecidas en el departamento.Atiende rápido y efectivamente el teléfono.Asigna y despacha correctamente los medicamentos a base de los NDC.Asiste al farmacéutico en el inventario de medicamentos y material médico quirúrgico.Procura hacer buena utilización de materiales y equipo.Sigue las instrucciones del supervisor realizando las tareas, estableciendo prioridades y utilizando su juicio crítico.Mantiene el área de trabajo limpia y organizada.Realizar proyectos especiales que le sean encomendados.Realizar otras tareas afines que le sean asignadas.Maneja correctamente la Guardia de Farmacia de acuerdo con el procedimiento establecido.Realizar limpieza adecuada de las máquinas de infusiones y rotular la fecha en que se realizó este procedimiento.Prepara los medicamentos en el cuarto limpio siguiendo técnicas asépticas adecuadas.Cumple con la norma de vestimenta establecidas en el cuarto limpio.Prepara adecuadamente quimioterapias y sustancias peligrosas en el cuarto limpio establecido, cumpliendo con las normas de preparación y vestimenta.Hace la limpieza como se establece del cuarto limpio (Soluciones intravenosas.)Cumple con las regulaciones establecidas por USP 797.Toda otra tarea de acuerdo con las necesidades de la empresa.Cumple con las disposiciones del Plan de Cumplimiento Corporativo de BOH, sus normas y procedimientos y Códigos de Conducta.

    NIVEL DE AUTORIDAD Y/O JUICIO INDEPENDIENTE

    Usual y regularmente, el puesto de Técnico de Farmacia ejerce un nivel bajo de autoridad y juicio independiente con respecto al desempeño de las tareas y funciones adscritas al mismo.

    NIVEL DEL PUESTO

    EDUCACIÓN:Grado Asociado de Farmacia y Registro por la Junta de Farmacia.EXPERIENCIA:1 a 2 años de experiencia en funciones relacionadas al puesto de Técnico de Farmacia. COMPETENCIAS: Conocimiento en el área de composición de medicamentos.Conocimiento en preparación de antibióticos, quimioterapias, nutriciones parenterales y medicamentos especializados. Conocimiento en procesar recetas de forma electrónica a pacientes. Destreza para entrar en sistema data correcta y rápida. Destreza para atender las necesidades del personal clínico. Destreza para dar prioridad al uso de apósitos y medicamentos que estén próximos a expirar para utilizar estos antes de que llegue la fecha de expiración. Alta capacidad analítica y de atención al detalle.

    Patrono con Igualdad de Oportunidad de Empleo

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  • A

    Test Technician  

    - 21152
    Job DescriptionJob DescriptionTEST TECHNICIAN 1, INSTRUMENTS – SPARKS,... Read More
    Job DescriptionJob Description

    TEST TECHNICIAN 1, INSTRUMENTS – SPARKS, MD

    Pay Rate: $25.00/hour

    JOB DETAILS

    Schedule: Monday–Friday | 7:00 AM – 3:30 PMInterviews: In-personPlease do not submit duplicate candidates previously interviewed or rejected.Candidates with strong work longevity preferred. Multiple short-term assignments may not be considered.

    POSITION OVERVIEW

    The Instrument Test Technician 1 is responsible for performing production assembly operations, system analysis, instrument testing, troubleshooting, and performance optimization in a manufacturing environment. This role supports quality, safety, and production standards while working closely with Manufacturing Engineering, Quality, Planning, and Purchasing teams.

    RESPONSIBILITIES

    Build, integrate, and understand complete assembly processes for production instruments.Perform functional and release testing on moderately complex instruments.Analyze testing data and determine pass/fail results.Troubleshoot electrical, mechanical, and software-related issues on non-functioning equipment.Provide system optimization solutions related to movement precision and lighting systems.Identify defects and recommend process or design improvements.Read and interpret drawings, work instructions, and workmanship standards.Train associates on mechanical and testing procedures as needed.Perform production activities in compliance with GMP, safety, and quality standards.Support material handling functions for raw materials and sub-assemblies.Maintain clean, safe, and organized work areas according to company policies.Collaborate with Manufacturing Engineering, Quality, Planning, and Purchasing departments.Follow all company operating procedures, safety requirements, and housekeeping standards.Work overtime as needed to support business demands.

    QUALIFICATIONS

    Associate degree in Mechatronics or related technical field with 0 years of experience ORMinimum of 5 years of experience in electrical, mechanical, or software troubleshootingStrong troubleshooting and analytical skillsAbility to interpret technical drawings and work instructionsExperience working in manufacturing or production environments preferredKnowledge of GMP and quality standards preferredAbility to work independently and within a team environment

    If you are interested, please reach out to Chin Yang at A-Line Staffing. 586-323-4194 | cyang@alinestaffing.com.

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  • A
    Job DescriptionJob DescriptionTest Technician ILocation: Sparks Glenco... Read More
    Job DescriptionJob Description

    Test Technician I
    Location: Sparks Glencoe, MD
    Schedule: Monday–Friday | Day Shift
    Pay Rate: $25.00/hour

    Job Overview

    The Test Technician I performs production assembly operations along with complete system analysis, testing, and performance optimization of moderately complex instruments. This role involves basic electrical, mechanical, and software troubleshooting to diagnose issues in non-functioning test equipment and implement solutions based on defined pass/fail criteria. The technician identifies and escalates testing issues and serves as a subject matter expert in instrument functional performance.

    Key Responsibilities

    Build, integrate, and understand the full assembly process and requirements for instruments in the production areaExecute and interpret test instructions for at least one moderately complex instrument, including functional and release testingAnalyze test results and data to determine pass/fail outcomes and recommend corrective actionsOptimize system performance, including precision of movement and/or light systems, using test dataIdentify defects and recommend design or process improvementsRead and interpret drawings, work instructions, and workmanship standardsTrain and support associates in mechanical assembly and testing activitiesComplete production activities in compliance with regulatory requirements and BD safety and quality standardsProcess and disposition Quality Notifications (QNs)Interface with Manufacturing Engineering, Quality, Planning, and Purchasing teams as neededPerform material handling for raw materials and sub-assembliesMaintain a safe, clean, and organized work environment in accordance with housekeeping standardsFollow Good Manufacturing Practices (GMP), safety policies, and company proceduresWork overtime as required to meet business needsPerform other duties as assigned

    Qualifications

    Education & Experience

    High School Diploma or GED with 6 years of manufacturing experience, orAssociate (AA) technical degree with 2 years of manufacturing experienceExperience working in a regulated manufacturing environment is required

    Required Skills & Competencies

    Ability to support testing of moderately complex instrumentsProven leadership skills with the ability to mentor and coach other associatesStrong accountability for results and continuous process improvementDemonstrated commitment to Continuous Improvement and Lean Manufacturing principlesExperience with mechanical tools (e.g., torque drivers, gauges, bits)Proficiency in reading drawings and measuring/interpreting dimensions and requirementsEffective time management across multiple production ordersStrong teamwork and collaboration skillsAbility to work within established quality systems and proceduresFlexibility to manage frequent changes in assignments

    Technical & Professional Skills

    Proficient in English (reading, writing, and basic documentation)Ability to analyze charts, follow diagrams, and perform basic arithmeticBasic computer skills, including use of Windows-based systemsStrong math and analytical capabilitiesAbility to use independent judgment to plan work, troubleshoot, and problem-solveStrong communication and leadership skills

    If you are interested, please send an up-to-date resume to jschafer@alinestaffing.com Read Less
  • T

    Data Analyst  

    - 68113
    Job DescriptionJob DescriptionThis position is for future workData Ana... Read More
    Job DescriptionJob Description

    This position is for future work

    Data Analyst

    Location: Offutt AFB, NE

    Clearance: Active TOP SECRET with eligibility for SCI.

    Join a Mission-Driven Team at The GARRETT GROUP

    At The GARRETT GROUP, we believe the best solutions begin with a great team of people. When you join us, you become part of a collaborative, mission-focused community committed to excellence in everything we do. We take pride in supporting our nation's most critical missions while creating an environment where our employees can thrive.

    Our team members enjoy a comprehensive benefits package-including a competitive 401(k) with company match, generous Paid Time Off, flexible work schedules, medical, dental, and vision coverage, short-term disability, and company-paid life insurance-because taking care of you enables you to take care of the mission.

    Position Overview

    The GARRETT GROUP is seeking an experienced Data Analyst to support advanced analytical, data management, and machine learning initiatives in a dynamic Department of Defense environment. The selected candidate will be responsible for designing and implementing enterprise-level data collection strategies, managing and analyzing large and complex datasets, and delivering actionable insights to support operational and strategic decision-making.

    This role requires strong technical expertise in data science methodologies, machine learning model development, statistical analysis, and business intelligence tools. The ideal candidate will possess the ability to lead analytical projects, collaborate across multidisciplinary teams, and communicate complex findings to technical and non-technical stakeholders.

    Key Responsibilities

    The Data Analyst will design and manage data collection processes, analyze large and complex datasets, develop machine learning models, and create analytical products using Python, R, SQL, and Business Intelligence tools. The role supports mission decision-making through data visualization, automation, project leadership, Agile collaboration, and delivery of actionable insights to technical and senior leadership teams.

    Required Qualifications

    Bachelor's degree or higher in Data Science, Computer Science, Statistics, Mathematics, Engineering, Information Systems, or a related technical discipline. Minimum of 7 years of experience designing and implementing data collection strategies, data management solutions, and advanced analysis of large, complex datasets. Demonstrated experience leading analytical or technical projects and coordinating cross-functional teams. Direct experience developing, testing, and deploying Machine Learning models. Expertise with: Python R Business Intelligence tools Data cleaning and data wrangling methodologies Proficiency with: Structured Query Language (SQL) Database management concepts and practices Familiarity with Agile methodologies and participation in sprint planning, backlog grooming, and retrospectives. Strong analytical, problem-solving, and critical-thinking skills. Excellent written and verbal communication skills, including the ability to brief senior leadership.

    The GARRETT GROUP is an Equal Opportunity Employer.



    Job Posted by ApplicantPro
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  • T

    Front End Developer  

    - 68113
    Job DescriptionJob DescriptionNote: This position is for future work.... Read More
    Job DescriptionJob Description

    Note: This position is for future work.

    Front End Developer

    Location: Offutt AFB, NE

    Clearance: Active TOP SECRET with eligibility for SCI.

    Join a Mission-Driven Team at The GARRETT GROUP

    At The GARRETT GROUP, we believe the best solutions begin with a great team of people. When you join us, you become part of a collaborative, mission-focused community committed to excellence in everything we do. We take pride in supporting our nation's most critical missions while creating an environment where our employees can thrive.

    Our team members enjoy a comprehensive benefits package-including a competitive 401(k) with company match, generous Paid Time Off, flexible work schedules, medical, dental, and vision coverage, short-term disability, and company-paid life insurance-because taking care of you enables you to take care of the mission.

    Position Overview

    The GARRETT GROUP is seeking an experienced Front End Developer to support the design, development, and enhancement of modern web-based applications and data visualization platforms in support of Department of Defense mission requirements. The selected candidate will develop responsive user interfaces using modern web technologies, with a strong emphasis on the React framework, while integrating data-driven applications, dashboards, and visualization capabilities to support operational analysis and decision-making.

    The ideal candidate will possess strong front-end development expertise, experience with MAVEN Smart Systems, and the ability to work collaboratively within Agile development environments supporting complex mission-focused initiatives.

    Key Responsibilities

    The Front End Developer will design and maintain responsive web applications and interactive dashboards using React and modern visualization libraries, while integrating APIs, RSS feeds, and database-driven solutions to support mission analysis and decision-making. The role includes automating workflows with Python or JavaScript, supporting data visualization and application performance, collaborating within Agile development teams, and delivering intuitive, scalable user interfaces for operational environments.

    Required Qualifications

    Bachelor's degree or higher in Data Science, Computer Science, Data Analytics, Business Analytics, Management Information Systems, Statistics, Applied Mathematics, Applied Physics, or a related technical discipline. Minimum of 7 years of combined front-end development and data visualization experience. Demonstrated experience developing user interfaces using the React framework and modern web technologies. Experience with MAVEN Smart Systems. Experience developing interactive web-based dashboards and visualizations using modern visualization libraries. Experience supporting database-driven applications, version control, and database normalization practices. Experience automating tasks using Python, JavaScript, or similar scripting languages. Experience querying external databases through APIs and RSS feeds. Familiarity with Agile development methodologies and working within cross-functional technical teams. Strong analytical, problem-solving, and communication skills.

    The GARRETT GROUP is an Equal Opportunity Employer.



    Job Posted by ApplicantPro
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  • V
    Job DescriptionJob DescriptionValidation & Engineering Group, Inc. (V&... Read More
    Job DescriptionJob Description

    Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

    We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

    Specialist QA (5:00 pm - 5:30 am)

    SUMMARY
    Perform one or more of the following duties and responsibilities in support of Quality Assurance program under minimal supervision.

    FUNCTIONS
    - Review and approve product MPs.
    - Approve process validation protocols and reports for manufacturing processes.
    - Request Quality on incident triage team.
    - Approve Environmental Characterization reports.
    - Release of sanitary utility systems.
    - Approve planned incidents.
    - Represent QA on NPI team.
    - Lead investigations.
    - Lead site audits.
    - Own site quality program procedures.
    - Designee for QA manager on local CCRB.
    - Review Risk Assessments.
    - Support Automation activities.
    - Support facilities and environmental programs.
    - Review and approve Work Orders.
    - Review and approve EMS/BMS alarms.
    - Approve NC investigations and CAPA records.
    - Approve change controls.
    - Provide lot disposition and authorize lots for shipment.

    EDUCATION
    -Doctorate OR
    -Masters + 2 years of directly related experience OR
    -Bachelors + 4 years of directly related experience OR

    Responsibilities
    • Execute Quality disposition (approval or rejection) of bulk drug substances.
    • Provide Quality oversight to ensure that operations for clinical and licensed pharmaceutical Drug Substance (API) are manufactured, tested, stored, and managed according to current Good Manufacturing Practices (cGMP), Good Laboratory Practices (cGLP), and other applicable regulations.
    • Ensure that deviations from established procedures are identified, reported, and documented per procedures.
    • Ensure that changes that could potentially impact drug substance quality are assessed according to procedures.
    • Ensure that production records and testing results are complete, accurate, and documented according to written procedures and cGMP requirements.
    • Ensure that facilities, equipment, materials, organization, processes, and procedures align with cGMP practices and other applicable regulations.
    • Champion continuous improvement initiatives, programs, and projects, including developing efficiency projects and supervising progress.
    • Ensure completion of required training and maintain assigned training adherence to support successful task execution.
    • Collaborate and partner cross functionally to ensure the Quality Management System (QMS) processes are completed in accordance with established procedures.
    • Support internal and external audits and inspections as part of the audit/inspection management team, including acting as Quality Unit representative as needed.
    • Alert senior management of quality, compliance, supply, and safety risks.
    • Provide support and oversight for New Product Introduction (NPI).

    Attributes:

    • Experience with key electronic systems, such as documentation platforms (e.g., CDOCS), Maximo, TrackWise, LIMS, MES/electronic batch record systems, and SAP.
    • Experience in computer systems validation (CSV) or computer systems quality assurance, including consulting level technical proficiency.
    • Experience with validation of GxP applications, including Validation Master Plans, GxP risk assessments, IQ/OQ/PQ protocols, test scripts, and summary/approval reports.
    • Robust knowledge of manufacturing and distribution processes, including QA, QC, and Process Development operations.
    • Validated experience serving as Quality Contact for complex projects involving packaging, inspection, commissioning, qualification, and new drug substances/products.
    • Strong organizational skills, with the ability to drive assignments through successful completion.
    • Demonstrated leadership, influencing, and negotiation skills, including interactions with regulatory agencies and evaluation of compliance issues.
    • Strong communication skills (written and oral), facilitation abilities, and full bilingual proficiency in English and Spanish, with the ability to work independently and effectively across all organizational levels.

    At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

    Excited to build something meaningful together? We look forward to hearing from you.

    Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

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  • I

    IT HelpDesk Manager  

    - 45651
    Job DescriptionJob DescriptionWe are seeking an IT HelpDesk Manager!Ce... Read More
    Job DescriptionJob Description

    We are seeking an IT HelpDesk Manager!

    Central & Southeastern Ohio Region

    Join our Team!

    Integrated Services for Behavioral Health (ISBH) is a community-minded, forward-thinking behavioral health organization helping people along the road to health and well-being. We meet people in their homes and communities and help connect them to the resources they need. We serve Southeastern and Central Ohio with a comprehensive array of behavioral health and other services, working with local partners to promote healthy people and strong communities. All of our services are intended to be collaborative and personalized for the individual.

    The IT Helpdesk Manager is responsible for the strategic oversight, operational management, and continuous improvement of the IT Helpdesk function across the organization. This role ensures the delivery of high-quality, responsive, and customer-focused technical support services while aligning helpdesk operations with organizational priorities, clinical workflows, and enterprise IT standards.

    In addition to maintaining hands-on technical competency, the Helpdesk Manager provides direct supervision, coaching, and performance management for a team of helpdesk technicians. The role is accountable for service delivery metrics, ticket management, staff development, process optimization, and the implementation of best practices that enhance end-user satisfaction and operational efficiency.

    The salary for this position is $75,006.00 to $95,190.00 annually, based on experience

    Essential Functions

    Provide leadership, oversight, and strategic direction for the Information Technology Helpdesk function, ensuring high-quality, customer-focused technical support services across the organization.Directly supervise, mentor, and manage a team of Helpdesk Technicians, fostering a positive, accountable, and high-performing work environment.Manage, prioritize, and oversee all inbound IT support tickets, ensuring timely resolution, appropriate escalation, and minimal operational disruption.Establish, monitor, and report on helpdesk performance metrics, including service level agreements (SLAs), response times, resolution times, and customer satisfaction.Serve as the primary escalation point for complex or high-impact technical issues, ensuring prompt resolution and clear communication with stakeholders.Develop, implement, and maintain helpdesk policies, procedures, and standard operating practices aligned with organizational and IT governance standards.Lead continuous improvement initiatives to optimize helpdesk workflows, ticket management processes, and service delivery outcomes.Oversee the creation and maintenance of comprehensive documentation, including knowledge base articles, troubleshooting guides, and training materials.Provide advanced technical troubleshooting support for hardware, software, network, and system-related issues as needed.Ensure proper account management processes, including user provisioning, access control, and security compliance.Oversee endpoint device lifecycle management, including deployment, maintenance, refresh, and decommissioning in accordance with established procedures.Monitor and ensure completion of preventative maintenance activities across all supported systems and endpoint devices.Lead onboarding and ongoing training for helpdesk staff, ensuring technical competency and adherence to service standards.Conduct training sessions for staff and end users to promote system knowledge, efficiency, and self-service capabilities.Collaborate with IT leadership and cross-functional departments to support system implementations, upgrades, and organizational initiatives.Maintain oversight of IT inventory management processes, ensuring accurate tracking and documentation of all equipment.Ensure all helpdesk interactions are properly documented within the ticketing system in a timely and consistent manner.Follow up on support requests and analyze trends to improve service quality and reduce recurring issues.Ensure adherence to cybersecurity protocols, including virus remediation, endpoint protection, and user awareness.Participate in organizational and IT governance initiatives, contributing to policy development and compliance efforts.Evaluate the performance of helpdesk staff, conduct formal performance reviews, and recommend appropriate personnel actions.Supervise and coordinate the activities of staff members through regular team meetings, coaching sessions, and ongoing communication.Adhere to the ISBH Confidentiality Policy.Participate in New-Hire Orientation as needed.Travel to offices throughout the service area is required.All other duties assigned.

    Minimum Requirements:

    Education/Licensure

    A high school diploma or GED equivalent is required.A bachelor’s degree in Information Technology, Computer Science, or a related field is required.

    Experience

    5 years of progressive IT support experience is required3 years of supervisory experience in IT or a related field is required.Experience managing helpdesk operations in a healthcare or similarly complex environment is preferred.Experience with account provisioning, system access controls, and security best practices is required.

    Knowledge, Skills, and Abilities

    Advanced knowledge of helpdesk ticketing systems, endpoint management, and user support processes is required.Proficiency in troubleshooting hardware, software, networking, and access-related issues is required.Ability to lead, motivate, and manage technical teams is required.Advanced organizational and process management skills are required.The ability to analyze performance metrics and implement data-driven improvements is required.Excellent communication and interpersonal skills with a strong customer service orientation.Ability to manage deadlines within a fast-paced, high-volume environment is requiredA valid driver's license is requiredAn appropriate level of auto insurance coverage is requiredThe ability to operate in an Internet-based, automated office environment is requiredThe ability to maintain a high-speed internet connection is required

    Physical Requirements

    Prolonged periods of sitting at a desk and working on a computer are requiredThe ability to transport IT equipment is requiredMust be able to lift up to 15 pounds at times

    Enjoy a great work environment with an excellent salary, generous paid time off, and a strong benefits package.

    Benefits include:

    MedicalDentalVisionShort-term DisabilityLong-term Disability401K w/ Employer MatchEmployee Assistance Program (EAP) provides support and resources to help you and your family with a range of issues.

    To learn more about our organization: https://ISBH.org

    OUR MISSION
    Delivering exceptional care through connection

    OUR VALUES
    Dignity - We meet people where they are on their journey with respect and hope

    Collaboration - We listen to understand and ask how we can best support the people and communities we serve

    Wellbeing - We celebrate one another's strengths, and we support one another in being well

    Excellence - We demand high-quality care for those we serve, and we are a leader in how we care for one another as a team

    Innovation - We deeply value a range of perspectives and experiences, knowing it is what inspires us to stretch past where we are and reach towards what we know is possible

    We’re an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

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  • V

    Analytical Services Scientist  

    - 00613
    Job DescriptionJob DescriptionValidation & Engineering Group, Inc. (V&... Read More
    Job DescriptionJob Description

    Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

    We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

    Analytical Services Scientist

    Summary:

    Will provide Analytical Technology expertise for Quality Control requirements within the introduction of new products to the Site, development / transfer / validation of analytical methodologies & technologies, instrumentation services & technologies, and the resolution of complex and critical analytical investigations. Will provide support to the QC Laboratory to ensure QC Systems maintenance. Participate as the Quality representative on steering committees, ad-hoc projects, introduction of new system, upgrades for the Quality Control Laboratory to ensure that requirements are identified and carried out following procedures and SLC (System Life Cycle processes) as required. Ensure the operational efficiency and excellence of the organization by designing, documenting and providing solutions to new business requirements, trends, and concepts appropriately through the latest technological paths. Will maintain Laboratory efficiency and capacity metrics. The incumbent understands the internal and external customer’s business requirements and business process management, and then translates them to process, system or software requirements.

    Responsibilities:

    Collaborate with functional areas to determine regulatory requirements, validation requirements, business & functional risks and work within cross-functional project teams in the development of validation deliverables or systems upgrades for Laboratory equipment and computer systems in Quality or within the Quality Systems.Generate, develop, evaluate, review and approval of Validation / Automation Documentation (validation plans, protocols and final reports), performance qualification, system life cycle approach to ensure compliance and regulatory requirements from the QC perspective.Coordination / direction and active participation in the validation of site laboratory equipment, facilities, utilities, processes and software in compliance with company policies, Federal Drug Administration (FDA) regulations, European current Good Manufacturing Practices (cGMP’s) and Good Automated Manufacturing Practice (GAMP) standards.Performs the method development, method validation, method transfer and method verification of new or existing products, guaranteeing implementation of a feasible and efficient process. Performs process Failure Mode and Effects Analysis (FMEA’s) and other process verification activities following current Regulatory Guidelines.Conduct, write and manage laboratory investigations.Must have excellent technical writing, experience on root cause analysis and CAPA plan determination.Maintenance of Investigations Metric to support Quality Council QC Metrics.Supports process activities to achieve a successful on time resolution of incidents and deviations and enhances quality and effectiveness of laboratory systems, including change control and Corrective Action /Preventive Action (CAPA) towards optimization laboratory processes to assure effectiveness, robustness, and compliance.Lead / Performs special project as assigned. Participate as a team leader or a member of the project teams where needed and help provide direction on future enhancements to the systems.Assist in solving problems during validation process, system upgrades or investigations and address or seek advice from SMEs (Subject Matter Experts) on issues such as deficiencies, deviations and change control.Administrate Quality Computer Systems and perform periodic review as required. Knowledge on Laboratory Information Management Systems (LIMS Vantage or LIMS Lab Ware) is desired. Full knowledge on Chromatographic Data Management System (CDMS) as Empower.Troubleshoot of methods, and or instruments as needed. Coordinate and manages outside services as required for calibration, maintenance, evaluations, quotes, etc. Perform calibration or maintenance as required. Manage, store, handle, dispose, label and inspect laboratory waste following Environmental Protection Agency (EPA), Environmental Quality Board (EQB) and site requirements procedures, guides and policy.Knowledge of Drug Enforcement Administration (DEA) regulations for controlled substances is required.Broad knowledge of Laboratory instruments as HPLC, UPLC, Dionex, GC, Dissolution baths, TOC, FTIR, NIR, Automatic Titrator, UV Spectrophotometer, KF, among others.Write protocols for new instrument introduction – IQ, OQ, PQ, PVT, costing and troubleshooting/PM/Calibration.Author or guide end users in writing system operational procedures, work instructions, system guides templates and SOPs (Standard Operating Procedures).Comply with all environmental and quality trainings, procedures, guidelines, practices, current cGMP’s, permit conditions and internal notifications of any environmental or quality event.Perform any other job-related duties as required or that may arise in the future.

    Requirements:

    Education /Experience.

    Bachelor degree in Science, Engineering or Computer Science from an accredited institution. Master’s degree is an added advantage. At least five (5) year of laboratory experience or systems validation in an FDA regulated environment is required.

    Licenses and/or Certifications

    CSQE Certified Software Quality Engineer from ASQ (American Society for Quality), preferred.Chemical Licensee, preferred.

    Technical Competencies

    Ability to effectively manage multiple projects at the same time with minimum supervision and to incorporate a wide array of technical principles, concepts and theories in innovative ways.Demonstrated analytical and problem-solving skills.Proven ability to teach others and transfer knowledge to end users. Able to work under pressure and self-starter.Ability to work cross functionally within an organization, being able to impact and influence other management teams that do not report to this position. Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Regulatory (FDA) industry experience, familiarity with cGMPs, GAMP (Good automated manufacturing practice), Laboratory Equipment / Instrumentation C&Q practices (Commissioning & Qualification) and current to Pharmacopeias requirements, changes and modifications.Proven ability to learn new computer software/systems and laboratory instruments with minimum of instruction and general understanding of SLC (system life cycle) and CSV (computer validation system). Knowledge and experience with systems and validation processes.Good organization skills and time management skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines, effective project management skills.Fully Bilingual, excellent oral and written communication in both English/Spanish languages.Skills in MS Office Suite applications of MS Project, Outlook, Word, and PowerPoint, and is skilled at performing data evaluation, formulas and metrics

    At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

    Excited to build something meaningful together? We look forward to hearing from you.

    Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

    Read Less
  • V

    Analytical Services Scientist  

    - 00652
    Job DescriptionJob DescriptionValidation & Engineering Group, Inc. (V&... Read More
    Job DescriptionJob Description

    Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

    We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

    Analytical Services Scientist

    Summary:

    Will provide Analytical Technology expertise for Quality Control requirements within the introduction of new products to the Site, development / transfer / validation of analytical methodologies & technologies, instrumentation services & technologies, and the resolution of complex and critical analytical investigations. Will provide support to the QC Laboratory to ensure QC Systems maintenance. Participate as the Quality representative on steering committees, ad-hoc projects, introduction of new system, upgrades for the Quality Control Laboratory to ensure that requirements are identified and carried out following procedures and SLC (System Life Cycle processes) as required. Ensure the operational efficiency and excellence of the organization by designing, documenting and providing solutions to new business requirements, trends, and concepts appropriately through the latest technological paths. Will maintain Laboratory efficiency and capacity metrics. The incumbent understands the internal and external customer’s business requirements and business process management, and then translates them to process, system or software requirements.

    Responsibilities:

    Collaborate with functional areas to determine regulatory requirements, validation requirements, business & functional risks and work within cross-functional project teams in the development of validation deliverables or systems upgrades for Laboratory equipment and computer systems in Quality or within the Quality Systems.Generate, develop, evaluate, review and approval of Validation / Automation Documentation (validation plans, protocols and final reports), performance qualification, system life cycle approach to ensure compliance and regulatory requirements from the QC perspective.Coordination / direction and active participation in the validation of site laboratory equipment, facilities, utilities, processes and software in compliance with company policies, Federal Drug Administration (FDA) regulations, European current Good Manufacturing Practices (cGMP’s) and Good Automated Manufacturing Practice (GAMP) standards.Performs the method development, method validation, method transfer and method verification of new or existing products, guaranteeing implementation of a feasible and efficient process. Performs process Failure Mode and Effects Analysis (FMEA’s) and other process verification activities following current Regulatory Guidelines.Conduct, write and manage laboratory investigations.Must have excellent technical writing, experience on root cause analysis and CAPA plan determination.Maintenance of Investigations Metric to support Quality Council QC Metrics.Supports process activities to achieve a successful on time resolution of incidents and deviations and enhances quality and effectiveness of laboratory systems, including change control and Corrective Action /Preventive Action (CAPA) towards optimization laboratory processes to assure effectiveness, robustness, and compliance.Lead / Performs special project as assigned. Participate as a team leader or a member of the project teams where needed and help provide direction on future enhancements to the systems.Assist in solving problems during validation process, system upgrades or investigations and address or seek advice from SMEs (Subject Matter Experts) on issues such as deficiencies, deviations and change control.Administrate Quality Computer Systems and perform periodic review as required. Knowledge on Laboratory Information Management Systems (LIMS Vantage or LIMS Lab Ware) is desired. Full knowledge on Chromatographic Data Management System (CDMS) as Empower.Troubleshoot of methods, and or instruments as needed. Coordinate and manages outside services as required for calibration, maintenance, evaluations, quotes, etc. Perform calibration or maintenance as required. Manage, store, handle, dispose, label and inspect laboratory waste following Environmental Protection Agency (EPA), Environmental Quality Board (EQB) and site requirements procedures, guides and policy.Knowledge of Drug Enforcement Administration (DEA) regulations for controlled substances is required.Broad knowledge of Laboratory instruments as HPLC, UPLC, Dionex, GC, Dissolution baths, TOC, FTIR, NIR, Automatic Titrator, UV Spectrophotometer, KF, among others.Write protocols for new instrument introduction – IQ, OQ, PQ, PVT, costing and troubleshooting/PM/Calibration.Author or guide end users in writing system operational procedures, work instructions, system guides templates and SOPs (Standard Operating Procedures).Comply with all environmental and quality trainings, procedures, guidelines, practices, current cGMP’s, permit conditions and internal notifications of any environmental or quality event.Perform any other job-related duties as required or that may arise in the future.

    Requirements:

    Education /Experience.

    Bachelor degree in Science, Engineering or Computer Science from an accredited institution. Master’s degree is an added advantage. At least five (5) year of laboratory experience or systems validation in an FDA regulated environment is required.

    Licenses and/or Certifications

    CSQE Certified Software Quality Engineer from ASQ (American Society for Quality), preferred.Chemical Licensee, preferred.

    Technical Competencies

    Ability to effectively manage multiple projects at the same time with minimum supervision and to incorporate a wide array of technical principles, concepts and theories in innovative ways.Demonstrated analytical and problem-solving skills.Proven ability to teach others and transfer knowledge to end users. Able to work under pressure and self-starter.Ability to work cross functionally within an organization, being able to impact and influence other management teams that do not report to this position. Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Regulatory (FDA) industry experience, familiarity with cGMPs, GAMP (Good automated manufacturing practice), Laboratory Equipment / Instrumentation C&Q practices (Commissioning & Qualification) and current to Pharmacopeias requirements, changes and modifications.Proven ability to learn new computer software/systems and laboratory instruments with minimum of instruction and general understanding of SLC (system life cycle) and CSV (computer validation system). Knowledge and experience with systems and validation processes.Good organization skills and time management skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines, effective project management skills.Fully Bilingual, excellent oral and written communication in both English/Spanish languages.Skills in MS Office Suite applications of MS Project, Outlook, Word, and PowerPoint, and is skilled at performing data evaluation, formulas and metrics

    At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

    Excited to build something meaningful together? We look forward to hearing from you.

    Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

    Read Less
  • V

    Analytical Services Scientist  

    - 00614
    Job DescriptionJob DescriptionValidation & Engineering Group, Inc. (V&... Read More
    Job DescriptionJob Description

    Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

    We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

    Analytical Services Scientist

    Summary:

    Will provide Analytical Technology expertise for Quality Control requirements within the introduction of new products to the Site, development / transfer / validation of analytical methodologies & technologies, instrumentation services & technologies, and the resolution of complex and critical analytical investigations. Will provide support to the QC Laboratory to ensure QC Systems maintenance. Participate as the Quality representative on steering committees, ad-hoc projects, introduction of new system, upgrades for the Quality Control Laboratory to ensure that requirements are identified and carried out following procedures and SLC (System Life Cycle processes) as required. Ensure the operational efficiency and excellence of the organization by designing, documenting and providing solutions to new business requirements, trends, and concepts appropriately through the latest technological paths. Will maintain Laboratory efficiency and capacity metrics. The incumbent understands the internal and external customer’s business requirements and business process management, and then translates them to process, system or software requirements.

    Responsibilities:

    Collaborate with functional areas to determine regulatory requirements, validation requirements, business & functional risks and work within cross-functional project teams in the development of validation deliverables or systems upgrades for Laboratory equipment and computer systems in Quality or within the Quality Systems.Generate, develop, evaluate, review and approval of Validation / Automation Documentation (validation plans, protocols and final reports), performance qualification, system life cycle approach to ensure compliance and regulatory requirements from the QC perspective.Coordination / direction and active participation in the validation of site laboratory equipment, facilities, utilities, processes and software in compliance with company policies, Federal Drug Administration (FDA) regulations, European current Good Manufacturing Practices (cGMP’s) and Good Automated Manufacturing Practice (GAMP) standards.Performs the method development, method validation, method transfer and method verification of new or existing products, guaranteeing implementation of a feasible and efficient process. Performs process Failure Mode and Effects Analysis (FMEA’s) and other process verification activities following current Regulatory Guidelines.Conduct, write and manage laboratory investigations.Must have excellent technical writing, experience on root cause analysis and CAPA plan determination.Maintenance of Investigations Metric to support Quality Council QC Metrics.Supports process activities to achieve a successful on time resolution of incidents and deviations and enhances quality and effectiveness of laboratory systems, including change control and Corrective Action /Preventive Action (CAPA) towards optimization laboratory processes to assure effectiveness, robustness, and compliance.Lead / Performs special project as assigned. Participate as a team leader or a member of the project teams where needed and help provide direction on future enhancements to the systems.Assist in solving problems during validation process, system upgrades or investigations and address or seek advice from SMEs (Subject Matter Experts) on issues such as deficiencies, deviations and change control.Administrate Quality Computer Systems and perform periodic review as required. Knowledge on Laboratory Information Management Systems (LIMS Vantage or LIMS Lab Ware) is desired. Full knowledge on Chromatographic Data Management System (CDMS) as Empower.Troubleshoot of methods, and or instruments as needed. Coordinate and manages outside services as required for calibration, maintenance, evaluations, quotes, etc. Perform calibration or maintenance as required. Manage, store, handle, dispose, label and inspect laboratory waste following Environmental Protection Agency (EPA), Environmental Quality Board (EQB) and site requirements procedures, guides and policy.Knowledge of Drug Enforcement Administration (DEA) regulations for controlled substances is required.Broad knowledge of Laboratory instruments as HPLC, UPLC, Dionex, GC, Dissolution baths, TOC, FTIR, NIR, Automatic Titrator, UV Spectrophotometer, KF, among others.Write protocols for new instrument introduction – IQ, OQ, PQ, PVT, costing and troubleshooting/PM/Calibration.Author or guide end users in writing system operational procedures, work instructions, system guides templates and SOPs (Standard Operating Procedures).Comply with all environmental and quality trainings, procedures, guidelines, practices, current cGMP’s, permit conditions and internal notifications of any environmental or quality event.Perform any other job-related duties as required or that may arise in the future.

    Requirements:

    Education /Experience.

    Bachelor degree in Science, Engineering or Computer Science from an accredited institution. Master’s degree is an added advantage. At least five (5) year of laboratory experience or systems validation in an FDA regulated environment is required.

    Licenses and/or Certifications

    CSQE Certified Software Quality Engineer from ASQ (American Society for Quality), preferred.Chemical Licensee, preferred.

    Technical Competencies

    Ability to effectively manage multiple projects at the same time with minimum supervision and to incorporate a wide array of technical principles, concepts and theories in innovative ways.Demonstrated analytical and problem-solving skills.Proven ability to teach others and transfer knowledge to end users. Able to work under pressure and self-starter.Ability to work cross functionally within an organization, being able to impact and influence other management teams that do not report to this position. Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Regulatory (FDA) industry experience, familiarity with cGMPs, GAMP (Good automated manufacturing practice), Laboratory Equipment / Instrumentation C&Q practices (Commissioning & Qualification) and current to Pharmacopeias requirements, changes and modifications.Proven ability to learn new computer software/systems and laboratory instruments with minimum of instruction and general understanding of SLC (system life cycle) and CSV (computer validation system). Knowledge and experience with systems and validation processes.Good organization skills and time management skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines, effective project management skills.Fully Bilingual, excellent oral and written communication in both English/Spanish languages.Skills in MS Office Suite applications of MS Project, Outlook, Word, and PowerPoint, and is skilled at performing data evaluation, formulas and metrics

    At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

    Excited to build something meaningful together? We look forward to hearing from you.

    Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

    Read Less
  • V

    Analytical Services Scientist  

    - 00612
    Job DescriptionJob DescriptionValidation & Engineering Group, Inc. (V&... Read More
    Job DescriptionJob Description

    Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

    We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

    Analytical Services Scientist

    Summary:

    Will provide Analytical Technology expertise for Quality Control requirements within the introduction of new products to the Site, development / transfer / validation of analytical methodologies & technologies, instrumentation services & technologies, and the resolution of complex and critical analytical investigations. Will provide support to the QC Laboratory to ensure QC Systems maintenance. Participate as the Quality representative on steering committees, ad-hoc projects, introduction of new system, upgrades for the Quality Control Laboratory to ensure that requirements are identified and carried out following procedures and SLC (System Life Cycle processes) as required. Ensure the operational efficiency and excellence of the organization by designing, documenting and providing solutions to new business requirements, trends, and concepts appropriately through the latest technological paths. Will maintain Laboratory efficiency and capacity metrics. The incumbent understands the internal and external customer’s business requirements and business process management, and then translates them to process, system or software requirements.

    Responsibilities:

    Collaborate with functional areas to determine regulatory requirements, validation requirements, business & functional risks and work within cross-functional project teams in the development of validation deliverables or systems upgrades for Laboratory equipment and computer systems in Quality or within the Quality Systems.Generate, develop, evaluate, review and approval of Validation / Automation Documentation (validation plans, protocols and final reports), performance qualification, system life cycle approach to ensure compliance and regulatory requirements from the QC perspective.Coordination / direction and active participation in the validation of site laboratory equipment, facilities, utilities, processes and software in compliance with company policies, Federal Drug Administration (FDA) regulations, European current Good Manufacturing Practices (cGMP’s) and Good Automated Manufacturing Practice (GAMP) standards.Performs the method development, method validation, method transfer and method verification of new or existing products, guaranteeing implementation of a feasible and efficient process. Performs process Failure Mode and Effects Analysis (FMEA’s) and other process verification activities following current Regulatory Guidelines.Conduct, write and manage laboratory investigations.Must have excellent technical writing, experience on root cause analysis and CAPA plan determination.Maintenance of Investigations Metric to support Quality Council QC Metrics.Supports process activities to achieve a successful on time resolution of incidents and deviations and enhances quality and effectiveness of laboratory systems, including change control and Corrective Action /Preventive Action (CAPA) towards optimization laboratory processes to assure effectiveness, robustness, and compliance.Lead / Performs special project as assigned. Participate as a team leader or a member of the project teams where needed and help provide direction on future enhancements to the systems.Assist in solving problems during validation process, system upgrades or investigations and address or seek advice from SMEs (Subject Matter Experts) on issues such as deficiencies, deviations and change control.Administrate Quality Computer Systems and perform periodic review as required. Knowledge on Laboratory Information Management Systems (LIMS Vantage or LIMS Lab Ware) is desired. Full knowledge on Chromatographic Data Management System (CDMS) as Empower.Troubleshoot of methods, and or instruments as needed. Coordinate and manages outside services as required for calibration, maintenance, evaluations, quotes, etc. Perform calibration or maintenance as required. Manage, store, handle, dispose, label and inspect laboratory waste following Environmental Protection Agency (EPA), Environmental Quality Board (EQB) and site requirements procedures, guides and policy.Knowledge of Drug Enforcement Administration (DEA) regulations for controlled substances is required.Broad knowledge of Laboratory instruments as HPLC, UPLC, Dionex, GC, Dissolution baths, TOC, FTIR, NIR, Automatic Titrator, UV Spectrophotometer, KF, among others.Write protocols for new instrument introduction – IQ, OQ, PQ, PVT, costing and troubleshooting/PM/Calibration.Author or guide end users in writing system operational procedures, work instructions, system guides templates and SOPs (Standard Operating Procedures).Comply with all environmental and quality trainings, procedures, guidelines, practices, current cGMP’s, permit conditions and internal notifications of any environmental or quality event.Perform any other job-related duties as required or that may arise in the future.

    Requirements:

    Education /Experience.

    Bachelor degree in Science, Engineering or Computer Science from an accredited institution. Master’s degree is an added advantage. At least five (5) year of laboratory experience or systems validation in an FDA regulated environment is required.

    Licenses and/or Certifications

    CSQE Certified Software Quality Engineer from ASQ (American Society for Quality), preferred.Chemical Licensee, preferred.

    Technical Competencies

    Ability to effectively manage multiple projects at the same time with minimum supervision and to incorporate a wide array of technical principles, concepts and theories in innovative ways.Demonstrated analytical and problem-solving skills.Proven ability to teach others and transfer knowledge to end users. Able to work under pressure and self-starter.Ability to work cross functionally within an organization, being able to impact and influence other management teams that do not report to this position. Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Regulatory (FDA) industry experience, familiarity with cGMPs, GAMP (Good automated manufacturing practice), Laboratory Equipment / Instrumentation C&Q practices (Commissioning & Qualification) and current to Pharmacopeias requirements, changes and modifications.Proven ability to learn new computer software/systems and laboratory instruments with minimum of instruction and general understanding of SLC (system life cycle) and CSV (computer validation system). Knowledge and experience with systems and validation processes.Good organization skills and time management skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines, effective project management skills.Fully Bilingual, excellent oral and written communication in both English/Spanish languages.Skills in MS Office Suite applications of MS Project, Outlook, Word, and PowerPoint, and is skilled at performing data evaluation, formulas and metrics

    At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

    Excited to build something meaningful together? We look forward to hearing from you.

    Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

    Read Less
  • V

    Analytical Services Scientist  

    - 00616
    Job DescriptionJob DescriptionValidation & Engineering Group, Inc. (V&... Read More
    Job DescriptionJob Description

    Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

    We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

    Analytical Services Scientist

    Summary:

    Will provide Analytical Technology expertise for Quality Control requirements within the introduction of new products to the Site, development / transfer / validation of analytical methodologies & technologies, instrumentation services & technologies, and the resolution of complex and critical analytical investigations. Will provide support to the QC Laboratory to ensure QC Systems maintenance. Participate as the Quality representative on steering committees, ad-hoc projects, introduction of new system, upgrades for the Quality Control Laboratory to ensure that requirements are identified and carried out following procedures and SLC (System Life Cycle processes) as required. Ensure the operational efficiency and excellence of the organization by designing, documenting and providing solutions to new business requirements, trends, and concepts appropriately through the latest technological paths. Will maintain Laboratory efficiency and capacity metrics. The incumbent understands the internal and external customer’s business requirements and business process management, and then translates them to process, system or software requirements.

    Responsibilities:

    Collaborate with functional areas to determine regulatory requirements, validation requirements, business & functional risks and work within cross-functional project teams in the development of validation deliverables or systems upgrades for Laboratory equipment and computer systems in Quality or within the Quality Systems.Generate, develop, evaluate, review and approval of Validation / Automation Documentation (validation plans, protocols and final reports), performance qualification, system life cycle approach to ensure compliance and regulatory requirements from the QC perspective.Coordination / direction and active participation in the validation of site laboratory equipment, facilities, utilities, processes and software in compliance with company policies, Federal Drug Administration (FDA) regulations, European current Good Manufacturing Practices (cGMP’s) and Good Automated Manufacturing Practice (GAMP) standards.Performs the method development, method validation, method transfer and method verification of new or existing products, guaranteeing implementation of a feasible and efficient process. Performs process Failure Mode and Effects Analysis (FMEA’s) and other process verification activities following current Regulatory Guidelines.Conduct, write and manage laboratory investigations.Must have excellent technical writing, experience on root cause analysis and CAPA plan determination.Maintenance of Investigations Metric to support Quality Council QC Metrics.Supports process activities to achieve a successful on time resolution of incidents and deviations and enhances quality and effectiveness of laboratory systems, including change control and Corrective Action /Preventive Action (CAPA) towards optimization laboratory processes to assure effectiveness, robustness, and compliance.Lead / Performs special project as assigned. Participate as a team leader or a member of the project teams where needed and help provide direction on future enhancements to the systems.Assist in solving problems during validation process, system upgrades or investigations and address or seek advice from SMEs (Subject Matter Experts) on issues such as deficiencies, deviations and change control.Administrate Quality Computer Systems and perform periodic review as required. Knowledge on Laboratory Information Management Systems (LIMS Vantage or LIMS Lab Ware) is desired. Full knowledge on Chromatographic Data Management System (CDMS) as Empower.Troubleshoot of methods, and or instruments as needed. Coordinate and manages outside services as required for calibration, maintenance, evaluations, quotes, etc. Perform calibration or maintenance as required. Manage, store, handle, dispose, label and inspect laboratory waste following Environmental Protection Agency (EPA), Environmental Quality Board (EQB) and site requirements procedures, guides and policy.Knowledge of Drug Enforcement Administration (DEA) regulations for controlled substances is required.Broad knowledge of Laboratory instruments as HPLC, UPLC, Dionex, GC, Dissolution baths, TOC, FTIR, NIR, Automatic Titrator, UV Spectrophotometer, KF, among others.Write protocols for new instrument introduction – IQ, OQ, PQ, PVT, costing and troubleshooting/PM/Calibration.Author or guide end users in writing system operational procedures, work instructions, system guides templates and SOPs (Standard Operating Procedures).Comply with all environmental and quality trainings, procedures, guidelines, practices, current cGMP’s, permit conditions and internal notifications of any environmental or quality event.Perform any other job-related duties as required or that may arise in the future.

    Requirements:

    Education /Experience.

    Bachelor degree in Science, Engineering or Computer Science from an accredited institution. Master’s degree is an added advantage. At least five (5) year of laboratory experience or systems validation in an FDA regulated environment is required.

    Licenses and/or Certifications

    CSQE Certified Software Quality Engineer from ASQ (American Society for Quality), preferred.Chemical Licensee, preferred.

    Technical Competencies

    Ability to effectively manage multiple projects at the same time with minimum supervision and to incorporate a wide array of technical principles, concepts and theories in innovative ways.Demonstrated analytical and problem-solving skills.Proven ability to teach others and transfer knowledge to end users. Able to work under pressure and self-starter.Ability to work cross functionally within an organization, being able to impact and influence other management teams that do not report to this position. Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Regulatory (FDA) industry experience, familiarity with cGMPs, GAMP (Good automated manufacturing practice), Laboratory Equipment / Instrumentation C&Q practices (Commissioning & Qualification) and current to Pharmacopeias requirements, changes and modifications.Proven ability to learn new computer software/systems and laboratory instruments with minimum of instruction and general understanding of SLC (system life cycle) and CSV (computer validation system). Knowledge and experience with systems and validation processes.Good organization skills and time management skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines, effective project management skills.Fully Bilingual, excellent oral and written communication in both English/Spanish languages.Skills in MS Office Suite applications of MS Project, Outlook, Word, and PowerPoint, and is skilled at performing data evaluation, formulas and metrics

    At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

    Excited to build something meaningful together? We look forward to hearing from you.

    Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

    Read Less
  • V

    Analytical Services Scientist  

    - 00688
    Job DescriptionJob DescriptionValidation & Engineering Group, Inc. (V&... Read More
    Job DescriptionJob Description

    Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

    We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

    Analytical Services Scientist

    Summary:

    Will provide Analytical Technology expertise for Quality Control requirements within the introduction of new products to the Site, development / transfer / validation of analytical methodologies & technologies, instrumentation services & technologies, and the resolution of complex and critical analytical investigations. Will provide support to the QC Laboratory to ensure QC Systems maintenance. Participate as the Quality representative on steering committees, ad-hoc projects, introduction of new system, upgrades for the Quality Control Laboratory to ensure that requirements are identified and carried out following procedures and SLC (System Life Cycle processes) as required. Ensure the operational efficiency and excellence of the organization by designing, documenting and providing solutions to new business requirements, trends, and concepts appropriately through the latest technological paths. Will maintain Laboratory efficiency and capacity metrics. The incumbent understands the internal and external customer’s business requirements and business process management, and then translates them to process, system or software requirements.

    Responsibilities:

    Collaborate with functional areas to determine regulatory requirements, validation requirements, business & functional risks and work within cross-functional project teams in the development of validation deliverables or systems upgrades for Laboratory equipment and computer systems in Quality or within the Quality Systems.Generate, develop, evaluate, review and approval of Validation / Automation Documentation (validation plans, protocols and final reports), performance qualification, system life cycle approach to ensure compliance and regulatory requirements from the QC perspective.Coordination / direction and active participation in the validation of site laboratory equipment, facilities, utilities, processes and software in compliance with company policies, Federal Drug Administration (FDA) regulations, European current Good Manufacturing Practices (cGMP’s) and Good Automated Manufacturing Practice (GAMP) standards.Performs the method development, method validation, method transfer and method verification of new or existing products, guaranteeing implementation of a feasible and efficient process. Performs process Failure Mode and Effects Analysis (FMEA’s) and other process verification activities following current Regulatory Guidelines.Conduct, write and manage laboratory investigations.Must have excellent technical writing, experience on root cause analysis and CAPA plan determination.Maintenance of Investigations Metric to support Quality Council QC Metrics.Supports process activities to achieve a successful on time resolution of incidents and deviations and enhances quality and effectiveness of laboratory systems, including change control and Corrective Action /Preventive Action (CAPA) towards optimization laboratory processes to assure effectiveness, robustness, and compliance.Lead / Performs special project as assigned. Participate as a team leader or a member of the project teams where needed and help provide direction on future enhancements to the systems.Assist in solving problems during validation process, system upgrades or investigations and address or seek advice from SMEs (Subject Matter Experts) on issues such as deficiencies, deviations and change control.Administrate Quality Computer Systems and perform periodic review as required. Knowledge on Laboratory Information Management Systems (LIMS Vantage or LIMS Lab Ware) is desired. Full knowledge on Chromatographic Data Management System (CDMS) as Empower.Troubleshoot of methods, and or instruments as needed. Coordinate and manages outside services as required for calibration, maintenance, evaluations, quotes, etc. Perform calibration or maintenance as required. Manage, store, handle, dispose, label and inspect laboratory waste following Environmental Protection Agency (EPA), Environmental Quality Board (EQB) and site requirements procedures, guides and policy.Knowledge of Drug Enforcement Administration (DEA) regulations for controlled substances is required.Broad knowledge of Laboratory instruments as HPLC, UPLC, Dionex, GC, Dissolution baths, TOC, FTIR, NIR, Automatic Titrator, UV Spectrophotometer, KF, among others.Write protocols for new instrument introduction – IQ, OQ, PQ, PVT, costing and troubleshooting/PM/Calibration.Author or guide end users in writing system operational procedures, work instructions, system guides templates and SOPs (Standard Operating Procedures).Comply with all environmental and quality trainings, procedures, guidelines, practices, current cGMP’s, permit conditions and internal notifications of any environmental or quality event.Perform any other job-related duties as required or that may arise in the future.

    Requirements:

    Education /Experience.

    Bachelor degree in Science, Engineering or Computer Science from an accredited institution. Master’s degree is an added advantage. At least five (5) year of laboratory experience or systems validation in an FDA regulated environment is required.

    Licenses and/or Certifications

    CSQE Certified Software Quality Engineer from ASQ (American Society for Quality), preferred.Chemical Licensee, preferred.

    Technical Competencies

    Ability to effectively manage multiple projects at the same time with minimum supervision and to incorporate a wide array of technical principles, concepts and theories in innovative ways.Demonstrated analytical and problem-solving skills.Proven ability to teach others and transfer knowledge to end users. Able to work under pressure and self-starter.Ability to work cross functionally within an organization, being able to impact and influence other management teams that do not report to this position. Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Regulatory (FDA) industry experience, familiarity with cGMPs, GAMP (Good automated manufacturing practice), Laboratory Equipment / Instrumentation C&Q practices (Commissioning & Qualification) and current to Pharmacopeias requirements, changes and modifications.Proven ability to learn new computer software/systems and laboratory instruments with minimum of instruction and general understanding of SLC (system life cycle) and CSV (computer validation system). Knowledge and experience with systems and validation processes.Good organization skills and time management skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines, effective project management skills.Fully Bilingual, excellent oral and written communication in both English/Spanish languages.Skills in MS Office Suite applications of MS Project, Outlook, Word, and PowerPoint, and is skilled at performing data evaluation, formulas and metrics

    At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

    Excited to build something meaningful together? We look forward to hearing from you.

    Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

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  • V

    QA Specialist II  

    - 00617
    Job DescriptionJob DescriptionValidation & Engineering Group, Inc. (V&... Read More
    Job DescriptionJob Description

    Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

    We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

    QA Specislist II

    Description:

    The Quality Analyst is responsible for resolution of issues with suppliers (investigations and corrective actions), maintenance of supplier status, evaluation and closure of supplier change notifications, supplier scorecards and SQA reports.

    Responsibilities:

    Coordinates resolution of problem relating to quality and performance of purchased materials with suppliers and Manufacturing Quality Assurance.The incumbent monitors and manages implementation of new and existing processes that ultimately impact vendor product quality assurance.Establish and document contact with suppliers concerning quality issues/concerns (i.e. nonconformity, deviation, defect report, waivers, etc.).Perform assessment of supplier change notification (SCN) of incoming material. Monitor supplier change notification review through Plant to ensure a timely completion.Evaluates Specification Acceptance Letter exception and assess need for elevation to area management, as needed.Updates and maintains the System Application Product (SAP) system with current specification date, approval of supplier sites and/or purchasing control.Interfaces with and maintains cooperative relationships with plant departments to assure the total integrity and usability of incoming materials.Serves as an effective liaison and maintains a cooperative relationship with other Quality areas, Plant departments, Bioresearch Center counterparts, and TPMs as needed.Assists section with the follow-up and close out of the management reviews action items upon their implementation.Ensures that all quality goals are met, and all practices and procedures comply with applicable policies and regulations for the Quality areas under his/her responsibility.The Quality Analyst is responsible for resolution of issues with suppliers (investigations and corrective actions), maintenance of supplier status, evaluation and closure of supplier change notifications, supplier scorecards and SQA reports.

    Qualifications:

    Bachelor’s degree in Natural Sciences, Biology, Chemistry or Engineering.Quality related work in the pharmaceutical or medical device Health Care Organization. Total combined minimum years of experience required - 2 years.Key Stakeholders: Suppliers, Purchasing, IQA, Materials Management, TPM's, Technical groups, Manufacturing, Quality Assurance, Compliance, Validation, etc.Good problem solving and analytical skillsGood interpersonal relations/communications skillsGood verbal and written communicationGood negotiation skillsQuality related work in the pharmaceutical or medical device Health Care Organization. Total combined minimum years of experience required - 5 years.Technical Skills:Good verbal and written communication.Good problem solving and analytical skills.Good interpersonal relations/communications skills.Good negotiation skills.Good analytical skills.Supplier Management Experience.Must be fully bilingual (English / Spanish).Must be proficient using MS Windows and Microsoft Office applications.Experience in pharmaceutical industry.Preference experience in incoming quality area.Available to work extended hours, possibility of weekends and holidays.

    At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

    Excited to build something meaningful together? We look forward to hearing from you.

    Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

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  • G

    Senior Full Stack Developer  

    - 00926
    Job DescriptionJob DescriptionJob Overview:We are seeking a highly ski... Read More
    Job DescriptionJob DescriptionJob Overview:

    We are seeking a highly skilled Senior Full Stack Developer to join our Technology team. This role is responsible for designing, developing, and leading enterprise-level applications across multiple platforms, including BackOffice 360, WIC Portal, Mi WIC PR, Clinic Monitoring System, and AI-driven chatbot solutions. The ideal candidate will have strong experience in full stack development, cloud technologies, and enterprise architecture.

    Responsibilities and Duties:Design and implement scalable enterprise architectures.Lead the development of applications using Angular and .NET technologies.Build and maintain RESTful APIs and microservices.Integrate AI-based solutions such as Azure OpenAI, AI Search, and chatbot technologies.Develop and deploy cloud-based solutions in Azure and AWS.Optimize and manage SQL Server databases for performance and reliability.Integrate external platforms such as Genesys Cloud.Collaborate with cross-functional teams to define technical and business requirements.Mentor and support junior developers and development teams.Troubleshoot, debug, and enhance enterprise applications and systems.Ensure best practices in coding standards, security, scalability, and system performance.Qualifications and Education Requirements:Bachelor’s degree in Computer Science, Information Technology, Software Engineering, or related field (or equivalent experience).Minimum of 7+ years of experience in full stack development.Strong experience with cloud platforms such as Azure and AWS.Advanced knowledge of SQL Server and database optimization.Experience designing and implementing enterprise architectures.Proficiency in Angular, JavaScript, .NET, and C#.Experience with API development, microservices, and system integrations.Familiarity with AI-driven technologies and enterprise application environments preferred.Bilingual in English and Spanish, both verbal and written, preferred.Skills Required:Strong problem-solving and analytical skills.Ability to lead technical projects and development teams.Excellent communication and collaboration skills.Ability to manage multiple projects and meet deadlines.High attention to detail and commitment to quality.Strong organizational and decision-making skills.

    We are an employer EEO/M/F/V/D.

    Job Type:

    Full-time

    Benefits:401(k)401(k) matchingDental insuranceHealth insuranceLife insurancePaid time offVision insuranceSchedule:8 hour shiftMonday to FridayOn callWork Location:

    In person.

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  • G

    Full Stack Developer  

    - 00926
    Job DescriptionJob DescriptionJob Overview:We are seeking a Full Stack... Read More
    Job DescriptionJob DescriptionJob Overview:

    We are seeking a Full Stack Developer to join our Technology team. This role is responsible for developing, maintaining, and enhancing enterprise systems such as WIC Portal, Vendor Systems, and mobile applications. The ideal candidate will have hands-on experience in full stack development, working with modern frameworks and supporting cloud-based solutions.

    Responsibilities and Duties:Develop and maintain frontend applications using Angular.Build and support backend services using .NET technologies.Work with SQL Server databases, including queries and basic optimization.Build and consume RESTful APIs.Support and maintain mobile applications using MAUI/Xamarin.Assist with cloud integrations in Azure and AWS.Troubleshoot, debug, and enhance existing systems.Collaborate with cross-functional teams to gather and implement requirements.Ensure code quality, system performance, and application scalability.Participate in testing, deployments, and ongoing system improvements.Qualifications and Education Requirements:Bachelor’s degree in Computer Science, Information Technology, Software Engineering, or related field (or equivalent experience).2–5 years of experience in full stack development.Knowledge of Angular and .NET frameworks.Basic knowledge of SQL Server and database management.Experience building and consuming RESTful APIs.Familiarity with HTML, CSS, and JavaScript.Experience with MAUI/Xamarin mobile applications preferred.Basic understanding of cloud platforms such as Azure and AWS.Bilingual in English and Spanish, both verbal and written, preferred.Skills Required:Strong problem-solving and analytical thinking skills.Ability to work independently and collaboratively within a team environment.Strong communication and interpersonal skills.Attention to detail and commitment to code quality.Time management skills with the ability to meet deadlines.

    We are an employer EEO/M/F/V/D.

    Job Type:

    Full-time

    Benefits:401(k)401(k) matchingDental insuranceHealth insuranceLife insurancePaid time offVision insuranceSchedule:8 hour shiftMonday to FridayOn callWork Location:

    In person.

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  • J
    Job DescriptionJob DescriptionAbout Company:JC Automation Corp. (JCA)... Read More
    Job DescriptionJob Description

    About Company:

    JC Automation Corp. (JCA) was founded in 1997 with the mission of filling a gap between technology and regulatory requirements in the life science manufacturing industry. The company offers highly capable resources at an affordable cost to build solutions and execute projects in: Automation, Control Systems Integration, Information Technology, System Integration and Regulatory Compliance.

    JCA is a HUBZone Certified Small Business Firm, NMSDC Certified Minority Business Enterprise, and Certified Critical Industry Supplier. It’s mission is to add value by delivering quality services & solutions on time all the time by transforming processes & technology into business advantages.

    ABOUT THE ROLE

    We are seeking a technically strong and operationally driven Project Engineer to lead the end-to-end installation and commissioning of pharmaceutical coating equipment in a regulated manufacturing facility. In this role, you will own the project from planning through qualification handover — managing schedules, controlling costs, supervising contractors, and coordinating across Engineering, Quality, and Manufacturing teams.

    This is a field-intensive position that requires both technical depth in equipment installation and the ability to navigate the regulatory requirements of a cGMP environment. You will be the central point of accountability for ensuring that every aspect of the installation is executed on time, within budget, and in full compliance with applicable standards.

    RESPONSIBILITIES

    Project Oversight & Installation: Lead the end-to-end installation and commissioning of manufacturing coating equipment, ensuring all technical specifications and operational requirements are met.Schedule & Activity Management: Rigorously monitor project schedules and daily activities, identifying potential bottlenecks and implementing proactive measures to ensure on-time delivery.Cost Control & Budget Compliance: Track project expenses and resource allocation to ensure all installation activities remain strictly within the approved budget and commercial guidelines.Operational Excellence: Supervise contractor performance and equipment vendor activities to guarantee that all mechanical and electrical integrations align with the facility's infrastructure.Qualification & Validation Support: Assist in the development and execution of FAT, SAT, and IQ/OQ protocols, ensuring that equipment meets all performance standards before final handover.cGMP & Safety Compliance: Ensure that all installation procedures strictly adhere to cGMP regulations, data integrity principles, and plant-specific safety standards.Cross-Functional Liaison: Serve as the primary point of contact between Manufacturing, Quality, and Engineering teams to facilitate seamless communication and resolve technical conflicts during the project lifecycle.Reporting & Documentation: Provide detailed progress reports on milestones, activity status, and financial variances to project leadership, ensuring transparency and accountability.

    REQUIREMENTS & QUALIFICATIONS

    Required

    Bachelor's degree in Mechanical, Chemical, Industrial, or Electrical Engineering, or a related technical discipline.Minimum 3–5 years of experience in project engineering or equipment installation within pharmaceutical or regulated manufacturing environments.Hands-on experience with pharmaceutical manufacturing equipment installation, including mechanical, electrical, and utility connections.Experience supporting or executing FAT, SAT, IQ, and OQ qualification activities.Working knowledge of cGMP regulations, data integrity principles, and safety standards applicable to pharmaceutical manufacturing.Bilingual in English and Spanish (oral and written).

    Preferred

    Direct experience with solid dosage or coating equipment (e.g., tablet coaters, fluid bed systems).PMP or equivalent project management certification.Familiarity with SAP or similar ERP systems for project cost tracking.Experience reading and interpreting engineering drawings, P&IDs, and equipment manuals.

    SKILLS

    Technical Skills

    Pharmaceutical equipment installation and commissioningFAT, SAT, IQ/OQ protocol development and executioncGMP compliance and data integrity principlesProject schedule management and critical path monitoringCost tracking and budget controlContractor supervision and vendor managementEngineering drawings, P&IDs, and technical documentationMicrosoft Office 365 — Project, Excel, Word, Teams

    Soft Skills

    Strong technical judgment and hands-on problem solvingClear and structured communication with cross-functional teamsProactive schedule and risk managementAccountability for deliverables from planning through closeoutAbility to operate effectively under pressure and tight deadlinesCollaborative leadership in multidisciplinary project environments Read Less
  • J

    Field Project Activity Coordinator  

    - 00729
    Job DescriptionJob DescriptionAbout Company:JC Automation Corp. (JCA)... Read More
    Job DescriptionJob Description

    About Company:

    JC Automation Corp. (JCA) was founded in 1997 with the mission of filling a gap between technology and regulatory requirements in the life science manufacturing industry. The company offers highly capable resources at an affordable cost to build solutions and execute projects in: Automation, Control Systems Integration, Information Technology, System Integration and Regulatory Compliance.

    JCA is a HUBZone Certified Small Business Firm, NMSDC Certified Minority Business Enterprise, and Certified Critical Industry Supplier. It’s mission is to add value by delivering quality services & solutions on time all the time by transforming processes & technology into business advantages.

    ABOUT THE ROLE

    We are looking for an experienced and organized Field Project Activity Coordinator to lead the daily coordination of equipment installation activities on the manufacturing floor of a pharmaceutical facility. In this role, you will be the operational bridge between project managers and the field — ensuring that contractors, vendors, and tradespeople execute their work safely, efficiently, and in strict alignment with cGMP requirements.

    This is a hands-on, floor-level role that demands strong situational awareness, discipline in permit and safety management, and the ability to keep multiple workstreams moving simultaneously. You will be responsible for real-time progress tracking, materials logistics, and direct oversight of all field execution activities.

    RESPONSIBILITIES

    Field Operations Oversight: Direct and coordinate daily installation and execution activities on the manufacturing floor for solid dosage equipment (e.g., coaters, blenders, granulators).Contractor Management: Supervise external vendors, mechanical contractors, and tradespeople, ensuring their tasks are executed efficiently and in strict alignment with the daily project schedule.Permit & Safety Logistics: Manage daily field logistics, including securing and maintaining necessary work permits (e.g., LOTO, hot work) and ensuring absolute adherence to plant safety protocols.cGMP Environment Compliance: Monitor work areas to guarantee that all field activities comply with cGMP guidelines, maintaining required cleanliness and operational standards for solid dose manufacturing zones.Materials & Staging: Coordinate the prompt delivery, staging, and safe storage of materials, tools, and equipment components on the floor to prevent any downtime during the installation process.Progress Tracking & Reporting: Maintain accurate daily logs of field progress, proactively resolving on-site roadblocks and escalating critical constraints to the Project Management team.Cross-Functional Communication: Act as the direct operational bridge between the engineering project managers and the executing field personnel, ensuring instructions are clearly understood and implemented.

    REQUIREMENTS & QUALIFICATIONS

    Required

    Bachelor's degree in Engineering, Construction Management, or a related technical field; or equivalent hands-on experience in a regulated manufacturing environment.Minimum 3 years of experience coordinating field construction, equipment installation, or maintenance activities in a pharmaceutical or regulated facility.Direct experience managing contractors and subcontractors in a field environment.Strong working knowledge of permit systems (LOTO, hot work, confined space) and plant safety requirements.Familiarity with cGMP guidelines applicable to solid dosage or pharmaceutical manufacturing operations.Bilingual in English and Spanish (oral and written).

    Preferred

    Experience working with solid dosage manufacturing equipment such as tablet coaters, blenders, or granulators.Exposure to commissioning and qualification (C&Q) activities during equipment installation or startup.OSHA 10 or OSHA 30 certification (General Industry or Construction).Experience using Smartsheet, MS Project, or similar tools for daily progress tracking.

    SKILLS

    Technical Skills

    Field construction and equipment installation coordinationContractor and vendor oversight in regulated environmentsWork permit management — LOTO, hot work, confined spacecGMP compliance monitoring on the manufacturing floorMaterials staging and logistics coordinationDaily progress logging and issue escalationEngineering drawings and installation documentationMicrosoft Office 365 — Excel, Word, Teams

    Soft Skills

    Strong situational awareness and real-time decision makingDirect, clear communication with contractors, vendors, and project managersDiscipline in safety compliance and permit adherenceHighly organized with ability to manage multiple parallel workstreamsProactive in identifying and escalating field risksReliable, accountable, and effective under schedule pressure Read Less
  • J

    Project Scheduler  

    - 00729
    Job DescriptionJob DescriptionAbout Company:JC Automation Corp. (JCA)... Read More
    Job DescriptionJob Description

    About Company:

    JC Automation Corp. (JCA) was founded in 1997 with the mission of filling a gap between technology and regulatory requirements in the life science manufacturing industry. The company offers highly capable resources at an affordable cost to build solutions and execute projects in: Automation, Control Systems Integration, Information Technology, System Integration and Regulatory Compliance.

    JCA is a HUBZone Certified Small Business Firm, NMSDC Certified Minority Business Enterprise, and Certified Critical Industry Supplier. It’s mission is to add value by delivering quality services & solutions on time all the time by transforming processes & technology into business advantages.

    ABOUT THE ROLE

    We are looking for a detail-oriented and proactive Project Scheduler to support the planning and execution of pharmaceutical equipment installation projects at our Canovanas facility. In this role, you will be the backbone of our project control’s function — building and maintaining comprehensive schedules, monitoring critical path performance, and enabling real-time visibility for all stakeholders through advanced use of Smartsheet.

    You will work directly alongside project managers, field leads, engineering teams, and contractors to ensure every milestone is tracked, every risk is flagged early, and every deliverable lands on time. This is a high-visibility, cross-functional role in a fast-paced, regulated manufacturing environment.

    RESPONSIBILITIES

    Schedule Development & Maintenance: Build and manage comprehensive project schedules for pharmaceutical equipment installation, ensuring all logic, dependencies, and constraints are accurately represented in Smartsheet.Critical Path Analysis: Monitor the project's critical path and near-critical paths to proactively identify potential delays, providing the PM team with early warnings and mitigation strategies.Progress Tracking & Reporting: Facilitate weekly schedule update meetings with field leads and contractors to capture real-time progress, reflecting accurate status in the master schedule.Smartsheet Optimization: Leverage advanced Smartsheet features — automated workflows, cross-sheet references, and dynamic dashboards — to streamline project reporting and stakeholder visibility.Resource Loading & Leveling: Support the allocation of labor and equipment resources across project activities to prevent over-allocation and ensure smooth execution in the field.Milestone Management: Track key project milestones and contractual deliverables, ensuring alignment with overall facility deadlines and commissioning targets.Baseline Management: Establish and maintain project baselines to perform variance analysis, comparing actual progress against planned performance to drive accountability.Cross-Functional Coordination: Collaborate with Engineering, Procurement, and Quality teams to ensure all prerequisites and post-installation activities are integrated into the master timeline.

    REQUIREMENTS & QUALIFICATIONS

    Required

    Bachelor's degree in Engineering, Project Management, Business Administration, or a related field.Minimum 3 years of experience in project scheduling or project controls in a regulated industry (pharmaceutical, biotech, medical device, or similar).Advanced proficiency in Smartsheet — including automated workflows, cross-sheet formulas, resource views, and dashboard creation.Demonstrated experience developing and managing integrated project schedules, including critical path and baseline analysis.Strong understanding of cGMP environments and regulatory compliance requirements.Bilingual in English and Spanish (oral and written).

    Preferred

    PMP or PMI-SP (Scheduling Professional) certification.Experience with MS Project or Primavera P6 as supplementary scheduling tools.Familiarity with pharmaceutical equipment installation, commissioning, or C&Q activities.Experience working within capital project environments in a pharmaceutical manufacturing site.

    SKILLS

    Technical Skills

    Smartsheet (advanced) — automated workflows, cross-sheet references, dynamic dashboardsMS Project / Primavera P6Critical path method & schedule logicBaseline management & variance analysisResource loading & levelingcGMP compliance & pharmaceutical regulatory frameworksMS Office 365 (Excel, PowerPoint, Word, Teams)

    Soft Skills

    Attention to detail and methodical approach to dataProactive communication and stakeholder managementProblem solving and early risk identificationStrong time management and organizational skillsCollaborative team player adaptable to fast-paced environmentsAccountability and ownership of deliverables Read Less

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