Validation Engineer Medical Devices UK, Oxford (Hybrid) (77545 N2711) Oxford, England
| Salary: | GBP45000 - GBP50000 per annum + Excellent Salary/Benefits Package |
Validation Engineer - Medical Devices -Oxford, UK - (Hybrid) (Temporary/Permanent Post)
Excellent Post in a Prestigious Medical Devices Company
A prestigious Medical Devices Company based in Oxford, UK with major Irish connections is seeking to recruit the following post:
Validation Engineer (Hybrid)
Job Purpose:
To manage, coordinate, execute and report on the validation of production processes, manufacturing and test equipment for active implantable medical device products.
Eligibility:
• Degree qualification or higher in technical engineering or science discipline
• Familiar with validation requirements in a regulated industry such as Medtec, pharma, etc.
• Familiar with quality systems such as ISO13485 or FDA QSR
• Six Sigma Green Belt or Similar
• Experience in the development and execution of validation protocols and reports including
associated test method validations.
• Participated in risk management activities such as PFMEA or DFMEA and have experience with
the impact of risk management on validation strategies.
Renumeration: Excellent Salary on offer (Negotiable)
Interested please email CV for immediate interview to:
coh@headhuntinternational.com
Alternatively, if you have a colleague who may interested and suitable, we are more than happy to consider
If interested please email CV to: sh@headhuntinternational.com
Or call 00353 87 947 3404 Christy - Ireland: 087 9473404
Excellent Post in a Prestigious Medical Devices Company
A prestigious Medical Devices Company based in Oxford, UK with major Irish connections is seeking to recruit the following post:
Validation Engineer (Hybrid)
Job Purpose:
To manage, coordinate, execute and report on the validation of production processes, manufacturing and test equipment for active implantable medical device products.
Eligibility:
• Degree qualification or higher in technical engineering or science discipline
• Familiar with validation requirements in a regulated industry such as Medtec, pharma, etc.
• Familiar with quality systems such as ISO13485 or FDA QSR
• Six Sigma Green Belt or Similar
• Experience in the development and execution of validation protocols and reports including
associated test method validations.
• Participated in risk management activities such as PFMEA or DFMEA and have experience with
the impact of risk management on validation strategies.
Renumeration: Excellent Salary on offer (Negotiable)
Interested please email CV for immediate interview to:
coh@headhuntinternational.com
Alternatively, if you have a colleague who may interested and suitable, we are more than happy to consider
If interested please email CV to: sh@headhuntinternational.com
Or call 00353 87 947 3404 Christy - Ireland: 087 9473404