Quality and Validation Officer

Quality and Validation Officer

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 and Friday 8.30am 2.30pm

At Accubio Ltd, we are dedicated to developing cutting-edge diagnostic solutions that improve lives. We are looking for a motivated Quality and Validations Associate to join our team and help ensure our products meet the highest standards of quality and compliance. If you re passionate about quality systems, validation, and continuous improvement within a fast-growing life sciences company, this is the role for you.

Why this role matters:

As our Quality and Validation Officer, you ll play a key role in validation, ensuring our technologies meet the highest quality standards. You won t just tick boxes - you ll elevate standards, drive innovation and embed excellence into everything we do. This is your chance to influence how life-saving technologies are made, tested and delivered.

What you ll be doing:

Your day-to-day will be dynamic, purposeful and full of opportunities to grow.

Key responsibilities include:

• 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. Creation, review, approval and update of quality and validation documentation.

• Personally responsible for 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 the group s quality goals and culture.

• Identify and highlight potential issues in processes, whilst continuously seeking opportunities for improvement.

What you bring:

We re looking for someone who s not just qualified - but driven, detail-oriented and ready to make a difference.

• 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 communicator - written and verbal

• High attention to detail with a methodical mindset

• Ability to meet deadlines, agile with priorities

• Self-motivated and collaborative.