LSC have a great contract opportunity for QA External Specialist to join a biopharmaceutical company in Dublin focused on serving patients with severe and ultra-rare disorders through the innovation, development, and commercialization of life-transforming therapeutic products
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- The Specialist for Drug Substance/Drug Product Manufacturing will be responsible, with management support, for providing oversight of quality activities associated with drug product manufacturing processes to contract manufacturing organisations.
- The Specialist contributes and guides completion of milestones associated with specific projects and supports ongoing quality assurance responsibilities in support of: Contract Manufacturing oversight and quality systems including Change Control, Deviations, and CAPAs.
- Performs all responsibilities in accordance with company policies, procedures, and federal regulations.
- The incumbent will be responsible for supporting Alexion drug product manufacturing and assessing the compliance of this program against best industry practice and current regulatory expectations.
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!
Apply via this advert or contact Gráinne Hodnett at LSC on 021-4777329 if you have any more questions about this role!