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We are seeking an experienced Environmental, Health & Safety (EHS) Specialist to provide short-term, onsite support at a UK-based, regulated manufacturing and life sciences environment. Short-term, high-impact role within a growing life sciences environment with a high potential for contract extensi

We are seeking a visionary and hands-on Head of Pipeline Biology to lead the biological development of our novel bispecific TCR therapeutics targeting AML and solid tumours. This is a pivotal role in our journey to bring first-in-class, first-in-human molecules to the clinic. You will work closely with the Chief Scientific Officer and Protein Science leadership to guide the non-clinical cellular testing of candidate molecules, enabling the selection of a lead candidate for full preclinical development. Your work will directly inform regulatory submissions and shape our clinical strategy. This role requires strong team leadership, scientific understanding, and expertise in immunology, cellular biology, and molecular biology including lentiviral transduction. In this role you will be accountable for: • Determining HLA-restriction, for the successful and appropriate in vitro characterisation of binding specificity of candidate and T cell activation and T cell mediated killing of bi-specific TCR molecules to cells., • in vivo characterization bi-specific TCR molecules would be desirable. Key Responsibilities Scientific Leadership & Strategy • Lead the preclinical biology group, overseeing in vitro and in vivo testing of bispecific TCR molecules., • Design and implement assays to assess binding specificity, T cell activation, and T cell-mediated killing., • Develop testing strategies to evaluate efficacy, safety, and mechanism of action., • Collaborate with Protein Engineering to optimize candidate molecules. Regulatory & Translational Impact • Drive the generation of data packages to support regulatory submissions (MHRA, FDA, EMA)., • Contribute to Clinical Trial Authorisation (CTA) and IND/NDA applications., • Engage with regulatory bodies and external experts to ensure alignment with global standards. Team & Operational Leadership • Manage and mentor a growing team of cell biologists (initially 3–4 scientists)., • Oversee budgets, timelines, and reporting for biological testing activities., • Present findings to the Senior Leadership Team and external stakeholders. Foster a culture of innovation, collaboration, and scientific excellence. Experience and Qualifications • PhD in Immunology, Cell Biology, Molecular Biology, or related field., • 5+ years of biotech/pharma experience in R&D, ideally in TCR therapeutics, bispecifics, or immuno-oncology., • Direct hands-on laboratory experience in testing the safety and efficacy of soluble high-affinity TCR molecules., • Proven track record in non-clinical development and regulatory engagement., • Experience contributing to successful regulatory filings and clinical trial enablement. Technical Expertise • Deep knowledge of T cell biology, cellular assays, and molecular techniques including cell binding assays, T cell activation, and T cell killing both in vitro and in vivo., • Hands-on experience with lentiviral transduction, cloning, and cell line engineering, particularly in generating isogenic cell lines using lentiviral transduction, growing a large array of cell lines, human organoids, and primary human cells., • Skilled in multi-colour flow cytometry, EliSpot, luminometry, and fluorescence-based assays. Leadership & Communication • Proven leadership skills, including successful development and implementation of scientific strategies, and ability to work with other leaders and support staff., • Excellent communication skills, with ability to present complex data to senior stakeholders., • Experience in cross-functional collaboration and strategic decision- making., • Experience in managing, mentoring, developing, and motivating teams of scientists., • Experience in managing budgets, agreeing and delivering timelines of work, and writing reports., • Ability to present work to the Senior Leadership Team., • Ability to publish and present work done by your team and in partnership with other team members., • Familiarity with requirements for development and submission of preclinical data packages for a Clinical Trial Authorisation to MHRA and a New Drug Application to the FDA and EMA. Why Join • Be at the forefront of next-generation immunotherapies., • Lead a high-impact team in a mission-driven, science-first environment., • Shape the future of TCR bispecifics and contribute to life-saving innovations.

We want to solve immune dysfunction. Many cancers and other diseases are caused, or resist treatment, because T cells can't recognize or target cells correctly. We're progressing first-in-class antigen modulators through the clinic, developed to treat disease by controlling T cell activation. Our technology modulates antigen presentation, flicking a switch inside cells to alter their appearance to the immune system. This approach marks a fundamental shift in how we treat people living with autoimmune disorders, cancers and infectious diseases. Role Overview: Due to ongoing growth, we are recruiting a new Clinical Supply Manager role to join the CMC team. This position is ideal for an enthusiastic, result-driven professional who thrives at the cross-functional interface between CMC, clinical supply management and Clinical Operations. You will be coordinating the planning, management and supply of IMP for all Greywolf’s global clinical trials. Core Responsibilities: • Managing all activities related to Clinical Supply Management including batch packaging, labelling, distribution strategy, expiry updates and label translations delivering IMP on time and right first time., • In collaboration with Head of CMC, own the clinical supply forecasting based on the clinical study design and any subsequent evolution of the clinical protocol through amendments., • Coordinating activities between internal stakeholders (Head of CMC, CMC Project Manager, GMP QA, Clinical Operations leads and Asset level Project Managers) and relevant CDMO partners to ensure timely delivery of the required clinical supplies., • Represent the CMC team at asset-specific Clinical Study Team (CST) and communicate effectively on project progress., • Partner with Clinical Operations Leads, Head of CMC and CMC Project Manager to understand clinical demand requirements and ensure alignment with study teams on clinical supply plans and timelines including the ability to interpret and advise on protocol design with respect to supplies., • Liaise with Clinical Operations Leads on site initiation and patient visit timings and ensure IMP is provided in a timely manner. While having an understanding of the IMP and Subject Matter Expert on Pharmacy activities and dosing aspects of the IMP., • Author Investigational Product Handling and Pharmacy Manuals, providing key drug supply and ancillary handling information., • Subject matter expert for the IRT (Interactive Response Technology) drug supply and reconciliation modules. Key member of sponsor team with a strong understanding of patient randomisation and strata and establishing IRT design and User Acceptance Testing supporting clinical teams., • Manage clinical supply inventory and IMP tracking, develop inventory reports and monitor upcoming expiry across all Greywolf clinical trials through to study close out., • Drive activities around PLD (packaging, labelling and distribution) including batch record reviews and reconciliation, CDMO and depot selection for the supply chain, contracting and management of out of scope activities, • Coordinate batch release with CDMOs for intermediate release and final release as well as Greywolf QA sponsor release, • Assist in monitoring and tracking product re-test/expiration for clinical supplies including re-labelling activities and country specific product release, • Assist QA/CMC team in the investigation of deviations related to clinical supplies, resolving shipment issues, recommending appropriate corrective and preventative actions, • Providing budget estimates and updates to Head of CMC during budget forecasting., • Manage and adhere to the supplies budget with PL&D vendors through the lifecycle of the program, communicating changes to the Head of CMC as appropriate, • Manage clinical supply CDMOs in inventory reconciliation and disposition for unlabelled and labelled packaged drug products., • Ensuring compliance with company internal procedures and GXP requirements by close collaboration with QA and Clinical Operations and approved vendors. Skills, Knowledge, Qualifications and Experience: • BSc or MSc in a relevant scientific discipline (chemistry, pharmaceutical science)., • Knowledge of global pharmaceutical regulatory requirements (e.g. cGMP, GCP)., • Knowledge of IRT system set-up, functionality and regular use., • 5+ years of experience in a clinical stage biotech/mid-size pharma or CDMO business (preferably a combination of both)., • Proven track record in clinical supply chain management., • Understanding of supply chain networks, Quality (GMP/GCP), clinical regulations, timelines and quality to facilitate communications to leadership and to develop efficient clinical supply solutions balancing multiple business objectives., • Ability to adapt and pivot following changes in the clinical study design including mid-study., • Ability to work in a fast-paced cross-functional environment., • Thinking out of the box and pre-empting issues. If you are passionate about Clinical Supply Chain Management and want to work in a fast growing and exciting company, we invite you to apply and contribute to our mission of advancing ground-breaking discoveries. What Sets You Apart: • Experience with adaptive clinical trials design., • Ability to work at the interface of multiple disciplines: CMC, Clinical Supplies and Clinical Operations. (Some of..) our Perks and Benefits: • 2 holiday office shut-down periods during July and December, in addition to 25 days annual holiday., • Flexible, hybrid working (you should be able to attend our office in Milton Park, Oxfordshire 1-2 times per week and travel to partner sites, board and other meetings, as required).

Senior Bioinformatics Data Engineer Are you a data engineer passionate about turning large-scale genomic data into actionable biological insight? Join a cutting-edge biotech at the forefront of functional genomics and therapeutic discovery. THE COMPANY This pioneering Oxford-based biotech is unlocking the non-coding genome to understand the root causes of human disease and enable new therapeutic targets. Combining high-throughput functional genomics with advanced computation and machine learning, the company’s platform integrates vast, complex datasets to drive precision drug discovery. As part of a cross-disciplinary Computational team, you’ll help expand and scale the data infrastructure that powers these discoveries, working at the interface of bioinformatics, data engineering, and software development. THE ROLE As Senior Bioinformatics Data Engineer, you will design, build, and maintain robust data systems that manage the flow of large-scale functional genomics data from raw, unstructured lab outputs to structured, accessible datasets used for analysis and decision-making. You’ll collaborate with bioinformaticians, machine learning specialists, and software engineers to ensure scalability, reliability, and performance across the entire data ecosystem. Key Responsibilities: • Develop and manage core data infrastructure enabling automated data flows from lab data to analytics-ready formats., • Build and optimise scalable biological data processing pipelines (Nextflow, Seqera)., • Maintain and develop cloud-based infrastructure with high uptime, failsafes, and modern DevOps/DataOps practices., • Implement data modelling solutions across relational and non-relational databases (PostgreSQL, Elasticsearch). ABOUT YOU You’ll thrive in this role if you have: • Industry experience within biotech, pharma, or large-scale computational research., • Expertise using Dagster and Nextflow., • Experience designing and implementing scalable data pipelines for biological data. This role can be hybrid or remote with monthly office commitments. If you’re ready to shape the data backbone of a platform redefining genomic discovery, apply now! I look forward to hearing from you!

Junior Account Manager – Medical Communications 📍 Oxfordshire - Hybrid An award-winning medical communications agency is looking for a proactive, organised and ambitious Junior Account Manager to join their growing client services team. If you’re currently an Account Executive with at least 18 months’ experience and looking for more responsibility, ownership, and opportunities to shine, this role is for you. 🌟 Why You’ll Love This Role You’ll be at the heart of delivering impactful, meaningful healthcare communication projects that make a real difference. From publications and educational materials to scientific meetings and digital initiatives, you’ll help drive high-quality work that supports global medical teams, healthcare professionals and patients. You’ll gain exposure to a wide variety of therapy areas, work closely with cross-functional scientific and creative teams, and contribute to both day-to-day project delivery and long-term client relationships. 💼 What You’ll Be Doing As a Junior Account Manager, you will: Deliver Outstanding Projects • Manage logistics and project delivery across a variety of medical communication activities (publications, slide decks, infographics, meetings, symposia and more), • Create and maintain project timelines, trackers and status reports, • Lead internal status meetings and take part in client calls with confidence, • Organise venues, AV, travel, faculty contracts and onsite preparedness, • Proactively communicate with internal teams, clients and external experts, • Monitor project budgets and highlight any variances, • Support forecasting, invoicing and financial reporting, • Identify risks and propose practical solutions early, • Build strong relationships across your team and the wider agency, • Mentor new Account Executives and graduates, • Support new business activities when required, • Expand your scientific understanding of client products and therapy areas, • Stay curious—seek feedback, learn, and grow with support from your manager You will thrive in this role if you are: • Already working as an Account Executive in a medical communications agency, • A natural organiser with excellent time management and attention to detail, • A strong communicator (written and verbal), confident with clients and internal teams, • Proactive, solutions-focused and comfortable juggling multiple tasks, • Calm under pressure and adaptable when priorities shift, • Join a respected, supportive and fast-growing med comms agency, • Work on exciting, high-impact scientific and medical projects, • Develop quickly with tailored training, mentoring and progression pathways, • Collaborate with passionate, talented colleagues across scientific, creative and digital teams, • Hybrid or remote working options to suit your lifestyle Ready to grow your med comms career? If you’re excited to take on more responsibility, work on diverse scientific projects and become a trusted partner to global clients, we’d love to hear from you, apply with your CV today.

Our PHARMA client is looking for a medical writer with 3-5 years writing experience in a pharma company or a healthcare communications agency to join their growing writing team. Oncology experience is essential (prostate, solid tumours, neuro-oncology or medical imaging would all be advantageous).

Company description: Oxford Biomedica is a quality and innovation-led viral vector CDMO that enables its clients to deliver life-changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, Oxford Biomedica has more than 25 years of experience in viral vectors, the driving force behind the majority of gene therapies. Cell and gene therapy is the treatment of disease by the delivery of therapeutic genetic material (DNA or RNA), into a patients cells. One highly effective approach to delivering genetic information is to re-engineer existing viruses to be safe delivery vehicles (vectors) to insert the genetic material into patients cells. This can be achieved either by directly administering the vector to the patient (often referred to as in vivo gene therapy), or by first introducing the genetic material to cells or tissue outside of the body, before administering the cells or tissue into the patient (often referred to as ex vivo gene therapy or gene-modified cell therapy). Oxford Biomedica collaborates with some of the world's most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. Oxford Biomedica's world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods and depth of regulatory expertise. Job description: Join Us in Changing Lives At OXB , our people are at the heart of everything we do. Were on a mission to enable life-changing therapies to reach patients around the worldand were looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful . Were currently recruiting for a Senior Maintenance Engineer for the Engineering team. In this role, you will utilize Good Engineering Practices (GEP) to establish and maintain the industrial process automation, building automation and operational technology systems required to support cGMP manufacturing and process development. As a system owner, you will be responsible for day-to-day operations support and troubleshooting, project execution, commissioning and qualification support, and optimizing process and utilities equipment within a regulated cGMP facility, playing a key part in advancing our mission and making a real difference. Your responsibilities in this role would be: Assuming ownership responsibility of control systems and other operational technologies by applying the engineering lifecycle to enable cGMP manufacturing. Organizing and leading all aspects of cross-functional internal projects including scope, schedules, and execution. Applying technical expertise in ensuring the reliability of complex process equipment, data, and building and utilities systems. Developing solutions and best practices for a variety of problems with moderate scope and complexity, and working collaboratively with Quality, Manufacturing, Facilities, Process Development, external supply partners, and vendors. Responding to support calls and troubleshoots equipment and uses evaluation, judgement, and interpretation to resolve issues and select best course of action. Being a Control Systems Engineering representative for capital projects involving building automation, process and utilities equipment for cGMP facilities. Profile description: We are looking for: Technical/ Complex equipment systems Control systems. Bioreactor/ Filling line background. Background in GMP/ Pharma/ regulated environments: Bachelor's degree in Electrical Engineering / Computer Science / Chemical Engineering or equivalent, with a minimum of 5 years of experience in a cGMP engineering environment, or advanced degree in lieu of experience. Significant knowledge and understanding of GMP engineering principles and practices in the gene therapy industry. Manufacturing control systems automation background focused specifically in the design, installation, programming, validation, and in lifecycle maintenance of automated equipment, specifically in a GMP environment. Knowledge of GAMP software development lifecycle, ANSI/ISA-S88 and S95 industry standards, and 21 CFR Part 11. Demonstrated experience with network architecture including TCP/IP, Routing, Switching, Network IDS/IPS, Active Directory, Domain Integration, and Firewalls. Able to accommodate changing priorities and deadlines and work independently solving complex process and equipment problems. We offer: Why Join Us? Competitive total reward packages Wellbeing programmesthat support your mental and physical health Career development opportunitiesto help you grow and thrive Supportive, inclusive, and collaborative culture State-of-the-art labs and manufacturing facilities A company that lives its values: Responsible, Responsive, Resilient, Respect We want you to feel inspired every day. At OXB, were future-focused and growing fast. We succeed togetherthrough passion, commitment, and teamwork. Ready to Make a Difference? Collaborate. Contribute. Change lives. TPBN1_UKTJ

Company description: OXB is a quality and innovation-led viral vector CDMO that enables its clients to deliver life-changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, OXB has more than 30 years of experience in viral vectors, the driving force behind the majority of gene therapies. Cell and gene therapy is the treatment of disease by the delivery of therapeutic genetic material (DNA or RNA), into a patients cells. One highly effective approach to delivering genetic information is to re-engineer existing viruses to be safe delivery vehicles (vectors) to insert the genetic material into patients cells. This can be achieved either by directly administering the vector to the patient (often referred to as in vivo gene therapy), or by first introducing the genetic material to cells or tissue outside of the body, before administering the cells or tissue into the patient (often referred to as ex vivo gene therapy or gene-modified cell therapy). OXB collaborates with some of the world's most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. OXB's world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods and depth of regulatory expertise. Job description: Join Us in Changing Lives At OXB , our people are at the heart of everything we do. Were on a mission to enable life-changing therapies to reach patients around the worldand were looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful . Were currently recruiting for a VP, Head of Site Services . In this role, you willlead, inspire and manage the strategic and operational performance of OXB UK site services functions on the Oxford Site to ensure high quality, compliant, timely and efficient services are provided to support all site activities. Site Service functions include Engineering, Facilities Management, Validation, and Safety, Health and Environment (SHE). The role works as a key member of the UK Site Leadership team to deliver a high quality, efficient, client-centric service, with a focus on delivery. The team works closely together to overcome challenges and manage resources according to specific needs of the business, playing a key part in advancing our mission and making a real difference. Your responsibilities in this role would be: Active Member of the Oxford Site Leadership Team Leading and inspiring a team of professionals, coaching and developing capability and competency within the team and ensuring effective management processes are in place to manage and recognise performance. Budgetary control, maintain and manage to budget. Work alongside the Procurement Team to drive savings and improve cost control Exemplify the OXB values of Responsible, Responsive, Resilient and Respect. Define and implement site, regulatory and corporate guidelines, policies, procedures and industry standards to ensure ongoing compliance of all service function team activities. Define the departmental structure ensuring optimal resources are in place for the cost-effective delivery of requirements. Use lean principles to drive safety, efficiency, quality and delivery. Set individual & team objectives, and performance manage to ensure ownership and delivery Ensure all GMP processes, systems (including computer systems) and equipment are validated in line with cGMP and includes a robust Science Risk based approach. Active member of Global Environment, Social, Environment (ESG) Group, to drive and integrate sustainable and ethical practices within the business whilst leading local site-based activities Agree and deliver against service levels required from site services to support other Site functions. Provide leadership across the site services functions (Engineering, Facilities, Validation and SHE) to: Deliver CAPEX, engineering and facility projects Ensure a safe and compliant working environment for all Oxford UK staff Deliver Facilities services across Oxford sites as per appropriate service level agreements Ownership of UK Business Continuity, and Environmental performance plans We are Looking For: Degree level qualified in a scientific or technical discipline Management experience in a highly regulated Biotech or Pharma environment, experience in engineering in a cGMP environment Skilled at using data to drive decision making. Be a change agent for the department and site. Drive safety, quality and project risk. Instils a culture of ownership and Continuous Improvement. Core competency in Lean/Operational Excellence. Driving Safety, Quality, Delivery and cost. Experience of implementing new computerized maintenance management systems Knowledge of the financial aspects of the business, including budget control, budget planning, as well as impact of cost on COGS. Demonstrates excellent judgment, mental agility and problem-solving skills, uses commercial acumen, strategic and big picture thinking to drive the business forward. Strong understanding of Validation Lifecycle, Engineering, Maintenance, Facilities management and Security. About Us: OXB is a quality and innovation-led viral vector CDMO with a mission to enable its clients to deliver life changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, we have more than 30 years of experience in viral vectors; the driving force behind the majority of gene therapies. OXB collaborates with some of the worlds most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. OXBs world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods, and depth of regulatory expertise. Why Join Us? ??Competitive total reward packages ??Wellbeing programmesthat support your mental and physical health ??Career development opportunitiesto help you grow and thrive ??Supportive, inclusive, and collaborative culture ??State-of-the-art labs and manufacturing facilities ?? A company that lives its values: Responsible, Responsive, Resilient, Respect We want you to feel inspired every day. At OXB, were future-focused and growing fast. We succeed togetherthrough passion, commitment, and teamwork. Ready to Make a Difference? Collaborate. Contribute. Change lives. We offer: Oxford Biomedica is a quality and innovation-led viral vector CDMO that enables its clients to deliver life-changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, Oxford Biomedica has more than 25 years of experience in viral vectors, the driving force behind the majority of gene therapies. Cell and gene therapy is the treatment of disease by the delivery of therapeutic genetic material (DNA or RNA), into a patients cells. One highly effective approach to delivering genetic information is to re-engineer existing viruses to be safe delivery vehicles (vectors) to insert the genetic material into patients cells. This can be achieved either by directly administering the vector to the patient (often referred to as in vivo gene therapy), or by first introducing the genetic material to cells or tissue outside of the body, before administering the cells or tissue into the patient (often referred to as ex vivo gene therapy or gene-modified cell therapy). Oxford Biomedica collaborates with some of the world's most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. Oxford Biomedica's world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods and depth of regulatory expertise. TPBN1_UKTJ

About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. Experience working with PET tracers, radiopharmaceutical supply chains, or related m

They are now looking to add an equity research associate to their Pharmaceutical equity research team. Writing pieces of equity research on European Pharma companies.

HR Business Partner- Permanent and Full-Time.A Chemical Manufacturing Company.Cornwall- Open to relocators within the UK.As a leading provider of engineered solutions for critical industrial applications, our company supports customers across aerospace, manufacturing, technology, and other high-perf

They are now looking to add an equity research associate to their Pharmaceutical equity research team. Writing pieces of equity research on European Pharma companies.

Planet Pharma are seeking highly experienced and strategic Directors of Biostatistics (both Oncology and Non-Oncology) to lead statistical activities across a portfolio of clinical trials, spanning early to late phase development.

EU-Remote Pharma / Biotech / Life Sciences / Cold Chain Packaging. Our products have consistently proven their performance in real-world applications, making them the first choice for leading pharmaceutical and food companies worldwide. We are looking for a true industry professionalsomeone who und

Xmoor Pharma is the only integrated cell and gene therapy CDMO with over 20 years of consultancy expertise embedded across every stage of the CMC journey — from early-phase strategy to process development, GMP manufacturing and commercialisation. You will support the site Pharmaceutical Quality Sy

A Global leader in Pharma is seeking a Scientific Publications professional to support global data dissemination and advance scientific and medical understanding of their products and therapeutic areas.

They are now looking to add an equity research associate to their Pharmaceutical equity research team. Writing pieces of equity research on European Pharma companies.

Planet Pharma are working with premier life sciences service provider that supports pharmaceutical and biotechnology companies across the entire drug development cycle. With capabilities in chemistry, biology, pharmacology, toxicology, and analytical sciences, it provides integrated solutions that h

Coach and develop senior consultants to build depth and capability in the UK Pharma Industry practice. Proven commercial leadership in consulting, data, or technology within the pharmaceutical or life sciences industry. The pharmaceutical industry is undergoing rapid transformation, driven by digita

An exciting opportunity has arisen for two.Reporting into a Regional Business Manager, you will play a pivotal role in shaping local account strategy, driving business performance, and supporting healthcare professionals to improve outcomes for patients living with chronic immunological conditions.T

Pharma, Biotech, MedTech or scientific innovation. Exposure to internationally recognised Pharma, Biotech and MedTech companies.

Proven experience in an EHS advisory or similar role, ideally within biotech, pharmaceutical, laboratory, or technical environments.

Nxera Pharma is establishing a new AI enabled discovery initiative to build a high throughput AI and physics driven GPCR discovery engine that augments our world class experimental capabilities and extensive proprietary structural and chemogenomic data assets originating from Heptares Therapeutics.

Previous pharmaceutical industry experience, ideally within secondary care or biologics.

A leading recruitment consultancy in the United Kingdom is seeking a Talent Partner to leverage a strong industry brand and drive business development in the pharmaceutical sector.

Pharma, biotech, healthcare, or broader life‑sciences data leadership.

A leading engineering company is seeking a Director of Structural Engineering for their Science & Pharma team in London.

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Planet Pharma is an American parented Employment Business/Agency that provides global staffing services w

We’re investing in our Pharma Industry practice to support organisations across R&D, manufacturing, supply chain, and commercial operations as they adopt digital, data, and AI‑driven transformation. You’ll collaborate with Valcon’s European Pharma network to share best practice and deliver i

Key Responsibilities Define and execute the organisation’s enterprise‑wide data strategy Lead data transformation initiatives across architecture, governance, quality, and operations Oversee creation of dat

Experience in clinical trials from CRO or pharma/biotech company or as an investigator.

The ideal candidate will lead teams in cheminformatics innovation and AI/ML platform integration, requiring a PhD and significant experience in pharma R&D. A leading pharmaceutical company located in the United Kingdom is seeking a Head of Cheminformatics and Data Architecture.

Planet Pharma is an Employment Business providing Global Staffing services. Interested? Apply now for immediate consideration or contact James Allen on +44 203 868 8607 – jallen@planet-pharma.

A leading consulting firm in the UK is seeking an experienced Partner to lead their Pharma and Life Sciences practice. The ideal candidate will bring significant commercial leadership experience within the pharmaceutical sector.

Medical Advisor - UK & Ireland (Migraine/CNS).Medical Affairs activities for migraine across the UK & Ireland.This role is ideal for someone passionate about scientific excellence, strategic impact and building strong relationships within the neurology community.Drive execution of the Medical Affair

Are you passionate about advancing Oncology clinical development?.Would you relish the challenge of working within a leading global organization; one where you will enjoy a high level of responsibility and autonomy, whilst able to focus on further enhancing your therapeutic expertise?.Our client has

Direct message the job poster from Planet Pharma. CRO/Pharma industry experience required. Interested? Apply now for immediate consideration or contact James Allen on +44 203 868 8607 – jallen@planet-pharma.

A unique opportunity to play a key leadership role within an exceptionally successful, extremely dynamic, and remarkably ambitious business.Having achieved unbridled success over recent years you can help lead the next phase of their growth, development and success.Do you have the passion, enthusias

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

Nxera Pharma is establishing a new AI enabled discovery initiative to build a high throughput AI and physics driven GPCR discovery engine that augments our world class experimental capabilities and extensive proprietary structural and chemogenomic data assets originating from Heptares Therapeutics.

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

Industries: Pharmaceutical Manufacturing and Biotechnology Research.

Planet Pharma are seeking highly experienced and strategic Directors of Biostatistics (both Oncology and Non‑Oncology) to lead statistical activities across a portfolio of clinical trials, spanning early to late phase development.

Define and implement Valcon’s Pharma Industry strategy in collaboration with European leadership. Coach and develop senior consultants to build depth and capability in the UK Pharma Industry practice. Deep understanding of pharma R&D, manufacturing, regulatory, and commercial operations.

A global biopharma company is seeking a skilled scientist to support non-clinical pharmacokinetics/pharmacodynamics (PKPD) and toxicokinetics strategy within early drug development. Industries: Pharmaceutical Manufacturing and Biotechnology Research. Get notified about similar Pharmacometrician role

An exciting senior VP or Director level opportunity to join the Healthcare Equity Research team in London, where you will analyse, model and write research on European Specialty Pharmaceuticals and communicate the results and recommendations to our global equity sales force, traders and investment f

A leading consultancy in Pharma is seeking a Partner to lead and expand their operations within the UK Pharmaceutical and Life Sciences industry.

This role involves analyzing European Specialty Pharmaceuticals and communicating findings globally to salesforce and clients. The ideal candidate should have extensive experience in biopharmaceuticals, strong analytical skills, and excellent communication abilities.