LSC have a requirement for a C&Q Engineer to join a leading biotech company based in Cork. For more than 25 years this company has been a global leader in the field of biomedicines, in particular pioneering monoclonal antibody technology a cutting-edge approach to producing medicines that launched a new generation of products to treat immune related diseases such as rheumatoid arthritis and plaque psoriasis.
The C&Q Engineer will be responsible for:
o Provide input into all aspects of validation i.e. from design through to the commissioning and qualification execution phases
o Participate in the design of systems and equipment to ensure that they comply with GMP requirements. o Develop validation documentation as required (e.g. specifications, plans, protocols, procedres).
o Review and approve documents prepared by the validation team, other departments and contractor organisations (e.g. commissioning test plans, impact assessments, change controls).
o Execute qualification protocols as required.
The C&Q Engineer will have:
o Minimum 3+ years experience in the Pharmaceutical Industry.
o Experience on commissioning, qualifying / verifying some of the following systems: Utilities (water for injection, clean steam, process gases, HVAC), fridges, freezers, LAF, BSC units, autoclaves and isolators
If you would like to hear more about this C&Q Engineer, then please contact Martin at LSC on 021-4777329 or apply directly through this advert.