Latest Pharmaceutical Scientist Jobs

Senior Principal Statistical Programmer

The Senior Principal Statistical Programmer leads statistical programming activities for multiple clinical studies or large projects, ensuring high-quality and timely deliverables. They collaborate with biostatistics, coordinate programming teams, and maintain compliance with industry standards.

Novartis London, United Kingdom

On-site Permanent

Principal Statistical Programmer

The Principal Statistical Programmer leads statistical programming activities for large or pivotal clinical studies, ensuring high-quality and timely deliverables. They collaborate with cross-functional teams, mentor other programmers, and maintain compliance with industry standards.

Novartis London, United Kingdom

On-site Permanent

DOCUMENT CONTROLLER

Compliance and Documentation AdministratorCrewe£28275 per annumFull-Time, PermanentAn excellent opportunity has arisen for an organised and detail-oriented Compliance and Documentation Adminitrator to join a successful and growing organisation operating within a highly regulated industry.This role is ideal for someone with strong...

KPI Recruiting Crewe Green, Cheshire, CW1 5UN, United Kingdom £28,275 pa

Connectivity Specialist

Evolve are partnering with a driven medical device manufacturer who are seeking a Connectivity Specialist to help shape the future of connected healthcare. This is an exciting opportunity to combine technical expertise, customer engagement, and project leadership to deliver innovative...

Evolve Selection Watford, Hertfordshire, United Kingdom

Production maintenance technician

Production Maintenance Technician – Night ShiftLocation: Plymouth, DevonSector: Medical Devices / Advanced ManufacturingEmployment Type: PermanentKinetic Business Solutions are supporting a leading medical devices manufacturer based in Plymouth with the appointment of a skilled Production Technician to join their night shift...

Kinetic Business Solutions Devon, United Kingdom £30,000 – £31,000 pa

Senior Specialist I, QA Clinical

The Senior Specialist I, QA Clinical is responsible for quality oversight in clinical development, supporting cross-functional relationships and ensuring compliance with GCP/GVP regulations. Key responsibilities include developing and implementing risk-based audit plans, conducting audits, and managing quality events. The role involves working closely with clinical project teams and external stakeholders, and maintaining the quality management system.

Autolus Stevenage, United Kingdom

Hybrid Permanent Flexible

Senior Engineering Technician /Secondment

This role involves providing hands-on engineering leadership to support the introduction and scale-up of new pharmaceutical products within a regulated manufacturing environment. The technician will ensure equipment and processes meet safety, compliance, and reliability standards, lead technical issue resolution, and coordinate engineering activities across teams during product launches and validation. Emphasis is placed on operational readiness, change control, and continuous improvement in a GMP-compliant setting.

GSK Barnard Castle, United Kingdom

On-site Contract

Associate Principal AI & ML Engineer – Evinova

As an Associate Principal AI & ML Engineer at Evinova, you will develop and integrate advanced algorithms and generative AI systems to optimize clinical trial design and improve drug development processes. Your role involves working with multi-source data, building production systems, and collaborating with cross-functional teams to drive impactful solutions.

AstraZeneca London, United Kingdom

Hybrid Permanent

Steriles Business Change Lead

Lead business change initiatives for sterile manufacturing at a GSK site in Barnard Castle, ensuring operational readiness across quality, compliance, and production systems. Coordinate cross-functional teams through commissioning, validation, and go-live phases, with a focus on safety, regulatory compliance, and sustainable performance improvement in a highly regulated pharmaceutical environment.

GSK Barnard Castle, United Kingdom

On-site Permanent

Master Scheduler, Engineering

Work with usOur team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working...

Autolus Stevenage, United Kingdom

ViiV Healthcare (GSK) Medical Director, ViiV R&D Physician Center of Excellence

This Medical Director role involves leading Phase 1-4 clinical trials, ensuring the successful planning, execution, and reporting of protocols for innovative HIV treatments. The role requires strong medical governance, safety expertise, and cross-functional collaboration with internal and external stakeholders to advance ViiV's mission of delivering long-acting HIV therapies.

GSK United States

On-site Permanent

ViiV Healthcare (GSK) Medical Director, ViiV R&D Physician Center of Excellence

This Medical Director role involves managing and overseeing Phase 1-4 clinical trials for ViiV Healthcare, focusing on the development of innovative HIV treatments. Key responsibilities include designing study protocols, ensuring medical governance, managing safety events, and collaborating with internal and external stakeholders to drive the success of clinical trials.

GSK

On-site Permanent

ViiV Healthcare (GSK) Medical Director, ViiV R&D Physician Center of Excellence

The Medical Director role at ViiV Healthcare focuses on managing and overseeing Phase 1-4 clinical trials, ensuring the successful planning, execution, and reporting of protocols. Key responsibilities include providing medical governance, managing safety events, and collaborating with internal and external stakeholders to develop groundbreaking HIV treatments.

GSK

On-site Permanent

Executive Director Clinical Operations, Program Management

This role leads global clinical program delivery within AstraZeneca’s Oncology portfolio, focusing on strategic planning, operational excellence, and cross-functional leadership across late-stage development. The Executive Director will manage senior program directors, drive standardization, resolve escalated issues, and strengthen internal and external partnerships to accelerate patient impact. It involves governance, resource planning, financial stewardship, and leading organizational change in a dynamic, science-driven environment.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Small Molecule CMC Leader - Senior Director

Leads Chemistry, Manufacturing and Controls (CMC) strategy and execution for small molecule, biopharm, or cell and gene therapy medicines from late-stage development through commercialisation. Oversees process development, regulatory filings, supply chain, and lifecycle management across global teams and external partners, ensuring readiness for approval and launch. Role involves high-level governance engagement, risk management, and transition to commercial supply.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent