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Quality Officer, GLP/ GMP

Russell Taylor Group

Bradford

On-site

GBP 32,000

Full time

30+ days ago

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Job summary

Ein etabliertes Unternehmen im Bereich GMP/GLP sucht einen engagierten Qualitätsbeauftragten zur Verstärkung seines QA-Teams. In dieser spannenden Rolle sind Sie verantwortlich für die Unterstützung der Qualitätsaktivitäten im Labor, die Verbesserung des Qualitätsmanagementsystems sowie die Durchführung von Schulungen zu GMP und GLP. Sie werden auch an Audits teilnehmen und sicherstellen, dass die Dokumentationssysteme eingehalten werden. Wenn Sie eine Leidenschaft für Qualitätssicherung haben und in einem dynamischen Umfeld arbeiten möchten, ist dies die perfekte Gelegenheit für Sie.

Qualifications

  • Abschluss in einem relevanten wissenschaftlichen / MINT-Fach oder umfangreiche QA-Erfahrung.
  • Erfahrung in qualitätsbezogenen Aufgaben und QMS-Frameworks.

Responsibilities

  • Unterstützung der Qualitätsaktivitäten in den Laborbereichen.
  • Wartung und Verbesserung des Qualitätsmanagementsystems (QMS).
  • Durchführung von Audits und Inspektionen.

Skills

Qualitätsmanagement
GMP
GLP
IT-Kenntnisse
Interpersonelle Fähigkeiten
Berichtsschreibung

Education

Abschluss in einem relevanten wissenschaftlichen / MINT-Fach

Job description

Quality Officer, GLP/ GMP

Type: Permanent
Location: Bradford (fully onsite)
Hours: Days
Salary: CIRCA £32,000

Our Client, a multi-sited GMP/GLP testing company is growing their QA team and looking to recruit a QA Officer to join their specialised QA team.

The Role:

  1. Supporting the quality activities of the laboratory areas.
  2. Maintaining & improving the Quality Management System (QMS).
  3. Training personnel in GMP, GLP and associated QMS requirements.
  4. Supporting the completion of agreed action plans arising from regulatory/customer audits of the facility.
  5. Maintaining and executing the site internal audit schedule.
  6. Maintaining the Supplier oversight programme.
  7. Perform audits and inspections as assigned, reporting any deficiencies to the Quality Manager and Operations Director to include: Facilities, equipment, systems (including Computerised systems), procedures, records, data and information.
  8. Review and approve production and analytical documentation necessary for the analysis of samples and Certificates of Analysis.
  9. Ensure that the document control system is maintained.
  10. Perform investigations on non-conformances/deviations/OOS, review information and draw conclusions in support of CAPAs, customer complaints etc.
  11. Assist with/host audits by customers and regulators/accreditation bodies.

The Person:
  1. Will hold a degree in a relevant Scientific / STEM subject or significant QA (GLP/ GMP) experience to counter this.
  2. Experienced in quality related/ QMS related duties - CAPA, deviations, OOs, documentation review etc with a GLP / GMP QMS framework.
  3. Strong IT literacy.
  4. Strong interpersonal skills and good report writing skills.

Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or GDPR please get in touch with us here.
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