- Quality assurance
- Batch record review
- Batch record release
- Audit
- CAPA
- Batch record
- SOP
- Compliance
- Document control
- GMP
- BS Degree preferred with minimum 2 years of directly related pharma experience
- Previous quality assurance experience
- GMP experience required
- 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
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Manufacturing Quality Associate - Raleigh, United States - Actalent
Description
Our client, a global pharma manufacturer, is seeking a Manufacturing Quality Associate to evaluate and review manufacturing activities (incoming material release, batch release, investigations, change controls, other activities as needed) in support of clinical and commercial batch production.
Skills:
Additional Skills & Qualifications:
Experience Level:
Intermediate Level
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.
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