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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!

EHS Specialist (Contract) We’re supporting a regulated life sciences site near Oxford that is seeking an experienced EHS Specialist to provide hands-on, onsite support on a short-term contract basis. Working alongside the site EHS lead, you will play a vital role in ensuring safe and compliant operations across laboratories, facilities, and contractor activities in a fast-moving, regulated environment. Key Responsibilities • Develop, review, and update risk assessments across laboratory, facility, and construction activities, • Prepare and deliver EHS training for site personnel, • Conduct and review COSHH assessments in line with UK legislation, • Draft, revise, and standardise SOPs to support compliant operations, • Support incident investigations, including root-cause analysis and corrective actions, • Review RAMS and Permits to Work for onsite contractors, • Provide day-to-day EHS guidance and advisory support to operational teams Requirements • Proven experience in an EHS advisory or specialist role within a regulated environment (pharma, biotech, laboratories, or similar), • Strong knowledge of UK HSE legislation and best practices, • Confident in producing clear, practical EHS documentation (risk assessments, SOPs, COSHH), • Excellent communication and stakeholder engagement skills, • NEBOSH General Certificate (or equivalent) required; NEBOSH Diploma preferred, • Must be able to work fully onsite

Takara Bio is dedicated to driving innovation in the life sciences through our advanced products and solutions. Our mission is to empower researchers and organizations to achieve their goals in academic, hospital, pharmaceutical, biotech, and government sectors. We foster a culture of collaboration, integrity, and excellence. About the Role The Sales Execution role is crucial for driving sales of Takara Bio’s products across key accounts. The successful candidate will achieve and exceed sales targets by maintaining existing business, expanding sales within current accounts, and developing new business opportunities. Responsibilities • Responsible for driving sales of the company’s products across Key Academic, Hospital, Pharma, Biotech, and Government accounts, while consistently delivering a high level of personal service to customers., • Achieve and exceed sales targets by maintaining existing business, growing sales within current accounts, and developing new customer relationships., • Prospect, map, and prioritize new accounts and customers, identifying opportunities for new product launches and cross-selling., • Maintain a high level of technical knowledge of Takara products and effectively position them against competitors., • Implement and execute corporate sales and marketing strategies, applying effective selling techniques, value propositions, and closing strategies., • Maintain Salesforce (CRM) by accurately updating opportunities, customer interactions, and key account information to ensure a clear and reliable pipeline for forecasting and tactical planning., • Communicate potential opportunities to the Sales Team and Product Managers through timely, accurate Salesforce updates., • Provide timely communication, quotations, and follow-up to customers, ensuring expectations are consistently met or exceeded., • Collaborate with Regional Sales Managers, European Sales Manager, Product Managers, and/or R&D to deliver impactful presentations, product demonstrations, and on-site visits., • Represent the company at trade shows, vendor events, and customer meetings as required., • Gather and provide market intelligence and competitive insights to the organization to inform strategy., • Analyse accounts, competitive activity, and product mix; identify areas of growth and implement actionable sales plans., • Contribute to the development and execution of the business plan to increase revenue within the territory. Qualifications • Mandatory: BSc in Molecular Biology or related life science discipline, • Desirable: MS or PhD in Molecular Biology or related life science discipline Required Skills • Mandatory: Minimum 2 years lab bench experience in Cell, Molecular Biology or related area., • Desirable: Minimum 2 years’ experience selling kits and reagents into the University of Oxford, University of Bristol, Cardiff University and other key accounts across the midlands to the south of the UK. Minimum 3 years sales experience selling life science kits and reagents into Life Science Market. An established network of contacts within above accounts. Preferred Skills • Mandatory: Driving License and right to work in the UK, • Desirable: Location and travel South of the UK near key accounts such as Oxford University, University of Bristol or University of Birmingham and travel to these key accounts on a regular basis. Equal Opportunity Statement This company is committed to diversity and inclusivity.

Location: Oxford, United Kingdom Department: Drug Discovery & Translational Sciences Reports to: Chief Scientific Officer About the Role We are seeking an exceptional scientific leader to build and scale a world-class AI-driven bioinformatics function in the heart of the UK’s life sciences ecosystem in Oxford. As Senior Director, AI & Bioinformatics, you will define and execute the company’s computational strategy across target identification, multimodal data integration, and predictive modelling to accelerate our drug discovery pipeline. This is a high-impact executive leadership role with full ownership of strategy, people, platform, and cross-functional integration. You will partner closely with Biology, Chemistry, Translational Medicine, and Clinical Development to transform data into differentiated therapeutics. Key Responsibilities Strategic Leadership • Define and deliver the AI & data strategy aligned with corporate R&D goals., • Build a scalable computational platform integrating genomics, transcriptomics, proteomics, imaging, and clinical data., • Drive adoption of AI/ML across early discovery through translational stages., • Lead development of predictive models for:, • Target identification and validation, • Biomarker discovery, • Patient stratification, • Drug response modelling, • Implement state-of-the-art approaches including:, • Foundation models for biology, • Graph neural networks, • Multi-omics integration, • Generative models for target prioritisation, • Recruit, mentor, and scale a multidisciplinary team of:, • Computational biologists, • Bioinformaticians, • ML engineers, • Data scientists, • Create a high-performance, collaborative culture embedded within wet-lab discovery teams., • PhD in Bioinformatics, Computational Biology, Machine Learning, Systems Biology, or related discipline., • 10+ years experience in biotech/pharma drug discovery., • Proven leadership experience building and managing high-performing computational teams., • Track record of deploying AI/ML models into real discovery pipelines (not just research prototypes)., • Deep expertise in:, • Multi-omics analysis, • Statistical genetics, • Python/R and modern ML frameworks, • Cloud computing (AWS/GCP/Azure), • Experience leading AI strategy in oncology, immunology, rare disease, or precision medicine., • Industry collaborations with UK/EU academic institutions., • Exposure to regulatory considerations for AI in drug development., • Executive-level compensation + equity participation, • Opportunity to shape a flagship AI-enabled biotech platform, • Access to Oxford’s leading academic and clinical ecosystem, • Flexible hybrid working model, • Generous pension, bonus, and long-term incentive plans

! Location: Need to be located close to Oxfordshire Start date: ASAP Shift Pattern: 2-2-3 (Panama Schedule) | 7:00am – 7:00pm Work Arrangement: Site-based (no remote work) Type of position: Freelance. Minimum 6 month contract with the view to extend Job Description Planet Pharma are working with a biotechnology company known for pioneering work in messenger RNA (mRNA) science. Its focus is on developing medicines that use mRNA to instruct the body’s cells to produce proteins that can prevent or treat disease. The organisation operates across infectious diseases, oncology, rare conditions, and immune disorders, and it became widely recognised for creating one of the first mRNA‑based vaccines during the global pandemic. Beyond vaccines, it continues to expand its therapeutic pipeline, invest heavily in research platforms, and partner with global health and scientific institutions to advance next‑generation treatments. Description: Joining this organisation offers the chance to contribute to a pioneering environment advancing the use of mRNA technology in modern medicine. With a broad and growing pipeline across multiple therapeutic areas, you will collaborate with talented colleagues and global partners, playing a direct role in improving health outcomes worldwide. As part of a long‑term commitment to strengthening onshore mRNA vaccine manufacturing in the UK, a state‑of‑the‑art research, development, and production facility is being established in Oxfordshire. This initiative will support respiratory vaccine manufacturing, create highly skilled roles, and promote collaboration with academic institutions, the NHS, and government partners across the country. We are seeking motivated and detail‑oriented professionals to support 24/7 manufacturing operations, with a focus on end‑to‑end warehouse and logistics activities. This Fixed‑Term Contract position is essential to maintaining compliant, efficient material flow for real‑time mRNA production. You will gain hands‑on experience with SAP, Quality Management Systems (QMS), and digital workflows—building strong foundations for future automation and AI‑enabled operational environments. Key Responsibilities • Receive and process inbound deliveries, ensuring documentation is accurate and resolving any discrepancies., • Upload delivery and quality records into the organisation’s QMS to maintain full GMP compliance., • Pick, verify, and stage materials required for mRNA manufacturing in line with production schedules., • Apply internal standards for labelling, handling, storage, and inventory control within a GxP‑regulated setting., • Perform daily SAP transactions related to inventory movements and stock accuracy., • Support outbound logistics, including shipment preparation and documentation., • Conduct cycle counts and reconcile physical inventory with SAP data., • Identify, segregate, and manage expired or non‑conforming materials., • Work closely with logistics and operations teams to ensure seamless support across the facility., • Complete all required training to meet compliance, quality, and safety expectations. Requirements: • Good experience in warehouse operations ideally in life science or food industry, • Experience working in a GMP / GDP environment., • Knowledge of Quality Management Systems (QMS)., • Ability to lift and move products safely., • Flexibility to meet operational demands., • Strong attention to detail with a collaborative, customer-focused approach. If this role isn’t suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help! 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. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognized by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

Biological and Chemical Safety Officer (BCSO) | Oxford (On-site) BioTalent are partnered with a highly ambitious scientific research institute in Oxford that is building a major new biology and genome engineering capability, backed by long-term funding and significant investment. This is not a standard lab safety role. The organisation is scaling rapidly, with a growing laboratory footprint and expanding research activity across biological agents, recombinant DNA work, and hazardous chemical programmes. They are now hiring a Biological and Chemical Safety Officer to help build and maintain the safety framework that will support hundreds of researchers as the institute grows. This role is ideal for someone who enjoys being hands-on in laboratory environments and wants genuine ownership over biosafety and chemical safety programmes, rather than operating as a purely administrative H&S function. The Role You will act as the biological and chemical safety lead within a major research institute, working closely with scientists, lab operations teams, and central EHS colleagues to ensure safe, compliant, and effective research activity. You will support risk assessment processes, lead audits and lab inspections, deliver training, and provide incident response expertise across a dynamic, fast-growing research environment. Key Responsibilities • Develop and implement biosafety procedures aligned to containment standards, • Support biological risk assessments for lab protocols and operational activities, • Provide expertise in pathogen handling, recombinant DNA work, and biohazard waste processes, • Lead chemical safety programmes including chemical hygiene practices and hazardous material oversight, • Review chemical risk assessments, SOPs, and SDS documentation, • Conduct routine lab walks, inspections, and safety audits, • Lead incident investigations and corrective/preventive action planning, • Deliver biological and chemical safety training to researchers and staff, • Support internal and external audits and maintain documentation frameworks, • Contribute to a proactive safety culture across a growing scientific organisation Who This Role Suits This role will suit someone who has worked in a laboratory safety function within biotech, pharma, research institutes, universities, or healthcare environments, and who is confident engaging directly with scientists and technical stakeholders. You will likely have experience as a Biological Safety Officer, Chemical Safety Officer, Laboratory Safety Officer, or EHS Specialist, with strong working knowledge of COSHH and UK safety compliance frameworks. Why Someone Would Move • Opportunity to join a major institute at a key scale-up stage, • High visibility role with real ownership and influence, • Strong scientific environment with long-term investment and growth, • Chance to shape safety systems properly from the ground up, • Excellent benefits package including bonus, travel allowance, private medical, and electric car scheme Location / Working Setup Oxford based, with strong on-site presence required. Candidates must live within commuting distance or be willing to relocate. Right to work in the UK is required, with sponsorship considered on a case-by-case basis. If you’d like to hear more, please apply or message directly for a confidential discussion.

! Location: Need to be located close to Oxfordshire Start date: ASAP Work Arrangement: Site-based (no remote work) Type of position: Freelance. Minimum 3 month contract with the view to extend Job Description Planet Pharma are working with a biotechnology company known for pioneering work in messenger RNA (mRNA) science. Its focus is on developing medicines that use mRNA to instruct the body’s cells to produce proteins that can prevent or treat disease. The organisation operates across infectious diseases, oncology, rare conditions, and immune disorders, and it became widely recognised for creating one of the first mRNA‑based vaccines during the global pandemic. Beyond vaccines, it continues to expand its therapeutic pipeline, invest heavily in research platforms, and partner with global health and scientific institutions to advance next‑generation treatments. Description: Joining this organisation offers the chance to contribute to a pioneering environment advancing the use of mRNA technology in modern medicine. With a broad and growing pipeline across multiple therapeutic areas, you will collaborate with talented colleagues and global partners, playing a direct role in improving health outcomes worldwide. As part of a long‑term commitment to strengthening onshore mRNA vaccine manufacturing in the UK, a state‑of‑the‑art research, development, and production facility is being established in Oxfordshire. This initiative will support respiratory vaccine manufacturing, create highly skilled roles, and promote collaboration with academic institutions, the NHS, and government partners across the country. We’re looking for a dynamic EHS Specialist to jump in and deliver high‑impact, short‑term onsite support to our Environmental, Health & Safety function. Partnering closely with the EHS Director, you’ll be at the heart of keeping our fast‑growing facility safe, compliant and running smoothly. This is your chance to make an immediate difference in a hands‑on, high‑visibility role. What You’ll Take Charge Of • Driving the creation and refresh of risk assessments across labs, facilities and active construction areas, ensuring every activity is safe and compliant., • Designing and delivering engaging EHS training that equips our teams with the knowledge to work confidently and safely., • Leading COSHH assessments and ensuring full alignment with UK regulatory requirements., • Writing, refining and standardising SOPs that elevate operational safety and consistency across the site., • Supporting incident investigations from start to finish — uncovering root causes and shaping corrective actions that prevent recurrence., • Reviewing contractor RAMS and Permits to Work to ensure all onsite activities meet our safety expectations., • Acting as a trusted EHS advisor to operational teams, providing practical guidance and proactive support. Requirements: • Demonstrated experience in an EHS advisory or similar role, ideally within biotech, pharma, laboratory, or technical environments, • Strong knowledge of UK HSE legislation and best practices, • Ability to produce clear, practical EHS documentation (risk assessments, SOPs, COSHH, etc.), • Excellent communication and stakeholder-management skills, • NEBOSH General Certificate (or equivalent) as a minimum, NEBOSH Diploma preferred If this role isn’t suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help! 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. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognized by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

Life Sciences Solicitor / 5 – 10+ PQE / Oxfordshire / £90-100K + DOE – A rare opportunity to join a leading UK life sciences practice, advising innovative businesses from start-ups to global pharma organisations, within a collaborative and highly ranked team – To apply please call Gemma on 020 7183 8586. JOB TITLE: Life Sciences Solicitor PQE REQUIRED: 5+ LOCATION: Oxfordshire SALARY: £90-100K DOE THE ROLE: An exciting opportunity has arisen for an experienced Commercial Solicitor to join a top-ranked life sciences team based in Oxfordshire. This specialist practice advises a broad spectrum of life sciences and technology-based clients, including biotech, biopharma, vaccines, medical devices, diagnostics, agbiotech and tech bio businesses, as well as universities, research institutes, charities and government bodies. You will undertake a wide range of commercial work including IP licensing and partnering transactions, clinical trial arrangements, research collaborations, supply and manufacturing agreements, regulatory matters, data protection issues and due diligence for corporate transactions. Working closely with senior members of a large and highly regarded commercial IP and IT team, you will play a key role in delivering strategic advice to innovative and high-growth clients operating at the forefront of scientific and technological development. THE CANDIDATE: The successful candidate will have at least five years’ post-qualification experience gained within a strong regional, City or in-house environment. You will demonstrate solid technical expertise in commercial law and have proven experience advising life sciences or technology-based businesses. Commercial awareness, enthusiasm for the sector and the flexibility to work across a varied caseload are essential. This role would suit a proactive and ambitious lawyer seeking to deepen their sector expertise within a leading specialist team. THE FIRM: This is an award-winning, Top 50 UK law firm with a strong national presence and an outstanding reputation across multiple practice areas. The firm is known for its collaborative culture, commitment to career development and strong sector focus. You will be joining one of the largest life sciences teams in the UK, consistently ranked in the legal directories and recognised for its depth of expertise and client service. PACKAGE: The firm offers a competitive salary and comprehensive benefits package, together with flexible and hybrid working arrangements. Ongoing professional development and a supportive, inclusive working environment form a core part of the firm’s culture. HOW TO APPLY: Contact Gemma at eNL on 020 7183 8586 or email with your CV, or simply call for a confidential discussion. eNL will never share your CV with a third party without your express permission. As part of our candidate care process, we aim to respond to all applications in 7 days. If you have not been contacted within this timescale, your application has been unsuccessful on this occasion. Please note our advertisements use PQE/salary levels purely as a guide. At eNL we value diversity and inclusion. We want to attract people at all levels and encourage applications from all suitably qualified candidates whatever your ethnicity, religion, age, physical or mental disability, sexual orientation, gender identity or any characteristics protected by law in the jurisdictions in which we operate.

A pioneering biotechnology company is seeking a Commercial Supply Chain Manager based in Oxford, UK. The ideal candidate will have 5-10 years of progressive supply chain management experience in pharmaceuticals. Responsibilities include supporting the management of global supply chain logistics, dev

A leading healthcare digital solutions provider in the UK is seeking a Director of Strategic Accounts to drive business growth within a portfolio of key clients.

MAA, contributing to EU regional clinical regulatory strategy and supporting EU Regulatory Leads across global development and lifecycle activities within a leading pharmaceutical organisation. Planet Pharma is an American parented Employment Business/Agency that provides global staffing services wi

We are currently looking for a well-established Senior Account Manager, with a strong background in health, pharma and medical marketing agencies to lead a client account, or set of accounts, focusing on helping develop the accounts further, keeping them highly profitable and growing. Operationally

We are currently supporting a global biopharmaceutical organisation in the search for a.

You will partner closely with SDRs, SalesOps, Product, Alliances, and Marketing to deliver a worldclass buyer experience in the pharmaceutical and health sectors. Build compelling value cases for a diverse set of senior stakeholders across pharmaceutical companies. Navigate pharma tenders and compl

You will partner closely with SDRs, SalesOps, Product, Alliances, and Marketing to deliver a worldclass buyer experience across the pharmaceutical and healthcare sectors. Build compelling value cases for a diverse set of senior stakeholders across pharmaceutical companies. Navigate pharma tenders

Regulatory Affairs Manager (EU) | Leading Pharma. MAA, contributing to EU regional clinical regulatory strategy and supporting EU Regulatory Leads across global development and lifecycle activities within a leading pharmaceutical organisation. Planet Pharma is an American parented Employment Busines

A leading marketing agency is looking for a Digital Marketing Executive to work in partnership with a prominent B2B client.You will be responsible for developing and executing marketing campaigns, managing various digital channels, and monitoring performance.The ideal candidate will have 2+ years of

Candidates should have a Bachelor of Science or Arts and experience in pharmaceutical manufacturing.

A leading pharmaceutical organization is looking for a Regulatory Affairs Manager to handle EU regulatory submissions and contribute to clinical regulatory strategies. The ideal candidate should have over 5 years of experience in pharma or biotech, especially in Regulatory Affairs, alongside a stron

A global organization in medical communication is seeking a Sales Consultant to develop and maintain client relationships with Pharma, Biotech, and Med Device clients. Candidates should have over 2 years in business development, a solid understanding of pharmaceutical market research, and strong org

A global pharmaceutical company is seeking a Supply Chain Director to oversee end-to-end operations on a permanent basis.

Own and grow Powtoon's Pharma & Life Sciences vertical, targeting pharmaceutical, biotech, and related healthcare organizations. A customer-facing sales professional who thrives on solving real business problems in the Pharma world. Experience selling solutions related to training, communication, en

A leading global healthcare company in the UK seeks a Regional Health Outcomes Manager to drive market access objectives across the Midlands region.The role focuses on building relationships with NHS decision-makers to ensure the accessibility of vital medications.Candidates should have a degree, a

A leading pharmaceutical recruitment agency is seeking a QC Technologist for an initial 12-month contract in Berkshire. A relevant degree in Science, Biochemistry, or Chemistry is required, along with industry experience in a pharmaceutical setting.

A medical technology company in Oxford is seeking a Software Quality Manual Test Analyst to ensure the safety and quality of digital health solutions.This role involves verifying software across medical device projects while collaborating with diverse teams.Candidates should have a relevant degree a

A leading biomedical company in the United Kingdom is seeking an Information Scientist with a passion for AI and content analytics.This role will involve designing AI-enabled workflows, applying NLP and machine learning for scientific analysis, and supporting R&D teams with high-quality information.

In our Business Areas Pharma, Supply Chain, and Technologies, we deliver products, solutions and services that inspire and create added value for customers.

The role involves safely completing daily pharmaceutical deliveries using a 3.

A leading research institute in Oxford is seeking an experienced Environmental Health and Safety Officer to lead the EHS strategy in a pharmaceutical setting.

ADVANZ PHARMA is a global pharmaceutical company with the purpose to improve patients’ lives by providing the specialty, hospital, and rare disease medicines they depend on. We partner with innovative biopharma and pharmaceutical development companies to bring medicines to patients. Selling skills

Referrals increase your chances of interviewing at SoftPace Pharma by 2x.

The role involves developing client relationships, presenting solutions to pharmaceutical companies, and promoting products within the scientific community.

A global pharmaceutical company is seeking a Senior Medical Information Officer to provide critical support in delivering high-quality medical information and managing inquiries.

A leading recruitment firm in the UK is looking for a Business Leader to drive customer-focused initiatives and enhance profitability.The role involves managing relationships with clients and overseeing complex projects.Ideal candidates should have a strong commercial background and excellent relati

A global biopharmaceutical company in London is seeking a Senior Specialist in QA to oversee quality oversight of service providers involved in clinical studies. Applicants should have extensive experience in the pharmaceutical industry, preferably in quality roles supporting medical affairs or R&D.

Are you passionate about advancing Oncology clinical development?.This is a career defining opportunity where you will play a key role in the vision and strategy of a dynamic Biotechnology Company bringing novel immunotherapy drugs into development to benefit cancer patients.Our client has enjoyed u

A leading contract manufacturer in the pharmaceutical sector is looking for a Global Project Manager to oversee critical engineering projects and ensure operational excellence.

A leading healthcare distribution firm in the United Kingdom is hiring a Multi Drop Van Driver to ensure the prompt delivery of pharmaceuticals to pharmacies and hospitals.

Pharma-Search Ltd – grant@pharma-search. This is a unique opportunity to join a leading Global Pharmaceutical Company as they undertake an unprecedented level of investment and activity in Cell and Gene Therapy Research to deliver upon their ambition to become a leader in this field. Our client is

A leading research organization in the UK is seeking a Senior Regulatory & Scientific Writer to produce high-quality documents supporting pharmaceutical development and commercialization.

Ideal candidates will have a background in customer service or operations, especially in the pharma industry, and experience with ERP systems.

A unique opportunity to play a key role within an exceptionally successful, dynamic, and remarkably ambitious business.Having achieved unbridled success over the last 5 years, you will help define, lead and shape the next phase of their growth, development and success.Do you have the ability to lead

The role requires proven B2B sales excellence and a strong network within the pharma market.

A leading Global Clinical Research Organisation is seeking a Vice President of Project Management to develop and implement long-term strategies across Europe, AsiaPacific, and Africa.You will lead the Project Management team, ensuring efficient operations and strong client relationships.Ideal candid

This specialist IP firm has a leading reputation for advising on pharmaceutical and life sciences patent litigation.

Achieve individual annual sales target based on selling to pharmaceutical clients across the offering suite to attain TCV quotas as assigned. Proven success in managing and growing strategic accounts within mid-size and large pharma. IQVIA is seeking a high-impact Director/Senior Director of Busines

A global organization is looking for an Executive Assistant to support a senior legal leader.In this permanent role, you will manage complex diaries, handle sensitive communications, and coordinate meetings.The ideal candidate will have extensive experience in an in-house legal environment and advan