Quality Specialist

Talentmark; Runcorn; On-site; GBP 17,000 - 25,000; Full time

Job summary

Talentmark is recruiting a Quality Specialist for a 6-month contract based in Runcorn. The role involves maintaining quality documentation, archiving records, and ensuring controlled copies with strict versioning, in line with good documentation practices.

You will support the Quality team, handle retention rules, and contribute to improvement projects. UK work entitlement is essential, hours are Mon-Fri 9am-5pm, salary £15.38 per hour, based in the site.”

Qualifications

• Accurate and detail-focused in handling information.
• Well organized and able to meet deadlines.
• Clear communicator across site colleagues.
• Experience in regulated environments is a plus.
• Entitlement to work in the UK is essential.

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• Check document identification, version and approval status, issuing controlled copies and withdrawing superseded versions.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

Attention to detail

Organised

Communication

Confidentiality

Job description

Talentmark are recruiting for a Quality Specialist to join a global pharmaceutical company on a contract basis for 6 months. This role is based in Runcorn.

Company

Our client's aim is to be a global leader in generics and biopharmaceuticals, improving the lives of patients across the world.

Salary

£15.38 per hour Rates are dependent upon experience

Mon-Fri, 9 am to 5 pm

Quality Specialist Role

• 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• Check document identification, version and approval status, issuing controlled copies and withdrawing superseded versions.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.

Your Background

• Excellent accuracy and attention to detail when checking, handling and recording information.
• Well organised, 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 (pharmaceutical, healthcare, finance or similar) would be useful.

It is essential that applicants hold entitlement to work in the UK.

Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check