Summary: The role of Quality Specialist at a global pharmaceutical client in Moorgate, London, involves ensuring compliance with GMP and regulatory standards through the review of clinical batch records. This temporary contract position offers exposure to a variety of investigational medicinal products and requires strong communication skills and attention to detail. The position is hybrid and includes a competitive hourly rate based on experience. The role also involves conducting audits and collaborating with global functions to support the clinical supply chain.

Key Responsibilities:

• Conduct routine audits of data, procedures, equipment, and systems to ensure compliance with SOPs and GMPs.
• Review and approve production and analytical documentation for the release of API and clinical supply lots.
• Communicate and resolve audit comments with client areas.
• Perform audits or inspections of assigned areas or systems under supervision or as part of a team.
• Issue reports summarizing deficiencies and work with areas to execute remedial action.
• Notify appropriate management of inspection results.

Key Skills:

• Experience in the pharmaceutical/chemical industry or government drug-regulatory agency.
• Working knowledge of cGMP regulations.
• Effective oral and written communication skills.
• Interpersonal skills necessary for collaboration.
• Experience in a QA or similar role in a GMP environment preferred.
• Bachelor’s degree in a relevant field for new science graduates.
• Willingness to learn and adapt.

Salary (Rate): £29.39

City: London

Country: United Kingdom

Working Arrangements: hybrid

IR35 Status: undetermined

Seniority Level: Mid-Level

Industry: Other