LSC have a great contract opportunity for a Senior Lead MES Validation Engineer to join a consulting and manufacturing services provider for the life sciences industry.
If you have 5+ years validation experience in a highly automated Life Sciences manufacturing environment and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
o Lead validation activities in the implementation of Manufacturing Execution Systems (MES) and Electronic Batch Records (EBR).
o Work closely with business management and validation departments to strategically define validation approaches and solutions that add value to clients, and to project delivery.
o Partner with business clients and multi-disciplinary Accenture delivery teams to determine appropriate validation strategy and approach for specific MES projects (including interfaces to other systems).
o Develop or provide guidance on the Validation deliverables including Quality Assurance Plans, Validation and Testing Plans, Design Documents, Test Protocols and Summary Reports, Traceability Matrix etc.
o Co-ordinate and conduct informal and formal testing of MES solutions.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
o Bachelors' degree in Science, Engineering or relatable technical degree
o Knowledge of FDA and GMP guidelines a necessity
o Working knowledge of software Development Life Cycle (SDLC) and support methodologies required.
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 Paul O'Driscoll at LSC on 021-4777329 if you have anymore questions about this Senior Lead MES Validation Engineer opportunity