Latest Quality Management Jobs

Medical Writer III, Oncology

The Medical Writer III role involves writing and coordinating complex clinical and regulatory documents for oncology, leading cross-functional document planning and review meetings, and mentoring junior staff. The position requires 6+ years of pharmaceutical/scientific industry experience, including 4+ years in regulatory medical writing, and proficiency in internal systems and processes.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Medical Writer III, X-TA

This 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 may be located in multiple European countries.

Johnson & Johnson MedTech Netherlands

Medical Writer III, X-TA

The Medical Writer III role involves writing and coordinating clinical and regulatory documents, leading cross-functional document planning 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

Medical Writer III, X-TA

The Medical Writer III role involves writing and coordinating clinical and regulatory documents, leading cross-functional document planning meetings, and mentoring junior staff. The position is hybrid, with 3 days onsite weekly, and may be located in multiple European countries.

Johnson & Johnson MedTech

Medical Writer III, X-TA

This 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

Medical Safety Officer - PALM

This role involves leading the safety assessment and risk management of pharmaceutical products across their lifecycle, with a focus on evaluating safety data from clinical trials, literature, and post-market sources. The Medical Safety Officer provides medical expertise to cross-functional teams, contributes to regulatory submissions, and ensures compliance with global pharmacovigilance standards. A key responsibility is leading Safety Management Teams and guiding risk mitigation strategies in collaboration with regulatory authorities and internal stakeholders.

Johnson & Johnson MedTech

Medical Safety Officer - PALM

This role involves leading the safety assessment and risk management of pharmaceutical products across their lifecycle, with a focus on evaluating safety data from clinical trials and real-world sources. The Medical Safety Officer provides strategic medical oversight to cross-functional teams, contributes to regulatory submissions, and ensures compliance with global pharmacovigilance standards. Key responsibilities include leading Safety Management Teams, developing risk mitigation strategies, and communicating safety findings to internal leadership and health authorities.

Johnson & Johnson MedTech

Medical Safety Officer - PALM

This role involves leading the medical safety assessment of pharmaceutical products throughout their lifecycle, with a focus on signal detection, risk management, and regulatory compliance. The Medical Safety Officer provides scientific leadership across cross-functional teams, contributes to key regulatory documents, and communicates safety findings to internal stakeholders and health authorities. The position requires strong expertise in pharmacovigilance, clinical trial safety, and global regulatory standards.

Johnson & Johnson MedTech

Medical Safety Officer - PALM

This role involves leading the safety assessment and benefit-risk oversight of pharmaceutical products across their lifecycle, with a focus on proactive risk management and regulatory compliance. The Medical Safety Officer provides medical expertise to cross-functional teams, contributes to clinical and regulatory documentation, and communicates safety findings to internal leadership and external health authorities. Key responsibilities include signal detection, risk mitigation strategy design, and medical oversight of safety evaluations.

Johnson & Johnson MedTech

Sr. Manager, Safety/PSM

Leads environmental, health, safety, and Process Safety Management (PSM) programs at a manufacturing site, ensuring regulatory compliance and driving a strong safety culture. Focuses on risk-based safety integration, incident investigation, and continuous improvement in regulated environments. Serves as a key advisor to leadership on safety strategy and regulatory interactions.

Johnson & Johnson MedTech United States £122,000 – £245,000 pa

On-site Permanent

Sr. Manager, Safety/PSM

The Sr. Manager, Safety/PSM role involves leading and managing global safety and Process Safety Management (PSM) programs, ensuring compliance with regulations, and driving a strong safety culture. Key responsibilities include developing safety policies, conducting audits, and partnering with site leadership to mitigate risks.

Johnson & Johnson MedTech

Sr. Manager, Safety/PSM

The Sr. Manager, Safety/PSM leads and manages global safety and Process Safety Management (PSM) programs, ensuring compliance with regulations and driving a strong safety culture. Key responsibilities include leading safety audits, developing safety policies, and partnering with site leadership to mitigate risks.

Johnson & Johnson MedTech £122,000 – £245,000 pa

Sr. Manager, Safety/PSM

Leads environmental, health, and safety (EHS) and Process Safety Management (PSM) programs at a manufacturing site, ensuring regulatory compliance and driving a strong safety culture. Responsibilities include managing PSM elements such as hazard analysis, management of change, and incident investigation, while partnering with operations and leadership to mitigate risks. Focuses on continuous improvement of safety systems and performance through data analysis, audits, and cross-functional collaboration.

Johnson & Johnson MedTech US$122,000 – US$245,000 pa

On-site Permanent

Sr. Manager, Safety/PSM

The Sr. Manager, Safety/PSM leads and manages global environmental, health, safety, and Process Safety Management (PSM) programs. Key responsibilities include ensuring regulatory compliance, driving a strong safety culture, and integrating risk-based safety practices into manufacturing and operational activities.

Johnson & Johnson MedTech £122,000 – £245,000 pa

Medical Writer III, Oncology

The Medical Writer III role involves writing and coordinating clinical and regulatory documents for oncology treatments, leading cross-functional teams, and mentoring junior staff. Responsibilities include document planning, content review, and process improvement.

Johnson & Johnson MedTech Belgium