Im currently looking for a Quality Specialist to join a leading API business based in the Oxfordshire area. As the Quality Specialist you will be responsible for participating in leading Quality Systems improvement projects across the site as well as the following:

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the Quality Specialist will be varied however the key duties and responsibilities are as follows:

Participate in the improvement, update, alignment and maintenance of the existing quality system, including processes, procedures and associated tools, such as, Change control, deviations, CAPA, Validation, Qualification & Risk Management.

Responsible for the maintenance of the Quality IT systems, including eDMS & eQMS.

Promotes and contributes to Continuous improvement activities

Provide advice and guidance to other departments across the business to ensure they are compliant to company policies, best practices and cGMP.

ROLE REQUIREMENTS:

To be successful in your application to this great opportunity as the Quality Specialist we are looking to identify the following on your profile and past history:

1. Proven industry experience within a Pharmaceutical GMP business within a Quality Assurance position.

Experience of validation, including Computer System Validation.

3. A working knowledge and practical experience of Quality Management Systems

Key Words: QA, Quality Assurance, GMP, API, QMS, Quality Management System, CSV, Computer System Validation, Pharmaceutical

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.