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Form of workOur 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. You will 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. Your expertise will help in identifying deviations from established standards, in the manufacturing of clinical and commercial batches. You will make sure that product and process documents match the specifications based on established sampling and statistical process control procedures. In the relevant cases you will approve minor investigations and participate in minor change control activities to ensure compliance to procedures/GMPs.
Candidates must have the following:
Batch record review
Batch release
Pharmaceutical GMP experience (minimum 1-2 years)
Monday-Friday
3rd shift
Additional Skills & Qualifications:
BS Degree with minimum 2 years of directly related pharma experience
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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Hiring diverse talent
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