Biotech Document Reviewer (1 Year Contract)
Core
Reviewing QC records, validation reports, and OOS/deviation documentation to ensure compliance with SOPs and client protocols in a pharmaceutical laboratory.
Role type
QC Document Reviewer
Builds
Validated QC records and compliance reports for pharmaceutical clients
Domain
Pharmaceutical Quality Control / Regulatory Compliance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Chemistry/Biochemistry/Biology/Microbiology knowledge, LIMS data entry, audit trail verification, SOP adherence, OOS/deviation closure, calibration document auditing, KPI trending
Preferred skills
Experience with SGS SOPs, method transfer verification
Technologies
LIMS
Responsibilities
Review QC records against methods and SOPs, identify areas for SOP/method improvement, close OOS and deviations before QA release, audit calibration and QC documents, input data for departmental KPIs
Seniority
Mid-level, hands-on IC