QA Officer

RBW Consulting; Croydon; On-site; GBP 32,000 - 43,000; Full time

Job summary

RBW Consulting is seeking a QA Officer for a GMP manufacturing site in South West London. The role supports production, warehousing and QC to ensure compliant manufacturing and product release.

You will work within a collaborative Quality team, handling deviations, CAPAs, change controls and investigations, and contributing to audits and supplier quality programs. Strong cross-functional communication is essential.

Qualifications

• Scientific Degree.
• 2-3 years of experience within QA or QC in a GMP-regulated pharmaceutical, healthcare, food or cosmetics environment.
• Strong understanding of GMP and quality systems.
• Knowledge of ALGOA & Data Integrity.
• Experience with deviations, CAPAs, change controls and investigations.
• Strong communication skills and the ability to work cross-functionally.
• Excellent organisational skills with a proactive approach to problem solving.

Responsibilities

• Running Initial Impact Assessment for Production Floor.
• Supporting batch release activities and quality decision making.
• Managing deviations, CAPAs, change controls and customer complaints.
• Reviewing batch documentation, laboratory data and Certificates of Analysis.
• Reviewing and approving SOPs and GMP documentation.
• Supporting internal audits, supplier quality activities and inspections.

Skills

GMP knowledge

Quality systems

Deviations handling

Cross-functional team

Education

Scientific Degree

Job description

QA Officer

South West London | GMP Manufacturing | Permanent

An exciting opportunity has arisen for a QA Officer to join a well-established GMP manufacturer experiencing significant growth and investment. This role offers the chance to work within a collaborative Quality team, supporting manufacturing, warehousing and QC operations while helping drive GMP compliance and quality culture across the site.

The Role

As QA Officer, you will play a key role in supporting production, warehouse and Quality teams in ensuring products are manufactured and released in compliance with GMP and regulatory requirements. The position combines quality systems, batch review, investigations, customer complaints, supplier quality activities and cross-functional quality support.

Responsibilities

• Running Initial Impact Assessment for Production Floor.
• Supporting batch release activities and quality decision making.
• Managing deviations, CAPAs, change controls and customer complaints.
• Reviewing batch documentation, laboratory data and Certificates of Analysis.
• Reviewing and approving SOPs and GMP documentation.
• Supporting internal audits, supplier quality activities and inspections.

Requirements

• Scientific Degree.
• 2-3 years of experience within QA or QC in a GMP-regulated pharmaceutical, healthcare, food or cosmetics environment.
• Strong understanding of GMP and quality systems.
• Knowledge of ALGOA & Data Integrity.
• Experience with deviations, CAPAs, change controls and investigations.
• Strong communication skills and the ability to work cross-functionally.
• Excellent organisational skills with a proactive approach to problem solving.

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