QA Document Reviewer

JR United Kingdom; Stirling; On-site; GBP 25,000 - 35,000; Full time

Job summary

Join a dynamic life science organization as a QA Document Reviewer, perfect for early-career professionals. This role offers the chance to engage in document and batch record reviews, ensuring compliance with regulatory standards. You'll collaborate with the Quality Assurance Manager, providing vital support in maintaining master documents and data integrity. With opportunities for future development, this position is ideal for those eager to grow in a thriving environment. If you're detail-oriented and passionate about quality assurance, this could be your next career step!

Qualifications

• Educated to HNC/HND as minimum; degree preferred.
• Experience in document review in a regulated (GMP) environment.

Responsibilities

• Review quality and batch documentation.
• Maintain a status tracker for batch record review.
• Assist in compliance with GMP regulations.

Skills

Document Review

Communication Skills

Organizational Skills

Analytical Problem Solving

IT Literacy

Education

HNC/HND

Degree

Tools

Microsoft Office

Job description

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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!