LSC have a great contract opportunity for a Quality Specialist to join a leading biotech company based in Dublin.
If you have 3 years of experience and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Provide direct Quality support to production and support areas.
- Provides presence on the shop floor to support compliance and data integrity.
- Review and approve executed production documentation such as electronic batch records and logbooks to ensure accuracy and compliance with cGMPs.
- QA support, review and approval of C&Q, Performance qualification (PQ) & Process Validation documents.
- Support sustaining activities such as change management, deviations, CAPAs, equipment requalification, periodic review, site maintenance & Calibration Programs.
- Provides support to internal audits and regulatory inspections.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Bachelor degree, in a scientific or engineering field
- 3 years of relevant post-degree experience in a GMP environment: manufacturing, laboratory, quality, operations, technical, or regulatory function.
- Lean Six-sigma and problem-solving tools
- MES experience desirable
For our contracting positions in Ireland's pharmaceutical industry, applicants must possess a Stamp 1G or a Stamp 4 visa. We apologize for any inconvenience, as visa sponsorship is not available currently.
Apply via this advert or contact Grainne Hodnett on 021 4777 329 if you have any more questions about this opportunity!
