Jobs in Reading

Trial Vendor Senior Manager

This role involves managing all vendor-related aspects of global clinical trials, ensuring study outcomes are delivered within schedule, budget, and quality standards. The Senior Manager will collaborate with the Vendor Start-up Manager and other team members, oversee vendor service delivery, and manage risks and performance.

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom

Hybrid Permanent

Trial Vendor Senior Manager

This role involves managing all vendor-related aspects of global clinical trials, ensuring study outcomes are delivered on schedule, within budget, and to quality standards. You will collaborate closely with the Clinical Trial Team and vendor start-up managers, overseeing vendor interfaces, cost control, and service excellence.

Novartis United Kingdom

Hybrid Permanent Flexible

Field Service Engineer

As a Field Service Engineer, you will be the primary point of contact for customers in the Manchester area, providing technical support and maintenance for state-of-the-art robotics and automation solutions in the pharmaceutical and biotechnology industries. You will handle service calls, perform diagnostics, and ensure customer satisfaction through timely and professional communication.

Wallace Hind Selection Bolton, United Kingdom £52,000 – £56,000 pa

On-site Permanent

Member of Technical Staff, Applied AI

Member of Technical Staff, Applied AIThe opportunityWe are looking for a Member of Technical Staff with deep expertise in generative modelling to work at the interface between our frontier models and the customers who depend on them. You will join...

Latent Labs London, United Kingdom, United Kingdom

Hybrid Permanent

Forward Deployed AI Engineer

Forward Deployed AI EngineerThe opportunityWe are looking for a Forward Deployed AI Engineer to serve as the critical bridge between Latent Labs’ frontier generative models and the customers who rely on them. You will work directly with pharmaceutical and biotech...

Latent Labs London, United Kingdom, United Kingdom

Hybrid Permanent

Senior SME - MSAT EM Tech Ops DS DP

This role involves collaborating with internal and external stakeholders to support the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, providing lifecycle support, and ensuring compliance with GMP standards. The role also focuses on continuous improvement and managing technical transfers between contract manufacturing organizations (CMOs).

GSK East Hertfordshire, United Kingdom

On-site Permanent

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

The Data QC Specialist will perform detailed quality control reviews of laboratory data and documentation to ensure accuracy, traceability, and compliance with regulatory standards. This role involves working closely with laboratory scientists and data management teams to resolve data discrepancies and maintain inspection readiness.

Moderna Oxford, United Kingdom

On-site Temporary

SME - MSAT EM Technical Operations DS/DP

This role involves collaborating with internal and external stakeholders to support the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, managing product lifecycle activities, and ensuring compliance with GMP standards. The position also involves supporting CMOs in audits, technical transfers, and continuous improvement initiatives.

GSK United States

On-site Permanent

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

The Data QC Specialist will perform detailed quality control reviews of laboratory data and documentation to ensure accuracy, traceability, and compliance with regulatory standards. This role involves working closely with laboratory scientists and data management teams to resolve discrepancies and maintain inspection readiness.

Moderna

On-site Temporary

Senior Director of Operational Technology (Operations)

This role involves leading the execution of OT strategy across AstraZeneca's global manufacturing network, ensuring alignment with business priorities and improving reliability, safety, and compliance. Key responsibilities include lifecycle management, risk mitigation, capability building, and regulatory readiness.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

Vice President, Head of Clinical Operations

This role involves leading the clinical operations strategy and execution across Recursion’s full clinical portfolio, from early-stage studies to pivotal trials and submission support. The VP will build scalable operating models, manage global trials, and ensure operational excellence in a data-driven, patient-centered, and technology-enabled environment.

Recursion North Tyneside, NE29 8EP, United Kingdom

On-site Permanent

Vice President, Head of Clinical Operations

This role involves leading the clinical operations strategy and execution across Recursion’s development portfolio, from study planning to study closeout. You will build and mentor a high-performing team, manage global trials, and ensure operational excellence in an AI-native TechBio company.

Recursion United Kingdom

On-site Permanent

Design Lead - Drug Delivery Systems

The Design Lead role involves leading complex research projects and the design and development of novel infusion pumps and active implantable technology. You will work with a multidisciplinary team, providing technical and strategic leadership, and hands-on design work. The company values innovation and is focused on developing life-saving medical devices.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director at Pfizer is responsible for developing and maintaining quality plans, ensuring inspection and audit readiness, and providing quality oversight of process deviations and investigations. This role involves interpreting and applying global regulations, driving compliance, and collaborating with stakeholders to identify and mitigate risks, ensuring the quality and integrity of Pfizer's medicines and vaccines.

Pfizer Sandwich, United Kingdom

On-site Permanent

Quality & Regulatory Associate

This role involves supporting the development and maintenance of a Quality Management System aligned with ISO13485 and FDA requirements in a growing med-tech company. The candidate will manage regulatory documentation, design controls, and quality processes, contributing to audit readiness and continuous improvement. It's a hands-on position with direct impact on product compliance and regulatory submissions.

Taylorollinson Manchester, United Kingdom £35,000 – £45,000 pa

Hybrid Permanent