Project Engineer - Validation & Commissioning (Medical/Pharma)

Rise Technical Recruitment Ltd
£55000 - £57000 per annum
30 Nov 2017
08 Dec 2017
Contract Type
Full Time
Project Engineer - Validation & Commissioning (Medical/Pharma)

£55000-57000 per annum
plus holiday, excellent pension, permanent health insurance, childcare vouchers

2-3 year fixed term contract

Bedfordshire, commutable from Leighton Buzzard, Luton, Dunstable, Milton Keynes, Hemel Hempstead, Aylesbury

Are you an experienced Engineer with experience in operations, process and equipment validation looking for long term 2-3-year contract to start in the new year?

This fantastic company design, manufacture and supply packaging to household names within the Pharmaceutical sector and have an excellent reputation in their market.

This is a challenging newly created position offering a chance to make a real impact on the business. The position will be based in Bedfordshire but will have an international feel and will involve some travel.

The ideal Engineer will be involved in a new project and will provide operations, quality, and technical support to both internal and external operations. This includes Service Centre operations, process and equipment validation. A background in manufacturing, or quality audit role would be desirable as would previous experience in the pharmaceutical or medical device industry.

The role

*Working with senior engineering staff to understand potential business partners and vendors' quality management systems, capabilities, processes, and programs. Working with business partners to implement corrective actions for identified gaps and/or potential risks

*Execute test protocols at potential business partner sites and report results to ensure compliance with program requirements

*Support external business partners from initial validation and deployment, through ongoing technical and engineering service operations activities

*Provide global process and technical support for services equipment and processes. Support, train, and audit applicable test protocols and standard operating procedures (SOPs) across global service centre operations (including external business partners)

The Person

*Bachelor's degree in engineering or equivalent recognized engineering qualification with one to three years of related experience in an engineering, manufacturing, or quality audit role. Global pharmaceutical or medical device industry experience is preferred.

*Must be able to operate in a fast-paced organization, manage multiple projects simultaneously and possess strong organizational skills with the ability to meet deadlines

*Must be able to interact effectively and diplomatically with customers, vendors and employees at all levels within the company

*Ability to travel up to 50% of time both domestically and internationally as required to meet objectives

*Must be flexible with work schedules and be available to work on evenings and weekends, with or without advanced notice

This roles are for an immediate start so please send an up-to-date CV ASAP to Sarah Hibberd

Keywords : Manufacturing Engineer, Engineer, Field Engineer, Thermal Engineering, Quality Manager, Engineering, Quality

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