Quality Records Specialist - Pharmaceutical Compliance

Talentmark; Preston on the Hill; On-site; GBP 17,000 - 25,000; Full time

Job summary

Talentmark are recruiting a Quality Specialist to join a global pharmaceutical company on a contract basis for 6 months. The role is based in Runcorn, UK, with a rate of £15.38 per hour and standard Mon-Fri, 9 am to 5 pm hours.

You will maintain controlled quality documentation, check versions and approvals, index and archive records, apply retention rules and provide general admin support to the Quality team. DBS checks may be required.

Qualifications

• Excellent accuracy and attention to detail when checking, handling and recording information.
• Well organized, able to manage your own workload to deadlines and keep confidentiality.
• Clear, friendly communicator who is comfortable working with colleagues across the site.
• Reliable and resilient, with a willingness to learn, follow procedures and ask for help when needed.
• Experience in a regulated or compliance-focused environment would be useful.

Responsibilities

• Maintain controlled, accessible and traceable quality documentation and archived records, in line with good documentation practices.
• Check document identification, version and approval status, issuing controlled copies and withdrawing superseded versions.
• Index, file and archive paper and electronic records, logging locations, retrievals and returns accurately.
• Apply retention and access rules, protecting record integrity and escalating errors or missing and damaged records.
• Provide general administrative support to the Quality team and help with improvement projects as needed.

Skills

Accuracy

Organization

Communication

Reliability

Regulated environment experience

Job description

Talentmark are recruiting a Quality Specialist to join a global pharmaceutical company on a contract basis for 6 months. The role is based in Runcorn, UK, with a rate of £15.38 per hour and standard Mon-Fri, 9 am to 5 pm hours.

You will maintain controlled quality documentation, check versions and approvals, index and archive records, apply retention rules and provide general admin support to the Quality team. DBS checks may be required.