LSC have a great contract opportunity for a Validation Lead 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:
- Coordinates and supervises all validation activities.
- Approves validation planning documents detailing overall strategy for the project.
- Develops and approves the master list of validation test documents and activities.
- Reviews and approves all C&Q summary reports and validation summary reports.
- Ensures all Validation Engineers who perform validation activities have relevant training assigned.
- Assist in the development of User Requirement Specifications (URS's) and Quality Risk Assessment for Equipment and Automated Systems (QRAES).
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- BS degree with 7+ years of experience in Validation, Engineering, Microbiology or Quality.
- Extensive knowledge and demonstrated experience managing validation activities for Pharmaceutical/Biotechnology projects.
- Experience of sterile/biotech equipment within the pharmaceutical industry is preferred.
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 Kathy Gillen on 021 4777329 if you have anymore questions about this role!
