QA Documentation Specialist — GMP/ISO Regulated

SRG (United Kingdom); City Of Stirling; Vor Ort; AUD 65.000 - 90.000; Vollzeit

Zusammenfassung

SRG is seeking a Quality Assurance Associate to support the QA function and ensure documentation excellence across the business in a regulated environment. You will review quality and batch documentation, maintain trackers, and support archiving and data accuracy.

Reporting to the QA Manager, you will coordinate SOP reviews, ensure revisions meet timelines, and contribute to GMP compliance and continuous QA improvement, with strong written and verbal communication and proficient office skills.

Qualifikationen

• Experience reviewing quality or batch documentation in a regulated GMP environment.
• Strong written and verbal communication at all levels.
• Analytical approach to problem solving and decision making.
• Excellent organisational skills and ability to work independently and as part of a team.
• Proficiency in Microsoft Office and confident data entry skills.

Aufgaben

• Review quality and batch documentation with accuracy and attention to detail
• Provide document control functions, support, and guidance across the business
• Maintain trackers and generate accurate status reports to support batch compilation activities
• Support document archiving, ensuring controlled and compliant material movement
• Coordinate SOP review cycles and ensure revisions meet required timelines
• Ensure all documents are updated, mastered, and maintained according to established procedures
• Contribute to GMP compliance activities and continuous QA improvement

Kenntnisse

Strong communication

Analytical thinking

Organisational skills

Independent worker

Ausbildung

Relevant QA/Regulatory experience

Tools

Microsoft Office

Data entry

Jobbeschreibung

SRG is seeking a Quality Assurance Associate to support the QA function and ensure documentation excellence across the business in a regulated environment. You will review quality and batch documentation, maintain trackers, and support archiving and data accuracy.

Reporting to the QA Manager, you will coordinate SOP reviews, ensure revisions meet timelines, and contribute to GMP compliance and continuous QA improvement, with strong written and verbal communication and proficient office skills.