Scientific Officer – Quality Assurance

JobsTrackR; Greater Manchester; On-site; GBP 28,000 - 34,000; Part time

Job summary

An established industry player is seeking a detail-oriented Scientific Officer for a part-time role in Quality Assurance. This position is crucial for maintaining high standards in clinical research, requiring collaboration across scientific and operational teams. The ideal candidate will have a BSc in a scientific discipline and experience in QA or compliance. Responsibilities include managing QA documentation, conducting audits, and ensuring adherence to regulatory standards. This role offers flexibility in working hours while emphasizing team collaboration, making it an exciting opportunity for those passionate about quality assurance in a scientific setting.

Qualifications

• Experience in QA or compliance within a scientific or regulated environment.
• Familiarity with GCP, GLP, or GCLP standards.

Responsibilities

• Maintain accurate QA documentation and equipment records.
• Support planning and delivery of internal audits and inspections.
• Assist in managing non-conformances and implementing CAPAs.

Skills

Quality Assurance

Attention to Detail

Communication Skills

Regulatory Compliance

Team Collaboration

Education

BSc in a Scientific Discipline

Tools

LIMS

Electronic QMS Systems (e.g., Q-Pulse)

Job description

Scientific Officer – Quality Assurance
Manchester
£28,000 – £34,000 per annum (pro rata), depending on experience
Part Time (17.5 hours per week) –2 Years Fixed Term
Job Description:
We are recruiting on behalf of a prominent research organisation for a part-time Scientific Officer to join a dedicated Quality Assurance (QA) team. This role plays a vital part in maintaining the standards and systems that support high-quality clinical research. You’ll contribute to the management and development of the organisation’s Quality Management System (QMS), conduct internal audits, support compliance activities, and help maintain the documentation and procedures required to meet Good Clinical Practice (GCP) and other regulatory standards.
This is a fantastic opportunity for a detail-oriented individual with experience in QA or compliance within a scientific or regulated environment to work collaboratively across a range of scientific and operational teams.
Key Responsibilities:

• Maintain accurate QA documentation, equipment records, and procedural logs.
• Support the planning and delivery of internal audits and inspections.
• Assist in the management of non-conformances and the implementation of CAPAs.
• Contribute to the review and development of Standard Operating Procedures (SOPs).
• Provide advice on GCP and other relevant regulatory standards.
• Liaise with multidisciplinary teams to support consistent quality practices across laboratories.

About you:

• A BSc in a scientific discipline or equivalent relevant experience.
• Experience working in a QA or compliance role within a regulated academic or industrial lab.
• Familiarity with GCP, GLP, or GCLP standards.
• Strong attention to detail and accurate record-keeping skills.
• Excellent communication skills and a collaborative mindset.
• Experience with LIMS or electronic QMS systems (e.g., Q-Pulse) is desirable.

Working Pattern
The working pattern for this position is negotiable, designed to offer flexibility while ensuring strong team collaboration:

• The role is 0.5 FTE (17.5 hours per week).
• Preferred options include 2.5 days per week (ideally over three consecutive days: two full days and one half day) or five half days across the working week.
• Start and end times are flexible, but presence during core hours (10am–12pm and/or 2pm–4pm) is expected.
• The role is fully on-site, with remote working considered only in exceptional circumstances. Candidates looking to compress all hours into two days would not meet the operational needs of the post.

If this sounds like the perfect role for you then please submit your CV

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