Description
Optimus Search are an industry leading Recruitment Consultancy currently working with some of the world's most renowned companies.My client is a leading Medical Devices company based in Milton Keynes, together we are looking for a Validation and Verification specialist to join their team on a 6-month contract.
Ideal applicants will have a minimum 5 years' experience in a similar role.
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.
Tasks & Requirements;
As the validation and verification expert will lead and manage the activities related to Medical Drug delivery device to ensure that the final product meet the intended use. Including:
- End-to-End System Test Requirements within validation
- Review & approve supplier test plans, protocols and validation reports
- Develop and execute validation and verification protocols
- Plan and implement quality assurance and quality control for all test activities related to the validation project
- Training to software development life cycle, preferably in the medical device domain (21 CFR 820, IEC 62304, FDA software guidelines ISO 13485 and ISO 11608)
- Experience in working within a regulated medical device development environment, particularly based on the FDA Quality System Regulation and ISO 13485.
- Knowledge of Medical drug delivery device with embedded software in validation