Quality Control Specialist (hybrid)
Job Code: RK22140
Duration: 11 Months
Location: Carlow
We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Carlow. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
Position Overview:
This position will support all aspects of New Material Introduction process and associated supplier changes ensuring effective interaction with other departments/global teams on matters related to new material introduction and associated qualification as well as support selection and management of external testing Laboratories ensuring all outsourced methods are validated and suitable for the product/material required.
Duties:
1. Work as directed by the Quality Control Manager according to Company safety policies, cGMP and cGLP.
2. Facilitate and drive effective communication to ensure success through representation of QC team on tier meetings.
3. Support all aspects of New Material Introduction process ensuring effective interaction with other departments/global teams/external contract testing labs on matters related to new material introduction, supplier changes and associated qualification.
4. Participate and support Internal/External Investigations.
5. Coordinate the creation/update to Quality standards for raw materials and components at Carlow. Complete impact assessments for change controls related to Carlow processes.
6. Coordinate any efficiency/increased Lab capability projects as detailed by Quality Control Manager.
7. Provide support with audit/inspection requirements to ensure department compliance/readiness. Participate in internal and external audits and inspections, taking the role of auditee for assigned areas of responsibility.
8. Coordination, ownership, and author as required for Annual Product Review.
9. Participate in Quality Risk Management.
Education and Experience:
1. Bachelor’s Degree or higher preferred; ideally in a science related discipline.
2. 2-4 years of experience in a cGMP laboratory environment.
3. Knowledge of or previous experience in New Material Introduction process.
If interested in this posting please feel free to contact Rachel Kent on +353 (0)87 427 8808 or rachel.kent@lifescience.ie for further information.
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