Research and Development Technical Specialist in York

Research and Development Technical Specialist in York

York Full-Time 30000 - 40000 Β£ / year (est.) No working from home possible
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At a Glance

  • Tasks: Lead technical investigations and coordinate product improvements in medical devices.
  • Company: GBUK, a leading medical device manufacturer making a real difference in patient care.
  • Benefits: Collaborative team culture, professional development, and the chance to impact lives.
  • Other info: Opportunity for career growth and working with experienced professionals.
  • Why this job: Join us to innovate and improve healthcare solutions that truly matter.
  • Qualifications: Experience in technical, quality or R&D roles; strong analytical skills required.

The predicted salary is between 30000 - 40000 Β£ per year.

R&D Technical Associate

Location

Head Office, North Duffield, Selby

Help improve medical devices that make a difference.

At GBUK, we're passionate about developing high-quality medical devices that improve patient care across the world.

As our R&D Technical Associate, you'll play a key role in ensuring our products continue to meet the highest standards of quality, safety and regulatory compliance.

Working closely with colleagues across Research & Development, Quality Assurance and Manufacturing, you'll lead technical investigations, coordinate product improvements and help ensure our products remain compliant throughout their lifecycle.

If you enjoy solving technical problems, working collaboratively and making a tangible impact on patient safety, we'd love to hear from you.

What you'll be doing

As an R&D Technical Associate, you'll be responsible for supporting the ongoing quality, performance and compliance of GBUK products by:

  • Leading investigations into product performance, customer complaints and non-conformation
  • Coordinating R&D actions relating to CAPAs, change controls and quality investigations, ensuring activities are completed accurately and on time.
  • Working closely with external manufacturing partners to investigate issues and maintain accurate product specifications.
  • Supporting root cause analysis and implementing effective corrective and preventive actions.
  • Planning, coordinating and carrying out product testing, including writing protocols, analysing data and producing technical reports.

Ensuring product specifications and technical documentation remain current and compliant.

  • Supporting internal and external quality and regulatory audits.
  • Providing technical guidance and training to colleagues where required.
  • Escalating product quality or patient safety concerns appropriately.
  • Identifying opportunities to improve products, processes and ways of working.

About you

We're looking for someone who enjoys working with technical detail and has a collaborative approach to problem-solving.

You'll ideally have

Essential

  • Experience working within a technical, quality or R&D environment in the medical device, pharmaceutical or food manufacturing industries.

Working knowledge of ISO13485.

Strong analytical and investigative skills with excellent attention to detail.

Confidence communicating with both internal teams and external manufacturing partners.

  • Good IT skills, including Microsoft Office. A full UK driving licence and access to your own vehicle.

Desirable

  • A degree in a scientific, engineering or medical discipline.
  • Knowledge of Medical Device Regulation (MDR), MDCG guidance and relevant UK, EU or FDA regulatory requirements.
  • Familiarity with ISO 14971 (Risk Management), ISO 10993 (Biological Evaluation) and other applicable medical device standards.
  • Knowledge of regulations and standards relating to In Vitro Diagnostic (IVD) devices.

What success looks like...

You'll help ensure

  • Technical investigations are completed thoroughly and within agreed timescales.
  • CAPAs, non-conformances and change control actions are delivered on time.
  • Product specifications remain accurate, controlled and up to date.
  • Products continue to meet regulatory, quality and customer requirements.
  • Continuous improvements are identified and implemented across products and processes.

Why join GBUK?

GBUK is a leading medical device manufacturer supplying innovative healthcare solutions to customers across the UK and internationally.

Our products make a real difference to patients every day, and our people are at the heart of everything we do.

When you join GBUK, you'll become part of a collaborative team where innovation, continuous improvement and professional development are encouraged.

You'll have the opportunity to contribute to meaningful projects, work alongside experienced technical professionals and help shape products that improve lives.

Our Values

At GBUK, we look for people who share our values

Integrity – We do the right thing.

Collaboration – We achieve more together.

Innovation – We continually look for better ways to improve.

Solutions Focused – We solve problems with purpose.

Adaptability – We embrace change and new opportunities.

Research and Development Technical Specialist in York employer: GBUK

At GBUK in North Duffield, Selby, we pride ourselves on being an excellent employer that values collaboration and leadership. Our supportive work culture fosters employee growth through continuous training and development opportunities, ensuring that your contributions are recognised and impactful. Join us to be part of a dynamic team where your leadership can truly make a difference in our operations.

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Contact Details:

GBUK Recruitment Team

We think you need these skills to ace Research and Development Technical Specialist in York

Technical Investigations
Quality Assurance
Regulatory Compliance
Root Cause Analysis
CAPA Management
Change Control
Product Testing