LSC have a great contract opportunity for a Validation Engineer to join a global Biopharmaceutical company in Cork. The facility specialises in the fermentation, purification and sterile filling of biotech products, as well as supporting product development and clinical trials.
If you have minimum 6 years experience in a regulated manufacturing environment and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT – KEY RESPONSIBILITIES:
o Ensure highest Quality, Compliance and Safety standards are adhered to.
o Protocol/report authoring/execution/oversight/approval as appropriate
o Recommend technical approaches in line with global and local standards.
o Ensure supply of high quality product through ensuring equipment availability; maximize team member performance through continuous process improvement initiatives.
o Benchmark and remain current with development of new technologies in the vaccine and biopharmaceutical processing field of expertise and seek to deploy process improvements through innovation and utilization of these technological advances.
ABOUT YOU – ARE YOUR SKILLS A MATCH?
o Hon. Degree or Masters in a Science or Engineering discipline
o Demonstrated knowledge in validation and other pharmaceutical or Biopharmaceutical operations (e.g. manufacturing, technology, engineering, quality, analytical)
o Previous experience of delivering technical/validation projects
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 Kathy Gillen at LSC on 021-4777329 if you have anymore questions about this Validation Engineer opportunity!