A company is looking for a QA Compliance Specialist III in Third Party Manufacturing.
Key Responsibilities
Maintain effective liaison with Quality, Regulatory, Technical, and Supply Chain areas
Ensure production at TPM sites complies with current good manufacturing practices and specifications
Review and approve manufacturing directions, investigations, and annual Product Quality Reviews
Required Qualifications
Bachelor's degree in Engineering or Science
Six years of experience in Pharmaceutical operations, preferably in Biologic manufacturing
Knowledge of GMP regulations and standards for pharmaceutical products
Experience with change notifications and third-party manufacturing
Familiarity with SAP and LRMS is highly preferred
Compliance Specialist • Oklahoma City, Oklahoma, United States