Latest Quality Management Jobs

Medical Writer III, X-TA

The Medical Writer III role involves writing and coordinating clinical and regulatory documents, leading cross-functional document planning and review meetings, and mentoring junior staff. The position is hybrid, with 3 days onsite weekly, and supports key therapeutic areas within the Integrated Data Analytics & Reporting (IDAR) business.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Exp Anlst Reg Aff

The Lead Content Compliance Specialist role involves coordinating and optimizing advertising and promotional material approval processes across EMEA. Key responsibilities include managing complex submissions, driving process improvements, and ensuring compliance with regulatory standards.

Johnson & Johnson MedTech Leeds, United Kingdom

Trainee Medical Sales

This role involves driving new business and developing existing customer relationships in the medical devices sector, with a focus on NHS and private healthcare customers. The trainee will receive comprehensive training and support while promoting a respected range of medical products in an operating room environment.

Wallace Hind Selection Slough, Berkshire, United Kingdom £35,000 – £40,000 pa

Surgical Medical Sales Representative

This role involves driving new business and developing existing customer relationships for surgical oncology medical implant products. The job is highly consultative, requiring preparation of quotations, equipment demonstrations, and participation in industry fairs and congresses.

Wallace Hind Selection Swindon, Wiltshire, United Kingdom £45,000 – £50,000 pa

Medical Writer III, Oncology

The Medical Writer III role involves writing and coordinating complex clinical and regulatory documents for oncology, leading cross-functional teams, and mentoring junior staff. Responsibilities include document planning, content review, and championing best practices in medical writing.

Johnson & Johnson MedTech Canada

Associate Director, Safety Analysis Scientist

Leads safety evaluation and risk management for pharmaceutical products across development and post-marketing phases, providing scientific analysis to inform regulatory decisions and benefit-risk assessments. Works cross-functionally within Global Medical Safety to conduct proactive data reviews, support safety documentation, and guide strategy. Serves as subject matter expert and may oversee training, audits, and process improvements.

Johnson & Johnson MedTech United States US$137,000 – US$235,750 pa

Hybrid Permanent

Associate Director, Safety Analysis Scientist

This role involves leading safety evaluations for pharmaceutical products in development and on the market, with a focus on analyzing complex medical data, supporting global safety teams, and ensuring regulatory compliance. The scientist will act as a subject matter expert, contribute to safety strategy, and provide oversight on critical safety documentation and risk management. Based in the U.S., the position operates in a hybrid model with significant autonomy and cross-functional collaboration.

Johnson & Johnson MedTech US$137,000 – US$235,750 pa

Hybrid Permanent

Associate Director, Safety Analysis Scientist

This role involves leading the scientific safety assessment of pharmaceutical products across development and post-marketing stages, with a focus on analyzing complex medical data, supporting global safety teams, and ensuring regulatory compliance. The Associate Director will serve as a subject matter expert, driving safety evaluations, contributing to key clinical documents, and advising on risk management strategies. They will also lead training initiatives, support audits, and innovate processes for safety data interpretation and reporting.

Johnson & Johnson MedTech £137,000 – £235,750 pa

Hybrid Permanent

Manager, 3PL Partner Excellence

This role involves managing 3PL partner relationships, deploying standardized processes, and ensuring alignment with transformation objectives. Responsibilities include contract management, performance tracking, and governance activities across the EMEA distribution network.

Johnson & Johnson MedTech

Manager, 3PL Systems & Integration

This role involves defining and maintaining business process integration requirements for 3PL WMS operations, ensuring consistent and scalable execution across the global distribution network. The Manager will collaborate with various teams to align warehouse processes, operational standards, and system interaction points, driving governance and continuous improvement initiatives.

Johnson & Johnson MedTech United Kingdom

Hybrid Permanent

Manager, 3PL Systems & Integration

This role involves defining and maintaining business process integration requirements for 3PL WMS operations, ensuring consistent and scalable execution across the global distribution network. The Manager will work closely with global Transformation, IT, and regional teams to align warehouse processes, operational standards, and system interaction points.

Johnson & Johnson MedTech

Manager, 3PL Systems & Integration

This role involves defining and integrating Warehouse Management System (WMS) capabilities across 3PL-operated distribution sites. Responsibilities include aligning warehouse processes, operational standards, and system interaction points to ensure consistent execution across the global distribution network. The position works closely with global Transformation, IT, and regional teams to support the asset-light operating model and drive continuous improvement.

Johnson & Johnson MedTech

OT Cyber Security Lead

The Manufacturing Systems Cybersecurity Global Lead will develop and maintain the global OT cybersecurity strategy and standards for DePuy Synthes manufacturing sites. Responsibilities include evaluating cybersecurity technologies, driving standardization, and conducting assessments to enhance security and operational resilience.

Johnson & Johnson MedTech Leeds, United Kingdom

Manager, Medical Writing, Immunology

Leads medical writing activities for clinical documents in the Immunology therapeutic area, providing scientific and strategic leadership. Manages a team of medical writers, mentors junior staff, and collaborates cross-functionally to ensure regulatory compliance and high-quality documentation. Works within a global regulatory environment, contributing to process improvements and departmental best practices.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

OT Cyber Security Lead

The Manufacturing Systems Cybersecurity Global Lead will develop and maintain the global OT cybersecurity strategy and standards for DePuy Synthes manufacturing sites. Responsibilities include evaluating cybersecurity technologies, driving standardization, and conducting assessments to enhance security and operational resilience across the global manufacturing network.

Johnson & Johnson MedTech Ireland