Job Title: Quality Auditor / QA Specialist – Contract (6 Months)

Location: London (Hybrid – 2–3 days on-site)

We are seeking an experienced Quality Auditor / QA Specialist to join a global pharmaceutical development team on a 6-month contract.

This role offers exposure to a wide range of investigational medicinal products, from small molecules to complex biologics, and an opportunity to make a tangible impact on the delivery of life-changing medicines.

What You’ll Do:

• Conduct routine audits of data, procedures, equipment, systems, and facilities to ensure compliance with GMP/SOPs and international regulations
• Review and approve production and analytical documentation for API, clinical supply, and investigational medicinal products
• Communicate and resolve audit findings with client teams and support corrective actions
• Compile audit reports and work with operational teams to implement improvements
• Collaborate with global clinical supply chain and manufacturing teams

What We’re Looking For:

• Proven experience in pharmaceutical manufacturing or regulatory agency QA
• Strong cGMP / GMP knowledge and practical audit experience
• Excellent attention to detail, communication, and interpersonal skills
• Ability to work independently, manage multiple priorities, and support cross-functional teams
• Proficient in Trackwise, LMS, ERP systems, and Microsoft Office
• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or related field
• Minimum 3 years applied QA experience in the pharmaceutical industry

Why This Role Is Exciting:

• Work in a dynamic global development environment with exposure to innovative therapies
• Opportunity to influence quality standards across manufacturing and clinical supply
• Hybrid working model: collaborate onsite and remotely