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Senior Local Trial Manager

The Senior Local Trial Manager is responsible for overseeing clinical trials in the UK, ensuring compliance with protocols, SOPs, and regulatory standards. Key responsibilities include coordinating trial activities, managing site selection, and maintaining relationships with external and internal stakeholders. The role involves process improvement, mentoring team members, and delivering high-quality data.

Johnson & Johnson MedTech High Wycombe, United Kingdom
Hybrid Permanent

Technology Director, Make EMEA

This role leads the EMEA manufacturing technology strategy for DePuy Synthes, focusing on digital solutions like MES, automation, and data integration across regulated MedTech sites. The director partners with operations and quality leaders to ensure compliant, efficient, and standardized systems while leading regional teams and shaping global strategy. Key initiatives include digital manufacturing, cybersecurity, and data-driven decision-making in a highly regulated environment.

Johnson & Johnson MedTech Ireland
Hybrid Permanent
Medtronic logo

Product Portfolio Marketing Specialist

In this role, you will shape the competitive landscape for bladder and bowel neurostimulation therapies, driving international product launches and marketing strategies. You will collaborate with cross-functional teams to ensure successful market entry and growth, while gathering market intelligence and supporting sales teams with marketing expertise.

Medtronic Watford, United Kingdom
Remote Permanent
Medtronic logo

Product Portfolio Marketing Specialist

This role involves shaping the competitive landscape for bladder and bowel neurostimulation therapies internationally. You will lead product launches, develop marketing strategies, and collaborate with cross-functional teams to ensure successful market penetration and growth. The position requires a strong background in medical device marketing and the ability to work in a fast-paced, international environment.

Medtronic Italy
Remote Permanent

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. They actively participate in risk management activities, maintain clinical quality plans, and communicate risk updates to stakeholders through regular reviews and governance meetings.

Johnson & Johnson MedTech
On-site Permanent

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. Key responsibilities include active participation in study activities, regular risk reviews, maintaining clinical quality plans, and facilitating risk updates to R&D colleagues.

Johnson & Johnson MedTech
On-site Permanent

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

Product Marketing Lead Electrophysiology

This role involves leading the Product Marketing team for electrophysiology across EMEA, driving the execution of the regional commercial plan, and developing customer engagement programmes. The position requires deep expertise in MedTech, particularly in electrophysiology and cardiovascular treatments, and involves collaborating with various stakeholders to ensure successful product launches and commercial performance.

Johnson & Johnson MedTech France
On-site Permanent

Product Marketing Lead Electrophysiology

This role involves leading the Product Marketing team for electrophysiology across EMEA, driving the execution of new product launches, developing customer engagement programmes, and ensuring commercial performance. The position requires deep expertise in MedTech, particularly in electrophysiology and cardiovascular treatments, and a strong track record in product marketing and commercial execution.

Johnson & Johnson MedTech
On-site Permanent

Product Marketing Lead Electrophysiology

This role involves leading the Product Marketing team for electrophysiology across EMEA, driving the execution of the regional commercial plan, and developing customer engagement programmes. The position requires deep expertise in MedTech, particularly in electrophysiology and cardiovascular treatments, and a strong track record in product marketing and commercial execution.

Johnson & Johnson MedTech
On-site Permanent

Specialist, Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, works with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. They actively participate in study activities, maintain clinical quality plans, and communicate risk updates to R&D colleagues through regular review cycles.

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

Director, 3rd Party RM. Program (BPO)

The Director, 3rd Party RM Program provides strategic leadership for an enterprise-wide third-party risk management program, focusing on anti-bribery and anti-corruption risks. Key responsibilities include setting global standards, developing risk assessment frameworks, overseeing due diligence processes, and partnering with Legal and IT to implement technology solutions.

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

Associate Director, RA UK & Ireland

The role involves leading and overseeing regulatory affairs activities for the UK market, ensuring compliance with UK and EU regulations, and managing regulatory risk. The Associate Director will partner with various teams to support product registrations, lifecycle management, and business initiatives, while also leading the UKCA marking strategy and coaching regulatory team members.

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

Sr. Source Reg Compliance Specialist

The Sr. Source Regulatory Compliance Specialist is responsible for ensuring suppliers and externally provided processes comply with regulatory requirements and quality standards. Key responsibilities include executing supplier audits, supporting compliance oversight, and maintaining documentation. The role involves close collaboration with Quality, Regulatory Affairs, Supply Chain, and Procurement teams to maintain product quality and supply continuity.

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

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