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. 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)
Schedule:
Monday-Friday
3rd shift
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