QA Document Reviewer

SRG; Stirling; On-site; GBP 25,000 - 35,000; Full time

Job summary

A leading life science organisation is seeking a QA Document Reviewer in Stirling. This role is ideal for early-career professionals with document review experience in a GMP environment. The successful candidate will ensure compliance with regulatory requirements and maintain quality documentation, providing a solid foundation for future career development.

Qualifications

• Educated to HNC/HND as minimum; degree preferred.
• Experience in document review in a regulated (GMP) environment.
• Excellent written and verbal communication skills.

Responsibilities

• Review quality and batch documentation.
• Maintain a status tracker and provide accurate status reports.
• Assist in compliance with GMP regulations.

Skills

Communication

Organisational skills

Analytical problem solving

IT literacy

Education

HNC/HND

Degree (preferred)

Tools

Microsoft Office

Job description

SRG are working with an exciting and growing life science organisation to help them find a QA Document Reviewer.

This is a great opportunity for someone early in their career and some document/batch record review experience. You will be joining a dynamic organisation with great opportunity for future development.

Reporting to the Quality Assurance Manager, the successful candidate will be responsible for maintaining all activities associated with master and working documents, data and records, ensuring compliance with regulatory requirements and company policies/ procedures.

The Role:

• Review quality and batch documentation
• Provide document control functions and advice
• Maintain a status tracker and provide accurate status reports on batch record review to support batch compilation activities.
• Support document archiving activities when required to ensure the movement of material to and from the archive is properly controlled and documented
• Coordinate the company activities to ensure that SOP are reviewed / revised within the documented revision time span
• Ensure that all documents are updated and mastered according to existing procedures
• Assist in compliance with GMP regulations

Requirements:

• Educated to HNC/HND as minimum- degree preferred
• Experience in document review in a regulated (GMP) environment
• Excellent written and verbal communication skills; able to communicate effectively with all levels within the organisation
• Knowledge of Quality Systems would be beneficial
• Excellent organisational skills
• Ability to work independently and as a member of a team
• Analytical approach to problem solving and decision making
• IT literate with proficiency in Microsoft Office and data entry

If you think this could be the role for you, please apply online!

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Science and Quality Assurance

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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