LSC have a great contract opportunity for a Validation Engineer to join a global Biopharmaceutical company in Carlow.
If you have prior related work experience; ideally in manufacturing, preferably GMP setting and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT – KEY RESPONSIBILITIES:
o Serve as technical and/or validation support as required for manufacturing and new product introduction.
o Design/Author/Review/Approve/Execute process development studies in support of new product introduction and ongoing manufacturing support.
o Provide technical input into quality notification by authoring/reviewing/approving investigations.
o Execution of equipment commissioning and qualification programs
o Execution of equipment/qualification validation programs; including re-qualification and revalidation
o Design/Author/Review/Approve/Execute qualification/validation documentation and studies in line with the standard approval process
o Perform data analysis and make informed decisions/recommendations around conclusions reached from data analysis Support continuous improvement through Lean Six Sigma methodologies.
ABOUT YOU – ARE YOUR SKILLS A MATCH?
o Bachelor’s Degree or higher preferred; ideally in a Science, Engineering or other Technical discipline
o Relevant experience and a particular skill set in their area of expertise that adds value to the business; ideally in a manufacturing, preferably in a GMP setting
o SME in multiple aspects of aseptic processing.
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!