Job Title

Medical Devices Validation Engineer – Galway

The Role

  • Medical Devices Validation Engineer
  • Galway
  • Onsite role
  • Permanent or Contractor Role

Role Brief

The successful candidate will work across a range of medical devices projects, liaising with various departments, giving guidance, reviewing documentation and ensuring the company validation policies & procedures are being adhered to.

The role will be part of and support a large team focusing on a specific medical device and be tasked with ensuring all assigned validation responsibilities are carried out in line with the site validation master plan and regulations.

Skills Brief

  • Medical devices validation experience and knowledge of EUMDR regulations would be an advantage but is not essential. Validation experience in Pharma, Biotech or Life Sciences will be considered
  • Validation experience in another regulated manufacturing environment may also be considered
  • Coordinating the preparation, review & approval of the Validation tasks assigned by the Validation Lead
  • Coordinating the preparation, review & issuing of Validation protocols & reports
  • Preparing & coordinating validation documentation (risk assessments, traceability matrices, validation reports)
  • Contributing to team and site projects and initiatives as required
  • Contributing to continuous improvement activities with the validation team

Person Brief

Candidates must have a relevant science or engineering tertiary qualification with ideally 1 or more years’ experience in the medical devices industry.

Pharmaceutical, biotech or life sciences industry experience in Equipment & Process Validation will also be very positively considered.

A candidate with experience in a regulated manufacturing environment but with no GMP environment experience can also be considered with the right profile and attitude.

The ideal candidate will have excellent collaboration and communication skills, with a demonstrated understanding of manufacturing processes and related process equipment. In addition to this, strong attention to detail and an excellent understanding of validation concepts and documentation is required.

The role will be based in Galway and onsite. You should be living within a reasonable commute of the Galway area and be available to be onsite daily.

Opportunity Brief

This is an excellent opportunity to work with clients who are global leaders in their field, helping to develop and improve upon industry leading technology solutions. SL Controls offers a supportive environment committed to employee development and wellness, along with a competitive and rounded compensation and benefits package, which rewards high performers.

Company Brief

SL Controls are experts in the area of Equipment System Integration and System Support. We specialise in assisting our customers, including many of the world’s top multinational companies in the medical device and pharmaceutical sectors, achieve their Six Sigma and OEE targets.

Over the past 20 years we have grown our business from a Sligo based enterprise into an international business with additional offices in Galway, Limerick, Leinster and Florida USA.

We pride ourselves on our expertise in industrial IT integration and regulatory compliance in support of global end users, OEM’s and Technology providers.

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