Biotechnology Jobs

Engineering Technician (12 month secondment)

This role involves providing hands-on engineering support within a sterile pharmaceutical manufacturing environment, focusing on maintenance, compliance, and continuous improvement of production systems. The technician will work across complex equipment and processes, ensuring GMP standards, managing SAP systems, and supporting projects such as new product introductions. Key responsibilities include breakdown repairs, PPM activities, calibration, and supervision of contractors in a regulated, shift-based operation.

GSK Barnard Castle, United Kingdom

On-site Temporary

Senior Principal Statistician

This role involves providing advanced statistical expertise to support oncology clinical development across all phases, from early-stage trials to late-phase studies. The Senior Principal Statistician will lead the design and analysis of clinical trials using innovative methodologies such as Bayesian statistics and simulation techniques, working closely with cross-functional teams. The position emphasizes methodological innovation, risk assessment, and decision-making support within a global biopharma environment.

GSK Stevenage, United Kingdom

Hybrid Permanent

Medical Information Specialist

This role involves providing high-quality medical information to healthcare professionals, developing digital content for HCP and patient websites, and generating insights to support brand strategies. You will work closely with cross-functional teams to ensure clear and compliant scientific communication, focusing on Respiratory, Immunology, and Vaccines.

AstraZeneca London, United Kingdom

On-site Permanent

Scientist – Peptide Chemistry

This role involves conducting laboratory-based experimental work in peptide chemistry, designing and synthesizing peptides using solid-phase techniques, and contributing to the development of new peptide medicines. The position offers opportunities for personal and professional growth within a dynamic and collaborative team.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Director, CMC Regulatory Affairs

Leads global CMC regulatory strategy for small molecule medicines, working across R&D, supply, quality, and commercial functions to ensure regulatory compliance and uninterrupted patient supply. Provides strategic direction on regulatory submissions, mentors regulatory staff, and engages with global authorities. Focuses on solving complex regulatory challenges while aligning with business objectives and patient impact.

GSK

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role focuses on strengthening the operational and digital foundations of GSK's Supported Studies program. The Associate Director will lead data governance, system ownership, and digital integration efforts, ensuring data integrity, compliance, and efficiency across platforms like Veeva and IdeaPoint. The position acts as a bridge between business and technology, driving process improvements and digital transformation in a regulated clinical environment.

GSK US$154,275 – US$257,125 pa

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role leads operational excellence for Supported Studies at GSK, focusing on data integrity, system governance, and digital transformation. The individual will own the data and dashboard ecosystem, act as Business System Owner for key platforms like IdeaPoint and Veeva, and ensure compliance with regulatory requirements such as Transfer of Value. They will bridge business and technology to drive process improvements, enable resource planning, and enhance data transparency across clinical operations.

GSK £154,275 – £257,125 pa

Hybrid Permanent

Product Manager - Regulatory Vault

Are you passionate about making impactful contributions to the world of medicines and vaccines? GlaxoSmithKline (GSK) invites you to join our dynamic R&D Digital and Tech Team as a Product Manager - Regulatory Vault. In this pivotal role, you will...

GSK United Kingdom

Commercial Operations Director, ViiV UK

Leads UK commercial operations for ViiV Healthcare, driving marketing strategy, cross-functional projects, and operational performance across the HIV portfolio. Focuses on customer engagement, launch readiness, and data-driven decision-making in close collaboration with sales, medical, and market access teams.

GSK United Kingdom

Hybrid Permanent

Therapy Supply Chain Manager

Leads end-to-end supply planning and execution for a designated therapy area, ensuring uninterrupted patient access to medicines. Works cross-functionally across planning, manufacturing, quality, and commercial teams to resolve supply disruptions, drive inventory optimisation, and implement continuous improvement initiatives using data analysis and planning systems. Focuses on risk mitigation, regulatory compliance, and performance monitoring within a global pharmaceutical supply chain.

GSK United Kingdom

Hybrid Temporary

Principal Medical Writer

The Principal Medical Writer will lead the creation of high-quality clinical and regulatory documents, working closely with cross-functional teams to ensure scientific rigor and clear communication. This role involves strategic planning, project management, and translating complex data into clear narratives, with a focus on regulatory compliance and process improvement.

GSK United States

On-site Permanent

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for clinical programs in oncology, working closely with cross-functional teams to design robust clinical trials and contribute to regulatory strategy. The position also focuses on methodological innovation and mentoring colleagues to build statistical capability and quality.

GSK

Hybrid Permanent

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for oncology clinical programs, working closely with cross-functional teams to design robust clinical trials and drive methodological innovation. You will mentor colleagues and contribute to regulatory strategy, using advanced statistical methods and simulations to inform trial design and risk assessment.

GSK

Hybrid Permanent

Principal Programmer / Analyst

This role involves leading programming activities for complex clinical studies, ensuring high-quality and timely outputs. You will collaborate with cross-functional teams, mentor junior programmers, and support regulatory interactions, while fostering quality assurance and innovation.

GSK

Hybrid Permanent

Principal Medical Writer

The Principal Medical Writer will lead the creation of high-quality clinical and regulatory documents, working closely with cross-functional teams to ensure scientific rigor and compliance. This role involves strategic planning, project management, and translating complex data into clear narratives, with a focus on regulatory submissions and process improvements.

GSK

On-site Permanent