LSC have a great contract opportunity for a Validation Engineer to join a multinational medical device company based in Cork. The Cork facility is a global centre for product development, manufacturing and supply chain.
If you have minimum 5 years post qualification experience as a Validation Engineer within a medical device, pharmaceutical, or similar regulated industry and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT – KEY RESPONSIBILITIES:
o Responsible for ensuring conformance with current equipment, process, and systems validation regulations
o Responsible for determining the implications of validations upon; Product Quality, Patient Safety, and Data Integrity.
o Responsible for completing gauge R&R qualifications.
o Participate in Worldwide equipment, process, and software development
o Responsible for determining and implementing control measures to reduce the occurrence and possible impact of failures.
o Responsible for determining process inputs and factors for variation where process capability is required.
ABOUT YOU – ARE YOUR SKILLS A MATCH?
o Degree level qualification in Engineering or Equivalent.
o Minimum 5 years post qualification experience as a Validation Engineer within a medical device, pharmaceutical, or similar regulated industry.
o Experience in aspects of QA, validation and ISO 13485.
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 Martin Taggart at LSC on 021-47777329 if you have more questions about this Validation Engineer opportunity!