Quality Assurance Officer

Talentmark; England; Presencial; GBP 30.000 - 38.000; Jornada completa

Descripción de la vacante

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

You will provide GMP compliance support to the site, report to the QA Manager and help prepare, review and approve quality documentation, deliver GMP training, and assist with audits, deviations, validation and batch documentation.

Formación

• Degree in related scientific discipline.
• Relevant quality experience in a pharmaceutical environment.
• Previous manufacturing / production experience preferred in a GMP environment.
• Competent in MS Word & Excel.

Responsabilidades

• 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.

Conocimientos

GMP compliance

Quality control

MS Word

MS Excel

Educación

Degree in related scientific discipline

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.

Salary

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.

Essential Skills

• 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.