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QA Document reviewer

TN United Kingdom

Stirling

On-site

GBP 30,000 - 50,000

Full time

6 days ago
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Job summary

An exciting opportunity awaits at a growing life science organization for a QA Document Reviewer. This role is ideal for candidates with document and batch record review experience, offering a chance to contribute to compliance with regulatory standards. The successful applicant will work closely with the Quality Assurance Manager, ensuring that all documentation meets the required standards and is managed effectively. Join a dynamic team where your skills in communication, organization, and problem-solving will be valued, and help shape the future of quality assurance in life sciences.

Qualifications

  • Minimum HNC/HND required; degree preferred.
  • Experience in document review in a regulated environment.

Responsibilities

  • Review quality and batch documentation for compliance.
  • Maintain status tracker and provide reports on batch records.

Skills

Document Review
Communication Skills
Organizational Skills
Analytical Skills
Problem Solving

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 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!

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