Quality Control Specialist
2 days ago
CPL in partnership with our Client Pfizer are seeking a highly skilled Quality Control Specialist to join their team at their state-of-the-art site in Dublin, Grange Castle for a contingent 11-month fixed-term contract. This is an on-site role.
Key Responsibilities:
- Develop and maintain quality programs, processes, and procedures that ensure compliance with established standards and agency guidelines.
- Contribute to quality risk management by tracking commitment, interpreting policies, managing site complaints, and working directly with operating entities to provide process analysis oversight.
- Ensure the quality assurance program and policies are maintained and modified regularly, ensuring uniform standards worldwide and best practice sharing.
Requirements:
- A third-level qualification in Science, Engineering, or equivalent.
- Experience working in a QC laboratory, preferably in a biotech, pharmaceutical, or bio-pharmaceutical manufacturing environment.
- Demonstrated experience with analytical techniques, including bioassay/potency testing, ELISA, blotting, flow cytometry assays, PCR, molecular biology techniques.
- Excellent interpersonal and communication skills, with a detail-oriented approach and quick decision-making abilities.
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