Enable job alerts via email!

Quality Officer, GLP/ GMP

Russell Taylor Group Ltd

West Yorkshire

On-site

GBP 32,000

Full time

10 days ago

Boost your interview chances

Create a job specific, tailored resume for higher success rate.

Job summary

An established industry player in the GMP/GLP testing sector is seeking a dedicated Quality Officer to enhance their QA team. This role involves supporting quality activities, maintaining and improving the Quality Management System, and ensuring compliance with GMP and GLP standards. You will train personnel, perform audits, and handle non-conformances while fostering a culture of quality and continuous improvement. If you are passionate about quality assurance and possess a strong scientific background, this opportunity offers a chance to make a significant impact in a growing organization.

Qualifications

  • Degree in a relevant Scientific / STEM subject or significant QA experience.
  • Experienced in QMS duties like CAPA, deviations, and documentation review.

Responsibilities

  • Support quality activities and maintain the Quality Management System.
  • Train personnel in GMP, GLP, and QMS requirements.
  • Perform audits and inspections, reporting deficiencies.

Skills

Quality Management System (QMS)
GMP
GLP
CAPA
Interpersonal Skills
Report Writing
IT Literacy

Education

Degree in a relevant Scientific / STEM subject

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 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.
Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.