QA Document reviewer

SRG; United Kingdom; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading life science organization seeks a QA Document Reviewer to ensure compliance with regulatory requirements and maintain master documents. This role involves meticulous documentation review, communication across all levels, and supporting batch compilation activities. Ideal candidates will have document review experience in a GMP environment and strong organisational skills.

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.
• Ensure compliance with GMP regulations.

Skills

Document Review

Communication

Organisation

Analytical Problem Solving

IT Literacy

Education

HNC/HND or Degree

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 with document/batch record review experience and offers the chance to join a growing and dynamic company.

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!

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.