Description
Optimus Search are an industry leading Recruitment Consultancy currently working with some of the world's most renown companies.My client is a leading Medical Device company based in Livingston, together we are looking for a Validation Engineer to join their team on a 6-month contract.
My client would like to interview candidates for this role immediately. If you are interested in finding out more about this role, then please send your CV over to , and we can arrange a time to talk in more detail.
Validation Engineer required to support key engineering projects at the manufacturing facility in Livingston.
Main duties include:
* Creation and processing of validation documentation including:
o Manufacturing Equipment Installation Qualifications (IQ's)
o Equipment and process Operational Qualifications (OQ's)
o Equipment and Process Performance Qualifications (PQ's)
o Computer System Validation (CSV) IQ/OQ's
o CSV Test Scripts
* Protocol & Report writing
* Technical Documentation
* Processing Protocols/report through the Quality System Lifecycle management system (ADAPTIV)
* Creation of manufacturing and Risk management Documents (Work Instructions, pFMEA's)
* Creation and updating of Project status using relevant Microsoft tools.
- Candidates should have excellent communication skills - both verbal and written.
- Must have strong computer skills in order to interact with Validation System (ADAPTIV) and be fluent in Microsoft applications i.e. Word/Excel/Powerpoint/Project.
- Experience of working in a regulated industry such as the Medical Device, Pharmaceutical industries preferred but not essential.
- Experience of working to Quality Systems Requirements are essential.
Ability to work on their own initiative and be flexible in order to meet strict deadlines is essential. - Experience in a Manufacturing environment preferred but not essential.