QA Manufacturing Specialist, Visp e/v/e/r/y/o/n/e
Core
QA Manufacturing Specialist ensuring GMP compliance on the pharmaceutical manufacturing shop floor.
Role type
QA Manufacturing Specialist
Builds
Injectable treatments for patients
Domain
Pharmaceutical manufacturing
Required skills
GMP knowledge, aseptic process understanding, deviation management, batch record review, environmental monitoring, root cause analysis, coaching
Preferred skills
Communication, decision-making in fast-paced settings
Technologies
GMP documentation systems, environmental monitoring tools
Responsibilities
Perform on-the-floor quality assurance support during manufacturing and cleaning; Witness and verify critical process steps and in-process controls; Review and document line clearances; Identify and report deviations; Support investigations and CAPAs; Conduct routine compliance checks and audits; Provide on-the-job coaching to operators.
Seniority
Mid-level, hands-on IC
