Jobs in Exeter

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities across EMEA and other highly regulated markets. You will evaluate compliance with GMP, regulatory requirements, and quality systems, and provide sterile manufacturing expertise. The role requires strong communication and stakeholder engagement skills.

GSK

Hybrid Permanent

Head of RTSM (Randomization and Trial Supply Management)

This role involves leading the RTSM function in the US, partnering with clinical development, operations, quality, and external vendors to design and deliver patient-focused randomization and clinical supply solutions. Responsibilities include managing cross-functional teams, risk assessments, process improvements, and fostering collaboration across internal and external partners.

GSK United States

Hybrid Permanent

Senior Clinical Development Medical Director - Renal

The Senior Clinical Development Medical Director will lead the strategy and execution of renal clinical development programs, from early to late phases. Responsibilities include providing clinical leadership, developing regulatory documents, ensuring patient safety, and collaborating with global teams and stakeholders.

Novartis

On-site Permanent

Senior Principal Biostatistician

This role involves leading the implementation of innovative trial designs and statistical models, collaborating with clinical and regulatory teams, and contributing to exploratory analyses and statistical consultations. The position requires a strong background in biostatistics and the ability to drive quantitative decision-making in clinical trials.

Novartis London, United Kingdom

Hybrid 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 Oversight and Compliance Director

The Quality Oversight and Compliance Director at Pfizer will be responsible for developing and maintaining quality plans, ensuring inspection and audit readiness, and providing 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 United Kingdom

On-site Permanent

MSAT Drug Product Lead (Parenteral Products)

This role involves managing the technical delivery of drug product manufacturing, primarily for GSK's sterile injectable products. Responsibilities include leading New Product Introduction (NPI), technology transfers, process verification, and regulatory submissions. The position requires strong technical expertise, collaboration across functions, and a focus on quality and compliance.

GSK East Hertfordshire, United Kingdom

On-site Permanent

MSAT Drug Product Lead (Parenteral Products)

This role involves managing the technical delivery of drug product manufacturing, primarily for GSK's sterile injectable products. Responsibilities include leading New Product Introduction (NPI), technology transfers, process verification, and regulatory compliance. The position requires strong technical expertise, collaboration across functions, and a focus on quality and patient safety.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

Global Study Manager

The Global Study Manager role involves leading the operational delivery of clinical studies from initiation to archiving, ensuring timelines, quality, and budget adherence. Key responsibilities include crafting delivery plans, leading the Operational Working Group, and collaborating with the Global Study Lead to achieve study deliverables. The role emphasizes innovation, risk management, and stakeholder communication.

GSK Stevenage, United Kingdom

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working closely with internal and external teams to ensure studies are delivered on time, on budget, and in compliance with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK Poland

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 on time, on budget, and compliant with standards. Key responsibilities include monitoring study conduct, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

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 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

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 clinical documents, coordinating meetings, managing study communications, and overseeing clinical supply and investigational product delivery.

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, and managing study communications and budgets.

GSK

Hybrid Permanent