Temp - Associate QC Compliance Specialist
Core
Support quality, compliance, and continuous improvement activities across QC laboratories (Chemistry, Bioassay, Microbiology, Virology) in a GMP-regulated environment.
Role type
Associate QC Compliance Specialist
Builds
Quality control operations and compliance processes for life-changing medicines
Domain
Pharmaceutical manufacturing / Quality Control
Deliverable
dashboards & analysis
Required skills
Laboratory investigation, deviation management, non-conformance handling, root cause analysis, CAPA implementation, trend identification, GMP compliance, report writing, cross-functional collaboration
Preferred skills
Experience with investigations, deviations, CAPAs, and root cause analysis in cGMP environment
Responsibilities
Lead and support laboratory investigations, deviations, and non-conformance activities; Write and review investigation reports and associated quality documentation; Perform root cause analysis and partner with teams to identify effective CAPAs; Support the timely implementation and monitoring of corrective and preventative actions; Identify recurring trends and recommend process improvements to strengthen Quality Control operations
Seniority
Associate Specialist, entry-level to mid-level IC