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Quality and Validation Officer

Job in Alva, Tillicoultry, Clackmannanshire, FK13, Scotland, UK
Listing for: AccuBio Ltd
Full Time position
Listed on 2026-01-02
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist / Manager, Quality Control / Manager
Salary/Wage Range or Industry Benchmark: 28711 - 33702 GBP Yearly GBP 28711.00 33702.00 YEAR
Job Description & How to Apply Below
Location: Alva

Job Title: Quality and Validation Officer – Accu Bio Ltd

Location: Office based, Alva, Clackmannanshire - FK12 5DQ

Salary: £28,711 - £33,702 per annum, DOE plus benefits

Contract: Permanent, Full time

Hours: Monday to Thursday 8.30am – 5.00pm, Friday 8.30am – 2.30pm

At Accu Bio Ltd, we are dedicated to developing cutting‑edge diagnostic solutions that improve lives. We are looking for a motivated Quality and Validation Officer to join our team and help ensure our products meet the highest standards of quality and compliance.

Why This Role Matters

As our Quality and Validation Officer, you will play a key role in ensuring our technologies meet the highest quality standards. You will move beyond ticking boxes to elevate standards, drive innovation, and embed excellence into everything we do—shaping how life‑saving technologies are made, tested, and delivered.

What You’ll Be Doing
  • Maintain the company’s QMS procedures, standards, and specifications.
  • Demonstrate and maintain cGMP, IVDR, and ISO 13485:2016 compliance with respect to process quality and product validation.
  • Establish key validation criteria, requirements and specifications.
  • Drive and support validation activities across various processes and systems, ensuring compliance and effectiveness.
  • Creation, review and approval of quality, validation, and manufacturing records, protocols and reports; update documentation as needed.
  • Personally responsible for the maintenance of site validation procedures, processes, and templates.
  • Actively assist Quality and Operational teams and advise Managers and Staff on quality compliance, ensuring alignment with group quality goals and culture.
  • Identify and highlight potential issues in processes while continuously seeking improvement opportunities.
What You Bring
  • A relevant degree or equivalent professional qualification.
  • Minimum three years’ experience in medical devices, pharma or a similarly regulated industry.
  • Proven success in a Quality Assurance/Validation role.
  • Strong organisational and administrative skills.
  • Clear, confident communication – written and verbal.
  • High attention to detail with a methodical mindset.
  • Ability to meet deadlines, agile with priorities.
  • Self‑motivated and collaborative.
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