Quality Assurance Officer

Ck Group; West End; Presencial; GBP 32.000 - 44.000; Jornada completa

Descripción de la vacante

Talentmark are recruiting for a Quality Assurance Officer on behalf of a Life Science and Pharmaceutical Manufacturing Company. The role is based at their site in Norfolk, England, and is a full-time, permanent position.

The successful candidate will provide GMP compliance support and report to the QA Manager. Responsibilities include preparing and reviewing quality documentation, delivering GMP training, supporting change controls, deviations, validation, SOPs and batch documentation,

Formación

• Degree in related scientific discipline.
• Relevant quality experience in a pharmaceutical environment.
• Previous manufacturing / production experience in GMP environment is preferred.

Responsabilidades

• Prepare, review and approve quality documentation.
• Assist with GMP and quality training programmes, including delivering training.
• Support quality procedures such as change controls, deviations, validation, SOPs and batch documentation.
• Assist with internal audits.
• Review batch documentation prior to release.
• Support quality projects and report writing.

Conocimientos

GMP experience

Quality documentation

Training delivery

Batch documentation review

MS Word

MS Excel

Educación

Degree in life sciences

Herramientas

MS Word

MS Excel

Descripción del empleo

Talentmark are recruiting for a Quality Assurance Officer on behalf of a Life Science and Pharmaceutical Manufacturing Company.

This role will be based at their site in

Norfolk and is a full-time, permanent position.

The salary for this role is competitive, dependent on experience.

The Role

The Quality Assurance Officer is responsible for providing GMP compliance support to the site. The successful candidate will report to the QA Manager.

Responsibilities:

• Prepare, review and approve quality documentation.
• Assist with development of GMP and quality related training programmes, including delivering training.
• Support with quality procedures such as change controls, deviations, validation, SOPs and complete precise batch documentation.
• Assist with internal audits.
• Review batch documentation prior to release.
• Support quality projects and assist with report writing.
• Degree in related scientific discipline.
• Relevant quality experience in a pharmaceutical environment.
• Previous manufacturing / production experience is preferred, specifically in a GMP environment.
• Competent in computer packages, including MS Word & Excel.

Quality Assurance Officer • Norfolk, England, GB