LSC have a great contract opportunity for a Validation Lead Engineer 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 project for you!
Duties & 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 the Validation schedule is developed and maintained.
Experience and Qualifications:
- 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.
- Demonstrated strong Communication and Leadership skills.
- Demonstrated ability to collaborate with senior stakeholders to achieve optimal outcomes.
- Experience with AVS (Airflow Visualization) Studies.
Applicants interested in our contracting opportunities within the pharmaceutical sector in Ireland are required to have a Stamp 1G or a Stamp 4 visa. Please note that we are unable to provide visa sponsorship. Thank you for your understanding.
Apply via this advert or contact Siobhan Cummins on 021 4777 329 if you have any more questions about this opportunity!
