Quality Assurance Professional

Who We Are

Since 1990, we’ve grown into a global leader in personalized medicine. Today, our +5,000 energetic employees are based in +80 locations in Europe, North America, South America, Africa and Asia-Pacific and are working together to support over 200,000 customers worldwide.

From compounding and natural products to software, equipment, and genomics — we deliver smart, ready-to-use solutions that make healthcare better.

We’re passionate, science-driven, and always looking for new ways to improve lives.

Explore your future at Fagron Career Site.

About The Job

• Assist in the preparation, review, issuance, distribution, and archival of quality documents, including Standard Operating Procedures (SOPs), forms, specifications, and work instructions
• Maintain document control systems and ensure only current, approved documents are in use
• Support the review of Batch Manufacturing Records (BMRs), Batch Packaging Records (BPRs), and associated documentation for compliance
• Assist in the administration of the Quality Management System (QMS), including deviations, CAPAs, change controls, customer complaints, and non-conformance records
• Track quality events to ensure timely investigation and closure
• Support data collection and preparation of quality metrics and reports
• Perform routine GMP inspections of manufacturing, packaging, warehouse, and laboratory areas
• Report quality issues or compliance concerns to the QA Supervisor or Quality Lead
• Coordinate GMP and quality-related training records
• Monitor employee training compliance and maintain training documentation
• Assist in onboarding new employees regarding quality procedures
• Support internal audits, self-inspections, supplier audits, and regulatory inspections
• Assist in preparing audit documentation and tracking corrective actions
• Ensure quality records are readily available during inspection
• Assist with documentation for equipment qualification, process validation, cleaning validation, and computerized system validation
• Maintain validation files and ensure documentation is complete and current
• Maintain accurate and organized quality records
• Participate in continuous improvement initiatives to enhance quality systems and compliance
• Collaborate with Manufacturing, Quality Control, Warehouse, Procurement and Operations departments
  
  

Set yourself apart

You possess the following qualifications, background and abilities:

• Bachelor’s degree (Pharmacy, Chemistry, Biology, Chemical Engineering, Biochemistry and relevant fields)
• 2+ years experience is preferable
• Excellent written and verbal communication skills
• Fluent in English
  
  

What's on offer?

At Fagron, you’ll find plenty of chances to grow — both personally and professionally. We work in an open, dynamic environment where your ideas and talents can shine.

We’re proud to be an equal opportunity employer. Diversity makes us stronger, and we’re committed to creating an inclusive workplace where everyone feels welcome.

Ready for the challenge?

Take the next step and join us in shaping the future of personalized medicine. Apply today at careers.fagron.com.

Please note: we do not accept agency referrals for this position.