Position: Quality & Validation Specialist Plasma Operations
Duration: 6 Months
Start date: End of September (ideally)
Rate: 60 per hour (Inside IR35)
Location: Liverpool/ Merseyside
CPL Life Sciences is currently partnered with one of the large Pharmaceutical Companies based in Merseyside, and they are on the lookout for an experienced Quality & Validation Specialist, with experience in the Pharmaceutical Industry.
Conducts a compliant validation process for quality information technology systems which requires formal validation documentation (including standard operating procedures) under appropriate government regulations.
Coordinates activities with clients, programmers/developers and operating personnel, domestic and, as appropriate, global.
Identifies current and anticipated requirements for compliant computerized operations and suggests methods for the identification, implementation and maintenance of the procedures, actions and documentation necessary to assure compliance according to the appropriate federal and international regulations which govern the user's applications.
Reports on the status of validation activities to fulfil regulatory requirements.
Keeps abreast of changing federal and international regulatory requirements, government audit policies, and the availability of current techniques. May perform system administration and configuration of quality information technology systems.
If you think that you are suitable for this position then please either apply through this advert, or email your CV to Daniel.firstname.lastname@example.org
- Agency: Cpl Life Sciences
- Contact: Daniel Mooney
- Reference: JO-2108-474472
Website: Cpl Life Sciences
- Posted: 15th September 2021
- Expires: 13th October 2021