LSC have a great contract opportunity for a QA Technical Support Specialist to join a South Dublin based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging.
If you have 7 years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Accountable for Quality oversight of processes and procedures related to Packaging, inspection Process Development, Validation, Engineering, Facilities/Utilities.
- Quality review and approval of Validation and qualification documentation and SOPs to support site validation activities:
Review of DS & QRAES documents - Review of validation Plans, Protocols, IOQ, PQ and associated validation documents
- Review of executed validation documents and reports
- Quality review and approval of Validation and qualification documentation and SOPs to support site validation activities:
- Perform all activities in compliance with safety standards and SOPs
- Be involved in all Validation Cross Functional Teams (CFTs) at the site to ensure adherence to required policies and procedures.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- University degree. Science or Engineering related discipline preferred.
- Relevant experience (7 yrs +) working in the pharmaceutical or biotechnology industry as a Subject Matter Expert providing quality direction of introduction of automation / IS projects
- Ability to work independently and remotely with minimum direct supervision.
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 Siobhan Cummins on 021 4777329 if you have anymore questions about this role!
