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Validation Engineer - R&D - Scotland

This job is no longer available

Employer
Paramount Recruitment
Posted
Friday, August 10, 2012
Closes
Friday, September 07, 2012
Ref
VENG12
Contact
Ekta Multani
Location
Scotland
Contract Type
Permanent
Hours
Salary
Negotiable

Further information


Validation Engineer - Medical Devices - Scotland


An innovative Medical Devices company in Scotland is on the lookout for a Validation Engineer to join their rapidly expanding team. This global organisation develops health care products. This Quality and Validation Engineering team works to ISO 13485 regulations and develop and implement Master Validation plans along with R&D activities.


As a Validation Engineer, you will be a responsible for product issues including process improvement activities, assist in complying and review process design specification, Ensure validation efforts are conducted in an appropriate and timely manner. , complete internal audits per the audit schedule engineer support and technical writing Protocols. The successful candidate will also ensure that all investigation and handling customer complaints are adhered to correctly, Ability to work within a regulated environment along with other tasks as necessary.


The ideal applicant will have experience in Engineering, Medical Devices or a regulatory industry experience. You will also be expected to have a good working knowledge of CAPA systems. In Addition, you will be working as a part as a team to identify potential problems using the correct tools and procedures where necessary. They looking for someone to come in and be a good communicator and a great influencer to the team providing solutions along with strengthening a team. It is essential that you have a degree within an engineering/Science discipline.


If successful, you will be rewarded with a generous salary, excellent benefits package, including healthcare and a company pension scheme, Life Assurance.
If you have the drive and enthusiasm to be a part of this exciting opportunity, please contact Ekta Multani, Recruitment Consultant at Paramount Recruitment 0121 616 3474.


Keywords: Regulatory Affairs, Quality Assurance, Medical Devices, ISO 9001, ISO 13485, Quality Systems, Ireland, CAPA, Medical Device Directive, Audit Design, 21 CFR part 820, Quality Control, Management, Six Sigma, LEAN, GMP, PFMEA, Quality Engineering Manager, Validation, Engineer, FDA, New Product Development, R&D
Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities.

Paramount Recruitment


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