Executive - Quality Assurance
Centrient Pharmaceuticals Netherlands(4 years ago)
About this role
A Quality Assurance Associate in the pharmaceutical industry ensures that products meet customer specifications and applicable regulatory standards (cGMP/GLP/ICH/USFDA/ISO). The role supports quality governance across manufacturing operations, maintaining documentation and records to demonstrate compliance. It also contributes to safety and environmental health practices to ensure a safe workplace.
Required Skills
- Vendor Qualification
- Auditing
- Regulatory Compliance
- Product Release
- COA Creation
- Batch Records
- Data Review
- Complaint Investigation
- Sampling Procedures
- Safety Compliance
+2 more
Qualifications
- Post-Graduation in Chemistry
About Centrient Pharmaceuticals Netherlands
centrient.comCentrient Pharmaceuticals is a sustainable leader in the production of antibiotics, statins, and antifungals. The company focuses on delivering high-quality healthcare solutions while prioritizing environmental sustainability and social responsibility. Centrient is committed to addressing pressing health challenges such as antimicrobial resistance through innovation and collaboration, ensuring that medicines reach those who need them most. With a strong emphasis on corporate governance and sustainability initiatives, Centrient fosters a responsible approach to pharmaceutical manufacturing.
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