Latest Managed Services Jobs

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Responsibilities include monitoring study progress, drafting key documents, coordinating meetings, managing communications, and overseeing clinical supplies and budget tracking.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are delivered on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, managing study communications, and overseeing clinical supply and investigational product delivery.

GSK

Hybrid Permanent

Head of Data & BI Platform Engineering

Leads Pfizer's enterprise data and BI platform engineering, overseeing critical data infrastructure including data warehouses, ETL pipelines, and visualization tools. Responsible for platform strategy, reliability, governance, and enabling AI/ML workloads through scalable, secure data services. Works closely with federated analytics teams to ensure high availability, performance, and compliance across global data platforms.

Pfizer US$274,000 – US$456,600 pa

Hybrid Permanent

Head of Data & BI Platform Engineering

Leads Pfizer's enterprise data and BI platform engineering, overseeing critical data warehousing, integration, and visualization systems that underpin AI and analytics initiatives. Responsible for platform strategy, SLA-driven operations, and cross-functional collaboration to ensure reliable, governed access to data across the organization. Focuses on scaling cloud-based platforms like Snowflake and Databricks while aligning with AI-ready data standards and regulatory compliance.

Pfizer US$246,600 – US$411,000 pa

Hybrid Permanent

Associate Production Manager /Secondment

This role involves supporting pharmaceutical manufacturing operations at AstraZeneca’s Macclesfield site, focusing on formulation, filling, packaging, and process performance. The Associate Production Manager will gain hands-on experience in cGMP compliance, deviation management, and Manufacturing Excellence initiatives while developing leadership and coaching skills. Working in a science-driven, patient-focused environment, the role emphasizes safety, operational standards, and continuous improvement within a collaborative team setting.

AstraZeneca Macclesfield, United Kingdom

On-site Contract

Global Labelling Manager, Content

The Global Labelling Manager, Content will lead the development and maintenance of high-quality global labelling documents for pharmaceutical products. Key responsibilities include organising cross-functional discussions, conducting research on competitor labels and regulatory guidance, and ensuring compliance with global standards across the product lifecycle.

Novartis London, United Kingdom

Hybrid Permanent

Global Program Regulatory Manager - Neuroscience

This role involves driving regulatory strategy and execution for neuroscience products across global markets, with a focus on preparing and submitting clinical trial applications, managing health authority interactions, and ensuring compliance throughout the product lifecycle. The manager will work cross-functionally to translate scientific data into regulatory submissions and support timely approvals. It is a hybrid role based in London, requiring strong expertise in pharmaceutical regulatory affairs.

Novartis

Hybrid Permanent

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

Director, CMC Regulatory Affairs

Lead the development and execution of global CMC regulatory strategies for small molecule drugs in clinical trials and marketing applications. Author and manage high-quality regulatory submissions across the US, EU, and rest of world, while advising cross-functional teams on compliance, risk mitigation, and evolving GMP standards. Collaborate closely with internal and external stakeholders to ensure timely delivery of regulatory deliverables and support clinical development programs.

Recursion London, W1C 2QP, United Kingdom

Remote Permanent

Associate Director, CMC Regulatory Affairs

This role involves leading the development and implementation of CMC regulatory strategies for small molecule drugs in global clinical trials. Responsibilities include managing CMC submissions, providing regulatory guidance, and collaborating with cross-functional teams to ensure compliance with US, EU, and ROW regulations.

Recursion United Kingdom £176,400 – £228,250 pa

Hybrid Permanent Flexible

Quality Engineer - Medical Devices - Didcot

Quality Engineer - Medical Devices - DidcotA pioneering medical device company in Didcot is looking to appoint a Quality Engineer to support the continued development, manufacture and improvement of its life‑changing technology. Newton Colmore is recruiting for this position exclusively,...

Newton Colmore Didcot, Oxfordshire, United Kingdom

Manufacturing Technician

This role involves supporting the production and testing of medical devices in a regulated manufacturing environment. The technician will maintain equipment, calibrate systems, and ensure accurate documentation while adhering to strict quality and safety standards. Work is conducted as part of a laboratory and manufacturing team with a focus on precision and compliance.

Manpower Birmingham, West Midlands (county), United Kingdom £14 ph

On-site Temporary

Regulatory Affairs Specialist

This role involves maintaining technical documentation and ensuring compliance with UK and EU MDR regulations for Class I and IIa medical devices. The specialist will support regulatory submissions, post-market surveillance, and quality management system development within a regulated environment. Collaboration with the QA Manager and ongoing product lifecycle support are key aspects of the position.

Cure Talent Upper Marlbrook, Worcestershire, B61 0RT, United Kingdom £45,000 – £50,000 pa

On-site Permanent

Embedded Software Engineer

This role involves designing and maintaining embedded C/C++ firmware for medical and mechatronic devices, taking full ownership of the software lifecycle, and establishing internal processes such as version control and documentation standards. The engineer will work hands-on with hardware teams, debug using test equipment, and lead the transition of firmware development from external contractors to in-house. It’s a rare opportunity to shape software engineering practices from the ground up within a small, mission-driven team focused on life-changing technology.

YT Technologies Belle Isle, West Yorkshire, WF1 5PS, United Kingdom £45,000 – £60,000 pa

Hybrid Permanent

Internal Sales Engineer - Laboratory Technologies

This role involves providing technical sales and customer support for precision laboratory components and systems, handling inquiries, quotations, and order processing. The engineer will work closely with external sales and internal teams, using SAP and CRM systems to manage customer information. Communication with customers is conducted via phone, email, and live chat, ensuring accurate and efficient service throughout the sales cycle.

ETS Technical Witney, Oxfordshire, United Kingdom £30,000 – £32,000 pa

On-site Permanent