Exciting Contract Opportunity: QA Auditor Compliance Manager - 12-Month Full-Time Contract, Biopharmaceutical Sector
Join a pioneering biopharmaceutical company in Europe's thriving biotech hub who are currently seeking a QA Auditor Compliance Manager for a 12-month full-time contract.
This role is crucial for ensuring the highest standards of GMP/GDP compliance in pharmaceutical products. If you have a passion for upholding quality in the dynamic world of biopharmaceuticals, this could be your next project.
Your Role as QA Auditor Compliance Manager:
- Oversee GMP/GDP compliance across third-party providers and internal facilities.
- Develop and execute external QA audits and internal self-inspection plans.
- Conduct GMP/GDP audits, coordinating with internal teams and suppliers for smooth execution and follow-up.
- Report critical inspection findings to key personnel and management.
- Implement and maintain Quality Agreements with vendors.
- Liaise between quality, regulatory, compliance, and operational teams, ensuring regulatory compliance and understanding.
Experience and Qualifications for the QA Auditor Compliance Manager Role:
- University degree in Pharmacy, Chemistry, or related science field (Master's level minimum).
- Minimum 3 years' experience in Auditing, ideally including a role as Lead Auditor.
- Comprehensive knowledge of drug product development, manufacturing processes, and quality control.
- Expertise in GMP/GDP and international quality regulations (e.g., ICH, ISO, WHO, PIC, FDA, EU GMP Guide).
- Skilled in project management, prioritisation, and attention to detail.
- Experience in Medical Devices is beneficial.
This contract role is a great opportunity to contribute significantly to a leading biopharmaceutical company.
If you're interested in this position, apply now for immediate consideration. For similar contract opportunities in the sector, feel free to reach out directly.