Microbiology Quality & Documentation Specialist

Connected Search Group

Buxton

On-site

GBP 33,000 - 36,000

Full time

14 days+
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Job summary

Connected Search Group is seeking a Documentation Officer to join an established microbiology laboratory in Derbyshire. The role combines quality, documentation and technical microbiology, with involvement in investigations, compliance, reporting and technical support.

Working within a GMP and ISO 17025 environment, you will ensure day-to-day quality and compliance while contributing to microbiological testing when required, and supporting customers with technical and testing requirements.

Qualifications

  • A degree in Life Sciences, Microbiology or a related discipline. BTEC or equivalent qualifications may also be considered.
  • Experience in a microbiology laboratory to UKAS/GMP standards.
  • Strong understanding of quality and documentation requirements.

Responsibilities

  • Manage quality event investigations including non-conformances, OOS investigations, CAPAs and change controls.
  • Generate, review and approve laboratory test reports.
  • Review and authorise laboratory data and perform data trending.
  • Prepare and review SOPs, test methods and other controlled documentation.
  • Provide technical support and troubleshooting to laboratory staff.
  • Assist with scheduling and prioritisation of test samples.
  • Liaise with customers regarding technical and testing requirements.
  • Support microbiological testing and plate reading as required.
  • Ensure activities comply with GMP and ISO 17025.

Skills

Life sciences background
Quality assurance
Analytical skills
Attention to detail
Communication skills

Education

Bachelor's degree in Life Sciences or Microbiology

Job description

Connected Search Group is seeking a Documentation Officer to join an established microbiology laboratory in Derbyshire. The role combines quality, documentation and technical microbiology, with involvement in investigations, compliance, reporting and technical support.

Working within a GMP and ISO 17025 environment, you will ensure day-to-day quality and compliance while contributing to microbiological testing when required, and supporting customers with technical and testing requirements.

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