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Validation Engineer

3 weeks ago

South West England, United Kingdom Hyper Recruitment Solutions Ltd Full time

We are currently looking for a Validation Engineer to join a Medical Devices company in the West of England. As the Validation Engineer you will take a lead role in validation activities for this site and you will play a significant part in supportingthe site validation program. Please note this is a 6 month contract (Strong chance of extension) and has been assessed Outside IR35.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Validation Engineer will be varied however the key duties and responsibilities are as follows:
1. Provide strategic direction on the site verification and validation plan.
2. Write and execute process and equipment validation activities. Execute full Validation lifecycle (IQ/OQ/PQ/VMP/PFMEA).
3. Support with new product validation and Computer Systems Validation (CSV).
4. The Validation Engineer will adhere to GMP and ISO13485 at all times.
ROLE REQUIREMENTS:
1. Relevant degree in a Scientific or Engineering discipline.
2. Proven industry experience in process and equipment validation within a Medical Devices setting (ISO13485).
3. A working knowledge and practical experience with CSV would be an advantage.
Key Words: Validation Engineer / Validation / IQ / OQ / PQ / VMP / Life Sciences / Medical Devices / GMP / ISO13485 / SOP's / Process Validation / Equipment Validation / Quality / CSV