SonicJobs Logo
Login
Left arrow iconBack to search

QA Document reviewer

SRG
Posted 8 days ago, valid for 6 days
Location

Stirling, Stirling FK8 2DG, Scotland

Salary

£28,000 - £33,600 per annum

info
Contract type

Full Time

By applying, a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.

Sonic Summary

info
  • SRG is seeking a QA Document Reviewer for a growing life science organization, offering an exciting opportunity for candidates with document and batch record review experience.
  • The role involves reviewing quality and batch documentation, maintaining master and working documents, and ensuring compliance with regulatory requirements and company policies.
  • Candidates should have a minimum of HNC/HND education, with a degree preferred, and experience in a regulated GMP environment.
  • Strong written and verbal communication skills, excellent organizational abilities, and proficiency in Microsoft Office are essential for this position.
  • The salary for this role is competitive, but specific figures were not provided, and candidates should have relevant experience in document review.

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.

Apply now in a few quick clicks

By applying, a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.