Scientific Officer Quality Assurance

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

Job summary

Ein etabliertes Forschungsunternehmen sucht einen detailorientierten Scientific Officer für die QA-Abteilung. In dieser spannenden Rolle tragen Sie zur Entwicklung und Verwaltung des Qualitätsmanagementsystems bei, führen interne Audits durch und unterstützen die Einhaltung von GCP-Standards. Diese Position bietet die Möglichkeit, in einem dynamischen Team zu arbeiten, das sich der Verbesserung der klinischen Forschung widmet. Wenn Sie Erfahrung in QA oder Compliance haben und eine Leidenschaft für wissenschaftliche Exzellenz mitbringen, ist dies die perfekte Gelegenheit für Sie.

Qualifications

• Erfahrung in QA oder Compliance in einem regulierten Umfeld.
• Fähigkeit zur genauen Dokumentation und Aufzeichnung.

Responsibilities

• Wartung von QA-Dokumentationen und Aufzeichnungen.
• Unterstützung bei internen Audits und Inspektionen.

Skills

Qualitätsmanagement

GCP

GLP

Aufmerksamkeit für Details

Kommunikationsfähigkeiten

Education

BSc in einem wissenschaftlichen Fach

Tools

LIMS

Q-Pulse

Job description

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 will 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

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

About You

1. A BSc in a scientific discipline or equivalent relevant experience.
2. Experience working in a QA or compliance role within a regulated academic or industrial lab.
3. Familiarity with GCP, GLP, or GCLP standards.
4. Strong attention to detail and accurate record-keeping skills.
5. Excellent communication skills and a collaborative mindset.
6. 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:

1. The role is 0.5 FTE (17.5 hours per week).
2. 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.
3. Start and end times are flexible, but presence during core hours (10am-12pm and/or 2pm-4pm) is expected.
4. 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.

This vacancy is being handled by Aspire Recruitment. Please be aware we receive a high volume of applications and regularly receive applications from candidates who exceed the job credentials. We will only contact you within the next 14 days if you are selected for interview.

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