Biotechnology Jobs

98 jobs for “Sustainable Manufacturing”

Results

Senior Medical Director, External Innovation and New Products Strategy

Last week

Ipsen London

Leads medical evaluation of external innovation and business development opportunities across Ipsen's oncology portfolio, assessing unmet need, clinical value and target product profiles. Sits on the Global Oncology Medical Leadership team, shaping cross-asset strategy and preparing new products for integration, while engaging external experts and scientific societies.

Hybrid
Ellison Institute of Technology logo

Postdoctoral Research Fellow (Rehm Lab) - Generative Biology Institute

7 months ago

Ellison Institute of Technology Oxford £40,000 pa

Designs and troubleshoots experiments in continuous evolution, engineering orthogonal replication systems for targeted gene evolution while preserving host viability. Involves computational analysis of complex datasets, publishing high-quality research, mentoring junior staff, and pursuing IP and translational opportunities within a new Oxford institute.

On-site Permanent
Ellison Institute of Technology logo

Postdoctoral Research Fellow (van Bijsterveldt Lab)-Generative Biology Institute

7 months ago

Ellison Institute of Technology Oxford £40,000 pa

Designs and troubleshoots experiments in synthetic chromosome engineering, including centromere design, mitotic segregation and meiotic recombination in mammals and plants. Involves large DNA construct assembly, cell culture, NGS, live-cell imaging and FISH, plus computational analysis, publishing, mentoring junior researchers and pursuing IP and translational opportunities.

On-site Permanent
GSK logo

Principal Medical Writer

3 months ago

GSK Durham, United States

Lead authoring and strategic planning for clinical and regulatory documents, including protocols, clinical study reports, briefing documents and submission dossiers. Manages end-to-end writing projects, coordinating contributors, timelines and quality checks, and acts as subject matter expert on medical writing standards, CTD structure and regulatory expectations while driving process improvement and audit readiness.

GSK logo

Principal Medical Writer

3 months ago

GSK London

Lead authoring and strategic planning of clinical and regulatory documents such as protocols, clinical study reports, briefing documents and CTD submission dossiers. Manage end-to-end writing projects, coordinating contributors, timelines and quality checks, and act as subject matter expert on medical writing standards and regulatory expectations while driving process improvement and audit readiness.

Medical Science Liaison - Neuroscience

Last week

Ipsen London

Field-based medical affairs role acting as a scientific partner to healthcare professionals and thought leaders across the East Midlands, Yorkshire and East of England. Involves non-promotional scientific exchange, medical education, advisory boards, and supporting investigator-sponsored and real-world evidence studies within a neuroscience portfolio, working closely with UK, Ireland and global teams.

Remote Permanent

Medical Science Liaison - Haematology

Last week

AstraZeneca Liverpool

Field-based medical role providing scientific leadership across the NHS haemato-oncology landscape in the North West, Midlands and East of England. You will plan territory engagement, build stakeholder partnerships, support research and evidence generation, and use digital channels to demonstrate medical impact while complying with the ABPI Code.

Hybrid Permanent

Medical Science Liaison - Haematology

Last week

AstraZeneca Birmingham

Field-based medical role providing scientific leadership across the NHS haemato-oncology landscape in the North West, Midlands and East of England. You will build stakeholder partnerships, support research and evidence generation, and use digital channels and insight-led planning to demonstrate medical impact while complying with the ABPI Code.

Clinical Specialist

3 weeks ago

Danaher Cambridge

Educates and trains clinicians on Masimo monitoring technologies, running product demonstrations, evaluations and deployments alongside account managers across the Eastern UK territory. Requires critical care, NICU, PICU or emergency nursing background and involves around 60% travel with overnight stays.

Hybrid Permanent

Program Lead - FSP Clinical Operations

2 months ago

Parexel London

Leads the success of assigned Functional Service Provider clinical operations programs, covering service delivery, financial performance, resource optimization and regulatory compliance. Provides strategic direction to FSP management teams, builds scalable delivery frameworks and performance metrics, and partners with functional and regional leaders to expand service offerings and grow client relationships.

Remote

Medical Director, Companion Diagnostics and Advanced Assays

Last month

Danaher Newcastle upon Tyne

Provides medical and clinical leadership for the development of novel diagnostic and companion diagnostic assays and platforms supporting precision medicine. Acts as subject matter expert for R&D projects, clinical studies and regulatory submissions, and supports pharma partnerships and pathology education. Hybrid role based in Newcastle Upon Tyne with 30-40% international travel.

Hybrid

Clinical Development Manager| Johnson & Johnson MedTech | Electrophysiology | South of the UK

Last week

Johnson & Johnson Innovative Medicine Southampton

Field-based clinical development role leading launch and adoption of pulsed field ablation technologies (VARIPULSE, Dual Energy STSF) across southern UK EP centres. Manages four New Technology Specialists, drives site readiness, first-case support and routine utilisation, and partners with the northern counterpart to set national clinical standards.

On-site Permanent

FSP Principal Medical Writer (Regulatory) - Client-Dedicated

4 months ago

Thermo Fisher Scientific United Kingdom

Lead medical writer dedicated to a single client, authoring and reviewing clinical study reports, protocols, IBs, INDs and MAAs while advising on document strategy and regulatory requirements. Provides senior review, mentoring and training to junior writers and program managers, and leads process improvement initiatives. Therapeutic experience in neurology, immunology, oncology or vaccines is valued.

Remote

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