Senior Quality Manager – Systems & Compliance

R&D Partners; City Of London; Presencial; GBP 60.000 - 90.000; Jornada completa

Descripción de la vacante

R&D Partners in the United Kingdom seeks a dedicated QA Manager to oversee quality systems, ensuring compliance with GxP regulations and readiness for inspections.

You will lead audits, train teams, review procedures, monitor supplier compliance, and drive continuous improvement across functions. Strong communication and leadership are essential; science degree preferred.

Formación

• Strong knowledge of pharmaceutical quality assurance and GxP regulations.
• Experience implementing effective and compliant quality management systems.
• Ability to prepare for, host, and follow up on audits and inspections.
• Leadership skills to manage and develop a high-performing team.
• Excellent communication, collaboration, and problem-solving abilities.

Responsabilidades

• Maintain and enhance quality systems to meet regulatory standards.
• Prepare for and manage audits and inspections.
• Provide training and support to teams on quality assurance practices.
• Review and update procedures to align with current regulations.
• Lead key quality meetings and ensure follow-up actions are completed.
• Monitor supplier compliance and audit schedules.
• Track and share performance metrics related to quality operations.
• Collaborate with other departments to improve processes and efficiency.
• Ensure documentation and data integrity comply with industry standards.
• Manage team workloads, priorities, and training needs.

Conocimientos

QA/GxP knowledge

Quality management systems

Audits & inspections

Leadership

Communication & collaboration

Problem solving

Science degree preferred

Educación

BSc/MSc in science

Descripción del empleo

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

R&D Partners is recruiting a dedicated and experience manager to oversee and improve quality systems, ensuring compliance with industry regulations and readiness for inspections. You will play a key role in supporting and training teams, managing audits, and driving a culture of quality across the organization.

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

Responsibilities

• Maintain and enhance quality systems to meet regulatory standards.
• Prepare for and manage audits and inspections.
• Provide training and support to teams on quality assurance practices.
• Review and update procedures to align with current regulations.
• Lead key quality meetings and ensure follow-up actions are completed.
• Monitor supplier compliance and audit schedules.
• Track and share performance metrics related to quality operations.
• Collaborate with other departments to improve processes and efficiency.
• Ensure documentation and data integrity comply with industry standards.
• Manage team workloads, priorities, and training needs.

Key Skills and Requirements

• Strong knowledge of pharmaceutical quality assurance and GxP regulations.
• Experience implementing effective and compliant quality management systems.
• Ability to prepare for, host, and follow up on audits and inspections.
• Leadership skills to manage and develop a high-performing team.
• Excellent communication, collaboration, and problem-solving abilities.
• Science-based degree (e.g., BSc or MSc) preferred.
• Familiarity with sterile manufacturing principles and guidelines.