Product Development Validation Engineer

Recruiter
Quality Start
Location
Watford
Posted
14 Apr 2018
Closes
14 May 2018
Sector
Engineering
Contract Type
Permanent
Hours
Full Time

Product Development Validation Engineer – Hertfordshire

Opportunity:

Are you currently working within the medical device industry? Does your experience include new product development as well as process development and optimisation of manufacturing equipment? Want to work for a global medical device manufacturing company? If yes then please read on.

Your role as a Product Development Validation Engineer based in Hertfordshire will involve developing new and existing medical device products, product enhancements and the introduction of product line extensions into manufacturing.

Duties and responsibilities include:

  • Designing and executing product development trials utilising design of experiment (DoE) principles.
  • Developing experiments and methods based on statistical techniques to support innovation projects.
  • Conducting pilot plant trials to support of new product development (NPD).
  • Performing and writing validations of product, processes and equipment in accordance with FDA and ISO guidelines.
  • Designing and process evaluations including development of material and product specifications, test methods and risk analysis (e.g. DFMEA, PFMEA).
  • Identifying and introducing suitable test and inspection methods using appropriate equipment and gauging and benchmark against best practice and relevant standards including measurement system analysis and calibration control.
  • Continuous improvement using DFSS, EMS, Kaizen, Lean and Six Sigma problem solving.

This is a full time permanent role with a great salary of £40,000 - £45,000 per annum and excellent benefits including Life insurance, Pension, Childcare Vouchers, 25 days holiday plus bank holidays on top, Employee share purchase plan and much more.

Skills:

To apply for the Product Development Validation Engineer role you will have the following:

  • Significant level of project engineering or project management experience gained within a medical device GMP development environment.
  • Experience of validation life cycle – equipment and process.
  • Experience in Lean, Six Sigma and DFSS.

How to Apply:

To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat.

My contact details are:

Miss Rashida Khan

0113 225 1547

If this sounds like the role for you or a colleague then please don’t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information.

For a list of our current vacancies, please visit www.qualitystart.co.uk

If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role.

Quality Start are acting as a specialist recruitment consultancy for this role.


This job was originally posted as www.totaljobs.com/job/80959842

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