Job Search

QA Auditor Compliance Manager

  • Negotiable
  • Allschwil, Basel-Country
  • Contract

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.

Isobel Abernethy Associate Consultant, Quality Assurance

Apply for this role

Copyright © All Rights Reserved SEC Life Sciences
Site by Venn