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Computer systems Validation Engineer 6675

Ref: 117 Date Posted: Tuesday 22 Aug 2017
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Job Title               Computer Systems Validation Engineer

Employer              Medical Technology Business

Job Type               Contract

Location               Inverness

Salary                  Competitive

Consultant          Gabrielle

Contact                0161 2600 193

                                Gabrielle@medicalengineers.co.uk

Job Description:

Our clients Manufacturing Business Centre plays a key role in the development and manufacture of new, sophisticated medical and industrial products. Working with colleagues in Europe, the USA and Japan, our multi-disciplinary team of R&D engineers is fully equipped with the latest computer-aided design and modelling technologies, to enable them to develop medical workstations and fluid management products & accessories, and industrial Remote Visual Inspection devices.
Producing world class products in terms of Quality, Cost and Delivery isn't just desirable, it's essential. Therefore, in today's fast moving, ever changing world, we continue to invest in both our people and the latest equipment and processes to remain at the forefront in manufacturing technology.

 

 

 

Your Responsibilities:

  • Provide support on validation activities especially computerised systems including training/awareness support in current computer/computerised systems regulations that must be adhered to, to achieve and maintain compliance in a timely manner.
  • Organise lead validation working parties associated with computerised systems and provide timely validation support to identified stakeholders. 
  • Motivating and influencing validation working parties through effective communication to ensure validation is carried out in a compliant and timely manner. 
  • Generate and/or perform reviews of validation deliverables in accordance with local and global established processes. 
  • Provide validation periodic review support to the business in all aspects of system development lifecycle processes. 

 

Requirements:

  • in depth knowledge of medical device or pharmaceutical industry regulations.
  •  Minimum of 3 year’s experience working in a regulated industry carrying out verification & validation activities. 
  • Knowledge of bespoke software and/or hardware build, testing, documentation and deployment as part of software and/or system development lifecycle.
  • Knowledge of document and change management process.
  • Working knowledge and application of risk management tools e.g. FMEA, FTA or SRA.
  • Proactive problem resolution. 

Self-directed; ability to work with minimal supervision as part 

Specialists in consultancy


At Medical Engineers we have a range of technical consulting jobs in the medical engineering industry throughout the UK. Requiring a broad range of technical and management skills and most importantly the ability to communicate effectively. Consultancy roles require candidates with unique abilities. Roles vary in length of contract depending on clients’ requirements.

Our degree qualified consultants have specialist knowledge of the UK medical engineering consultancy job market. We have a successful track record in finding the best candidates for our clients who know and trust Medical Engineers to understand their business requirements.

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