Validation Engineer – Medical Devices -Oxford, UK – (Hybrid)

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