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QA Officer

Scientific / Pharma
Date Posted:
11 Sep 2019
Vacancy Type:
Job Description

Our client is seeking an individual to join our team in the position of QA Officer.

If successful, you will be joining a team of motivated and self-driven individuals with a passion for ensuring the success of this exciting project.

Please note, QA experience in a Pharmaceutical background is essential.

Salary: Competitive salary and benefits offered.

Permanent and full time

Role Summary

To provide QA support to all departments.

Key Accountabilities

  • Maintain and develop the Quality Management System
  • Ensure all pre-production documentation is submitted to QA, checked and approved prior to use of any materials.
  • Ensure all post- production documentation is submitted to QA, checked and approved prior to batch release.
  • Ensure all input materials meet required specifications.
  • Complete QA approval of batch records in a timely manner.
  • Undertake QA approval of Q.C analytical worksheets prior to production use.
  • Participate in QA meetings.
  • Complete QA review and approval of deviations, C.A.P. A’s, change controls, complaints, out of specifications and other documentation such as SOP’s and forms.
  • Assist the QA manager with internal audits.
  • Ensure internal audit schedule are carried out in a timely manner.
  • Ensure quality related investigations are carried out in a timely manner.
  • Adhere to strict GMP compliance guidelines.
  • Ensure all documentation and staff meet GMP compliance expectations.
  • Write and develop policies.
  • Write and develop SOP’s and forms that may be required
  • Ensure quality agreements and quality questionnaires are in place with external companies.
  • Undertake external audits.
  • Manage and develop the company training matrix.
  • Complete three-monthly quality reviews on employee training record folders.
  • Provide the management team with compliance percentages for employee training.
  • Provide QA support to the production and QC departments.
  • Develop and update logbooks for the facility as and when required.


  • Quality Assurance: 1 year (Required)
  • GMP: 2 years (Required)

About Morgan Jones:

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