QA Engineer (Pharmaceuticals)
Salary undisclosed
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Job Title: Quality Assurance Engineer
Job Description
Will serve as Quality Assurance oversight for Quality Control (QC) data, documentation, and projects as well as Validation documentation and projects. The position will also assist with these activities for third party manufacturers. This position works directly with QC, Validation, and Project management to integrate Quality into industrial operations.
Hard Skills
This is a permanent position.
Work Site
This is a fully on-site position in BRIDGETON, Missouri.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.
Job Description
Will serve as Quality Assurance oversight for Quality Control (QC) data, documentation, and projects as well as Validation documentation and projects. The position will also assist with these activities for third party manufacturers. This position works directly with QC, Validation, and Project management to integrate Quality into industrial operations.
- Serve as QA reviewer and approver of QC release, stability and raw material data
- Serve as QA reviewer and approver of site validation protocols including production equipment, computer systems, laboratory equipment and methods
- Review SOPs for accuracy and compliance; draft revisions for updates as necessary
- Review and approve OOS/OOT investigations for raw materials, intermediates and finished product testing
- Review and approve investigations as it related to the execution of the project or validation
- Provide QA reviews and approvals of QC and/or Validation procedures, methods, change controls, CAPAs, deviations, and other documents, as necessary
- Support Annual Product Review responsibilities for the site
Hard Skills
- Understanding of validations from a technical standpoint
- Ability to review analytical data
- Chemistry or lab experience
- Experience in a contract lab setting or pharma manufacturing environment
- Ability to work independently and with guidance as needed
- Conservative yet problem-solving approach
This is a permanent position.
Work Site
This is a fully on-site position in BRIDGETON, Missouri.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
- Hiring diverse talent
- Maintaining an inclusive environment through persistent self-reflection
- Building a culture of care, engagement, and recognition with clear outcomes
- Ensuring growth opportunities for our people
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.
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