Quality Manager, RP

Hobson Prior International Ltd; Weybridge; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading life sciences recruiter is seeking a Quality Manager - Responsible Person (RP) to ensure adherence to quality management systems and regulatory requirements. This pivotal role involves overseeing compliance with GMP, GDP, and UK regulations, managing the quality issue resolution process, conducting audits, and leading training initiatives. The position requires a degree in life sciences and experience in quality assurance within the pharmaceutical industry.

Qualifications

• Degree in Pharmacy, Chemistry, Biology, or Pharmaceutical Sciences.
• Knowledge of UK/EU GMP and GDP regulations.
• Experience in quality assurance within manufacturing and distribution.

Responsibilities

• Oversee and improve the Quality Management System (QMS).
• Ensure compliance with quality and regulatory standards.
• Manage quality-related issues across the supply chain.

Skills

Problem-Solving

Organization

Communication

Leadership

Education

Degree in life sciences

Job description

Are you passionate about quality and precision? Join our client in this managerial position and help ensure top-tier standards every day.

Hobson Prior is seeking a Quality Manager - Responsible Person (RP) to ensure compliance with Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), and UK regulatory requirements for the manufacturing, importation, and distribution of medicinal products. In this role, you will oversee quality management systems, supply chain compliance, and act as the designated Responsible Person (RP) for Wholesale Distribution Authorisations (WDA(H)). This position is critical in maintaining high standards of product quality and regulatory adherence.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Oversee and improve the Quality Management System (QMS), including handling deviations, changes, complaints, and corrective actions.
• Ensure suppliers, manufacturers, and service providers meet quality and regulatory standards.
• Manage quality-related issues across the supply chain, including risk assessments and corrective action plans.
• Conduct audits of external partners and ensure follow-up on any required improvements.
• Maintain documentation for manufacturing processes and product specifications.
• Lead stability programs for licensed and unlicensed products.
• Provide training on GMP and GDP compliance to staff as needed.
• Act as the named Responsible Person (RP) for GDP compliance, ensuring proper storage, transportation, and handling of products.
• Ensure inspection readiness for UK sites holding WDA(H) licenses.

Key Skills and Requirements:

• Degree in life sciences (e.g., Pharmacy, Chemistry, Biology, or Pharmaceutical Sciences).
• Knowledge of UK/EU GMP and GDP regulations, including Human Medicines Regulations 2012.
• Experience in quality assurance within manufacturing and distribution environments.
• Eligible to act as a Responsible Person under MHRA guidelines.
• Strong problem-solving, organizational, and communication skills.
• Ability to lead, make decisions, and build effective relationships with teams, suppliers, and regulators.

For more information, please contact Frankie Cunnigham.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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