Quality Assurance Specialist

S3 Science Recruitment; Manchester; On-site; GBP 30,000 - 40,000; Part time

Job summary

Join a leading centre of excellence in clinical research as a Quality Assurance Specialist. This part-time role involves ensuring compliance with Good Clinical Practice in clinical trials, conducting audits, and supporting regulatory standards. Make a meaningful impact in biomedical science while working with a specialized team dedicated to patient-focused research.

Qualifications

• Experience in QA or compliance in GxP-regulated labs.
• Working knowledge of GCP, CAPA, internal audits, and quality systems.

Responsibilities

• Ensure compliance with GCP and clinical trial regulations.
• Conduct internal audits and manage documentation reviews.
• Maintain and improve Quality Management System (QMS).

Skills

Attention to Detail

Compliance

Quality Assurance

Education

BSc or equivalent experience

Tools

LIMS

QPulse

Job description

S3 Science Recruitment provided pay range

This range is provided by S3 Science Recruitment. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

Direct message the job poster from S3 Science Recruitment

Senior Recruitment Consultant - S3 Science Recruitment

QA Specialist

Join a Leading Centre of Excellence in Clinical Research!

A unique part-time opportunity has opened up for a detail-oriented and proactive Quality Assurance Specialist to contribute to a world-renowned research hub driving breakthroughs in cancer diagnostics and treatment.

In this pivotal role, you’ll be part of a specialised team ensuring compliance with Good Clinical Practice (GCP) in clinical trials. From managing internal audits and non-conformances to guiding teams on regulatory standards, you’ll be at the heart of initiatives that directly support patient-focused research.

The Role:

1. Ensure compliance with GCP and clinical trial regulations
2. Conduct internal audits and manage documentation reviews
3. Handle non-conformances and support CAPA implementation
4. Maintain and improve Quality Management System (QMS)
5. Activate and track projects in the Laboratory Information Management System (LIMS)
6. Provide QA guidance and basic training to staff
7. Support external audit preparation and regulatory inspections

You’ll Bring

• Experience in QA or compliance in GxP-regulated labs
• Working knowledge of GCP, CAPA, internal audits, and quality systems like LIMS and QPulse
• A science background (BSc or equivalent experience) and a meticulous eye for detail

This is more than a job—it’s your chance to make a meaningful impact while working with brilliant minds on some of the most exciting challenges in biomedical science today.

Apply now and be part of something that matters.

Seniority level

• Entry level

Employment type

• Part-time

Job function

• Quality Assurance

Industries

• Staffing and Recruiting