1 to 2 of 2 Permanent Validation Engineer Jobs in Hertfordshire

Senior Verification & Validation Engineer Cambridgeshire £40k - £55k (dep on exp) + bonus and excellent benefits! A fantastic opportunity for a Senior Verification & Validation Engineer has arisen at a Cambridge based cutting edge leading medical device development company whose innovative technology is reshaping the medical, life science … and diagnostics sectors! You will be leading the verification and validation activities for this groundbreaking and market disruptive point-of-care diagnostics device! As the Senior Verification & Validation Engineer, you will use your previous experience in product development within a regulated environment to draft V&V protocols … of this product, you will need to adhere to the requirements of medical device regulations – ISO 13485/FDA environments. As the Senior Verification & Validation Engineer, your responsibilities will include: Lead the planning of verification activities for the system, including both the Instrument and test consumable. Ensure tests more »

of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants are working on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across Belgium, Switzerland, Germany, Denmark France, and Canada. Thanks to our excellent team, we support manufacturers in all stages … a stimulating environment, with a lot of opportunities for your professional and personal development. Job Summary We are seeking an experienced Commissioning, Qualification, and Validation (CQV) Engineer to join our team. The CQV Engineer will play a crucial role in ensuring that all systems and equipment are … qualified, and validated according to industry standards and regulatory requirements. Responsibilities Lead CQV activities for pharmaceutical manufacturing projects. Develop and execute commissioning, qualification, and validation protocols. Ensure compliance with industry regulations and standards, such as cGMP and FDA guidelines. Collaborate with cross-functional teams to ensure the successful implementation more »