Job DescriptionJob Description

Compensation: $68,000–$70,000 annually, commensurate with experience.
Position Type: Full-time (Exempt)
Schedule: Monday–Friday, 8:30 AM – 5:00 PM. Occasional weekend work may be required. This position is fully on-site; remote work is not available for this role.
Work Location: The Institute for Food Safety and Health (IFSH), 6502 S Archer Rd., Bedford Park, IL 60501.
Benefits: Our commitment to employee well-being is reflected in our competitive benefits package located here.

Summary

The Research Scientist-Microbiology leads the Sprout Safety Alliance at Illinois Tech’s Institute for Food Safety and Health (IFSH). This position plans, designs, and executes collaborative and contract research projects in support of food safety initiatives and public health objectives. The role maintains laboratory equipment, resolves routine technical issues independently, and provides guidance to staff and students on research and safety related matters, as needed. As part of one of the FDA’s centers of excellence in food safety, this position supports research that advances FDA’s public health mission and provides the food industry with critical food safety information. The position collaborates with governmental agencies, academia, and food industry stakeholders, with success measured by collaborative research outcomes, project execution, and programmatic impact.

Key Responsibilities and Accountabilities

50% – Leads the IFSH Sprout Safety Alliance and provides training and technical assistance to sprout growers as part of alliance activities. Works collaboratively with governmental agencies, academic institutions, and industry stakeholders to support program objectives and food safety initiatives. Provides supervision, training, and guidance to Support Scientists and students, as needed.

50% – Leads collaborative research projects and develops a research program focused on the microbiological safety of foods and the detection of foodborne pathogens and toxins in foods. Drafts proposals and secures external funding through FDA collaborative research, competitive grants, and industry sponsored contract research. Executes research projects to meet objectives, milestones, and deliverables; prepares reports for funding entities; presents findings at scientific conferences; and publishes results in peer reviewed scientific journals.

Qualifications

- Ph.D. in Microbiology, Food Science, Agriculture, Biological Sciences, or a related field, or a master’s degree with at least three years of food safety related experience, or an equivalent combination of education and experience
- Experience conducting laboratory-based research involving foodborne pathogens, with knowledge of food safety issues related to food, produce, and or sprouts preferred
- Strong organizational, project management, and communication skillsAbility to communicate and present technical research clearly and concisely in written, verbal, and electronic formats to scientific, academic, industry, and government audiences
- Ability to work collaboratively with governmental agencies, academic institutions, and industry stakeholders
- Proficiency in Microsoft Office, including Word, Excel, PowerPoint, and Outlook

Supervision & Budget Authority

- May supervise and train Support Scientists and students, as needed, and perform budget related duties, as assigned

Service Standards and Performance Expectations

- Works with minimal supervision, responds to complex queries, and proactively seeks solutions- Maintains exceptional attention to detail when documenting and maintaining scientific notebooks, research records, and related documentation
- Effectively communicates with colleagues and stakeholders to encourage participation and seeks input from others to resolve issues as they arise
- Mentors staff and students, as directedIndependently solves routine laboratory or research problems
- Drafts grant proposals and proprietary contracts, as required

Physical Requirements

- Works extensively in a laboratory environment involving foodborne pathogens and strict safety procedures
- Regularly works with various chemical sanitizers in accordance with all applicable safety requirements
- Must be able to stand up to 50% of the workday to perform experiments and laboratory maintenance tasks
-May perform repetitive motions for up to 20% of the workday, including data entry and instrument manipulation
-May occasionally lift up to 10 pounds

EEOC Statement

Illinois Institute of Technology is an EEO/AA/Title VI/Title IX/Section 504/ADA/ADEA employer dedicated to building a community of excellence, equity, inclusion, and diversity. It is committed to fostering an inclusive environment and actively seeks applications from individuals of all backgrounds and identities, regardless of race, color, sex, marital status, religion, national origin, disability, age, unfavorable discharge from the military, status as a protected veteran, sexual orientation, including gender identity and expression, order of protection status, and/or genetic information. All qualified applicants will receive equal consideration for employment.

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Job DescriptionJob Description

Hillis-Carnes Engineering Associates (HCEA) is an ENR Top 500, regional, multi-disciplined engineering firm with advanced capabilities in geotechnical and geostructural engineering, environmental consulting, specialty construction, construction materials engineering and testing, and third-party inspections.

We are currently seeking a full-time Structural/Geostructural Senior Project Engineer to join our team in our Salisbury, MD office.

This exciting and dynamic position requires excellence in the following competencies: .

Client Management: Enhance our client satisfaction ratings by providing thorough, professional service and maintaining communication to develop long term relationships. Engineering Competence: Must have practical understanding and experience in reinforced concrete design with emphasis on foundations, retaining walls, and support of excavation (SOE), and misc. structures. The work will involve design and some field work.Project Management: Must be experienced in project management, with the ability to control schedules, budgets, resources, and provide the highest level of client services.

Job Requirements

Skills to collaborate and interface with Staff, Management, and Clients Working knowledge of geotechnical analysis and design preferredMinimum of 10 years of relevant experience in Structural/Geostructural EngineeringPE license required

Hillis-Carnes offers an excellent compensation and benefits package, including health (some plans include an Health Savings Plan Account), health wellness discount program, short disability, company life and long term disability, 401k with company match, Employee Stock Ownership Plan (ESOP), employee assistance program, generous paid time off and more.

Hillis-Carnes is proudly an Equal Opportunity Employer. Minorities and Women are encouraged to apply.

Job Posted by ApplicantPro
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Job DescriptionJob Description

PETN Chemical Operator
Austin Powder is seeking a skilled and reliable PETN Chemical Operator to join our explosive manufacturing team. This role involves operating production line equipment, handling raw materials and finished goods, monitoring chemical processes, and maintaining safety and quality standards. The ideal candidate will have mechanical and chemical aptitude, strong communication skills, and the ability to work rotating shifts in a physically demanding environment.
This position follows a rotating four-week block schedule with 12-hour shifts from 5:00 a.m. to 5:30 p.m. or 5:00 p.m. to 5:30 a.m., repeating throughout the year:
Responsibilities and Duties:
•
Operate chemical production equipment and loading machinery.
•
Handle and package finished goods and load raw materials.
•
Monitor production processes and perform basic quality checks.
•
Maintain clean and organized work areas and equipment.
•
Log production data and report equipment issues to supervision.
•
Follow Standard Operating Procedures (SOPs) and safety protocols without deviation.
•
Crosstrain into all positions within the PETN process.
Lift up to 50 lbs., climb stairs, and wear required PPE.
Qualifications:
• High school diploma or equivalent required.
• Basic understanding of computers and ability to use Microsoft Word and Excel.
• Must be able to work in a chemical manufacturing environment.
• Ability to work overtime and rotating shifts.
• Must be a self-starter and capable of working independently or as part of a team.
• Authorization to work in the United States.
• 1 year of experience in chemical operations.
• Prior experience in explosive or chemical manufacturing.
• Familiarity with Process Safety Management (PSM).
• Mechanically inclined.
Skills, Knowledge, and Abilities
• Strong mechanical and chemical aptitude.
• Excellent verbal and written communication skills.
• Good organizational and record-keeping abilities.
SINCE 1833,
IMPROVING THE WORLD WE LIVE IN.
Austin Powder has been making explosives for over 190 years and we take great pride in improving the world we live in.
In 1833, the Austin family created the company to produce black powder that would help break the rock, mine the minerals and build the canals and railroads to develop the frontier. Initially along the banks of the Cuyahoga River near Akron, Ohio, we grew as the country grew.
Today, Austin Powder is a world leader in the industrial explosives industry with a passionate commitment towards safety, a relentless customer focus, a family culture work environment, and a demonstration of respect towards all.
As in our early years, our mission continues to be to improve the world we live in through the safe and responsible use of explosives.
Our success has been based on our core values and this has proven to be universally true around the globe as the company has expanded to be one of the leading providers of industrial explosives and blasting services in the world.
Rev. 10.1.2024
• Ability to troubleshoot and report issues accurately.
• High attention to detail and safety awareness.
• Ability to work under pressure and adapt to changing conditions.
Work Environment
Industrial chemical manufacturing setting.
Exposure to loud noise, chemical odors, and varying temperatures.
Physically demanding role requiring standing, climbing, lifting, and wearing PPE.
Fast-paced, safety-focused environment with strict compliance standards.
Required to wear protective gear including gloves, safety glasses, respirators, and uniforms.
Austin Powder is an Equal Opportunity and Affirmative Action Employer and is committed to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job-related reasons regardless of an applicant's race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, marital status, genetic information, protected veteran status, or any other status protected by law. Austin Powder also participates in E-Verify.

Job Posted by ApplicantPro
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Job DescriptionJob Description

Vintun LLC is an SBA-certified Small Disadvantaged Business established under the Native Hawaiian Organization-Owned (NHO) program. As a professional services firm specializing in consulting and advisory services, Vintun is committed to improving operational efficiency and achieving organizational objectives for its clients.  We serve as a leading provider for information services and business management solutions to the Federal Government, delivering impactful solutions that yield lasting results. Headquartered in Stafford, Virgina, with a client support office in Hawaii, Vintun offers a highly competitive benefits package that reflects our commitment to attracting and retaining top industry talent.

Vintun is seeking a Senior Operations Research Analyst to support Commander, Fleet Readiness Centers (COMFRC). The ideal candidate will possess subject matter expertise in   data management and applied mathematics, with demonstrated experience in logistics and program management. Candidate must be comfortable working in a government environment and have prior Department of Defense (DoD) experience.

This position is contingent upon contract award.

This position is located at NAS Patuxent River, MD 

Job Tasks:

• Formulate and apply mathematical modeling, simulation, and other optimization methods to develop and interpret information that assists management with decision making, policy formulation, and other managerial functions. 

• Collect and analyze data and develop decision support software, services, or products. 

• Develop and supply optimal time, cost, or logistics networks for program evaluation, review, or implementation.

• Direct the collection, integration, and analysis of data from NAVAIR, Navy, Marine Corps, and other DoD sustainment systems (e.g., DECKPLATE, Vector, RAMP, IPSMS, AMSRR)

• Develop and refine predictive and prognostic models for early identification of cost and readiness degraders across fleet aircraft.

• Develop and maintain dashboards to display readiness and sustainment-related cost performance metrics. 

• Perform sustainment cost analysis, including Life Cycle Cost Estimates, Business Case Analyses (BCAs), and Total Ownership Cost analyses. 

• Analyze supply chain performance metrics and management to assess potential causes and solutions to readiness degraders. 

• Review independent investigations of proposed weapons systems changes and assess impacts on readiness, Level of Repair (LOR), and total ownership cost.

• Support the development of conceptual models, CONOPS documents, and system requirements documentation using agile software development methodology. 

• Mentor and oversee journeyman and junior analysts and manage assigned staff efforts.

Job Requirements:

• Bachelor’s Degree in a technical or business-related field Operations Research, Mathematics, Statistics, or Data Science preferred.

• 15+ years of experience in operational research, quantitative analysis, or a closely related field.

• Demonstrated expertise in mathematical modeling, forecasting, simulation, and statistical methods.

• Extensive experience with DoD/NAVAIR readiness, logistics, and sustainment data systems (e.g., DECKPLATE, Vector, RAMP, IPSMS, AMSRR).

• Experience performing Life Cycle Cost Estimates, BCAs, and Total Ownership Cost analyses.

• Experience developing predictive and prognostics models for early identification of cost and readiness degraders. 

• Experience with supply chain performance analysis and management. 

• Knowledge of agile software development methodology for developing conceptual models and system requirements documentation. 

• Proven ability to work on high-visibility, mission-critical programs.

• Knowledge of data management and visualization products.

• Proficiency with MS Excel and MS Access.

• Experience developing technical documentation and/or business process documentation.

• Ability to obtain and maintain a favorably adjudicated Tier-3 investigation (Secret clearance).

• Must be a US citizen.

Physical Requirements:

Work may involve sitting or standing for extended periods of time. Position may require typing and reading from a computer screen. Must have sufficient mobility, including but not limited to bending, reaching, and kneeling to complete daily duties in a timely and efficient manner. There is a possibility that due to parking availability and location of work, walking moderate to long distance may be required. Possible lifting up to 25lbs.

Due to this being a contract position working for the US government all candidates must be a U.S. citizen and pass a criminal and financial background check as well as a drug test.

Please note: Vintun LLC reserves the right to change or modify job duties and assignments at any time. The above job description is not all encompassing. Positions functions and qualifications may vary depending on business needs.

Vintun LLC is an equal opportunity employer and does not discriminate against applicants based on race, color, creed, religion, medical condition, legally protected genetic information, national origin, sex (including pregnancy, childbirth, or related medical condition), sexual orientation, gender identity and expression, age, disability, or Vietnam era, or other eligible veteran status or legally protected characteristics.

Vintun LLC is a professional services firm that provides consulting and advisory services to clients to improve operational efficiency and to accomplish organizational objectives. Vintun is headquartered in Stafford, VA with client support offices in San Diego and Hawaii. Vintun offers a highly competitive benefits package that reflects our objective of employing top industry performers.

Company DescriptionVintun LLC is a professional services firm that provides consulting and advisory services to clients to improve operational efficiency and to accomplish organizational objectives. Vintun is headquartered in Stafford, VA with client support offices in San Diego and Hawaii. Vintun offers a highly competitive benefits package that reflects our objective of employing top industry performers.Company DescriptionVintun LLC is a professional services firm that provides consulting and advisory services to clients to improve operational efficiency and to accomplish organizational objectives. Vintun is headquartered in Stafford, VA with client support offices in San Diego and Hawaii. Vintun offers a highly competitive benefits package that reflects our objective of employing top industry performers. Read Less

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:

Technical Services Scientist

Responsibilities:

Under limited supervision and in accordance with the laws, federal regulations, and applicable state and local policies, procedures and guidelines, this position has the following tasks and duties.Provide technical oversight for spray dry and solid dosage manufacturing processes, leveraging a strong technical foundation and previous experience supporting these processes.Participate in resolution of technical issues, including those related to control strategy and manufacturing.Authoring of deviations and change controls.Build, manage, and maintain internal and external relationships, site management, development and central technical organization, and cross-functional teams.Ensure that manufacturing processes are compliant, capable, in control, and maintained in a validated or qualified state.Understand, justify, and document the state of process validation with data that evaluates the capability of the manufacturing process to meet its stated purpose.Maintain processes in a state of compliance with US and global regulations, including cGMPs and applicable global regulatory manufacturing guidance.Support ongoing manufacturing at External Partners through process monitoring, issue response, and process improvements where necessary.

Requirements:

Bachelor's degree (minimum) in scientific disciplines of Biotech, Chemistry, Biochemistry, Biology, Pharmacy, or Engineering.3+ years of demonstrated hands-on working experience and proficiency with spray dry and/or solid dosage manufacturing.Strong understanding of regulatory requirements, their application, and expectations in a manufacturing environment (cGMPs and applicable global regulatory guidance).Proficient in data management practices across manufacturing operations.Proven ability to effectively communicate and influence across diverse teams.Demonstrated project management expertise with a track record of coordinating and executing multifaceted projects.Available to support 24/7 operations and issue resolutions across multiple time zones as needed.Excellent technical writing capabilities and documentation in English, and communication skills.Ability to manage multiple priorities and work independently with limited supervisionAvailable 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.

Read Less

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:

Technical Services Scientist

Responsibilities:

Under limited supervision and in accordance with the laws, federal regulations, and applicable state and local policies, procedures and guidelines, this position has the following tasks and duties.Provide technical oversight for spray dry and solid dosage manufacturing processes, leveraging a strong technical foundation and previous experience supporting these processes.Participate in resolution of technical issues, including those related to control strategy and manufacturing.Authoring of deviations and change controls.Build, manage, and maintain internal and external relationships, site management, development and central technical organization, and cross-functional teams.Ensure that manufacturing processes are compliant, capable, in control, and maintained in a validated or qualified state.Understand, justify, and document the state of process validation with data that evaluates the capability of the manufacturing process to meet its stated purpose.Maintain processes in a state of compliance with US and global regulations, including cGMPs and applicable global regulatory manufacturing guidance.Support ongoing manufacturing at External Partners through process monitoring, issue response, and process improvements where necessary.

Requirements:

Bachelor's degree (minimum) in scientific disciplines of Biotech, Chemistry, Biochemistry, Biology, Pharmacy, or Engineering.3+ years of demonstrated hands-on working experience and proficiency with spray dry and/or solid dosage manufacturing.Strong understanding of regulatory requirements, their application, and expectations in a manufacturing environment (cGMPs and applicable global regulatory guidance).Proficient in data management practices across manufacturing operations.Proven ability to effectively communicate and influence across diverse teams.Demonstrated project management expertise with a track record of coordinating and executing multifaceted projects.Available to support 24/7 operations and issue resolutions across multiple time zones as needed.Excellent technical writing capabilities and documentation in English, and communication skills.Ability to manage multiple priorities and work independently with limited supervisionAvailable 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.

Read Less

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:

Technical Services Scientist

Responsibilities:

Under limited supervision and in accordance with the laws, federal regulations, and applicable state and local policies, procedures and guidelines, this position has the following tasks and duties.Provide technical oversight for spray dry and solid dosage manufacturing processes, leveraging a strong technical foundation and previous experience supporting these processes.Participate in resolution of technical issues, including those related to control strategy and manufacturing.Authoring of deviations and change controls.Build, manage, and maintain internal and external relationships, site management, development and central technical organization, and cross-functional teams.Ensure that manufacturing processes are compliant, capable, in control, and maintained in a validated or qualified state.Understand, justify, and document the state of process validation with data that evaluates the capability of the manufacturing process to meet its stated purpose.Maintain processes in a state of compliance with US and global regulations, including cGMPs and applicable global regulatory manufacturing guidance.Support ongoing manufacturing at External Partners through process monitoring, issue response, and process improvements where necessary.

Requirements:

Bachelor's degree (minimum) in scientific disciplines of Biotech, Chemistry, Biochemistry, Biology, Pharmacy, or Engineering.3+ years of demonstrated hands-on working experience and proficiency with spray dry and/or solid dosage manufacturing.Strong understanding of regulatory requirements, their application, and expectations in a manufacturing environment (cGMPs and applicable global regulatory guidance).Proficient in data management practices across manufacturing operations.Proven ability to effectively communicate and influence across diverse teams.Demonstrated project management expertise with a track record of coordinating and executing multifaceted projects.Available to support 24/7 operations and issue resolutions across multiple time zones as needed.Excellent technical writing capabilities and documentation in English, and communication skills.Ability to manage multiple priorities and work independently with limited supervisionAvailable 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.

Read Less

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:

Technical Services Scientist

Responsibilities:

Under limited supervision and in accordance with the laws, federal regulations, and applicable state and local policies, procedures and guidelines, this position has the following tasks and duties.Provide technical oversight for spray dry and solid dosage manufacturing processes, leveraging a strong technical foundation and previous experience supporting these processes.Participate in resolution of technical issues, including those related to control strategy and manufacturing.Authoring of deviations and change controls.Build, manage, and maintain internal and external relationships, site management, development and central technical organization, and cross-functional teams.Ensure that manufacturing processes are compliant, capable, in control, and maintained in a validated or qualified state.Understand, justify, and document the state of process validation with data that evaluates the capability of the manufacturing process to meet its stated purpose.Maintain processes in a state of compliance with US and global regulations, including cGMPs and applicable global regulatory manufacturing guidance.Support ongoing manufacturing at External Partners through process monitoring, issue response, and process improvements where necessary.

Requirements:

Bachelor's degree (minimum) in scientific disciplines of Biotech, Chemistry, Biochemistry, Biology, Pharmacy, or Engineering.3+ years of demonstrated hands-on working experience and proficiency with spray dry and/or solid dosage manufacturing.Strong understanding of regulatory requirements, their application, and expectations in a manufacturing environment (cGMPs and applicable global regulatory guidance).Proficient in data management practices across manufacturing operations.Proven ability to effectively communicate and influence across diverse teams.Demonstrated project management expertise with a track record of coordinating and executing multifaceted projects.Available to support 24/7 operations and issue resolutions across multiple time zones as needed.Excellent technical writing capabilities and documentation in English, and communication skills.Ability to manage multiple priorities and work independently with limited supervisionAvailable 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.

Read Less

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:

Technical Services Scientist

Responsibilities:

Under limited supervision and in accordance with the laws, federal regulations, and applicable state and local policies, procedures and guidelines, this position has the following tasks and duties.Provide technical oversight for spray dry and solid dosage manufacturing processes, leveraging a strong technical foundation and previous experience supporting these processes.Participate in resolution of technical issues, including those related to control strategy and manufacturing.Authoring of deviations and change controls.Build, manage, and maintain internal and external relationships, site management, development and central technical organization, and cross-functional teams.Ensure that manufacturing processes are compliant, capable, in control, and maintained in a validated or qualified state.Understand, justify, and document the state of process validation with data that evaluates the capability of the manufacturing process to meet its stated purpose.Maintain processes in a state of compliance with US and global regulations, including cGMPs and applicable global regulatory manufacturing guidance.Support ongoing manufacturing at External Partners through process monitoring, issue response, and process improvements where necessary.

Requirements:

Bachelor's degree (minimum) in scientific disciplines of Biotech, Chemistry, Biochemistry, Biology, Pharmacy, or Engineering.3+ years of demonstrated hands-on working experience and proficiency with spray dry and/or solid dosage manufacturing.Strong understanding of regulatory requirements, their application, and expectations in a manufacturing environment (cGMPs and applicable global regulatory guidance).Proficient in data management practices across manufacturing operations.Proven ability to effectively communicate and influence across diverse teams.Demonstrated project management expertise with a track record of coordinating and executing multifaceted projects.Available to support 24/7 operations and issue resolutions across multiple time zones as needed.Excellent technical writing capabilities and documentation in English, and communication skills.Ability to manage multiple priorities and work independently with limited supervisionAvailable 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.

Read Less

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:

Technical Services Scientist

Responsibilities:

Under limited supervision and in accordance with the laws, federal regulations, and applicable state and local policies, procedures and guidelines, this position has the following tasks and duties.Provide technical oversight for spray dry and solid dosage manufacturing processes, leveraging a strong technical foundation and previous experience supporting these processes.Participate in resolution of technical issues, including those related to control strategy and manufacturing.Authoring of deviations and change controls.Build, manage, and maintain internal and external relationships, site management, development and central technical organization, and cross-functional teams.Ensure that manufacturing processes are compliant, capable, in control, and maintained in a validated or qualified state.Understand, justify, and document the state of process validation with data that evaluates the capability of the manufacturing process to meet its stated purpose.Maintain processes in a state of compliance with US and global regulations, including cGMPs and applicable global regulatory manufacturing guidance.Support ongoing manufacturing at External Partners through process monitoring, issue response, and process improvements where necessary.

Requirements:

Bachelor's degree (minimum) in scientific disciplines of Biotech, Chemistry, Biochemistry, Biology, Pharmacy, or Engineering.3+ years of demonstrated hands-on working experience and proficiency with spray dry and/or solid dosage manufacturing.Strong understanding of regulatory requirements, their application, and expectations in a manufacturing environment (cGMPs and applicable global regulatory guidance).Proficient in data management practices across manufacturing operations.Proven ability to effectively communicate and influence across diverse teams.Demonstrated project management expertise with a track record of coordinating and executing multifaceted projects.Available to support 24/7 operations and issue resolutions across multiple time zones as needed.Excellent technical writing capabilities and documentation in English, and communication skills.Ability to manage multiple priorities and work independently with limited supervisionAvailable 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.

Read Less

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:

Technical Services Scientist

Responsibilities:

Under limited supervision and in accordance with the laws, federal regulations, and applicable state and local policies, procedures and guidelines, this position has the following tasks and duties.Provide technical oversight for spray dry and solid dosage manufacturing processes, leveraging a strong technical foundation and previous experience supporting these processes.Participate in resolution of technical issues, including those related to control strategy and manufacturing.Authoring of deviations and change controls.Build, manage, and maintain internal and external relationships, site management, development and central technical organization, and cross-functional teams.Ensure that manufacturing processes are compliant, capable, in control, and maintained in a validated or qualified state.Understand, justify, and document the state of process validation with data that evaluates the capability of the manufacturing process to meet its stated purpose.Maintain processes in a state of compliance with US and global regulations, including cGMPs and applicable global regulatory manufacturing guidance.Support ongoing manufacturing at External Partners through process monitoring, issue response, and process improvements where necessary.

Requirements:

Bachelor's degree (minimum) in scientific disciplines of Biotech, Chemistry, Biochemistry, Biology, Pharmacy, or Engineering.3+ years of demonstrated hands-on working experience and proficiency with spray dry and/or solid dosage manufacturing.Strong understanding of regulatory requirements, their application, and expectations in a manufacturing environment (cGMPs and applicable global regulatory guidance).Proficient in data management practices across manufacturing operations.Proven ability to effectively communicate and influence across diverse teams.Demonstrated project management expertise with a track record of coordinating and executing multifaceted projects.Available to support 24/7 operations and issue resolutions across multiple time zones as needed.Excellent technical writing capabilities and documentation in English, and communication skills.Ability to manage multiple priorities and work independently with limited supervisionAvailable 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.

Read Less

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:

Technical Services Scientist

Responsibilities:

Under limited supervision and in accordance with the laws, federal regulations, and applicable state and local policies, procedures and guidelines, this position has the following tasks and duties.Provide technical oversight for spray dry and solid dosage manufacturing processes, leveraging a strong technical foundation and previous experience supporting these processes.Participate in resolution of technical issues, including those related to control strategy and manufacturing.Authoring of deviations and change controls.Build, manage, and maintain internal and external relationships, site management, development and central technical organization, and cross-functional teams.Ensure that manufacturing processes are compliant, capable, in control, and maintained in a validated or qualified state.Understand, justify, and document the state of process validation with data that evaluates the capability of the manufacturing process to meet its stated purpose.Maintain processes in a state of compliance with US and global regulations, including cGMPs and applicable global regulatory manufacturing guidance.Support ongoing manufacturing at External Partners through process monitoring, issue response, and process improvements where necessary.

Requirements:

Bachelor's degree (minimum) in scientific disciplines of Biotech, Chemistry, Biochemistry, Biology, Pharmacy, or Engineering.3+ years of demonstrated hands-on working experience and proficiency with spray dry and/or solid dosage manufacturing.Strong understanding of regulatory requirements, their application, and expectations in a manufacturing environment (cGMPs and applicable global regulatory guidance).Proficient in data management practices across manufacturing operations.Proven ability to effectively communicate and influence across diverse teams.Demonstrated project management expertise with a track record of coordinating and executing multifaceted projects.Available to support 24/7 operations and issue resolutions across multiple time zones as needed.Excellent technical writing capabilities and documentation in English, and communication skills.Ability to manage multiple priorities and work independently with limited supervisionAvailable 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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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:

Technical Services Scientist

Responsibilities:

Under limited supervision and in accordance with the laws, federal regulations, and applicable state and local policies, procedures and guidelines, this position has the following tasks and duties.Provide technical oversight for spray dry and solid dosage manufacturing processes, leveraging a strong technical foundation and previous experience supporting these processes.Participate in resolution of technical issues, including those related to control strategy and manufacturing.Authoring of deviations and change controls.Build, manage, and maintain internal and external relationships, site management, development and central technical organization, and cross-functional teams.Ensure that manufacturing processes are compliant, capable, in control, and maintained in a validated or qualified state.Understand, justify, and document the state of process validation with data that evaluates the capability of the manufacturing process to meet its stated purpose.Maintain processes in a state of compliance with US and global regulations, including cGMPs and applicable global regulatory manufacturing guidance.Support ongoing manufacturing at External Partners through process monitoring, issue response, and process improvements where necessary.

Requirements:

Bachelor's degree (minimum) in scientific disciplines of Biotech, Chemistry, Biochemistry, Biology, Pharmacy, or Engineering.3+ years of demonstrated hands-on working experience and proficiency with spray dry and/or solid dosage manufacturing.Strong understanding of regulatory requirements, their application, and expectations in a manufacturing environment (cGMPs and applicable global regulatory guidance).Proficient in data management practices across manufacturing operations.Proven ability to effectively communicate and influence across diverse teams.Demonstrated project management expertise with a track record of coordinating and executing multifaceted projects.Available to support 24/7 operations and issue resolutions across multiple time zones as needed.Excellent technical writing capabilities and documentation in English, and communication skills.Ability to manage multiple priorities and work independently with limited supervisionAvailable 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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Job DescriptionJob Description

Austin Powder is seeking to hire a full-time Manufacturing Chemical Engineer to join our team at our Red Diamond Manufacturing plant. This engineering position provides technical support to produce chemically manufactured energetic materials and the production of packaged explosives.

The Manufacturing Chemical Engineer enjoys a competitive wage and generous benefits. Our benefits include medical, dental, vision, a 401(k), a flexible spending account, life insurance, AD&D insurance, short-term disability, and an employee assistance program (EAP). If this sounds like the opportunity that you've been searching for, apply today!

ABOUT AUSTIN POWDER

Austin Powder manufactures a full line of industrial explosives and provides blasting services to customers in the quarrying, mining, construction, and oil and gas industries -- all for the purpose of providing aggregate, energy, and mineral products to consumers. The Red Diamond Plant is a stand-alone site of approximately 250 employees operating five major production areas to supply packaged explosive products to customers all over the country.

Our values of commitment to safety, attention to detail, and the power of family are the very bedrock upon which our company's culture is built. We truly value our team which is why we offer competitive opportunities for career growth and advancement.

A DAY IN THE LIFE OF A MANUFACTURING CHEMICAL ENGINEER

As a Manufacturing Chemical Engineer at the Red Diamond plant, you offer technical assistance to produce energetics and packaged explosives. You drive continuous improvement in capital and non-capital projects through reliability, cost, quality, and operability focus. Working with engineering, production, maintenance, and other support functions, you grow your expertise in engineering capacity to drive long-term sustainability and improvement at the plant.

You troubleshoot problems as they arise alongside team members. Identifying improvement opportunities, you work to optimize new solutions for the most impact. You help identify opportunities related to reliability, operability, raw material yields, capacity, energy, quality, product safety, and the environment.

Your skills will continue to develop in project management, process engineering, equipment troubleshooting, and continuous improvement as you take on managing projects from start to finish -- details like developing and updating flow diagrams, process safety, environmental documentation, and operational procedures. You will leverage or gain valuable experience in project management, detailed engineering, OSHA PSM, chemical manufacturing, equipment reliability, reactive chem, and more! As a highly motivated individual, you enjoy the challenge of finding engineering solutions and feel great satisfaction in improving production at the Red Diamond plant!

QUALIFICATIONS

B.S. Chemical Engineering degree OR equivalent degreeKnowledge of process control systemsExperience with chemical manufacturing equipment is a plus.Computer skills including Microsoft Office suiteAbility to perform work in a manufacturing environment which includes ascending and descending stairs and ladders.Entry level or Experienced engineers

Do you have strong written and verbal communication skills? Are you a problem solver with great decision-making abilities? Can you work on and balance multiple assignments at once? Are you attentive to safety? If so, you may be perfect for this position!

ARE YOU READY TO JOIN OUR TEAM?

If you feel that you would be right for this engineering position, please fill out our initial 3-minute, mobile-friendly application. We look forward to meeting you!

This contractor and subcontractor shall abide by the requirements of 41 CFR 60-1.4(a), 60-300.5(a) and 60-741.5(a). These regulations prohibit discrimination against qualified individuals based on their status as protected veterans or individuals with disabilities and prohibit discrimination against all individuals based on their race, color, religion, sex, sexual orientation, gender identity, national origin, and for inquiring about, discussing or disclosing compensation. Moreover, these regulations require that covered prime contractors and subcontractors take affirmative action to employ and advance in employment individuals without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.

Job Posted by ApplicantPro
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Job DescriptionJob Description

Compensation: $68,000–$70,000 annually, commensurate with experience.
Position Type / Schedule: Full-time (Exempt). Monday–Friday, 8:30 AM – 5:00 PM. Occasional weekend work may be required. This position is fully on-site; remote work is not available for this role.
Work Location: The Institute for Food Safety and Health (IFSH), 6502 S Archer Rd., Bedford Park, IL 60501.
Benefits: Our commitment to employee well-being is reflected in our competitive benefits package located here.

Summary

The Research Scientist – Chemistry will work at the IIT Institute for Food Safety and Health (IFSH) on the joint Proficiency Testing program with the U.S. Food and Drug Administration (FDA), located at the Moffett Campus of IIT. The joint IFSH-FDA Proficiency Testing program is ISO 17043 accredited. Under minimal supervision, the Scientist responds to complex scientific inquiries and resolves method/instrument issues. The Scientist also takes a lead role in drafting scientific papers/presentations.

Key Responsibilities & Accountabilities

20% - Contributes to the Proficiency Testing Chemistry programs by performing lab tests and analyses in accordance with required specifications, established procedures and customer service standards to provide accurate research data.

20% - Conducts analyses in a timely, accurate, and cost-effective manner. Manages lab processes and supplies and operates and maintains laboratory equipment (e.g., HPLC, GC, MS, ICP-MS, and other analytical instruments) to achieve maximum output.

20% - Assists in developing, documenting, updating, and maintaining approved procedures for
assigned Proficiency Testing Chemistry projects. Plans, schedules, and prioritizes project
activities.

20% - Accurately estimates the time required to complete tasks, respects timelines and priorities of others.
Works with industry partners and participates in cross-functional teams to drive project results.

10% - Develops client/grant/internal proposals for funding. Develops internal status updates, reports, and scientific presentations/publications.

10% - Directs students and other project contributors with small projects and projects of limited focus. Recommends ideas to
enhance department effectiveness. Ensures that all safety procedures are in effect and tracked. Communicates to encourage teamwork and a proactive approach to meet customer needs. Performs other duties as assigned.

Qualifications

- M.S. degree in Food Science, Chemistry or related field with 3 or more years’ related experience, or equivalent combination of education and experience
- Strong working knowledge of Microsoft Word and Excel- Excellent technical writing skills
- Strong verbal communication skills, including presenting papers and scientific findings

Supervision & Budget Authority

- No budget authority or supervision of staff
- May direct up to 3 students on small projects

Service Standards and Performance Expectations

- Works with minimal supervision, responds to complex queries and is proactive in seeking solutions
- Exceptional attention to detail, demonstrated through consistent performance, in maintaining and documenting scientific notebooks and papers
|- Effectively communicates to encourage participation and seeks input from others to resolve issues as they arise

Physical Qualifications

- Approximately 75% of work time will be spent in an ISO 17043-accredited laboratory and approximately 25% in an office environment.
- May have to lift up to 10 pounds on occasion and perform repetitive motions up to 20% of the time during the workday, including data entry and instrument manipulation.

EEOC Statement

Illinois Institute of Technology is an EEO/AA/Title VI/Title IX/Section 504/ADA/ADEA employer dedicated to building a community of excellence, equity, inclusion, and diversity. It is committed to fostering an inclusive environment and actively seeks applications from individuals of all backgrounds and identities, regardless of race, color, sex, marital status, religion, national origin, disability, age, unfavorable discharge from the military, status as a protected veteran, sexual orientation, including gender identity and expression, order of protection status, and/or genetic information. All qualified applicants will receive equal consideration for employment.

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Job DescriptionJob Description

We are current seeking a geotechnical engineer, P.E. preferred, to join our team in Salisbury, Maryland and participate on a wide variety of geotechnical, testing and monitoring related projects. Projects are primarily located within Maryland, Virginia, DC, Delaware, and Pennsylvania. Candidate will have the opportunity to collaborate with personnel at other HCEA offices throughout the company.

General Responsibilities:

Support the office's Geotechnical Group and other departments as required.Prepare technical proposals, cost estimates, plans, technical specifications, and reports, including day to day correspondence.Perform geotechnical analyses based on site conditions and requirements to support project designs.Evaluate laboratory and field data for inclusion in reports.Review and interpret data and test results.Prepare field reports, internal correspondence and engineering reports.Follow company safety standards, site safety standards, and provide all required permitting.Contact vendors; research literature and regulatory requirements; prepare designs.Support field instrumentation and monitoring activities.Develop and maintain clients and actively participate in professional and related industry organizations.

Candidate Qualifications:

B.S. Civil Engineering, Geotechnical Engineering, M.S. preferred.5 - 10 years of related experienceP.E. preferredEnthusiastic, self-starter with desire to provide excellent service to clientsStrong communication skills (oral and written)Computer literate (Word, Excel, Outlook, AutoCAD)Valid driver's licenseWilling to travel and work out of town for short periods of timePhysical requirements may require lifting up to 50 pounds and traverse over rugged terrain.

BENEFITS:

We are proudly an Equal Opportunity Employer and offer an appealing benefit package. A few of these perks include: 100% Employer-Paid Benefits (Long-Term Disability, Basic Life & Employee Assistance Program), Health (W/ Health Savings Account Option), Disability, 401k w/ Company Match, Generous Compensation for Employee-Referrals, Tuition Reimbursement and many more!

Need another reason to join in on the success? We offer an Employee Stock Ownership Plan (ESOP) in which employees are given shares in the company and the more successful the company is, the more valuable the shares become.

Want to grow with us? Apply Now!

Minorities and Women are encouraged to apply.

EOE

Job Posted by ApplicantPro
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Job DescriptionJob DescriptionREQUIRED:Active TS/SCI clearanceOnsite – Offutt AFB, NE7+ years all-source intelligence analysisPREFERRED:USSTRATCOM UCP mission experienceDESCRIPTION:

Constellation West is a 29-year WOSB and Prime Federal Contractor bidding on recompeting Joint Exercise, Training, Assessment and Related Support for USSTRATCOM/J7.

Qualified incumbent personnel currently supporting this mission will be afforded Right of First Refusal (ROFR) for applicable positions, consistent with contract requirements and contingent upon continued eligibility, performance, and government approval.

ABOUT US:

Constellation West is an award-winning company that delivers Information Technology (IT) engineering services and solutions and non-IT subject matter expertise worldwide. Established in 1997, Constellation West is an industry leader, partnering with key organizations across the Department of Defense and civilian agencies.

BENEFITS:

• Competitive 401(k) plan with employer matching
• Competitive Health Benefits with employer contributions
• 11 Paid Holidays per year
• 15 Days starting PTO for new hires
• Tuition/CE reimbursement
• Relocation Assistance
• Veteran Hiring Preference
• Employee Stock Ownership Plan (ESOP)

EEO:

Constellation West is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.

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Job DescriptionJob Description

AI Signal Research, Inc. (ASRI) is recruiting for the NAWCAD AID effort in Patuxent River, MD.

Education: Bachelor’s degree in a technical discipline.

Months/Years of Experience: N/A

Required Qualifications: U.S. Citizen. Must have a DoD security clearance.

Duties: Performs research into fundamental computer, network, software and information technology systems. Conducts research into problems in the field of computer hardware and software with a focus on system security and vulnerability. Conducts research into information technology architectures and infrastructure. The application of, or research into, computer science methods and techniques to store, manipulate, transform or present information by means of computer systems. The primary requirements of the work are (a) professional competence in applying the theoretical foundations of computer science, including computer system architecture and system software organization, the representation and transformation of information structures, and the theoretical models for such representations and transformations; (b) specialized knowledge of the design characteristics, limitations, and potential applications of systems having the ability to transform information, and of broad areas of applications of computing which have common structures, processes, and techniques; and (c) knowledge of relevant mathematical and statistical sciences.

Comments: Compliance with health mandates as dictated by the contract may be required as a condition of employment.

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Job DescriptionJob Description

En Alivia Specialty Pharmacy buscamos un Técnico/a de Farmacia para el área de Manejo de Casos LDD (Medicamentos de Distribución Limitada), enfocado en coordinar terapias especializadas y apoyar a nuestros pacientes durante su tratamiento.

Responsabilidades principales:

Evaluar y procesar recetas para terapias especializadas.

Coordinar la documentación requerida entre pacientes, médicos y aseguradoras.

Orientar a nuevos pacientes sobre sus tratamientos y costos asociados.

Gestionar reclamaciones de seguros, autorizaciones y asistencia económica disponible.

Dar seguimiento a entregas, recargas y continuidad de terapias.

Cumplir con los estándares de calidad y regulaciones estatales y federales.

Requisitos:

✔ Grado Asociado como Técnico/a de Farmacia
✔ Licencia vigente de Técnico/a de Farmacia
✔ Dominio del inglés y español (oral y escrito), requerido
✔ Formación especializada en acceso a beneficios médicos y de farmacia
✔ Experiencia en Farmacia Especializada (preferible)

EEOC F/M/V/D

¡Sé parte de un equipo que transforma la experiencia de salud de nuestros pacientes!

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Job DescriptionJob Description

Resumen:

Impartirá enseñanza a grupo(s) de estudiantes en el área de Ciencias de la Salud con Especialidad en Ciencias a nivel certificado técnico:

Requisitos:

Bachillerato concentración en su programa con 12 créditos o más en el área de especialidad a enseñar2 años de experiencia mínimo

“Patrono con Igualdad de Oportunidades en el Empleo y Acción Afirmativa para Mujeres, Veteranos y trabajadores con Discapacidad”.

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