Manufacturing Process Verification Specialist
2 days ago
About the Role
Zoetis, the world's largest manufacturer and supplier of animal pharmaceuticals, is seeking a skilled Manufacturing Process Verification Specialist to join our team in Lincoln, NE.
Key Responsibilities
- Support various activities within media preparation operations, including closing of process in SAP, GMP review of batch records, audit of batch records, CAPA, and change management.
- Understand, follow, and complete process documentation in support of GMP.
- Understand and follow safety policies as it relates to biological and chemical components and equipment to protect personnel and maintain product quality.
- Participate in daily manufacturing/Quality assurance meeting.
- Train colleagues on GMP documentation and ensure team compliance during execution and throughout review of batch records.
- Act as a liaison and collaborate with manufacturing support groups (quality assurance and mAb technical support) to ensure respect of GMP practice and appropriate CAPA defined.
- Assist as needed the production team with production tasks.
Requirements
- Relevant BS or equivalent degree required; MA/MS preferred.
- Preference given to applicants with relevant experience in GMP regulated manufacturing environment.
- Functional skills:
- Ability to read and follow written directions.
- Ability to communicate effectively both verbally and in writing.
- Ability to think critically.
- Ability to function independently when required.
- Ability to meet deadlines and keep organized methods of tracking standard work.
- Technical skills:
- Basic computer skills (Word and Excel).
- Proficiency in SAP.
- Ability to troubleshoot.
- Knowledge in GMP environment.
Physical Position Requirements
Exposure to chemicals, fumes, odors, noise, live steam, temperature fluctuations, biohazards, continuous standing and lifting to a maximum of 50 lbs.
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