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Quality Assurance Officer

CV-Library

Posted on Jul 13, 2026 by CV-Library
Kent, United Kingdom
Pharmaceutical
Immediate Start
£28k - £35k Annual
Full-Time
ROLE OVERVIEW:

A leading pharmaceutical company based in Sandwich, Kent is seeking a dedicated Quality Assurance Officer to join their expanding team. This is a great opportunity for an individual with QA experience from a GMP environment that is looking for a role that offers ownership, the chance to influence decisions, and the opportunity to make a meaningful contribution to a growing organisation.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as Quality Assurance Officer will be varied however key duties and responsibilities are as follows:

1. Maintaining and continually improving the Quality Management System (QMS).

2. Reviewing and approving batch manufacturing documentation prior to batch release.

3. Managing Deviations, CAPAs, Change Controls, Complaints, and OOS investigations.

4. Supporting internal and supplier audits, as well as customer and regulatory audits.

ROLE REQUIREMENTS:

To be successful in your application to this exciting role as Quality Assurance Officer we are looking to identify the following:

1. Relevant degree in a scientific discipline.

2. Proven industry experience in GMP Quality Assurance within a pharmaceutical manufacturing environment.

3. A working knowledge and practical experience with QMS, CAPAs, Deviations, and Change Controls.

Key Words:Quality Assurance / GMP / Pharmaceutical / QMS / CAPA / Deviation Management / Batch Release / Regulatory Audits / Supplier Audits / Quality Systems / Continuous Improvement

Reference: 225366057

https://jobs.careeraddict.com/post/113553030
CV-Library

Quality Assurance Officer

CV-Library

Posted on Jul 13, 2026 by CV-Library

Print
Kent, United Kingdom
Pharmaceutical
Immediate Start
£28k - £35k Annual
Full-Time
ROLE OVERVIEW:

A leading pharmaceutical company based in Sandwich, Kent is seeking a dedicated Quality Assurance Officer to join their expanding team. This is a great opportunity for an individual with QA experience from a GMP environment that is looking for a role that offers ownership, the chance to influence decisions, and the opportunity to make a meaningful contribution to a growing organisation.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as Quality Assurance Officer will be varied however key duties and responsibilities are as follows:

1. Maintaining and continually improving the Quality Management System (QMS).

2. Reviewing and approving batch manufacturing documentation prior to batch release.

3. Managing Deviations, CAPAs, Change Controls, Complaints, and OOS investigations.

4. Supporting internal and supplier audits, as well as customer and regulatory audits.

ROLE REQUIREMENTS:

To be successful in your application to this exciting role as Quality Assurance Officer we are looking to identify the following:

1. Relevant degree in a scientific discipline.

2. Proven industry experience in GMP Quality Assurance within a pharmaceutical manufacturing environment.

3. A working knowledge and practical experience with QMS, CAPAs, Deviations, and Change Controls.

Key Words:Quality Assurance / GMP / Pharmaceutical / QMS / CAPA / Deviation Management / Batch Release / Regulatory Audits / Supplier Audits / Quality Systems / Continuous Improvement
Print

Reference: 225366057

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