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Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Responsibilities include active participation in study activities, maintaining clinical quality plans, and facilitating regular risk reviews and updates.

Johnson & Johnson MedTech
On-site Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, collaborates with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include participating in risk assessments, maintaining clinical quality plans, and communicating risk updates to R&D colleagues through regular review cycles.

Johnson & Johnson MedTech Belgium
On-site Permanent
Medtronic logo

Product Portfolio Marketing Specialist

This role involves shaping the competitive position of bladder and bowel neurostimulation therapies internationally. You will lead product launches, develop marketing strategies, and collaborate with cross-functional teams to drive growth and deliver measurable business impact.

Medtronic
Remote Permanent
Medtronic logo

Product Portfolio Marketing Specialist

This role involves shaping the competitive position of bladder and bowel neurostimulation therapies internationally. You will lead product launches, develop marketing strategies, and collaborate with cross-functional teams to drive growth and deliver measurable commercial results.

Medtronic
Remote Permanent

EMEA HEMA Associate Manager

The EMEA HEMA Associate Manager supports the development and execution of Health Economics & Market Access activities across EMEA, working closely with country HEMA Leads. Responsibilities include coordinating EMEA initiatives, generating evidence, developing value tools, and ensuring compliance with governance standards.

Johnson & Johnson MedTech
On-site Permanent

EMEA HEMA Associate Manager

The EMEA HEMA Associate Manager supports the regional development and execution of Health Economics & Market Access activities across EMEA. Key responsibilities include coordinating EMEA initiatives, generating evidence, developing value tools, and ensuring compliance with regulatory standards.

Johnson & Johnson MedTech
On-site Permanent

D&A and Master Data Specialist

The role involves maintaining and ensuring the accuracy of master data across multiple platforms, implementing data governance strategies, and collaborating with various departments to enhance data processes. The position also includes developing analytical reports and supporting the implementation of new MDM systems.

Johnson & Johnson MedTech
On-site Permanent

D&A and Master Data Specialist

This role involves maintaining and ensuring the accuracy of master data across multiple platforms, implementing data governance practices, and collaborating with various departments to enhance data processes. The position also includes developing analytical reports and supporting the implementation of new MDM systems.

Johnson & Johnson MedTech
On-site Permanent

Associate Director, Regulatory Policy

The Associate Director, Regulatory Policy, provides leadership in regulatory compliance and policy, ensuring alignment with global and regional requirements. Key responsibilities include interpreting regulatory policies, developing internal guidelines, and supporting cross-functional teams to manage regulatory risks and enable informed decision-making.

Johnson & Johnson MedTech United Kingdom
On-site Permanent

Medical Writer II, Oncology

This role involves writing and coordinating clinical and regulatory documents for oncology treatments, including Phase 1-3 protocols, CSRs, and IB updates. The Medical Writer II will work in a team environment, applying internal standards and regulatory guidelines, and may lead writing projects under supervision.

Johnson & Johnson MedTech High Wycombe, United Kingdom
On-site Permanent

Manager, Safety Analysis Scientist

The Manager, Safety Analysis Scientist role involves leading the safety assessment of assigned products, preparing scientific safety analyses, and collaborating with cross-functional teams to ensure regulatory compliance. The role requires in-depth product knowledge, mentoring team members, and supporting safety management teams.

Johnson & Johnson MedTech High Wycombe, United Kingdom
Hybrid Permanent

Product Manager - EMEA

As a Product Manager, you will lead cross-functional teams to develop innovative AI and digital solutions that transform the orthopaedics supply chain. You will collaborate with business partners to implement data-driven, scalable solutions that enhance patient care and streamline processes.

Johnson & Johnson MedTech Leeds, United Kingdom
On-site Permanent

Manager, EUDAMED & Data Transparency

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through...

Johnson & Johnson MedTech Leeds, United Kingdom

Manager, Medical Writing, Immunology

The Manager, Medical Writing, Immunology role involves preparing and finalizing clinical documents, leading cross-functional teams, and guiding team members on processes and best practices. The position focuses on the Immunology therapeutic area, working with a high level of independence to ensure timely and scientifically sound document delivery.

Johnson & Johnson MedTech High Wycombe, United Kingdom
On-site Permanent

Associate Director, Safety Analysis Scientist

This role involves leading scientific safety evaluations for pharmaceutical products across development and post-marketing stages, with a focus on analyzing complex medical data, shaping safety strategies, and supporting regulatory compliance. The scientist will serve as a subject matter expert, lead cross-functional safety reviews, contribute to key clinical documents, and drive innovation in safety analysis methodologies. Emphasis is placed on proactive risk assessment, collaboration with global teams, and ensuring high-quality, timely safety reporting.

Johnson & Johnson MedTech High Wycombe, United Kingdom
Hybrid Permanent

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