LSC have a great contract opportunity for a Senior QC Specialist to join a South Dublin based Biopharmaceutical company that specialises in secondary manufacturing activities such as Formulation, Fill Finish and Packaging.
If you have at least 5 years in a cGMP regulated environment and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT – KEY RESPONSIBILITIES:
o QC Representative for site / laboratory upgrade projects
o Plan and manage QC related activities from site projects.
o QC Representative for NPI activities and routine Product meetings
o Plan and Perform non-core testing related to NPI activities
o Manage all sample management activities related to NPI activities throughout the site Sample shipments and temperature monitoring activities for NPI activities
o Create/own and approve protocols, sample plans, SOP and documentation related to NPI
o Responsible for their own training and safety compliance.
o Assist with resource management, QC Project Management and other work streams as required by the lab management.
o Authoring, executing and documenting the qualification of existing laboratory equipment in a cGMP regulated environment. Writing equipment validation protocols and associated summary reports.
ABOUT YOU – ARE YOUR SKILLS A MATCH?
o NPI and Method Transfer experience is a must
o Routine testing background with the technical know how, moved into project NPI/Method transfer roles
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!
To apply, submit your CV via this advert or contact Aaron Kingston at LSC on 021-4777329 if you have anymore questions about this Senior QC Specialist opportunity!