Your new company

Your new role

• Batch Record Review & material release to ensure compliance with GMP requirements.
• Carries out tasks related to the administration of event management systems, including Review & Approval of review, Deviations, and customer complaints.
• Compiles Annual Product Reviews.
• Supports all validation activities on site as described in the Site Validation Master Plan.
• Approves and compiles appropriate validation protocols and reports (analytical, cleaning, computer, process, equipment, etc.).

What you'll need to succeed

• Bachelor’s Degree in a scientific/technical discipline required
• A minimum of 3–5 years’ experience in a quality, validation or compliance role within the biological and/or pharmaceutical industry.
• Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals. The ability to apply GMP regulations and other FDA and international guidelines to all aspects of the position.

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.