MidContractENAsia/Pacific
Document QC Specialist – Summary
This is a junior-level Quality control role in a pharmaceutical / biotech / healthcare organization, focused on checking and managing regulated documents.
What you’ll do
• Review documents (SOPs, batch records, clinical reports) for accuracy and compliance
• Ensure proper formatting, version control, and standards
• Manage documents in a document system (upload, track approvals)
• Identify errors and flag issues
• Support documents for regulatory submissions
• Keep documentation audit-ready
Who it’s for
• Freshers or up to 2 years experience
• Background in Life Sciences / Pharmacy / Chemistry / Healthcare-related fields
• Basic knowledge of GxP (GMP/GCP/GLP)
• Strong attention to detail
