Pharma QA Officer: Quality & Compliance Champion

SRG; Stirling; On-site; GBP 38,000 - 48,000; Full time

Job summary

SRG in Stirling, UK, seeks an experienced QA Officer to own quality activities across new products, campaigns and change projects within a fast-paced pharmaceutical environment.

You will review critical documentation, support investigations and audits, and collaborate with Production, QC and R&D to maintain product quality, regulatory compliance and patient safety.

Key responsibilities include deviations handling, CAPA, change controls and ensuring timely QA sign-offs.

Qualifications

• Candidates must have a degree in a relevant scientific discipline and substantial QA experience in the pharmaceutical sector.
• Strong knowledge of GMP/GxP requirements and regulatory expectations.
• Experience with QMS and controlled documentation is essential.

Responsibilities

• Review and approve manufacturing batch records, packaging records, laboratory data and process instructions.
• Act as QA representative for new products, campaigns and change projects.
• Manage and support deviations, non-conformances, investigations and CAPA.
• Contribute to root cause analysis and CAPA implementation.
• Participate in change controls, risk assessments, validation activities and product quality reviews.
• Support internal audits, customer audits and regulatory inspection readiness.
• Maintain QMS documentation, including SOPs, protocols, reports and quality records.
• Support material and product disposition activities.
• Collaborate with Production, QC, R&D and other departments to resolve quality issues.
• Prepare quality trend reports and communicate findings to stakeholders.
• Promote a strong culture of quality, compliance and continuous improvement.

Skills

Quality Assurance

GMP/GxP knowledge

Regulatory compliance

Analytical thinking

Attention to detail

Education

Degree in Pharmacy, Chemistry, Biology

Tools

Quality Management System (QMS)

Job description

SRG in Stirling, UK, seeks an experienced QA Officer to own quality activities across new products, campaigns and change projects within a fast-paced pharmaceutical environment.

You will review critical documentation, support investigations and audits, and collaborate with Production, QC and R&D to maintain product quality, regulatory compliance and patient safety.

Key responsibilities include deviations handling, CAPA, change controls and ensuring timely QA sign-offs.