Quality Assurance Technician – Process & Cleaning Validation
Sector: Pharmaceutical Manufacturing
Employment Type: Full-Time, Permanent
Join a leading pharmaceutical manufacturing site with a strong reputation for quality and innovation. This is a pivotal role within the Validation team, focused on ensuring robust process and cleaning validation across both sterile and non-sterile product lines. Offering excellent long-term career prospects, this position will see you act as a technical reference point, working cross-functionally to maintain the highest standards of GMP compliance.
Key Responsibilities:
Validation Strategy: Develop and implement Validation Master Plans for process and cleaning validation activities.
Protocol & Reporting: Prepare detailed validation protocols, reports, and supporting documentation in line with GMP and internal quality policies.
Cross-Functional Collaboration: Work closely with Production, Quality Control, and Engineering teams to align validation activities with site operations.
Quality & Compliance: Conduct risk assessments, support CAPA activities, and manage change controls.
Audit & Inspection Support: Contribute to the preparation and hosting of site audits and inspections, including internal, client, and regulatory reviews.
Continuous Improvement: Drive enhancements to the quality system and contribute to the revalidation of ISO certifications.
Qualifications & Experience:
Education: Degree in Pharmacy or Life Sciences.
Industry Expertise: Minimum of 5 years’ experience in pharmaceutical validation, ideally with exposure to sterile manufacturing.
GMP Knowledge: Strong understanding of GMP requirements and validation best practices.
Technical Skills: Proficiency in quality management systems such as TrackWise, SAP, or similar.
Language Proficiency: High level of English, both written and spoken.
Professional Skills: Exceptional attention to detail, strong technical writing skills, and proven ability to work effectively in cross-functional teams.
Why Join Us?
This is an opportunity to play a central role in ensuring product quality and patient safety within a high-performing pharmaceutical site. You will work alongside experienced professionals, gain exposure to complex validation projects, and contribute to the continuous improvement of site operations.
Apply Now
If you are ready to take the next step in your pharmaceutical quality career, please submit your CV.
Link to Privacy Policy: https://www.gxpeople.com/cm/privacy