Validation Engineer - Medical Devices -Oxford, UK - (Hybrid) (ID - 77545) Oxford, England
| Salary: | GBP45000 - GBP50000 per annum + Excellent Salary/Benefits Package |
A prestigious Medical Devices Company based in Oxfordshire, UK with major Irish connections is seeking to recruit the following post:
VALIDATION ENGINEER
JOB PURPOSE:
To manage, coordinate, execute and report on the validation of production processes, manufacturing and test equipment for active implantable medical device products.
KEY RESPONSIBILITIES:
The validation engineering role is responsible for optimizing and overseeing the production and test processes to ensure the timely and cost-effective manufacturing of products. This role involves collaboration with cross-functional teams, developing equipment, implementing process improvements, and maintaining quality and safety standards.
QUALIFICATIONS:
• 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.
REMUNERATION:
- An attractive Salary/Benefits Package on offer.
WORKING ARRANGEMENT: A hybrid working arrangement is offered with limited travel to the UK.
APPLICATION: If interested in applying for this post, please submit your CV in WORD FORMAT to:
coh@headhuntinternational.com
INFORMAL ENQUIRIES: Can be made to Christy on 00353 87 9473404
www.headhuntinternational.com
VALIDATION ENGINEER
JOB PURPOSE:
To manage, coordinate, execute and report on the validation of production processes, manufacturing and test equipment for active implantable medical device products.
KEY RESPONSIBILITIES:
The validation engineering role is responsible for optimizing and overseeing the production and test processes to ensure the timely and cost-effective manufacturing of products. This role involves collaboration with cross-functional teams, developing equipment, implementing process improvements, and maintaining quality and safety standards.
QUALIFICATIONS:
• 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.
REMUNERATION:
- An attractive Salary/Benefits Package on offer.
WORKING ARRANGEMENT: A hybrid working arrangement is offered with limited travel to the UK.
APPLICATION: If interested in applying for this post, please submit your CV in WORD FORMAT to:
coh@headhuntinternational.com
INFORMAL ENQUIRIES: Can be made to Christy on 00353 87 9473404
www.headhuntinternational.com