Latest Life Sciences Jobs

Production Engineer (Nights)- Pharmaceuticals

This role involves providing engineering support during night shifts in a pharmaceutical manufacturing environment, focusing on maintaining and improving production processes. The engineer will monitor performance, troubleshoot issues, and ensure compliance with GMP and safety standards. The position emphasizes continuous improvement, change control, and deviation management within a regulated production setting.

Smart4Sciences North Yorkshire, United Kingdom

On-site Permanent

Senior Automation Engineer - Pharmaceuticals

Lead the design and optimisation of automation systems within a pharmaceutical manufacturing environment, focusing on PLC, SCADA, HMI, and DCS platforms. Collaborate with cross-functional teams to support continuous improvement, capital projects, and system validation. Provide technical leadership and mentorship to junior engineers while ensuring high reliability and compliance in controlled processes.

Smart4Sciences North Yorkshire, United Kingdom

On-site Permanent

Plant Quality Manager

Lead quality assurance and control operations at a regulated manufacturing site producing both cosmetic and medical device products. Oversee compliance with GMP, ISO 13485, and ISO 22716 standards, support audits, and drive continuous improvement initiatives. Collaborate with cross-functional teams including operations, engineering, regulatory affairs, and R&D to ensure product quality and regulatory alignment.

New Appointments Group Folkestone, Kent, United Kingdom

On-site 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

Trial Vendor Associate Director

This role involves managing all clinical vendor-related aspects of global clinical trials, including vendor service delivery, contract negotiations, cost control, and user-acceptance testing for eCOA and IRT systems. You will collaborate closely with the study team and ensure vendor service excellence throughout the trial lifecycle.

Novartis United Kingdom

Remote Permanent

Capital Project Engineering Manager - Pharmaceuticals

Lead and deliver capital engineering projects in a GMP-regulated pharmaceutical environment, from concept to commissioning and handover. Oversee multidisciplinary teams, manage CAPEX budgets, and ensure compliance with regulatory and safety standards. Drive innovation and continuous improvement in engineering solutions while supporting long-term site development strategies.

Smart4Sciences North Yorkshire, United Kingdom

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also supports site selection, protocol training, and continuous improvement initiatives to enhance clinical trial execution.

Pfizer Manchester, M1 4HD, 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

Translational Medicine Expert – Dermatology, Associate Director

This role involves leading translational medicine strategies in dermatology, spanning early to late-stage drug development. The expert will drive clinical pharmacology, biomarker development, and regulatory strategies while collaborating across research, development, and external stakeholders. Key responsibilities include study design, safety oversight, and scientific leadership in global project teams.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Senior Manager, Planning and Production Solutions—Label Operations

This role involves leading label design, production, and system operations for clinical trial supplies within a GMP and regulatory-compliant environment. The Senior Manager ensures accurate and timely delivery of packaging and labeling solutions using enterprise systems like PRISYM360 and EMD365, while driving process improvements and digital innovation. Collaboration with internal teams and external vendors is key to supporting global clinical studies and advancing supply chain traceability and efficiency.

Pfizer Sandwich, United Kingdom

Hybrid Permanent

Investigator Contracts Lead, Sr. Manager

Leads clinical trial site contract negotiations and budget management for global studies, overseeing agreements and amendments with investigator sites. Acts as a key point of contact for complex contracting strategies, collaborates with legal and finance teams, and mentors junior negotiators. Focuses on risk mitigation, timeline adherence, and process improvements in a remote, matrixed environment.

Pfizer London, SW7 2AP, United Kingdom

Remote Permanent

Senior Manager, HTA, Value and Evidence (HV&E), Rare Disease

This role involves developing and executing high-quality HTA, Value & Evidence strategies to support patient access and reimbursement for Rare Disease treatments. The Senior Manager will manage health economics and outcomes research, collaborate with cross-functional teams, and ensure a consistent evidence generation strategy across markets.

Pfizer United States

On-site Permanent

Senior Manager, HTA, Value and Evidence (HV&E), Rare Disease

This role involves developing and executing high-quality HTA, Value & Evidence strategies to support patient access and reimbursement for Rare Disease treatments. The Senior Manager will lead the generation of health economics and outcomes research, manage global value dossiers, and coordinate with cross-functional teams to ensure a consistent and robust evidence strategy.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

Senior Manager, HTA, Value and Evidence (HV&E), Rare Disease

The Senior Manager, HTA, Value & Evidence (HV&E) role involves developing and executing strategic efforts to support patient access and reimbursement for rare disease treatments. Responsibilities include managing health economics and outcomes research, generating real-world evidence, and collaborating with cross-functional teams to demonstrate the value of Pfizer's rare disease medicines.

Pfizer

On-site Permanent

Senior Manager, HTA, Value and Evidence (HV&E), Rare Disease

The Senior Manager, HTA, Value & Evidence (HV&E) role involves developing and executing strategic efforts to support patient access and reimbursement for rare disease treatments. This includes managing health economics and outcomes research, generating real-world evidence, and collaborating with cross-functional teams to demonstrate the value of Pfizer's medicines.

Pfizer

On-site Permanent