Role details

Validation Engineer

Blackpool   •  Permanent

Bullet points

  • Validation Engineer - Medical Devices, Regulatory Industry
  • Blackpool

About Our Client

Our client is a well-known household organisation that supply a variety of products globally. This North West site focuses predominately on Medical Devices.

Job Description

For the role of Validation Engineer, reporting to the Quality Manager, based in Blackpool you will responsible for but not limited to the following:

  • On site training for new starters
  • Chair the Validation Steering Committee
  • Support all validation activities on site
  • Active Leadership in site validation activities
  • Supporting validation activities through reviewing and approving all validation
  • Review of periodic validation

The Successful Applicant

To be considered for the role of Validation Engineer, based in Blackpool you must be able to demonstrate the following:

  • Preferably educated to degree level within Engineering/Science/Quality
  • Previous experience working in quality, technical or manufacturing roles in a regulated industry.
  • In depth knowledge of Quality, Compliance and Validation, with ISO 9000, ISO 13485, FDA QSRs.
  • Being a proficient user with Quality toolbox including FMEA, Root cause investigations Lean and Six Sigma tools & techniques.
  • Organised and able own a number of projects and activities.
  • Good time management and good interpersonal skills
  • Positive attidute and professional approach at all times.

What's on Offer

£Competitive + benefits

Apply for this job

Click the Apply or LinkedIn button below or contact Nicole Nielsen on +44 161 829 0433 quoting job reference 13723762
As you are using an Apple iOS device we are unable to offer you the CV upload function. Please apply with your Linkedin profile below or contact Nicole Nielsen on +44 161 829 0433 quoting job reference 13723762