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:
EngineerSummary:
Under general supervision, provides characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment. Applies basic engineering principles to the design and implementation of system modifications, experiments and/or capital projects. Organizes, analyzes and presents interpretation of results for operational issues or engineering projects of minor scope and complexity.
Attributes:
o Experience in data analysis.
o Optional knowledge of aseptic operation (filling and support).
o Recommended experience in engineering reliability elements and process excellence.
o Recommended experience in maintenance systems and asset management.
Qualifications:
Master’s degree ORBachelor’s degree in Engineering & 2 years of Engineering.Experience working knowledge of pharmaceutical/biotech processes.Familiarity with validation processes.Familiarity with documentation in a highly regulated environment.Ability to operate specialized laboratory equipment and computers as appropriate.Ability to interpret and apply GLPs and GMPs.Ability to apply engineering science to production.Able to develop solutions to routine technical problems of limited scope.Demonstrated skills in the following areas:Problem solving and applied engineering.Basic technical report writing.Verbal communication.Comprehensive understanding of validation protocol execution requirements.Demonstrated Skills in the following areas:Basic technical presentations.Personal Organization o Validation Protocol Writing.Dealing with and managing change.Technical (Equipment Specific).Analytical Problem Solving.Computer Literacy.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.
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 IDescription:
Responsible for auditing and reviewing batch records (electronic and paper) to ensure compliance with GMPs, internal procedures, and regulatory requirements. Supports quality release processes, deviation investigations, and continuous improvement of manufacturing operations.
Key Responsibilities:
Audit API and/or finished product batch records (electronic and paper) for GMP compliance.Approve MES exceptions and perform Quality Holds as required.Document and evaluate deviations and recommend corrective actions.Track and trend batch discrepancies; collaborate with Manufacturing, Tech Ops, MS&T, and MQA.Review manufacturing processes, equipment, and facilities for compliance.Disposition materials in SAP based on testing results and regulatory requirements.Prepare Certificates of Analysis and Compliance.Enter batch data into lot restriction systems.Assemble and manage batch record review packages per retention procedures.Prepare reports (Right First Time, Release Cycle Time, audit requests).Generate product quality review lot lists.Participate in cross-functional meetings regarding batch discrepancies.Serve as contact person for assigned projects.Ensure compliance with EHS standards.Manage QA Hold creation/removal in SAP.Qualifications:
Bachelor’s Degree in Science (Biology, Chemistry, Biotechnology) or Engineering.Knowledge of biotechnology manufacturing processes and GMPs (aseptic processing preferred).Experience in biotechnology manufacturing (quality and/or manufacturing areas) – minimum 2 years.Proficiency in English (bilingual English/Spanish preferred).Fully bilingual (English/Spanish) with strong communication skills.Proficiency in Microsoft Office and Windows environments.Strong knowledge of cGxP and regulatory compliance.Experience with:Design documentation (URS, DS)IQ, OQ, PQ protocol development and executionDeviations and investigation reportsSDLC, Risk Assessment, Data IntegrityFAT & SAT processesStrong technical writing and investigation skills.Availability for extended hours, 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.
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:
Project Scheduler (C&Q)Responsibilities:
Maintain integrated C&Q schedule (plan/actual/forecast).Support schedule impact analysis for C&Q reporting.Align with document preparation and execution phases and provide inputs for weekly/monthly forums.Escalate any concerns or issues that may be impacting the C&Q schedule.Work closely with the Project Integrator to ensure the latest updates on C&Q activities are captured and to stay current with changes in the overall project schedule.Run schedule scenarios as needed and assess/communicate impacts to the C&Q schedule.Qualifications:
Experience developing and maintaining integrated schedules for Commissioning & Qualification (C&Q) or comparable regulated project work.Proficiency with scheduling tools (e.g., Primavera P6 and/or Microsoft Project) and schedule controls practices (baseline management, progress updates, forecasting).Ability to perform schedule impact analysis and communicate drivers/risks for C&Q reporting (weekly/monthly).Strong coordination skills to align schedule with document readiness (protocols, test scripts, turnover packages) and field execution.Clear written and verbal communication; able to support forums and produce schedule visuals/metrics as needed.Additional Preferences:
Prior experience supporting CQV deliverables and turnover/handshake processes in GMP/regulated environments.Familiarity with progress measurement for C&Q (e.g., protocol readiness, execution, deviations/punchlist closure) and dashboard reporting.Experience working onsite and coordinating with construction, QA, engineering, and C&Q leads.Qualifications:
Bachelor's Degree in Science or Engineering.Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.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.
#LI-ZL1
Read LessValidation & 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:
Project Scheduler (C&Q)Responsibilities:
Maintain integrated C&Q schedule (plan/actual/forecast).Support schedule impact analysis for C&Q reporting.Align with document preparation and execution phases and provide inputs for weekly/monthly forums.Escalate any concerns or issues that may be impacting the C&Q schedule.Work closely with the Project Integrator to ensure the latest updates on C&Q activities are captured and to stay current with changes in the overall project schedule.Run schedule scenarios as needed and assess/communicate impacts to the C&Q schedule.Qualifications:
Experience developing and maintaining integrated schedules for Commissioning & Qualification (C&Q) or comparable regulated project work.Proficiency with scheduling tools (e.g., Primavera P6 and/or Microsoft Project) and schedule controls practices (baseline management, progress updates, forecasting).Ability to perform schedule impact analysis and communicate drivers/risks for C&Q reporting (weekly/monthly).Strong coordination skills to align schedule with document readiness (protocols, test scripts, turnover packages) and field execution.Clear written and verbal communication; able to support forums and produce schedule visuals/metrics as needed.Additional Preferences:
Prior experience supporting CQV deliverables and turnover/handshake processes in GMP/regulated environments.Familiarity with progress measurement for C&Q (e.g., protocol readiness, execution, deviations/punchlist closure) and dashboard reporting.Experience working onsite and coordinating with construction, QA, engineering, and C&Q leads.Qualifications:
Bachelor's Degree in Science or Engineering.Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.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.
#LI-ZL1
Read LessValidation & 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:
Project Scheduler (C&Q)Responsibilities:
Maintain integrated C&Q schedule (plan/actual/forecast).Support schedule impact analysis for C&Q reporting.Align with document preparation and execution phases and provide inputs for weekly/monthly forums.Escalate any concerns or issues that may be impacting the C&Q schedule.Work closely with the Project Integrator to ensure the latest updates on C&Q activities are captured and to stay current with changes in the overall project schedule.Run schedule scenarios as needed and assess/communicate impacts to the C&Q schedule.Qualifications:
Experience developing and maintaining integrated schedules for Commissioning & Qualification (C&Q) or comparable regulated project work.Proficiency with scheduling tools (e.g., Primavera P6 and/or Microsoft Project) and schedule controls practices (baseline management, progress updates, forecasting).Ability to perform schedule impact analysis and communicate drivers/risks for C&Q reporting (weekly/monthly).Strong coordination skills to align schedule with document readiness (protocols, test scripts, turnover packages) and field execution.Clear written and verbal communication; able to support forums and produce schedule visuals/metrics as needed.Additional Preferences:
Prior experience supporting CQV deliverables and turnover/handshake processes in GMP/regulated environments.Familiarity with progress measurement for C&Q (e.g., protocol readiness, execution, deviations/punchlist closure) and dashboard reporting.Experience working onsite and coordinating with construction, QA, engineering, and C&Q leads.Qualifications:
Bachelor's Degree in Science or Engineering.Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.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.
#LI-ZL1
Read LessValidation & 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:
Project Scheduler (C&Q)Responsibilities:
Maintain integrated C&Q schedule (plan/actual/forecast).Support schedule impact analysis for C&Q reporting.Align with document preparation and execution phases and provide inputs for weekly/monthly forums.Escalate any concerns or issues that may be impacting the C&Q schedule.Work closely with the Project Integrator to ensure the latest updates on C&Q activities are captured and to stay current with changes in the overall project schedule.Run schedule scenarios as needed and assess/communicate impacts to the C&Q schedule.Qualifications:
Experience developing and maintaining integrated schedules for Commissioning & Qualification (C&Q) or comparable regulated project work.Proficiency with scheduling tools (e.g., Primavera P6 and/or Microsoft Project) and schedule controls practices (baseline management, progress updates, forecasting).Ability to perform schedule impact analysis and communicate drivers/risks for C&Q reporting (weekly/monthly).Strong coordination skills to align schedule with document readiness (protocols, test scripts, turnover packages) and field execution.Clear written and verbal communication; able to support forums and produce schedule visuals/metrics as needed.Additional Preferences:
Prior experience supporting CQV deliverables and turnover/handshake processes in GMP/regulated environments.Familiarity with progress measurement for C&Q (e.g., protocol readiness, execution, deviations/punchlist closure) and dashboard reporting.Experience working onsite and coordinating with construction, QA, engineering, and C&Q leads.Qualifications:
Bachelor's Degree in Science or Engineering.Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.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.
#LI-ZL1
Read LessValidation & 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:
Project Scheduler (C&Q)Responsibilities:
Maintain integrated C&Q schedule (plan/actual/forecast).Support schedule impact analysis for C&Q reporting.Align with document preparation and execution phases and provide inputs for weekly/monthly forums.Escalate any concerns or issues that may be impacting the C&Q schedule.Work closely with the Project Integrator to ensure the latest updates on C&Q activities are captured and to stay current with changes in the overall project schedule.Run schedule scenarios as needed and assess/communicate impacts to the C&Q schedule.Qualifications:
Experience developing and maintaining integrated schedules for Commissioning & Qualification (C&Q) or comparable regulated project work.Proficiency with scheduling tools (e.g., Primavera P6 and/or Microsoft Project) and schedule controls practices (baseline management, progress updates, forecasting).Ability to perform schedule impact analysis and communicate drivers/risks for C&Q reporting (weekly/monthly).Strong coordination skills to align schedule with document readiness (protocols, test scripts, turnover packages) and field execution.Clear written and verbal communication; able to support forums and produce schedule visuals/metrics as needed.Additional Preferences:
Prior experience supporting CQV deliverables and turnover/handshake processes in GMP/regulated environments.Familiarity with progress measurement for C&Q (e.g., protocol readiness, execution, deviations/punchlist closure) and dashboard reporting.Experience working onsite and coordinating with construction, QA, engineering, and C&Q leads.Qualifications:
Bachelor's Degree in Science or Engineering.Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.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.
#LI-ZL1
Read LessValidation & 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:
Project Scheduler (C&Q)Responsibilities:
Maintain integrated C&Q schedule (plan/actual/forecast).Support schedule impact analysis for C&Q reporting.Align with document preparation and execution phases and provide inputs for weekly/monthly forums.Escalate any concerns or issues that may be impacting the C&Q schedule.Work closely with the Project Integrator to ensure the latest updates on C&Q activities are captured and to stay current with changes in the overall project schedule.Run schedule scenarios as needed and assess/communicate impacts to the C&Q schedule.Qualifications:
Experience developing and maintaining integrated schedules for Commissioning & Qualification (C&Q) or comparable regulated project work.Proficiency with scheduling tools (e.g., Primavera P6 and/or Microsoft Project) and schedule controls practices (baseline management, progress updates, forecasting).Ability to perform schedule impact analysis and communicate drivers/risks for C&Q reporting (weekly/monthly).Strong coordination skills to align schedule with document readiness (protocols, test scripts, turnover packages) and field execution.Clear written and verbal communication; able to support forums and produce schedule visuals/metrics as needed.Additional Preferences:
Prior experience supporting CQV deliverables and turnover/handshake processes in GMP/regulated environments.Familiarity with progress measurement for C&Q (e.g., protocol readiness, execution, deviations/punchlist closure) and dashboard reporting.Experience working onsite and coordinating with construction, QA, engineering, and C&Q leads.Qualifications:
Bachelor's Degree in Science or Engineering.Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.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.
#LI-ZL1
Read LessValidation & 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:
Project Scheduler (C&Q)Responsibilities:
Maintain integrated C&Q schedule (plan/actual/forecast).Support schedule impact analysis for C&Q reporting.Align with document preparation and execution phases and provide inputs for weekly/monthly forums.Escalate any concerns or issues that may be impacting the C&Q schedule.Work closely with the Project Integrator to ensure the latest updates on C&Q activities are captured and to stay current with changes in the overall project schedule.Run schedule scenarios as needed and assess/communicate impacts to the C&Q schedule.Qualifications:
Experience developing and maintaining integrated schedules for Commissioning & Qualification (C&Q) or comparable regulated project work.Proficiency with scheduling tools (e.g., Primavera P6 and/or Microsoft Project) and schedule controls practices (baseline management, progress updates, forecasting).Ability to perform schedule impact analysis and communicate drivers/risks for C&Q reporting (weekly/monthly).Strong coordination skills to align schedule with document readiness (protocols, test scripts, turnover packages) and field execution.Clear written and verbal communication; able to support forums and produce schedule visuals/metrics as needed.Additional Preferences:
Prior experience supporting CQV deliverables and turnover/handshake processes in GMP/regulated environments.Familiarity with progress measurement for C&Q (e.g., protocol readiness, execution, deviations/punchlist closure) and dashboard reporting.Experience working onsite and coordinating with construction, QA, engineering, and C&Q leads.Qualifications:
Bachelor's Degree in Science or Engineering.Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.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.
#LI-ZL1
Read LessValidation & 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:
Project Scheduler (C&Q)Responsibilities:
Maintain integrated C&Q schedule (plan/actual/forecast).Support schedule impact analysis for C&Q reporting.Align with document preparation and execution phases and provide inputs for weekly/monthly forums.Escalate any concerns or issues that may be impacting the C&Q schedule.Work closely with the Project Integrator to ensure the latest updates on C&Q activities are captured and to stay current with changes in the overall project schedule.Run schedule scenarios as needed and assess/communicate impacts to the C&Q schedule.Qualifications:
Experience developing and maintaining integrated schedules for Commissioning & Qualification (C&Q) or comparable regulated project work.Proficiency with scheduling tools (e.g., Primavera P6 and/or Microsoft Project) and schedule controls practices (baseline management, progress updates, forecasting).Ability to perform schedule impact analysis and communicate drivers/risks for C&Q reporting (weekly/monthly).Strong coordination skills to align schedule with document readiness (protocols, test scripts, turnover packages) and field execution.Clear written and verbal communication; able to support forums and produce schedule visuals/metrics as needed.Additional Preferences:
Prior experience supporting CQV deliverables and turnover/handshake processes in GMP/regulated environments.Familiarity with progress measurement for C&Q (e.g., protocol readiness, execution, deviations/punchlist closure) and dashboard reporting.Experience working onsite and coordinating with construction, QA, engineering, and C&Q leads.Qualifications:
Bachelor's Degree in Science or Engineering.Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.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.
#LI-ZL1
Read Less