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PE Global is currently recruiting for an experienced Global Procurement Analyst to join our pharma client based in Cambridge. \n \n The role is an initial 2-year contract. \n The rate for this role is between £23.69ph and £40.31ph PAYE, depending on experience. \n \n Candidates must be able to work on a hybrid basis, attending the Cambridge site approximately 2–3 days per week. \n \n Key Responsibilities \n \n\n • Lead contract negotiations and manage commercial relationships with key global suppliers, ensuring favourable terms, pricing, delivery and quality requirements.\n, • Develop and execute strategic sourcing plans for electronic components, sub-assemblies and contract manufacturing services.\n, • Lead cross-functional procurement and manufacturing optimisation projects, managing timelines, deliverables and cost-saving initiatives.\n, • Build and maintain strong relationships with global suppliers, monitoring supplier performance and driving continuous improvement.\n, • Support supplier selection, qualification and audits, assessing supplier capabilities, quality, cost, delivery and regulatory compliance.\n, • Establish and monitor supplier KPIs and SLAs, producing dashboards and reports for senior stakeholders and Quarterly Business Reviews.\n, • Identify and mitigate supply chain risks, including supplier, financial, geopolitical and market risks, while developing contingency and alternative sourcing strategies.\n, • Work closely with Procurement, Engineering, Quality, R&D, Manufacturing and other stakeholders to ensure supply assurance and successful project execution.\n\n \n Requirements \n \n\n • Bachelor’s degree in Supply Chain Management, Business, Engineering or a related technical/scientific discipline.\n, • Minimum 5 years’ professional experience in strategic sourcing, procurement or supplier management.\n, • At least 3 years’ experience within a regulated manufacturing environment such as Electronics/High-Tech, Medical Devices, Biotechnology or Pharmaceuticals.\n, • Strong experience in strategic sourcing, supplier relationship management, contract negotiation and commercial management.\n, • Proven experience leading cross-functional procurement projects and managing suppliers or contract manufacturing organisations.\n, • Experience with electronic components, PCBs, sensors, microchips or similar technical products is highly desirable.\n, • Strong understanding of Total Cost of Ownership (TCO), category management and global supply markets.\n, • Experience managing supplier KPIs, SLAs and performance reviews, with strong analytical and reporting capabilities.\n, • Proficiency with ERP and procurement systems such as SAP and SAP Ariba, with Power BI or advanced Excel experience highly desirable.\n, • Strong stakeholder management and communication skills, with the ability to present complex supply chain information to senior leadership.\n, • Experience managing international supplier networks and working across different cultures and time zones is desirable.\n, • Candidates must be able to work on a hybrid basis, attending the Cambridge site approximately 2–3 days per week.\n\n \n Please note PE Global cannot provide visa sponsorship for this role. Candidates will need the full right to live and work within the UK for at least the next 2 years.

The Company \n Ailux is an innovative biotechnology company focused on discovering and developing next-generation biologic therapeutics for chronic respiratory and immunological diseases with high unmet medical need. The company integrates advanced computational approaches with rigorous experimental and translational science across the drug discovery continuum, enabling faster and more informed decision-making from target identification through clinical candidate selection. \n As an AI-native biotech and wholly owned subsidiary of XtalPi, Ailux combines proprietary computational models with state-of-the-art wet lab capabilities to design differentiated therapeutics against challenging biological targets. The company has established strategic partnerships with leading pharmaceutical organisations, providing external validation of its scientific platform and discovery capabilities. Looking ahead, Ailux’s vision is to build a fully integrated, end-to-end drug discovery and development organisation capable of delivering the next generation of medicines for patients with chronic respiratory and immunological diseases. By combining advanced AI capabilities with deep biological, translational and clinical insight, the company aims to accelerate the development of differentiated therapeutics with meaningful impact for patients worldwide. \n Backed by an experienced leadership team, leading scientific advisors and a highly multidisciplinary organisation, Ailux is approaching a key inflection point as its first wave of therapeutic programmes advances toward clinical development. This is an opportunity to help shape the scientific foundations, pipeline and culture of a rapidly growing biotechnology company operating at the intersection of AI, translational science and next-generation therapeutics. \n \n Role Overview \n The Head of Translational Medicine & Biomarker Discovery (TMBD) is a senior scientific leadership role responsible for translating biological insights into clinical development strategies and patient-focused outcomes across the Ailux pipeline. The role provides strategic and scientific leadership across translational medicine, biomarker discovery and development, human target validation, target engagement, mechanism of action (MoA), and precision medicine and reports in to the Head of Translational Research. The Head of TMBD will ensure that robust, integrated translational strategies are established and executed across portfolio programmes, enabling high-quality decisions throughout the drug development lifecycle and increasing the probability of clinical and regulatory success. \n A key focus of the role is to establish and deliver fit-for-purpose biomarker strategies, from discovery through clinical deployment. This includes identifying and validating biomarkers that demonstrate target engagement, elucidate MoA, support patient selection and stratification, monitor pharmacodynamic effects, and inform clinical decision-making. The Head of TMBD will also lead the Biomarker Discovery and Assay team, driving the application of innovative and contemporary molecular technologies to identify, develop and operationalise clinically relevant biomarkers. The role will foster a culture of scientific excellence, innovation and collaboration, ensuring that emerging technologies are effectively translated into meaningful drug development applications. The role has accountability for the legally compliant, ethical and efficient management and use of human biological samples (HBS) across translational activities. This includes establishing appropriate sampling strategies within clinical development plans, ensuring operational feasibility for biomarker interrogation, maintaining robust governance and SOPs, and acting as the organisational focal point for HBS-related activities. As a member of the transitional leadership team, the Head of TMBD will contribute to the development and implementation of Ailux’s broader translational strategy and provide expert scientific leadership across multidisciplinary project teams. \n \n Key Accountabilities & Responsibilities \n Translational Medicine & Biomarker Strategy \n\n • Develop and execute integrated translational science strategies from early discovery through clinical development.\n, • Design and implement clinical biomarker strategies to guide decision-making, dose selection, risk mitigation, and patient stratification.\n, • Provide scientific expertise on human target validation, mechanism of action (MoA), target engagement, and clinical sampling strategies.\n\n Biomarker Discovery & Assay Development \n\n • Lead the Biomarker Discovery and Assay team in identifying, validating, and deploying target engagement and pharmacodynamic assays for clinical studies.\n, • Drive the application of innovative molecular technologies to accelerate biomarker discovery and translational insights.\n, • Integrate laboratory-based biomarker data with pharmacology and clinical datasets to inform programme decisions.\n\n Scientific & Organisational Leadership \n\n • Provide strategic scientific guidance across multidisciplinary project teams and serve as a subject-matter expert across Research and Development.\n, • Build external collaborations with academic institutions, biotech/pharma partners, and experts.\n, • Manage, mentor, and build organizational capabilities within the translational medicine team.\n\n Human Biological Samples (HBS) & Governance \n\n • Own the governance and operational framework for the compliant, ethical, and efficient use of HBS.\n, • Establish HBS sampling strategies within clinical development plans, maintaining SOPs and providing team training.\n, • Oversee the collection, processing, storage, and biobanking of HBS in compliance with legal, ethical, and regulatory standards.\n\n Quality, Compliance & Risk Management \n\n • Ensure team compliance with GLP, GCP, HSE, internal policies, and external regulations.\n, • Identify and mitigate scientific, operational, and regulatory risks across translational activities.\n\n \n Experience & Skills \n\n • Education & Experience: PhD (or equivalent) in a relevant scientific discipline with 10+ years in pharmaceutical R&D and drug development.\n, • Domain Expertise: Deep knowledge of immunology and/or respiratory disease biology, therapeutic mechanisms, and clinical development.\n, • Translational & Biomarker Leadership: Proven track record in developing translational/biomarker strategies, leading laboratory assay development, and deploying assays into clinical trials.\n, • HBS & Governance: Strong understanding of regulatory, ethical, and operational requirements for Human Biological Samples.\n, • Leadership & Collaboration: Demonstrated experience leading scientific teams, managing external collaborations, and communicating effectively with senior leadership.\n\n Desirable \n\n • Experience in precision medicine, patient stratification, or companion diagnostics (CDx).\n, • Track record of taking biomarkers from discovery through analytical validation to clinical implementation.\n, • Hands-on experience with advanced molecular profiling technologies (e.g., multi-omics).\n, • Experience supporting regulatory submissions/interactions or working in a fast-paced biotech environment.\n\n

Jim Gleeson is working in partnership with Nxera Pharma, to recruit an Associate Director / Director – Integrated Drug Discovery & Project Leadership. \n \n Location: \n Granta Park, Cambridge. You will need to be on-site for four days a week. \n \n About the company: \n Nxera Pharma is a technology-powered, global biopharmaceutical company advancing next-generation small molecule therapies from hit finding through early clinical development. The company combines deep GPCR biology expertise with structure-based drug design to generate highly differentiated, high-quality molecules with strong translational potential. \n Powered by its proprietary NxStar™ platform, Nxera’s discovery engine integrates structural biology, receptor pharmacology, computational design, and medicinal chemistry to unlock challenging GPCR targets. This platform-driven approach enables smart molecule design, rapid iteration, and disciplined progression into development. \n \n About the role: \n Reporting to the Head of Molecular Pharmacology this senior leadership position will provide scientific, strategic and people leadership across Nxera's discovery portfolio. The successful candidate will lead multidisciplinary scientists, provide project leadership for integrated drug discovery programmes, drive innovation across discovery technologies, and contribute to target identification, target validation and hit identification strategies. The role is intended to provide broad leadership capability across Molecular Pharmacology and Integrated Drug Discovery, ensuring delivery of high-quality assets while developing future scientific leaders. \n \n Responsibilities will include: \n\n • Leading integrated drug discovery projects from target validation through hit identification and lead optimisation in partnership with Biology, Chemistry, DMPK, Translational Sciences and Informatics.\n, • Provision of scientific leadership for cross-functional project teams, ensuring robust decision making and project progression to ambitious timelines.\n, • Supporting portfolio governance, prioritisation, forecasting and resource planning.\n, • Line managing and mentoring multidisciplinary scientists, fostering a culture of scientific excellence, innovation and accountability.\n, • Building an inclusive, collaborative and high-performing team.\n, • Providing strategic oversight of small molecule hit identification campaigns using internal and external capabilities.\n, • Working closely with medicinal chemistry and biology teams to design effective screening cascades and data-driven progression strategies.\n, • Provide scientific input into target assessment, translational relevance and portfolio opportunities.\n\n, • \n Skills and Experience: \n\n • PhD (preferred) or MSc in Pharmacology, Biochemistry, Molecular Biology or a related life sciences discipline.\n, • Extensive, industry-based experience within biotechnology and/or pharmaceutical drug discovery.\n, • Demonstrated success leading integrated drug discovery programmes.\n, • Proven experience line managing and developing multidisciplinary discovery science teams.\n, • Strong understanding of small molecule hit identification and screening strategies.\n, • Excellent communication, strategic thinking and stakeholder management skills.\n, • Familiarity with target identification and target validation approaches.\n, • Ideally with experience in GPCR pharmacology and an understanding of metabolic or endocrine disease.\n\n \n Apply: \n It is essential that applicants hold entitlement to work in the UK. Please quote job reference 197413 in all correspondence. \n

Supply Chain Specialist \n Location: Hybrid in Cambridge \n Job Type: Initial 3 Month contract (highly likely to be permanent after initial contract) \n \n About the Role \n We are looking for a highly organised and proactive Supply Chain Administrator to join our growing team. In this role, you'll be responsible for supporting the end-to-end supply chain process, ensuring the efficient coordination of purchase orders, freight movements, inventory updates, and shipping documentation. \n \n This is an excellent opportunity for someone with strong administrative skills, supply chain knowledge, and a passion for delivering exceptional operational support in a fast-paced environment. \n \n What You'll Be Doing: \n As our Supply Chain Specialist, you'll play a key role in keeping our supply chain running smoothly by: \n Purchase Order Management \n\n • Accessing and updating purchase orders within Atlas for stock distribution.\n, • Downloading and reviewing cockpit purchase orders to confirm quantities with internal stakeholders.\n\n Freight Coordination \n\n • Managing shipments from booking through to final delivery.\n, • Obtaining freight quotations and coordinating with freight forwarders on vessel collections, sailing schedules, and estimated arrival times.\n, • Ensuring shipments are delivered on time and in line with business requirements.\n\n Shipping Documentation \n\n • Preparing packing lists and commercial invoices using Excel templates.\n, • Producing compliance documentation, including Certificates of Origin and declarations.\n, • Creating and sending pro forma invoices and SAP delivery notes to the Commercial Operations team.\n\n Shipment Tracking \n\n • Monitoring shipments and updating production order schedules.\n, • Maintaining accurate information within the ComOps cockpit, including stock availability, quantity changes, and shipment delays.\n, • Providing regular ETA updates to internal stakeholders.\n\n Internal Collaboration \n\n • Liaising with UK and Rhein warehouses, freight partners, and internal departments.\n, • Supporting warehouse teams with inbound stock enquiries.\n, • Assisting the Commercial and Manufacturing teams with reporting, inventory updates, and operational support.\n\n Administration & Reporting \n\n • Maintaining accurate shipment records and filing documentation within Microsoft Teams.\n, • Providing data to support supply chain reporting and analytics.\n, • Undertaking additional administrative duties as required.\n\n \n You'll be successful in this role if you have: \n\n • Previous experience in a Supply Chain, Logistics or Operations Administration role.\n, • Strong knowledge of freight operations and inventory management.\n, • Experience using SAP for deliveries, stock allocation, or logistics processes.\n, • Advanced Microsoft Office skills, particularly Excel, Outlook and Word.\n, • Excellent organisational skills with exceptional attention to detail.\n, • Strong analytical and problem-solving abilities.\n, • Excellent communication and stakeholder management skills.\n, • The ability to prioritise multiple tasks and adapt in a fast-paced environment.\n\n \n Qualifications \n\n • Experience working with SAP.\n, • Proficiency in Microsoft Office, particularly Excel.\n, • Experience within supply chain, freight, logistics or inventory management is highly desirable.\n\n \n Apply directly if you feel you are a good fit for the role!

The Company \n Ailux is an innovative biotechnology company focused on discovering and developing next-generation biologic and peptide therapeutics for chronic respiratory and immunological diseases with high unmet medical need. The company integrates advanced computational approaches with rigorous experimental and translational science across the drug discovery continuum, enabling faster and more informed decision-making from target identification through clinical candidate selection. \n \n As an AI-native biotech and wholly owned subsidiary of XtalPi, Ailux combines proprietary computational models with state-of-the-art wet lab capabilities to design differentiated therapeutics against challenging biological targets. The company has established strategic partnerships with leading pharmaceutical organisations, providing external validation of its scientific platform and discovery capabilities. Looking ahead, Ailux’s vision is to build a fully integrated, end-to-end drug discovery and development organisation capable of delivering the next generation of medicines for patients with chronic respiratory and immunological diseases. By combining advanced AI capabilities with deep biological, translational and clinical insight, the company aims to accelerate the development of differentiated therapeutics with meaningful impact for patients worldwide. \n \n Backed by an experienced leadership team, leading scientific advisors and a highly multidisciplinary organisation, Ailux is approaching a key inflection point as its first wave of therapeutic programmes advances toward clinical development. This is an opportunity to help shape the scientific foundations, pipeline and culture of a rapidly growing biotechnology company operating at the intersection of AI, translational science and next-generation therapeutics. \n \n The Role \n We are seeking an experienced and strategic Head of Drug Safety to establish and lead Ailux’s translational safety sciences capability across its respiratory and immunology pipeline. Reporting to the VP, Head of In Vivo Bioscience, the role will shape nonclinical and translational safety strategies supporting the progression of novel biologics, multi-specific antibodies and peptide therapeutics from discovery through early clinical development. \n Working at the interface of computational design, translational biology and preclinical development, you will integrate mechanistic toxicology, pharmacology, DMPK and emerging clinical insights to enable informed, data-driven programme decisions and successful human translation. \n The role offers the opportunity to shape translational safety strategy across a next-generation respiratory and immunology pipeline spanning biologics, multi-specifics and peptide therapeutics. \n \n Key responsibilities \n Strategic leadership & portfolio impact \n\n • Lead the nonclinical safety strategy across Ailux’s pipeline\n, • Shape candidate selection and go/no-go decisions through integrated mechanistic and translational safety assessment, balancing target biology, therapeutic index, exposure margins and clinical risk.\n, • Partner closely with DMPK, bioscience, translational and clinical teams to integrate PK/PD, exposure-response and safety data into human dose prediction and first-in-human strategy\n, • Partner with Platform Science teams to evaluate and optimise emerging technologies.\n\n \n \n Scientific Oversight (Toxicology & Translational Safety) \n\n • Design and oversee nonclinical safety strategies supporting discovery through IND-enabling development for biologics, multi-specific antibodies and peptide therapeutics\n, • Provide strategic oversight across general toxicology, safety pharmacology, DART (developmental and reproductive toxicology), genotoxicity and investigative toxicology activities\n, • Integrate toxicology, pharmacology, DMPK, biomarker and translational datasets to support mechanistic interpretation and human risk assessment\n, • Interpret animal safety findings within the context of target biology, pharmacology and human relevance, including assessment of species translatability and exaggerated pharmacology risks\n, • Develop translational safety strategies incorporating exposure margins, toxicokinetics, biomarker approaches and emerging clinical data to support dose selection and clinical monitoring plans\n, • Contribute to optimisation of therapeutic index through integrated interpretation of efficacy, exposure and safety datasets\n, • Support first-in-human and early clinical programmes through integrated interpretation of nonclinical and emerging human safety data. Contribute to clinical risk mitigation strategies, safety monitoring approaches and dose escalation recommendations\n\n \n Execution & Programme Leadership \n\n • Oversee the design, execution and interpretation of GLP and non-GLP in vitro and in vivo safety studies across multiple species\n, • Apply quantitative and translational safety approaches, including toxicokinetic modelling and exposure-margin assessment, to support programme decision-making and clinical development strategy\n, • Define safety strategies for complex therapeutic modalities including multi-specific antibodies, engineered biologics, immune modulators, peptides and targeted delivery approaches\n, • Ensure delivery of high-quality, decision-enabling safety data packages supporting portfolio progression\n, • Act as Toxicology Lead on selected programmes, maintaining hands-on scientific contribution and strategic oversight\n\n \n Regulatory leadership \n\n • Lead nonclinical contributions to:\n, • IND / CTA / BLA / MAA submissions\n, • Regulatory briefing documents and responses\n, • Serve as a key scientific representative in regulatory interactions\n, • Ensure alignment between nonclinical findings, clinical strategy, and regulatory expectations\n\n \n Data interpretation & communication \n\n • Translate complex datasets into clear safety narratives and strategic recommendations\n, • Present nonclinical findings to:\n, • Internal leadership and governance boards\n, • External partners and regulators\n, • Ensure consistency and clarity across all safety communications\n\n External scientific presence \n\n • Maintain visibility in the scientific community through:\n, • Publications and conference presentations\n, • Engagement with external experts and advisors\n, • Help position Ailux as a leader in next-generation safety science\n\n Qualifications & experience \n\n • PhD (or equivalent) in toxicology, pharmacology, or related field\n, • ~10–15+ years in nonclinical safety within biotech/pharma\n, • Strong experience in:\n, • Designing toxicology strategies for regulatory submission\n, • GLP/non-GLP study oversight\n, • Regulatory interactions (FDA, EMA, etc.)\n\n Highly valuable \n\n • Experience supporting complex therapeutic modalities including multi-specific antibodies, engineered biologics, immune modulators, peptides and targeted delivery approaches\n, • Understanding of modality-specific safety considerations including exaggerated pharmacology, cytokine-mediated liabilities, immunogenicity, and tissue-specific toxicities\n, • Background in respiratory and Immunology indications preferable.\n, • Exposure to platform technologies or early-stage biotech environments\n\n Core competencies \n\n • Deep expertise in toxicology and nonclinical safety sciences\n, • Strategic thinking across the full drug development lifecycle\n, • Strong leadership with ability to scale teams in a growing company\n, • High adaptability in fast-paced, evolving environments\n, • Exceptional communication and regulatory writing skills\n\n

Jim Gleeson is working in partnership with Nxera Pharma, to recruit an Associate Director / Director – Integrated Drug Discovery & Project Leadership. Location: Granta Park, Cambridge. You will need to be on-site for four days a week. About the company: Nxera Pharma is a technology-powered, global biopharmaceutical company advancing next-generation small molecule therapies from hit finding through early clinical development. The company combines deep GPCR biology expertise with structure-based drug design to generate highly differentiated, high-quality molecules with strong translational potential. Powered by its proprietary NxStar™ platform, Nxera’s discovery engine integrates structural biology, receptor pharmacology, computational design, and medicinal chemistry to unlock challenging GPCR targets. This platform-driven approach enables smart molecule design, rapid iteration, and disciplined progression into development. About the role: Reporting to the Head of Molecular Pharmacology this senior leadership position will provide scientific, strategic and people leadership across Nxera's discovery portfolio. The successful candidate will lead multidisciplinary scientists, provide project leadership for integrated drug discovery programmes, drive innovation across discovery technologies, and contribute to target identification, target validation and hit identification strategies. The role is intended to provide broad leadership capability across Molecular Pharmacology and Integrated Drug Discovery, ensuring delivery of high-quality assets while developing future scientific leaders. Responsibilities will include: • Leading integrated drug discovery projects from target validation through hit identification and lead optimisation in partnership with Biology, Chemistry, DMPK, Translational Sciences and Informatics., • Provision of scientific leadership for cross-functional project teams, ensuring robust decision making and project progression to ambitious timelines., • Supporting portfolio governance, prioritisation, forecasting and resource planning., • Line managing and mentoring multidisciplinary scientists, fostering a culture of scientific excellence, innovation and accountability., • Building an inclusive, collaborative and high-performing team., • Providing strategic oversight of small molecule hit identification campaigns using internal and external capabilities., • Working closely with medicinal chemistry and biology teams to design effective screening cascades and data-driven progression strategies., • Provide scientific input into target assessment, translational relevance and portfolio opportunities. Skills and Experience: • PhD (preferred) or MSc in Pharmacology, Biochemistry, Molecular Biology or a related life sciences discipline., • Extensive, industry-based experience within biotechnology and/or pharmaceutical drug discovery., • Demonstrated success leading integrated drug discovery programmes., • Proven experience line managing and developing multidisciplinary discovery science teams., • Strong understanding of small molecule hit identification and screening strategies., • Excellent communication, strategic thinking and stakeholder management skills., • Familiarity with target identification and target validation approaches., • Ideally with experience in GPCR pharmacology and an understanding of metabolic or endocrine disease. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 197413 in all correspondence.

Vacancy Summary Job Title: Senior M&E Quantity Surveyor Job Type: Permanent Job Ref: #88987/1123 Location: Cambridgeshire Salary: c£75k-£85k+ basic (DOE) plus market leading benefits package inc car allowance, healthcare, pension etc Company & Project: A successful Cost Consultancy with an excellent reputation in the regional and national market are currently looking to grow their team with a talented Senior M&E Quantity Surveyor to join a recent major project win in the Life Science and Healthcare sectors. The successful business works across multiple sectors including Higher Education, Industrial, Science/Pharma, Commercial and Residential on projects from c£50m-£300m. They have an established team across Cambridgeshire of 20+ surveyors, working flexibly and on projects for long-term clients with repeat business. The team is currently expanding due to new project wins and a busy pipeline of secured work for the remainder of 2026 and into 2027/28. Our client has an excellent opportunity for a Senior M&E Quantity Surveyor that is looking to progress their career in a forward thinking and stable business with a clear pathway to Associate level. Duties & Responsibilities: The successful candidate will take responsibility for leading the Mechanical and Electrical packages/elements on projects between c£50m-c£300m+ within the Life Science and Healthcare sectors from feasibility through to project handover. You will undertake full quantity surveying/cost management/employer's agent duties, including pre-contract tenders, cost planning, and contract administration across JCT and NEC contracts including Design and Build. You will be expected to manage projects autonomously and work closely with the client. Therefore, excellent communication skills are essential. Desirable Experience: Previously held a Senior Quantity Surveyor role on projects £10m+. M&E or Building Services package specialist. Excellent client facing skills and able to lead and manage meetings. MRICS Chartership desirable or another relevant professional membership. Previous Roles: Project Quantity Surveyor OR Senior Quantity Surveyor OR MRICS Surveyor OR Associate OR QS OR Cost Consultant OR Cost Manager OR Building Services Quantity Surveyor OR M&E Cost Manager. Qualifications: BSc or MSc in Quantity Surveying or Construction Management or Building Surveying or BEng Mechanical Engineering, Electrical Engineering or Building Services. Engineering. Application Process: If you would like more information on this Senior M&E Quantity Surveyor position please contact Jess Quinn. Applications will be reviewed and you will be contacted within 48 hours if your CV is of interest. Services advertised by Apple Technical Recruitment are that of an Employment Agency/Business. TPBN1_UKTJ

Ethos is looking for experienced medical affairs professionals and MSLs from pharma/biotech to train our language model on professional presentations and slide deck tasks. Requirements include PharmD/MD/PhD with 4+ years in medical affairs, proven ability to produce compliant presentations, and expe

Ethos is seeking experienced medical affairs directors to help train AI models on professional presentation and slide deck tasks. The role requires 4+ years in medical affairs at pharma/biotech, an advanced degree (PharmD/MD/PhD), and expert PowerPoint skills for precise slide craftsmanship and clea

Ethos is seeking heads of medical affairs with 4+ years in pharma/biotech to train AI models on professional presentation tasks.

We're working with a leading foundational AI lab to find experienced heads of medical affairs from pharmaceutical companies who can help train their latest language model on professional presentation and slide deck tasks. We're looking for heads of medical affairs with 4+ years at a pharma or biotech company to create, evaluate, and refine AI-generated presentations and slide decks across core workflows: scientific presentation decks, KOL engagement slides, advisory board materials, medical education content, congress data readout presentations, and evidence summary slides. Compensation: $100/hour Commitment: Flexible, 5-20 hours per week (or more if desired) Location: Fully remote, work on your own schedule Start date: ASAP • Advanced degree (PharmD, MD, PhD) with 4+ years in medical affairs at a pharma or biotech company, • Experience producing compliant scientific presentations for external and internal audiences, • Expert-level PowerPoint and slide craftsmanship, with excellent written communication and attention to detail Ethos is a new expert network built by a McKinsey/SoftBank/DeepMind team and backed by world-leading investors like General Catalyst. We connect experts with investors and consultancies for paid expert calls, speaking engagements, and advisory opportunities. • Advanced degree (PharmD, MD, PhD) with 4+ years in medical affairs at a pharma or biotech company, • Experience producing compliant scientific presentations for external and internal audiences, • Expert-level PowerPoint and slide craftsmanship, with excellent written communication and attention to detail #J-18808-Ljbffr

You will guide target validation, hit identification and lead optimisation, while driving innovation in discovery technologies and portfolio strategies. Nxera Pharma is seeking an Associate Director/Director to provide scientific, strategic and people leadership across integrated drug discovery and

Vacancy Summary Job Title: Senior M&E Quantity Surveyor Job Type: Permanent Job Ref: #88987/1123 Location: Cambridgeshire Salary: c£75k-£85k+ basic (DOE) plus market leading benefits package inc car allowance, healthcare, pension etc Company & Project: A successful Cost Consultancy with an excellent reputation in the regional and national market are currently looking to grow their team with a talented Senior M&E Quantity Surveyor to join a recent major project win in the Life Science and Healthcare sectors. The successful business works across multiple sectors including Higher Education, Industrial, Science/Pharma, Commercial and Residential on projects from c£50m-£300m. They have an established team across Cambridgeshire of 20+ surveyors, working flexibly and on projects for long-term clients with repeat business. The team is currently expanding due to new project wins and a busy pipeline of secured work for the remainder of 2026 and into 2027/28. Our client has an excellent opportunity for a Senior M&E Quantity Surveyor that is looking to progress their career in a forward thinking and stable business with a clear pathway to Associate level. Duties & Responsibilities: The successful candidate will take responsibility for leading the Mechanical and Electrical packages/elements on projects between c£50m-c£300m+ within the Life Science and Healthcare sectors from feasibility through to project handover. You will undertake full quantity surveying/cost management/employer's agent duties, including pre-contract tenders, cost planning, and contract administration across JCT and NEC contracts including Design and Build. You will be expected to manage projects autonomously and work closely with the client. Therefore, excellent communication skills are essential. Desirable Experience: Previously held a Senior Quantity Surveyor role on projects £10m+. M&E or Building Services package specialist. Excellent client facing skills and able to lead and manage meetings. MRICS Chartership desirable or another relevant professional membership. Previous Roles: Project Quantity Surveyor OR Senior Quantity Surveyor OR MRICS Surveyor OR Associate OR QS OR Cost Consultant OR Cost Manager OR Building Services Quantity Surveyor OR M&E Cost Manager. Qualifications: BSc or MSc in Quantity Surveying or Construction Management or Building Surveying or BEng Mechanical Engineering, Electrical Engineering or Building Services. Engineering. Application Process: If you would like more information on this Senior M&E Quantity Surveyor position please contact Jess Quinn. Applications will be reviewed and you will be contacted within 48 hours if your CV is of interest. Services advertised by Apple Technical Recruitment are that of an Employment Agency/Business

We are seeking an experienced computational drug discovery leader to head a specialist CADD team within an established drug discovery organisation. This is a hands-on scientific leadership role, combining team leadership with direct involvement in multidisciplinary discovery programmes, from hit identification through lead optimisation and candidate nomination. The Role • Manage and lead a growing team of computational chemists and data scientists., • Responsible for directing computational strategy across structure- and fragment-based drug discovery programmes., • Apply and guide the use of docking, virtual screening, MD, QM and advanced computational methods., • Champion AI/ML, generative design and cheminformatics approaches that add value to drug discovery., • Work closely with cross-functional teams such as medicinal chemistry, structural biology, biophysics and biology teams., • Oversee computational workflows and analyse large-scale datasets, including DEL screening data., • Represent computational science with external partners and collaborators. About You You will have: • A PhD (or equivalent) in computational chemistry, CADD, cheminformatics or a related discipline., • Significant pharma/biotech drug discovery experience., • Strong hands-on expertise in CADD and structure-based drug design., • Practical experience applying AI/ML to drug discovery., • Proven experience leading and developing a team of computational scientists., • Strong communication skills and the ability to influence multidisciplinary project teams. Experience with fragment-based drug discovery, FEP, DEL data, cheminformatics and Python/software development would be highly advantageous. If you're looking for an opportunity to shape computational drug discovery strategy while remaining close to and hands on with the science, please apply! Keywords: Head of CADD, Head of Computational Chemistry, Head of Computational Drug Discovery, CADD Lead, Computational Chemistry Lead, Senior Computational Chemist, Principal Computational Scientist, CADD, Computational Chemistry, CADD, SBDD, Fragment-Based Drug Discovery, Virtual Screening, Molecular Docking, Molecular Dynamics, FEP, AI/ML, Cheminformatics, Drug Discovery, Hit ID, Hit-to-Lead, Lead Optimisation, Cambridge, Granta Park, Great Abington, South Cambridge, South Cambridgeshire, Duxford, Royston, Sawston, Saffron Walden, Haverhill, Hertfordshire, Essex, VRS9508MP. Follow VRS Recruitment on LinkedIn to view all our latest vacancies! Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website

Exciting opportunity to join an innovative, industry leading laboratory equipment distributor to drive Sales in the South East. Our client is a leading provider of analytical instruments in the UK with products ranging from sample preparation systems to elemental analysis instrumentation. This opportunity calls for an ambitious scientist looking to drive sales whilst providing excellent service to customers. Within this role, you will support customers by identifying their key pain points and advising which products in your portfolio would best serve their requirements. Your position will focus on managing existing accounts and identifying new customers in academic, CRO, biotech and pharma laboratories. You will be based remotely and are expected to travel ~60% of your time to customer sites across the Southeast for instrument demonstrations, presentations and negotiation. To be considered for this position you will have: • BSc minimum in Chemistry or related subject, • Eligibility to work in the UK without sponsorship, • UK driver’s license and willingness to travel, • Proven experience within scientific sales and understanding of the sales process is highly desirable For your work you will be provided with a competitive basic salary, commission scheme, car and additional employee benefits. Please apply below to receive more details! Keywords: chemistry equipment, laboratory equipment, consumables sales, capital sales, business development, account management, sales, sales executive, technical sales, technical sales specialist, London, Cambridge, Oxford, Kent, Leicester, Northampton, Ipswich, St. Albans, Luton, Watford, VRS9389PC Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website

Haleon, a leading consumer health company, is seeking a UK&I and Nordics Legal Counsel to provide strategic legal support across FMCG, pharmaceuticals, and European business units.

Blank Space Recruitment is recruiting an Account Director to lead a large-scale global pharma account across Congresses, exhibitions and life science events.

Reports to : Senior Director, Pharma Modeling LeadThis role is hybrid. Basic Qualifications & Skills :We are seeking professionals with the following required skills and qualifications to help us achieve our goals:Advanced degree in a relevant health discipline, such as, but not limited to, Pharmacy

Galderma, a leading dermatology specialist, is seeking a Head of Sales - Biologics to lead the UK sales function at a national level.You will oversee the Prescription Business Unit, delivering the sales plan and managing a high-performing team focused on a new Biologics launch in Dermatology.You wil

Ellipses Pharma is hiring a Medical Director in Greater London to oversee clinical trial protocols and strategy for oncology drug development. A PhD/MD with over 10 years in the pharmaceutical industry is preferred.

Business planning and Budget control: Delivering all sales performance goals relevant to the business in the UK Supporting Business Unit business development opportunities for the UK where needed Provide insight for product forecasting Support and co-ordinate where needed pre and post launch a

You will close high-value enterprise deals with pharma and biotech, shape the go-to-market playbook, and build a scalable commercial engine in a rapid-growth environment.

Piramal Critical Care in London is seeking a Senior Manager - Finance to act as the financial business partner to Sales and External Supply teams across European markets.You will influence pricing, profitability, and go-to-market strategies, drawing on expertise in contract manufacturing economics,

Veeva Systems is seeking a Global Program Manager to lead customer success across large pharma deployments, coordinating sales, product, and services.

Thriva are now looking to appoint a successful, experienced sales and business development executive adept at discovering, securing and managing strategic commercial partnerships across pharmaceutical companies with a focus on the UK market. Most importantly, within the first 12 months, be able to d

Experience working as a researcher in the biopharma sector, deep understanding of pharma R&D. Are you passionate about shaping commercial strategy and driving growth in the Pharma and Biotech segment?. Elsevier’s Life Sciences business focuses on the needs in segments including Pharma, biotech, me

Hyper Recruitment Solutions Ltd (HRS) is seeking a Head of Sales (Pharmaceutical & Life Sciences) to lead the UK growth strategy across specialist processing, containment and sterile manufacturing solutions. In this strategic leadership role, you will drive market expansion, align cross-functional t

Ellipses Pharma is an organisation that values the strength of collaboration, inclusive and quick decision making, knowledge sharing and a culture built on working together on site. Ellipses Pharma is a global clinical-stage drug development company focused on progressing first- or best-in-class onc

Strong pharmaceutical and life sciences experience through working in management consulting with pharmaceutical and life science clients. The firm works across energy and resources, financial services, government and public sector, consumer products and retail, pharmaceuticals and life sciences, man

Meeveem Limited is seeking a VP of Pharma Partnerships in London. This role involves discovering and managing strategic partnerships across pharmaceutical companies, focusing on the UK market.

Elsevier, a global leader in information and analytics, seeks a strategic leader to develop and execute segment-focused growth strategies across pharma and biotech.

Nxera Pharma seeks an Associate Director of Cybersecurity to lead and continuously improve cybersecurity across a globally distributed biopharmaceutical environment.

Piramal Critical Care (PCC), a business unit of Piramal Pharma, is the fourth-largest producer of inhaled anesthetics and a global player in hospital generics.

GlaxoSmithKline in the United Kingdom is seeking a Pharmaceutical Modelling Lead to shape reimbursement and access strategies through advanced economic models across therapeutic areas. Reporting to the Senior Director, Pharma Modelling Lead, the role is hybrid with 2–3 days in the office.

Ekco is seeking an experienced Enterprise Architect to define and govern the site technology architecture for a pharmaceutical manufacturing facility in a regulated GxP environment.

AVEVA is seeking an Industry Principal for Pharma/Life Science to create demand for our software and services across its industry groups in Europe with hybrid work.

A leading engineering firm in London is seeking a Director of Structural Engineering for their Science & Pharma Service Line.

Nxera Pharma is a technology‑powered biopharma company in pursuit of new specialty medicines to improve the lives of patients with unmet needs in Japan and globally. Nxera Pharma is a technology‑powered biopharma company, in pursuit of new specialty medicines to improve the lives of patients wit

Baringa, a global consulting firm, is expanding its Pharma and Life Sciences practice in Europe and the UK. You will work with leading pharmaceutical and life sciences clients across R&D to commercial, shaping operating models, data analytics and digital initiatives.

W Talent is seeking a Senior Finance Director / VP Finance for a private equity-backed pharmaceutical business in Greater London.

Being an influential leader within our organisation, as the most senior Structural Engineer within our London Science & Pharma team. You will be part of a dynamic 550 strong UK Buildings division, joining our ‘Science & Pharma’ Service Line team in London. Director of Structural Engineering - Sc

Norstella is seeking a Senior Data Scientist to drive AI/ML initiatives across pharmaceutical content and products. The role requires deep expertise in AI/ML techniques, LLMs, and strong communication to lead projects end-to-end in a fast-paced pharma-focused environment.

GlaxoSmithKline seeks a Senior Modelling Lead to drive cost-effectiveness and budget-impact models across therapeutic areas.You will shape reimbursement strategies, partner with cross-functional teams, and engage with HTA bodies to inform decision making.The role focuses on early modelling, performa

Industry principal Pharma/Life scienceApplylocations: London Cannon Street: Malmo, Sweden: Frankfurt, Germany: Manoteras, Spain: Paris, Francetime type: Full timeposted on: Posted Todayjob requisition id: R014012**AVEVA is creating software trusted by over 90% of leading industrial c

Oxygen 8 Recruitment is partnering with a leading healthcare digital communications name to recruit a Director, Strategic Accounts.This senior role focuses on turning strategic relationships into meaningful commercial growth across Europe.You will own 4-6 major accounts, craft strategic plans, and d

Verbatim Pharma are a boutique recruitment agency based in Hertfordshire that offer bespoke hiring solutions to clients in the clinical trial/pharmaceutical space, across the globe.

Clinical Development and Clinical Operations leadership within biotech or pharmaceutical organisations. Degree in Life Sciences, Biomedical Sciences, Pharmacy, Medicine, or a related discipline. Planet Pharma is an American parented Employment Business/Agency that provides global staffing services w

This is an opportunity to join a strategic, insight-led healthcare research consultancy known for delivering innovative, bespoke research that genuinely shapes pharmaceutical and biotech decision-making.