Quality & Site Leader, QMR - GMP/Regulated Med Devices

Vantive; Liverpool; Hybrid; GBP 110,000 - 140,000; Full time

Benefits offered by this job

Annual bonus

Pension contribution

Car allowance

25 days annual leave

Job summary

Vantive, a vital organ therapy company, seeks a Senior Manager, Quality and Site Quality Management Representative (QMR) for its Liverpool site. You will lead the Quality function, shape strategy and uphold compliance across GMP, ISO 13485 and regulatory requirements. You will sit on the Site Leadership Team and drive continuous improvement.

The role focuses on safeguarding product quality, maintaining regulatory compliance and developing the Quality team within a busy manufacturing site.

Qualifications

• Eight+ years of experience in Quality Assurance, Quality Control, Regulatory Affairs or related areas.
• Experience in pharmaceutical or medical device manufacturing.
• Experience with active pharmaceutical ingredient manufacturing and MHRA or FDA audits.
• Comprehensive knowledge of cGMP and EU/FDA/PIC/S requirements.
• Strong leadership, communication and project-management skills.
• Ability to take ownership and collaborate in a regulated environment.

Responsibilities

• Lead the Liverpool Quality team and sit on the Site Leadership Team.
• Represent Site Quality Management as QMR and ensure regulatory compliance.
• Ensure products manufactured and shipped meet quality and regulatory standards.
• Maintain site licenses and regulatory submission commitments.
• Oversee quality systems, qualification and validation activities.
• Drive improvements to strengthen quality, compliance and site performance.

Skills

People leadership

Project management

Communication

Problem-solving

Collaboration

Education

Scientific or engineering degree

Job description

Vantive, a vital organ therapy company, seeks a Senior Manager, Quality and Site Quality Management Representative (QMR) for its Liverpool site. You will lead the Quality function, shape strategy and uphold compliance across GMP, ISO 13485 and regulatory requirements. You will sit on the Site Leadership Team and drive continuous improvement.

The role focuses on safeguarding product quality, maintaining regulatory compliance and developing the Quality team within a busy manufacturing site.