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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!

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