Latest Project Services Jobs

Quality Validation and CSV Senior Specialist

This role involves leading validation and computerised systems validation (CSV) activities for manufacturing processes, equipment, and systems within a GMP-regulated environment. You will support new product introductions, ensure compliance through risk-based documentation and quality oversight, and collaborate with engineering, IT, and manufacturing teams. The position plays a key part in maintaining regulatory standards and advancing smart manufacturing initiatives at GSK’s Barnard Castle site.

GSK Barnard Castle, United Kingdom

Associate Director Predictive Agentic Target Biology

Lead the development and application of predictive computational models and agentic workflows to evaluate the tractability and safety of biological targets for drug discovery. Integrate multimodal data including genomics, proteomics, and functional screens to inform target prioritisation and mechanism of action. Collaborate with biologists, data scientists, and project teams to translate biological questions into robust, reproducible pipelines that guide go/no-go decisions in early drug development.

GSK Stevenage, United Kingdom

Hybrid Permanent

Senior Project Specialist, Clinical Supplies

This role involves coordinating clinical supply operations for Moderna’s mRNA-based therapeutics, ensuring investigational products are labeled, packaged, and distributed efficiently to clinical sites. The specialist will work cross-functionally with vendors and internal teams to maintain supply chain compliance, support IRT systems, manage temperature excursions, and drive digital innovation in supply operations.

Moderna Oxford, United Kingdom

Hybrid Permanent

Senior Project Specialist, Clinical Supplies

This role involves managing end-to-end clinical supply operations for Moderna’s mRNA-based therapeutic trials, including coordination of labeling, packaging, distribution, and temperature-controlled logistics. The specialist ensures investigational products are delivered on time and compliantly to clinical sites, supports IRT system testing, monitors vendor performance, and drives digital innovation and process improvements in supply chain execution.

Moderna

Hybrid Permanent

Director, Portfolio Development Process & Standards Lead

Lead the development and governance of processes, standards, and SOPs for CSL's global Portfolio Development function, ensuring high-quality clinical program execution. Drive cross-functional process improvement initiatives, change management, and training curriculum development. Collaborate with leadership and stakeholders across R&D to streamline decision-making and enhance operational excellence in a dynamic biotech environment.

CSL US$250,000 – US$280,000 pa

Hybrid Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic assets, engaging with key opinion leaders, and integrating innovation into portfolio planning. The position requires deep clinical expertise, a proven track record in deal-making, and strong collaboration with cross-functional teams.

CSL US$263,000 – US$328,000 pa

Hybrid Permanent

Connectivity Specialist

Evolve are partnering with a driven medical device manufacturer who are seeking a Connectivity Specialist to help shape the future of connected healthcare. This is an exciting opportunity to combine technical expertise, customer engagement, and project leadership to deliver innovative...

Evolve Selection Gloucester, Gloucestershire, United Kingdom

Senior Principal Statistical Programmer

Leads statistical programming for clinical studies across phases I-IV, ensuring high-quality, regulatory-compliant deliverables for regulatory submissions and clinical study reports. Develops and validates datasets and outputs using SAS, drives CDISC standards (SDTM/ADaM), and collaborates with biostatistics and cross-functional teams. Provides technical leadership, mentors junior programmers, and contributes to process improvements and programming specifications.

Novartis London, United Kingdom

On-site Permanent

R&D Scientist - Immunology

As an R&D Scientist, you will work in a state-of-the-art lab, generating high-quality immune profiling data using advanced cytometry and single-cell technologies. Your key responsibilities include performing flow cytometry assays, isolating immune cells from human blood, preparing samples for RNA sequencing, and maintaining quality control standards. You will collaborate with multidisciplinary teams and support ongoing research projects, with some weekend work required.

HAYS Specialist Recruitment London, United Kingdom £36,000 – £45,000 pa

On-site Permanent

Regulatory Affairs Specialist - Medical Devices

This role involves leading quality assurance and regulatory affairs initiatives within a global medical devices company, working across European, American, and Asian regulatory standards. You will develop and implement solutions for compliance and management systems in a highly technical R&D and manufacturing environment. The position offers exposure to emerging regulated industries and complex, international projects.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom £42,000 – £46,000 pa

On-site Permanent

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Research Scientist – In vitro display, Biologics discovery

This role involves the discovery and optimisation of peptides and biologics using in vitro display platforms such as phage, yeast, mRNA, and ribosome display. The scientist will design and execute experiments, analyse data, and collaborate with multidisciplinary teams to advance therapeutic programmes. The position emphasizes hands-on molecular biology, library generation, and selection techniques within a cutting-edge, AI-informed drug discovery environment.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

PhD Studentship in Computer Science: Programming Matter - Dynamic DNA Data Structures for Molecular Information Storage and Computing

This PhD studentship focuses on developing dynamic DNA data structures for molecular information storage and computing, combining computational design with experimental lab work. The project builds on pioneering research in DNA-based stack structures and aims to create novel molecular data structures such as queues, deques, and priority structures. The candidate will work within an interdisciplinary team, designing, modelling, and validating DNA/RNA systems and molecular circuits for in vitro or cellular applications.

Newcastle University Newcastle upon Tyne, Northern England, United Kingdom £21 pa

Contract

Validation/ Quality Assurance Specialist, Pharmaceutical

The Validation/Quality Assurance Specialist will plan and execute validation activities, author and maintain validation protocols, and collaborate with cross-functional teams to ensure compliance with GMP standards. The role involves maintaining validated status, supporting regulatory inspections, and contributing to the Site Validation Master Plan.

NMS Recruit Ltd t/a Russell Taylor Group Swadlincote, Derbyshire, DE11 0AG, United Kingdom £30,000 – £34,000 pa

On-site Permanent

Head of Computational-Aided Drug Discovery

Leads a computational chemistry and data science team embedded in multidisciplinary drug discovery projects, applying AI, machine learning, and structure-based methods to drive hit identification and lead optimisation. Directs scientific strategy, develops workflows, and contributes hands-on to project teams using biophysical and structural data. Focuses on integrating modern computational techniques with experimental insights to advance pre-clinical candidates.

Pure Resourcing Solutions Great Abington, Cambridgeshire, United Kingdom £100,000 pa

Director, Biostatistics

Lead statistical strategy for clinical development projects in inflammation and immunology, providing expert input on study design, analysis plans, and regulatory submissions. Collaborate with cross-functional teams to ensure robust data interpretation and compliance with global standards. Drive innovation in statistical methodology and support publication activities and product defense.

Pfizer Marlow, United Kingdom