LSC have a great contract opportunity for a Quality Control Specialist to a leading biotech company based in Dublin.
If you have Minimum 5 years of relevant post-degree or work experience in GMP Manufacturing and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Participates as the quality member on cross functional projects
- Responsible for review/approval of new and updated Master Batch Records / Electronic Batch Records
- Reviews executed production documentation such as electronic batch records and logbooks to ensure accuracy and compliance with cGMPs and company procedures and ensures completion of proper remediation of errors
- Provides presence on the shop floor to support compliance and data integrity
- Review & approve new and updated SOPs/ Work Instructions and Controlled Job Aides
- Actively participates in the Tier process and use this forum to make concerns visible and to partner with the functional area on resolution
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Evidence of leadership skills coupled with good oral and written communication skills
- Understanding of cGMPs and of regulatory requirements as they apply to the pharmaceutical field or a related area
- Demonstrated interpersonal skills including flexibility, collaboration and inclusion skills and ability to work in a team environment
Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!
Call in Cathal Rourke at LSC on 021 4777 329 to discuss this new role in detail or apply directly via this advert
