GMP QA Specialist

GMP QA Specialist

Full-Time 35000 - 38556 £ / year (est.) No working from home possible
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At a Glance

  • Tasks: Ensure quality standards in biopharmaceuticals and support audits and quality operations.
  • Company: Join a caring biopharmaceutical CRO in Livingston, Scotland.
  • Benefits: Competitive salary, enhanced leave, pension plan, and healthcare cash plan.
  • Other info: Flexible hours and global career progression opportunities await you.
  • Why this job: Make a real impact in quality assurance while growing your career.
  • Qualifications: 12 months experience in GMP/GLP lab; attention to detail is key.

The predicted salary is between 35000 - 38556 £ per year.

Location: Livingston, Scotland

Hours: 39 hours/week, Monday–Friday (flexible start/end times available)

Salary: Competitive + Excellent Benefits

Contract Type: Permanent, Full-Time

Visa Sponsorship: Unfortunately, not available for this role

Seeking an accomplished GMP QA professional to join a successful biopharmaceutical CRO in Livingston!

The Role:

As a Quality Assurance Specialist, you will play a key role in maintaining and improving the Quality Management System (QMS) in line with GMP and regulatory standards. You’ll support day-to-day quality operations, assist in audits, and ensure that quality metrics and systems are accurately maintained and reported.

Other key responsibilities will include:

  • Administration and development of LIMS and other IT systems
  • Review and approval of procedures, protocols, reports, and certificates of analysis
  • Management of quality KPIs and metrics
  • Support for internal audits, client audits, and regulatory inspections
  • Coordination of quality documentation and controlled substances processes
  • Delivery of QMS and eLIMS training to staff
  • Lead or support continuous improvement initiatives in the QMS
  • Deputising for QA Management where required

Applications are invited from candidates with a minimum of 12 months working within a GMP/GLP regulated laboratory. Experience within quality assurance would be a distinct advantage. You must have exemplary attention to detail and be confident liaising across multiple departments and externally.

What’s in it for you?

Join a company that genuinely cares about your growth and wellbeing. Employees benefit from:

  • Enhanced Annual Leave (including sell-back options and service-linked increases)
  • Company Pension Plan & Life Assurance (4x salary)
  • Free On-site Parking
  • Healthcare Cash Plan (after 6 months)
  • Enhanced Maternity, Adoption & Paternity Schemes
  • Global career progression opportunities
  • Access to Employee Assistance and Health & Wellbeing Programmes
  • Recognition for service, special achievements, and life events

Interested? Apply now through VRS Recruitment to take the next step in your Quality Assurance career within a supportive and forward-thinking organisation.

GMP QA Specialist employer: TieTalent

At TieTalent, we pride ourselves on being an exceptional employer that prioritises the growth and wellbeing of our employees. Located in Livingston, Scotland, we offer a supportive work culture with flexible hours, competitive salaries, and a comprehensive benefits package including enhanced annual leave and a robust pension plan. Join us to advance your career in a dynamic biopharmaceutical environment where your contributions to quality assurance will be recognised and valued.

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Contact Details:

TieTalent Recruitment Team

We think you need these skills to ace GMP QA Specialist

GMP
Quality Management System (QMS)
LIMS administration and development
Quality Assurance
Attention to Detail
Internal Audits
Regulatory Inspections