CareerAddict

Quality Assurance Officer

CV-Library

Posted on Jul 22, 2026 by CV-Library
Salisbury, Wiltshire, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Full-Time
Excellent opportunity for a GMP experienced QA professional to take on a challenging new role within a growing start-up!

As our client aims to achieve GMP accreditation, you will hold utmost responsibility for the management and maintenance of their QMS. Utilising your previous experience, you will contribute to inspecting the readiness for accreditation, working across departments to audit and self-inspect, whilst providing training across the teams in best practices.

Key responsibilities:

• Manage and maintain the site’s QMS, ensuring compliance across all departments

• Oversee quality events including deviations, CAPAs, and change controls

• Support Health & Safety compliance activities

• Review QC documentation to ensure accuracy and compliance

About you:

• Minimum 2 years’ QA experience in a GMP-regulated environment

• Confident and assertive, with strong communication skills to influence and engage at all levels

• Proactive and detail-oriented, with a drive for continuous improvement

In return, you will receive a highly competitive salary, with the opportunity to contribute to the success of a fast-growing business in rural Wiltshire!

Apply to be considered today!

Key words: QA, quality assurance, GMP, good manufacturing practice, laboratory, analytical, chemistry, QMS, audit, auditing, inspection, Wiltshire, VRS9487MP

Reference: 225402173

https://jobs.careeraddict.com/post/113593995
CV-Library

Quality Assurance Officer

CV-Library

Posted on Jul 22, 2026 by CV-Library

Print
Salisbury, Wiltshire, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Full-Time
Excellent opportunity for a GMP experienced QA professional to take on a challenging new role within a growing start-up!

As our client aims to achieve GMP accreditation, you will hold utmost responsibility for the management and maintenance of their QMS. Utilising your previous experience, you will contribute to inspecting the readiness for accreditation, working across departments to audit and self-inspect, whilst providing training across the teams in best practices.

Key responsibilities:

• Manage and maintain the site’s QMS, ensuring compliance across all departments

• Oversee quality events including deviations, CAPAs, and change controls

• Support Health & Safety compliance activities

• Review QC documentation to ensure accuracy and compliance

About you:

• Minimum 2 years’ QA experience in a GMP-regulated environment

• Confident and assertive, with strong communication skills to influence and engage at all levels

• Proactive and detail-oriented, with a drive for continuous improvement

In return, you will receive a highly competitive salary, with the opportunity to contribute to the success of a fast-growing business in rural Wiltshire!

Apply to be considered today!

Key words: QA, quality assurance, GMP, good manufacturing practice, laboratory, analytical, chemistry, QMS, audit, auditing, inspection, Wiltshire, VRS9487MP
Print

Reference: 225402173

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