Pharma Document Reviewer (Pharmaceutical Laboratory Experience is required)

📋 Description

• Document review and compliance with methods, specifications and SGS SOPs.
• Verify that records are complete and data entered into LIMS.
• Ensure validation/transfer/verification records align with client or SGS methods; review method
• Report test results on CofA or RofA depending on method status.
• Audit logbooks, calibration documents, and other QC records for approval and accuracy.
• Maintain training records and ensure binder currency according to training SOP.

🎯 Requirements

• Bachelor of Science in Chemistry or Microbiology (M.Sc preferred).
• Minimum 5 years of experience in a pharmaceutical laboratory or related company.
• Strong knowledge of cGMP and reference to compendia (USP required, EP preferred).
• Experience with TrackWise Digital or other QMS systems; familiarity with LIMS and instrument
• Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
• Good English communication and ability to manage multiple projects.

🎁 Benefits

• Hybrid work arrangement may apply depending on affiliate country; onsite for 2 to 6 months.
• Opportunity to engage in quality improvement initiatives and professional development.
• Join a global leader in testing, inspection and certification with a network of offices and labs.