Pharma Document Reviewer (Pharmaceutical Laboratory Experience is required)

📋 Description

• Document review and compliance in QC records
• Verify results entered into LIMS
• Audit records, calibration docs, and QC documents
• Review method development records per SGS SOPs
• Ensure test results reported on CofA or RofA as appropriate
• Support training and process improvements

🎯 Requirements

• Bachelor of Science in Chemistry or Microbiology; MSc preferred
• Minimum 5 years in a pharmaceutical lab
• Understanding of cGMP; USP knowledge required, EP preferred
• Experience with TrackWise Digital or other QMS
• Experience with LIMS and instrument software (e.g., Empower)
• Proficiency in MS Office

🎁 Benefits

• English communication skills required
• Strong project management and time management abilities
• Detail-oriented with ability to identify discrepancies
• Willingness to learn new tests and instruments
• Compliance with SGS quality, safety, and HR policies