Biotechnology Jobs

Senior NPI Quality Engineer

Senior NPI Quality EngineerElectronics & Medical DevicesCompetitive Salary plus Bonus & BenefitsRelocation Assistance Provided (If Required)Step into a pivotal leadership role as a Senior NPI Quality Engineer and help bring high-quality, regulated products to life from first design through to...

Jonathan Lee Recruitment Jersey Marine, West Glamorgan, SA10 6JJ, United Kingdom

Senior Biomedical Scientist Training Lead

Senior Biomedical Scientist Training Lead | Pathology | Full Time | Permanent | ManchesterJob PurposeTo assist in the organisation, management and development of services within a specialised area of the pathology service, or across a range of services provided by...

Spire Healthcare Manchester, United Kingdom

Pharmaceutical Manufacturing Manager

Leads pharmaceutical production operations, ensuring safety, quality, and regulatory compliance while driving continuous improvement through Lean Manufacturing. Oversees large manufacturing teams and collaborates with cross-functional departments to enhance site-wide performance. Focuses on operational excellence and strategic development within a regulated GMP environment.

Entrust Resource Solutions Devon, United Kingdom

On-site Permanent

Quality Assurance Specialist

This role involves maintaining and improving a Quality Management System in a medical device manufacturing environment, with a focus on regulatory compliance, documentation control, and audit management. The specialist will handle technical documentation, customer complaints, non-conformities, and CAPA activities while ensuring adherence to ISO13485 and EU MDR/IVDR standards. Close collaboration with senior management and external consultants is required to drive continuous quality improvements.

East Lancashire Services Manchester, United Kingdom

Hybrid 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

Quality Professional

This role involves maintaining and improving the Quality Management System for medical devices, ensuring compliance with ISO 13485 and FDA regulations. The professional will lead non-conformance investigations, manage CAPA processes, conduct risk assessments per ISO 14971, and support process validation and supplier quality activities. Close collaboration with R&D, manufacturing, and regulatory teams ensures quality is embedded across the product lifecycle.

Omega Resource Group Middleyard, Gloucestershire, United Kingdom

On-site Permanent

Project Quality Lead

This role involves leading quality strategy across the full product lifecycle in a pharmaceutical development environment. You'll drive design reviews, risk management, and quality system implementation while working closely with project teams and stakeholders. The position emphasizes proactive quality integration rather than post-hoc review, with a focus on influencing technical decisions and ensuring compliance through GMP and ISO standards.

Next Phase Recruitment United Kingdom

On-site Contract

Clinical & Validation Principal

Lead bioanalytical method development and validation activities within a GxP-regulated laboratory, overseeing HPLC, UPLC, and LC-MS/MS platforms. Manage a technical team, ensure regulatory compliance, and support audits and submissions. Focus on method optimisation, troubleshooting, and continuous improvement in a highly controlled environment.

Next Phase Recruitment Armagh, County Armagh, United Kingdom

On-site Permanent

Senior Scientist 2 MSAT

This role involves leading the transfer and scale-up of bioprocesses from development into GMP manufacturing environments. The scientist will design and oversee technical studies, ensure regulatory compliance, and support root cause analysis and process robustness. Working closely with cross-functional teams, they will drive successful process implementation in a highly collaborative, multidisciplinary setting.

SRG Darlington, County Durham, United Kingdom

On-site Permanent

Associate Director AI Acceleration Lead

The AI Acceleration Lead at GSK drives the design and execution of AI pilots to solve real operational challenges in clinical development. Working across clinical operations, technology teams, and external partners, the role focuses on testing AI solutions, validating impact, and guiding decisions on scaling. The position emphasizes hands-on use of AI tools, evidence-based evaluation, and change management to embed AI into clinical workflows and deliver measurable improvements in trial delivery and patient outcomes.

GSK

On-site Permanent

Associate Director AI Acceleration Lead

This role focuses on driving AI innovation within clinical operations at GSK, identifying high-impact use cases, designing and running AI pilots, and translating findings into scalable solutions. The position works across clinical teams, technology partners, and enterprise AI functions to validate AI tools, improve trial delivery, and deliver measurable operational value through hands-on prototyping and cross-functional collaboration.

GSK

On-site Permanent

Associate Director AI Acceleration Lead

Lead the design and execution of AI pilots to solve operational challenges in clinical development, working across clinical operations, technology teams, and vendors. Drive evidence-based scaling of AI solutions, validate feasibility using AI-native tools, and translate findings into strategic recommendations for enterprise adoption.

GSK United States

On-site Permanent

Associate Director AI Acceleration Lead

This role focuses on driving AI innovation within clinical operations at GSK by identifying high-impact opportunities, designing and running AI pilots, and translating results into scalable solutions. The AI Acceleration Lead will work across clinical, technical, and business teams to validate AI tools, measure value, and guide enterprise adoption—ensuring AI delivers measurable improvements in trial delivery and patient outcomes.

GSK

On-site Permanent

Associate Director AI Acceleration Lead

The AI Acceleration Lead will drive AI innovation in clinical development by identifying operational bottlenecks, designing and running AI pilots, and translating findings into scalable solutions. Working across clinical operations, technology teams, and external partners, the role focuses on validating AI use cases using rapid prototyping tools and agentic development platforms. The position emphasizes evidence-based decision-making to accelerate trial delivery and improve patient outcomes through measurable impact.

GSK

On-site Permanent

Associate Director AI Acceleration Lead

The role involves identifying and executing AI-driven pilot projects to solve operational challenges in clinical development, working closely with clinical teams, technology partners, and vendors. The focus is on validating AI solutions, measuring impact, and driving scalable adoption across GSK’s Development Operations. It emphasizes hands-on testing, evidence-based decision-making, and translating innovation into measurable improvements in trial delivery and patient outcomes.

GSK

On-site Permanent