Latest Professional Services Jobs

Field Service Engineer - Stoke-on-Trent to Wrexham

As a Field Service Engineer, you will provide essential technical support for Roche’s medical diagnostic systems, ensuring seamless operation and maximum uptime. Your responsibilities include troubleshooting complex faults, performing preventive maintenance, and training customers on the use of Roche’s innovative diagnostic equipment.

Roche

On-site Permanent

Field Service Engineer - Birmingham to Worcester Location

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive...

Roche United Kingdom

Global Study Lead

The Global Study Lead is responsible for managing the full lifecycle of clinical studies, from design and planning to execution and documentation. Key responsibilities include leading the study team, ensuring compliance with regulations, managing budgets, and collaborating with cross-functional teams and external partners to deliver high-quality study results.

Roche United States US$100,400 – US$186,400 pa

On-site Permanent

Global Study Lead

The Global Study Lead is responsible for overseeing the design, planning, execution, and documentation of clinical studies, ensuring compliance with regulatory requirements and delivering high-quality results within budget and timelines. The role involves leading cross-functional teams, collaborating with internal and external stakeholders, and managing study-level budgets and operational aspects.

Roche US$100,400 – US$186,400 pa

On-site Permanent

Sales Specialist - South West

This role involves driving sales of Roche's tissue-based diagnostic solutions within NHS pathology networks across the South West UK. The specialist will lead account strategy, engage with clinical and procurement stakeholders, and respond to complex tenders, leveraging digital tools and a deep understanding of cancer diagnostics workflows. The position plays a key role in shaping adoption of advanced diagnostic technologies in a changing healthcare landscape.

Roche United Kingdom

Hybrid Permanent

Product Specialist RCSC

This role involves providing remote technical and scientific support for Roche's Serum Work Area and Near Patient Care portfolio, including troubleshooting complex issues, conducting product training, and managing customer inquiries. The position also requires collaboration with field teams and sales managers to enhance customer satisfaction and service quality.

Roche Finland

Hybrid Permanent Flexible

Product Specialist RCSC

This role involves providing remote technical and scientific support for Roche's Serum Work Area and Near Patient Care portfolio, including troubleshooting complex issues, conducting product training, and managing customer inquiries. The position also requires collaboration with field teams and sales managers to enhance customer satisfaction and support commercial activities.

Roche

Hybrid Permanent Flexible

Biomededical Training Engineer

This role involves managing the full lifecycle of medical device refurbishment through Return to Base (RTB) processes, including inspection, repair, calibration, and compliance with MHRA, ISO 13485, and HTM standards. The engineer will also deliver hands-on technical training, mentor junior staff, and support continuous improvement initiatives. Collaboration with hospitals, OEMs, and internal teams ensures safe, compliant equipment is redeployed efficiently while improving service delivery.

Focus Resourcing Harlow, Essex, United Kingdom

On-site Permanent Clearance Required

Submission Readiness Document Manager

This role involves managing the submission-readiness of clinical documents to ensure they meet regulatory and quality standards for global submissions. The professional will oversee technical editing, support compliance with health authority guidelines, and work closely with cross-functional teams to improve document processes. It requires expertise in clinical documentation systems and a strong focus on operational excellence in a fast-paced, regulated environment.

Novartis London, United Kingdom £49,140 – £91,260 pa

Hybrid Permanent

Clinical Quality Assurance - Program Lead (Associate Director)

The Associate Director, Clinical Quality Assurance (QA) will lead quality oversight for clinical trials, ensuring compliance with health authority requirements and patient safety. Responsibilities include implementing quality strategies, monitoring risk management, and supporting governance for quality incidents. The role involves collaboration with key stakeholders and active participation in continuous improvement initiatives.

Novartis London, United Kingdom

Hybrid Permanent

Quality Professional

This role involves maintaining and improving the Quality Management System for medical devices, ensuring compliance with ISO 13485 and FDA regulations. The professional will lead non-conformance investigations, manage CAPA processes, conduct risk assessments per ISO 14971, and support process validation and supplier quality activities. Close collaboration with R&D, manufacturing, and regulatory teams ensures quality is embedded across the product lifecycle.

Omega Resource Group Middleyard, Gloucestershire, United Kingdom

On-site Permanent

Regulatory Transparency (Disclosures) Professional

In this role, you will manage the end-to-end execution of clinical trial registration and results posting, ensuring Roche complies with global regulations. You will lead the accurate and timely posting of clinical trial data, manage cross-functional teams, and ensure consistency and quality in all submissions.

Roche Welwyn Hatfield, United Kingdom

On-site Permanent

Regulatory Science Professional - Intelligence

This role involves managing regulatory intelligence for Roche’s pharmaceutical and medical device portfolio in the EU, with a focus on generating strategic, data-driven insights. The professional will leverage AI tools, maintain regulatory databases, and collaborate across global teams to inform decision-making and drive innovation in a dynamic regulatory environment.

Roche Welwyn Hatfield, United Kingdom

Hybrid Permanent

Quality Engineer

This role involves managing quality systems and asset calibration processes within a regulated medical devices environment. The Quality Engineer will oversee compliance with safety standards, maintain documentation integrity, and support audits while ensuring equipment is properly maintained. Training team members and improving health and safety performance are also key responsibilities.

Randstad Delivery Witney, Oxfordshire, United Kingdom £57,000 pa

On-site Contract

Director, Statistical Programming

This role involves leading and developing a team of programmers, providing strategic direction for statistical programming in clinical development, and ensuring quality, compliance, and continuous improvement. The Director will partner cross-functionally to drive business impact and maintain industry and regulatory knowledge.

AstraZeneca Cambridge, United Kingdom

On-site Permanent