Job Description
Quality Control Specialist (hybrid) is an exciting opportunity with an award-winning Pharmaceutical organization. This position supports New Material Introduction process, associated supplier changes, and external testing laboratories ensuring effective interaction with other departments and teams. Responsibilities include:
Work as directed by the Quality Control Manager according to Company safety policies, cGMP and cGLP
Facilitate communication to ensure success through representation of QC team on tier meetings
Support all aspects of New Material Introduction process ensuring effective interaction with other departments, global teams, and external contract testing labs
Participate in Internal/External Investigations
Coordinate the creation/update to Quality standards for raw materials and components
Complete impact assessments for change controls related to Carlow processes
Provide support with audit/inspection requirements to ensure department compliance/readiness
Participate in internal and external audits and inspections
Coordination, ownership, and author as required for Annual Product Review
Requirements:
Bachelors Degree or higher in a science related discipline
2-4 years of experience in a cGMP laboratory environment
Knowledge of or previous experience in New Material Introduction process
Strong quality control and GMP knowledge
We're an award-winning Pharmaceutical organization based in Carlow, and we're looking for a Quality Control Specialist to join our team.