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A leading pharmaceutical company in the Berkshire area is seeking a dedicated QA Specialist. As the QA Specialist, you will play a crucial role in ensuring the timely establishment and maintenance of customer Quality Agreements (QAA) between our client and its customers. This is an initial 12 month contract with a balanced work arrangement of 3 days onsite and 2 days from home.

Key Duties And Responsibilities

• Act as the primary point of contact for Quality Agreements, representing the company in negotiations and ensuring consistency between internal processes and commitments in QAAs.
• Set up and manage a system to track the completion status of QAAs, monitor requirements for periodic review, and initiate reviews as needed.
• Participate in global QAA SOP revision working groups, improve existing tracking tools, and create new solutions for QAA-related document life cycles.
• Provide training on the QAA structure and content to functional teams within the company.

Role Requirements

• Relevant degree in a science-related discipline.
• Extensive industry experience within a GMP-regulated pharmaceutical environment, ideally in biologics or biopharmaceuticals, and/or relevant QA experience.
• Working knowledge and practical experience with risk-based decision-making, problem-solving, and accurate data entry skills.

Key Words: Quality Agreements Specialist / QA Specialist / Quality Assurance Specialist / QAA / pharmaceutical industry / GMP-regulated / biologics / biopharmaceuticals / risk-based decision-making / data entry / customer relations / SOP revision / document life cycle

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.