CK Group are recruiting for a Quality Engineer to join a company in the pharmaceutical industry on a contract basis for 12 months.
Salary:
£25.98 ph PAYE or £18.79 - £29.12 ph UMB
Quality Engineer Role:
Lead design control and risk management activities for combination product development programs
Support and facilitation of effective risk management activities at external design companies and manufacturing facilities related to assigned projects
Ensure combination product development activities are compliant with quality and regulatory standards, both internal and external
Support device design and manufacturing investigations from devices used in clinical trials and commercial manufacture
Support the generation of all regulatory submission data and content for assigned device projects
Your Background:
Hold a relevant scientific or engineering degree, or have equivalent working experience
History of working in accordance with the requirements of ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation
Familiar with Human Factors Engineering - Usability Engineering
Familiar with device assembling manufacturing processes
Experience in design controls for combination products
Company:
Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year.
Location:
This role is based at our clients site in Cambridge. This is a hybrid role with 50% home working.
Apply:
For more information, or to apply for this Quality Engineer please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only).
It is essential that applicants hold entitlement to work in the UK
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
INDKA