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About the company: Factorytalk is a leading software implementation, development, and consulting company specialising in digitisation for life sciences manufacturers. We operate internationally between offices in the UK and Thailand, providing world-class digital solutions and consulting services. As a leading partner of Tulip Interfaces, Factorytalk supports multinational customers globally digitising their operations. Tulip is the leading Frontline Operations Platform, a cutting-edge no-code software platform recognised by The World Economic Forum, Gartner, Forester, Forbes and more. It enables the rapid building of connected digital apps to solve the most pressing challenges in manufacturing: error-proofing processes and boosting productivity, capturing and analyzing real-time data, and enabling continuous improvement. Job Description: Join us in supporting the creation and deployment of next generation digital manufacturing solutions using the Tulip () platform for Pharmaceutical and Biotech customers. This is groundbreaking work, reinventing the way life sciences manufacturers digitally transform using the very latest software tooling and methodologies. Openness to working in new ways with a flexible and creative mindset is key, as for most Pharma IT professionals this will be more agile and fast paced, and for people from non-regulated backgrounds work may require more structure and quality management. Work is delivered in tight collaborative teams with colleagues and customers, so a collaborative attitude and strong communications skills are essential. We are delivering a wide range of projects at any given time of differing sizes and type. You will be responsible for managing a group of projects and workstreams. Projects are generally either solution delivery, solutions roll-outs, integration projects, or platform related works. Solution delivery involves managing a team of colleagues and customer stakeholders through business processes analysis, requirements capture, solution design, development, validation, and go-live support. Roll-outs are where we are scaling a solution globally, and the rest involve implementing expansions or improvements to the underlying software platform. You will receive training on Tulip app delivery methods, attain certification and additional training on Factorytalk’s specialist App design, building, and validation methods. This will prepare you to excel by combining your project management skills with underlying knowledge of the Tulip software. You will also receive training in our project delivery methods to operate effectively internationally for some of the world’s largest companies. The successful person will be extremely proactive, and a natural communicator and stakeholder manager, with a passion for detail and being the central coordinator people rely on day to day. Location This position is based out of our Manchester, UK office. You will work with customers based all over the world. Work is hybrid and flexible, mostly done remotely or from one of our offices, however in person attendance at our offices will be required for onboarding and with some regularity. International travel to customer locations for key project meetings is required occasionally. Must have requirements: • 2–5 years’ experience in managing some IT system/software development and/or implementation projects., • Good understanding of the manufacturing process execution, with a strong preference for experience in pharmaceutical manufacturing., • Knowledge of software delivery projects, • Experience of managing multiple projects at a time, ranging from small to large scale and critical systems., • Expertise in typical project management tools for task, cost, time and quality management., • Excellent communication and soft skills including the ability to work effectively with internal and customer project teams internationally., • You will be an organized person with an attention to detail and a passion for ensuring compliance to project processes, • You should have an interest in improving business processes through digitisation using software., • Fluent in English both written and verbal., • Flexible mindset and comfortable in a fast-changing environment., • A global perspective and comfortable working with diverse cultures, • Necessary legal status to work in the UK. Beneficial requirements: • The closest relevant experience would be MES / EBR, eQMS, LIMS, ERP or other systems for GMP regulated manufacturers., • Experience of different project delivery methodologies including waterfall and agile, • Experience of client account management, • Knowledge of Computer System Validation is an advantage. Key Responsibilities: • Become an expert in project management for No-Code Tulip projects for life-sciences manufacturers, • Manage projects across the lifecycle from initial enquiry through to go-live, • Create plans, estimates, presentations, reports and track progress, • Support resource planning and management in conjunction with project leaders, • Collaborate and work closely with delivery teams, customer stakeholders, and partner organizations., • Successfully deliver project activities through to completion. Secondary Responsibilities: • Maintain a working knowledge of the Tulip product and solution delivery methodology., • Create and share documents and guidance on project management best practice, • Support the sales team process with new project opportunities., • Create and maintain project management documentation. Working at Factorytalk: Factorytalk is a place where exceptional teams come together to deliver their best work. We’re building a strong, diverse team that values hard work, families, and personal well-being. Benefits of working with us include: • Competitive salary and benefits packages, • Schedule and work location flexibility, • Company trips, • Personal development, education, and professional training support

Job title: HCPC registered Clinical Scientist Reports to: Head of Laboratory Location: Based onsite at Manchester Science Park Contract Type: Full-time, Permanent Salary & Benefits: Competitive Salary + Benefits Package About Yourgene Health: Yourgene Health is a leading integrated technologies and services business, enabling the delivery of genomic medicine. The group works in partnership with global leaders in DNA technology to advance diagnostic science. Our mission to enable scientific advances to positively impact human health remains at the core of our focus. It drives and motivates us to develop class leading products and services to meet our customers’ needs. Yourgene primarily develops, manufactures, and commercialises simple and accurate molecular diagnostic solutions, for reproductive health, precision medicine and infectious diseases. We have a comprehensive offering of non-invasive prenatal tests (NIPT) NGS workflows that have been built with labs in mind, and clinical prenatal screening services. The IONA® test was the pioneer, the first to market as an IVD product, changing the NIPT screening landscape back in 2015. Continuing to build on our expertise in cell-free DNA, our next generation size selection Ranger® Technology uses machine vision for superior precision. With multiple platforms for a range of clinical and research cfDNA sample preparation applications including NIPT, liquid biopsy, gene synthesis and long fragment recovery. In addition, we offer a portfolio of screening products in reproductive health, precision medicine and infectious disease including screening assays for cystic fibrosis and DPYD genotyping to prevent chemotoxicity. Yourgene Genomic Services provides a range of genetic analysis services for our clinical, research and pharma customers to support partners with DNA extractions, biobanking, genotyping, arrays and sequencing workflows (WES and WGS). Yourgene Genomic Services offers a Non-Invasive Prenatal Testing (NIPT) Service, enabling clinics to run their own NIPT service for pregnant women with our prenatal screening tests and service laboratory based in Manchester. Yourgene Health is part of the Novacyt group of companies and is headquartered in Manchester, UK with facilities in Singapore and Canada. Our Culture: Yourgene is a growing, vibrant and exciting place to work, we are looking for committed driven individuals to be part of our next growth journey. Our culture is described by our employee's as collegiate, friendly, professional, innovative, open and fast paced. We have many social and wellbeing initiatives run by our Nova Social and Charity Huddle that keep our sense of community and togetherness alive. At Yourgene we focus on putting values led programmes in place to ensure that we can attract, retain and develop our people. We want our people to have a career with Yourgene and we ensure that they are recognised and rewarded for their achievements and commitment, everyone plays a critical role in our growth journey. Description of role: We have an opportunity for a full-time and permanent HCPC registered Clinical Scientist to join our genomic services team based onsite at Manchester Science Park. As a clinical scientist you will lead a team of scientists delivering clinical molecular testing services including a Non-Invasive Prenatal Testing within a ISO15189, CQC accredited lab. You will use your expertise as a clinical scientist to lead the delivery of NIPT service laboratory ensuring compliance with quality and regulatory requirements. You will lead the development of new clinical services, leading the implementation and validation of new tests, ensuring the delivery of high quality testing services. You will lead the troubleshooting of assays and techniques both existing and in development. To implement laboratory procedures for sample receipt, processing, IQC, analysis, checking, interpretation, preparation of reports (both standard and complex) and reporting of results. You will supervise more junior members of the team and cultivate an open, continuous improvement culture in the lab. In partnership with others, to be responsible for the accuracy, timeliness and appropriateness of a variety of genetic testing, returning results to ordering clinicians and customers. Key areas of responsibility: • To run clinical genetic testing service providing NIPT and other complex genetic tests., • To supervise junior staff ensuring they are trained and maintain their competence in laboratory methods used to provide clinical tests., • To develop and implement lab procedures to receive, track and process clinical samples., • To provide expertise in the clinical interpretation of test results and communication of test results to clinicians., • To use your expertise as a clinical scientist to assist other departments with the development of leading products and services in precision medicine and reproductive health., • Conduct all activities in accordance with ISO 15189 and CQC requirements, following our quality management services and promoting a continuous improvement mindset., • Maintain patient data integrity and regulatory compliance for all projects and documentation, adhering to GDPR, GCLP and HTA regulations., • Identify and address non-conformities, deviations, and risks associated with laboratory activities., • Develop study plans/protocols, SOPs, and technical documents, ensuring compliance and approval., • Stand up new clinical services in accordance with the ISO15189 standards ensuring they assays are robust, verified/validated and offer our service customers state of the art molecular testing., • Lead internal meetings, audits, and communication with senior management to ensure transparency and alignment., • Liaise with the Quality Department to maintain correct documentation and SOPs., • Coordinate service schedules with senior management and project managers to meet business needs., • Ensure compliance with health and safety regulations, including COSHH systems., • Stay updated on scientific advancements and industry trends to align with company strategy. Qualifications, Skills and Abilities: • BSc in an appropriate biological science, • State Registered Clinical Scientist, • 3+ years’ experience working in a clinical laboratory carrying out molecular genetics testing, • Extensive experience working under ISO 15189 Quality Management System., • Strong understanding of genetics, NGS, bioinformatics, diagnostics, and precision medicine., • Experience in Oncology testing, whole genome sequencing and Reproductive Health is desirable., • Ability to critically analyse and interpret scientific data., • Ability to concentrate and work under pressure, • Excellent writing, oral communication, and presentation skills., • Experience working with the selection of suitable bioinformatics and clinical reporting tools preferred., • Demonstratable knowledge of patient consent, HTA, ethics and GDPR, • Confident communicator who is happy to communicate directly with external customers., • Experience in the supervision of junior staff Closing Date: Sunday 31st August, 2025 Equal opportunities: Yourgene Health and the Novacyt Group of companies provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law. Notice to Agency and Search Firm Representatives: Yourgene Health and the Novacyt Group of companies is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Yourgene Health and Novacyt Group employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Yourgene Health and the Novacyt Group of companies. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Location: Manchester, United Kingdom. Hybrid remote/onsite, flexible approx. 2 days per week in office. We will consider fully remote applicants however spending time in the office is an advantage. Employment Type: Full-Time About Us: Factorytalk is a leading provider of cutting-edge digital solutions including Manufacturing Execution System (MES) solutions for the Life Sciences industry. We are a leading partner of Tulip Interfaces having deployed Tulip successfully for top 10 Pharma to more than 30 sites worldwide. We are committed to delivering innovative technology solutions that enhance productivity, ensure regulatory compliance, and drive digital transformation for our clients. Position Overview: We are seeking a highly skilled and experienced Senior Solution Consultant to join our dynamic Tulip team. The successful candidate will play a key role in developing and delivering MES solutions on the Tulip platform for life sciences clients, including pharmaceuticals, biotechnology, and medical devices. They may also work across other use cases outside of MES as needed. This role involves collaborating with cross-functional teams to define requirements, design solutions, and support implementation to ensure successful project delivery. Key Responsibilities: • Engage with clients to understand business processes and identify MES requirements specific to the Life Sciences industry., • Design and architect MES solutions to address complex manufacturing and regulatory challenges., • Define integration approaches and design between MES and other systems such as ERP, devices, and machines., • Lead requirements gathering workshops and create detailed functional and technical specifications., • Collaborate with project managers, developers, and stakeholders to ensure seamless solution delivery., • Provide technical leadership and mentorship to junior consultants., • Support pre-sales activities including product demonstrations, proposal preparation, and solution design., • Stay up-to-date with industry trends, regulatory requirements, and emerging technologies., • Conduct training sessions and workshops to educate clients and internal teams. Qualifications & Experience: • Bachelor’s or Master’s degree in Engineering, Computer Science, Life Sciences, or related field., • Minimum of 5 years of experience in MES implementation, preferably within the Life Sciences industry., • Strong knowledge of MES platforms such as Siemens Opcenter, Werum PAS-X, Rockwell PharmaSuite, etc., • Knowledge and experience of Tulip, or other low/no-code tools, is an advantage but not essential as extensive technical training will be provided., • Proven experience in leading complex MES projects from concept to deployment., • Knowledge and understanding of Pharma and Biotech industry & processes., • Familiarity with GMP, FDA 21 CFR Part 11, GAMP5, and other relevant regulatory requirements., • Excellent problem-solving, communication, and interpersonal skills., • Ability to travel as required to client sites. What We Offer: • Competitive salary and benefits package., • Opportunities for professional growth and development., • A collaborative and innovative work environment. How to Apply: Please submit your resume and cover letter to with the subject line "Senior Solution Consultant, MES Life Sciences Application." Factorytalk is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

About the company: Factorytalk is a leading software implementation, development, and consulting company specialising in digitisation for life sciences manufacturers. We operate internationally between offices in the UK and Thailand, providing world-class digital solutions and consulting services. As a leading partner of Tulip Interfaces, Factorytalk supports multinational customers globally digitising their operations. Tulip is the leading Frontline Operations Platform, a cutting-edge no-code software platform recognised by The World Economic Forum, Gartner, Forester, Forbes and more. It enables the rapid building of connected digital apps to solve the most pressing challenges in manufacturing: error-proofing processes and boosting productivity, capturing and analyzing real-time data, and enabling continuous improvement. Job Description: Join us in supporting the creation and deployment of next generation digital manufacturing solutions using the Tulip () platform for Pharmaceutical and Biotech customers. This is groundbreaking work, reinventing the way life sciences manufacturers digitally transform using the very latest software tooling and methodologies. Openness to working in new ways with a flexible and creative mindset is key, as for most Pharma IT professionals this will be more agile and fast paced, and for people from non-regulated backgrounds work may require more structure and quality management. Work is delivered in tight collaborative teams with colleagues and customers, so a collaborative attitude and strong communications skills are essential. We are delivering a wide range of projects at any given time of differing sizes and type. You will be responsible for managing a group of projects and workstreams. Projects are generally either solution delivery, solutions roll-outs, integration projects, or platform related works. Solution delivery involves managing a team of colleagues and customer stakeholders through business processes analysis, requirements capture, solution design, development, validation, and go-live support. Roll-outs are where we are scaling a solution globally, and the rest involve implementing expansions or improvements to the underlying software platform. You will receive training on Tulip app delivery methods, attain certification and additional training on Factorytalk’s specialist App design, building, and validation methods. This will prepare you to excel by combining your project management skills with underlying knowledge of the Tulip software. You will also receive training in our project delivery methods to operate effectively internationally for some of the world’s largest companies. The successful person will be extremely proactive, and a natural communicator and stakeholder manager, with a passion for detail and being the central coordinator people rely on day to day. Location This position is based out of our Manchester, UK office. You will work with customers based all over the world. Work is hybrid and flexible, mostly done remotely or from one of our offices, however in person attendance at our offices will be required for onboarding and with some regularity. International travel to customer locations for key project meetings is required occasionally. Must have requirements: • 2–5 years’ experience in managing some IT system/software development and/or implementation projects., • Good understanding of the manufacturing process execution, with a strong preference for experience in pharmaceutical manufacturing., • Knowledge of software delivery projects, • Experience of managing multiple projects at a time, ranging from small to large scale and critical systems., • Expertise in typical project management tools for task, cost, time and quality management., • Excellent communication and soft skills including the ability to work effectively with internal and customer project teams internationally., • You will be an organized person with an attention to detail and a passion for ensuring compliance to project processes, • You should have an interest in improving business processes through digitisation using software., • Fluent in English both written and verbal., • Flexible mindset and comfortable in a fast-changing environment., • A global perspective and comfortable working with diverse cultures, • Necessary legal status to work in the UK. Beneficial requirements: • The closest relevant experience would be MES / EBR, eQMS, LIMS, ERP or other systems for GMP regulated manufacturers., • Experience of different project delivery methodologies including waterfall and agile, • Experience of client account management, • Knowledge of Computer System Validation is an advantage. Key Responsibilities: • Become an expert in project management for No-Code Tulip projects for life-sciences manufacturers, • Manage projects across the lifecycle from initial enquiry through to go-live, • Create plans, estimates, presentations, reports and track progress, • Support resource planning and management in conjunction with project leaders, • Collaborate and work closely with delivery teams, customer stakeholders, and partner organizations., • Successfully deliver project activities through to completion. Secondary Responsibilities: • Maintain a working knowledge of the Tulip product and solution delivery methodology., • Create and share documents and guidance on project management best practice, • Support the sales team process with new project opportunities., • Create and maintain project management documentation. Working at Factorytalk: Factorytalk is a place where exceptional teams come together to deliver their best work. We’re building a strong, diverse team that values hard work, families, and personal well-being. Benefits of working with us include: • Competitive salary and benefits packages, • Schedule and work location flexibility, • Company trips, • Personal development, education, and professional training support

Job title: Environment, Health & Safety Assistant Reports to: Facilities & EHS Manager Location: Onsite at our Manchester HQ (Manchester Science Park) Contract Type: Full-time, Permanent Salary & Benefits: Competitive Salary + Benefits Package About Yourgene Health: Yourgene Health is a leading integrated technologies and services business, enabling the delivery of genomic medicine. The group works in partnership with global leaders in DNA technology to advance diagnostic science. Our mission to enable scientific advances to positively impact human health remains at the core of our focus. It drives and motivates us to develop class leading products and services to meet our customers’ needs. Yourgene primarily develops, manufactures, and commercialises simple and accurate molecular diagnostic solutions, for reproductive health, precision medicine and infectious diseases. We have a comprehensive offering of non-invasive prenatal tests (NIPT) NGS workflows that have been built with labs in mind, and clinical prenatal screening services. The IONA® test was the pioneer, the first to market as an IVD product, changing the NIPT screening landscape back in 2015. Continuing to build on our expertise in cell-free DNA, our next generation size selection Ranger® Technology uses machine vision for superior precision. With multiple platforms for a range of clinical and research cfDNA sample preparation applications including NIPT, liquid biopsy, gene synthesis and long fragment recovery. In addition, we offer a portfolio of screening products in reproductive health, precision medicine and infectious disease including screening assays for cystic fibrosis and DPYD genotyping to prevent chemotoxicity. Yourgene Genomic Services provides a range of genetic analysis services for our clinical, research and pharma customers to support partners with DNA extractions, biobanking, genotyping, arrays and sequencing workflows (WES and WGS). Yourgene Genomic Services offers a Non-Invasive Prenatal Testing (NIPT) Service, enabling clinics to run their own NIPT service for pregnant women with our prenatal screening tests and service laboratory based in Manchester. Yourgene Health is part of the Novacyt group of companies and is headquartered in Manchester, UK with facilities in Singapore and Canada. Our Culture: Yourgene is a growing, vibrant and exciting place to work, we are looking for committed driven individuals to be part of our next growth journey. Our culture is described by our employee's as collegiate, friendly, professional, innovative, open and fast paced. We have many social and wellbeing initiatives run by our Nova Social and Charity Huddle that keep our sense of community and togetherness alive'. At Yourgene we focus on putting values led programmes in place to ensure that we can attract, retain and develop our people. We want our people to have a career with Yourgene and we ensure that they are recognised and rewarded for their achievements and commitment, everyone plays a critical role in our growth journey. Description of role: We are looking to recruit a full-time and permanent Environment, Health & Safety Assistant based onsite our Manchester HQ located at Manchester Science Park. The EHS Assistant will report to our Facilities & EHS Manager and will assist in ensuring compliance with statutory legislation, health & Safety, Health Technical Memoranda (HTM’s), Codes of Practice etc. Contribute to and support the maintenance of systems for collation, interpretation and analysis of the company’s green agenda and sustainability goals. Meeting internal and external reporting requirements and deadlines. Carry out site based audits to assess performance in line with procedures, identifying corrective actions. Assist and advise best practices and review Risk Assessments to ensure compliance. Key areas of responsibility: • Assist with the duties placed on employees by the Health and Safety at Work Act 1974 and all statutory duties appertaining to their work and processes., • Maintain communication lines to all employees as the first point of contact for Health and Safety related issues., • Assist with organising training and inductions for new starters., • Take responsibility for the monitoring of the H&S reporting tools and systems., • Attend H&S committee meetings., • Attend Green Team meetings. Qualifications, Skills and Abilities: • Proven experience in an administrative role, ideally within an EHS, quality, or compliance-related field, • Excellent organisational and time management skills with a strong attention to detail, • Proficient in using Microsoft Office, • Strong communication skills, both written and verbal, • A proactive and self-motivated approach with the ability to work independently and as part of a team, • A good understanding of basic EHS principles and regulations, • Be willing to attend training courses to gain qualifications such as IOSH. Closing Date: Sunday 31st August, 2025 Equal opportunities: Yourgene Health and the Novacyt Group of companies provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law. Notice to Agency and Search Firm Representatives: Yourgene Health and the Novacyt Group of companies is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Yourgene Health and Novacyt Group employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Yourgene Health and the Novacyt Group of companies. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Planet Pharma is seeking an Associate Director, AI Data Scientist to lead the design and implementation of innovative AI/ML/GenAI solutions that will transform clinical trial execution and digital healthcare. This is a highly visible, strategic role with the opportunity to impact patient recruitment, real-world data generation, and next-generation digital tools across global R&D. What you’ll do: 🔹 Lead AI/ML/GenAI initiatives to optimize clinical trial operations (patient recruitment, retention, data monitoring, automation). 🔹 Develop GenAI applications for automated clinical trial documentation (protocols, study reports, medical reports, patient narratives). 🔹 Create Digital Healthcare applications to support medical/scientific tools, patient engagement, and real-world evidence generation. 🔹 Design predictive models and generative AI solutions leveraging diverse healthcare data (clinical trials, EHRs, wearables, PROs, HEOR, Phase IV). 🔹 Collaborate with clinical, data science, RWE, and medical affairs teams to deliver AI-driven business value. 🔹 Build relationships with external experts (researchers, regulators, technology partners) to align solutions and stay at the forefront of innovation. 🔹 Ensure compliance with data privacy and regulatory standards while promoting knowledge sharing across teams. What we’re looking for: ✔️ Advanced degree (MS/PhD) in Data Science, Computer Science, Biostatistics, or related field ✔️ 7–10 years’ experience, with 3+ years applying AI/ML to healthcare or clinical research data ✔️ Expertise in Python, R, TensorFlow, PyTorch, and modern ML frameworks ✔️ Hands-on experience with LLMs, generative AI, and natural language processing for medical text ✔️ Familiarity with AWS, MLOps, and cloud-based platforms ✔️ Proven ability to partner with stakeholders and adapt AI solutions to complex healthcare challenges ✔️ Experience in digital healthcare tool development (advantageous) This is a unique opportunity to help shape the future of digital healthcare and clinical research by delivering AI solutions that improve patient outcomes and accelerate therapeutic innovation. At Planet Pharma, we connect top talent with impactful roles that drive innovation in life sciences — and this is one of them. For more information on this position, please apply now and one of our consultants will get in touch to discuss the opportunity with you in more detail.

Planet Pharma is seeking an Associate Director, AI Data Scientist to lead the design and implementation of innovative AI/ML/GenAI solutions that will transform clinical trial execution and digital healthcare. This is a highly visible, strategic role with the opportunity to impact patient recruitment, real-world data generation, and next-generation digital tools across global R&D. What you’ll do: 🔹 Lead AI/ML/GenAI initiatives to optimize clinical trial operations (patient recruitment, retention, data monitoring, automation). 🔹 Develop GenAI applications for automated clinical trial documentation (protocols, study reports, medical reports, patient narratives). 🔹 Create Digital Healthcare applications to support medical/scientific tools, patient engagement, and real-world evidence generation. 🔹 Design predictive models and generative AI solutions leveraging diverse healthcare data (clinical trials, EHRs, wearables, PROs, HEOR, Phase IV). 🔹 Collaborate with clinical, data science, RWE, and medical affairs teams to deliver AI-driven business value. 🔹 Build relationships with external experts (researchers, regulators, technology partners) to align solutions and stay at the forefront of innovation. 🔹 Ensure compliance with data privacy and regulatory standards while promoting knowledge sharing across teams. What we’re looking for: ✔️ Advanced degree (MS/PhD) in Data Science, Computer Science, Biostatistics, or related field ✔️ 7–10 years’ experience, with 3+ years applying AI/ML to healthcare or clinical research data ✔️ Expertise in Python, R, TensorFlow, PyTorch, and modern ML frameworks ✔️ Hands-on experience with LLMs, generative AI, and natural language processing for medical text ✔️ Familiarity with AWS, MLOps, and cloud-based platforms ✔️ Proven ability to partner with stakeholders and adapt AI solutions to complex healthcare challenges ✔️ Experience in digital healthcare tool development (advantageous) This is a unique opportunity to help shape the future of digital healthcare and clinical research by delivering AI solutions that improve patient outcomes and accelerate therapeutic innovation. At Planet Pharma, we connect top talent with impactful roles that drive innovation in life sciences — and this is one of them. For more information on this position, please apply now and one of our consultants will get in touch to discuss the opportunity with you in more detail.

Senior Associate Location: London office/hybrid/remote based Working Hours: Standard UK hours 9-5.30 OR 1pm – 9:30pm BST (due to increased demand and significant organic growth with US clients and Global HQ’s, a US hours team is being formed! This will present a great opportunity to gain expertise in the dynamic and evolving US market, boosting your CV and opening up more doors for the future!). Purpose: Conduct primary and secondary research and analysis; collect market insights and join the dots to bring to life complex market realities and deliver high impact presentations to varied client landscapes. This role will have significant exposure to the senior leadership team and an early opportunity to be involved in a wide variety of projects. About the Role I'm looking for a Senior Associate to join my clients UK based team. You’ll research, analyse, and translate complex market dynamics—particularly in pharma and biotech—into powerful insights and client-ready recommendations. This is a high-exposure role with early responsibility, direct interaction with senior leadership, and the chance to shape impactful projects from day one. What You’ll Do • Conduct primary and secondary market research, including attending key industry conferences., • Analyse findings and distil them into clear insights and high-impact recommendations., • Contribute to client deliverables, meetings, and presentations., • Support proposals and business development initiatives., • Mentor new team members and help shape a collaborative, high-performance culture. Ideal profile • BSc (or higher) in life sciences, physical sciences, or business-related fields., • 1–2 years’ experience in consulting, pharma/biotech, healthcare, or related industries (internships welcome)., • Strong analytical skills with the ability to connect the dots between qualitative and quantitative data., • Confident communicator, resilient under pressure, and motivated to deliver quality work., • Commercially aware, with an understanding of pharma/biotech product development., • Happy to work adjusted hours for a wealth of US based clients Why Join Us? • Early exposure to senior leaders and high-profile projects., • Opportunities to shape strategy and make real impact., • A collaborative, ambitious environment that values initiative and fresh thinking., • Get exposure to a highly buoyant, evolving and dynamic US Life Sciences market and client base For more info, apply now or reach me at

Senior Associate Location: London office/hybrid/remote based Working Hours: Standard UK hours 9-5.30 OR 1pm – 9:30pm BST (due to increased demand and significant organic growth with US clients and Global HQ’s, a US hours team is being formed! This will present a great opportunity to gain expertise in the dynamic and evolving US market, boosting your CV and opening up more doors for the future!). Purpose: Conduct primary and secondary research and analysis; collect market insights and join the dots to bring to life complex market realities and deliver high impact presentations to varied client landscapes. This role will have significant exposure to the senior leadership team and an early opportunity to be involved in a wide variety of projects. About the Role I'm looking for a Senior Associate to join my clients UK based team. You’ll research, analyse, and translate complex market dynamics—particularly in pharma and biotech—into powerful insights and client-ready recommendations. This is a high-exposure role with early responsibility, direct interaction with senior leadership, and the chance to shape impactful projects from day one. What You’ll Do • Conduct primary and secondary market research, including attending key industry conferences., • Analyse findings and distil them into clear insights and high-impact recommendations., • Contribute to client deliverables, meetings, and presentations., • Support proposals and business development initiatives., • Mentor new team members and help shape a collaborative, high-performance culture. Ideal profile • BSc (or higher) in life sciences, physical sciences, or business-related fields., • 1–2 years’ experience in consulting, pharma/biotech, healthcare, or related industries (internships welcome)., • Strong analytical skills with the ability to connect the dots between qualitative and quantitative data., • Confident communicator, resilient under pressure, and motivated to deliver quality work., • Commercially aware, with an understanding of pharma/biotech product development., • Happy to work adjusted hours for a wealth of US based clients Why Join Us? • Early exposure to senior leaders and high-profile projects., • Opportunities to shape strategy and make real impact., • A collaborative, ambitious environment that values initiative and fresh thinking., • Get exposure to a highly buoyant, evolving and dynamic US Life Sciences market and client base For more info, apply now or reach me at

Associate Director, AI Data Scientist.AI/ML/GenAI solutions that will transform clinical trial execution and digital healthcare.This is a highly visible, strategic role with the opportunity to impact patient recruitment, real-world data generation, and next-generation digital tools across global R&D

Overview You will be leading and managing the UK BIM & Piping team in terms of operational delivery and excellence, to resource allocation against projects and to Learning & Development of the team. You will play an active role in managing and developing client relationships and accounts as well as contributing to proposals and technical delivery and execution against projects. This is a highly visible and rewarding role within the UK business with a diverse range of responsibility. This role can be based out of the Birmingham or Manchester office. Responsibilities • Support the Process Group Manager to develop and deliver digital design services for Piping, MEP (REVIT), 3D coordination and project information elements of our projects., • Develop the team across the UK business units ensuring on-going personal development needs identified, so that the team has the correct mix of staff and contract resources., • Take technical responsibility for the team to ensure flawless delivery, working within hour budgets set by projects. Ensure the highest quality of design, engineering and advice on all projects., • Ensure the teams across the business units stay aligned with best practices in industry., • Actively input into PM Group Technology initiatives and drive the Group strategy in terms of PDP / BIM or other applications within your department., • Ensure compliance with PM Group and/or customer procedures, organise appropriate reviews (including peer reviews) and approve project documents for issue., • Coordinate with other disciplines to ensure the correct quality of deliverables are achieved in the correct timeframe based on the project schedule., • Support the Business Development team and Process Group Manager to provide support to proposals across UK Business Units as required., • Manage, develop and mentor resources in the department across the UK including supporting the Apprenticeship and NEXT Graduate Program., • Overseeing the recruitment, development and MEP Designers to meet project requirements., • Identify training and development needs and ensure appropriate support provided to personnel in your department., • Supporting the development and rollout of initiatives to improve efficiency and quality, • Bachelor Degree level and or qualification equivalent to IEng or Eng Tech registration., • Strong level of knowledge and experience within the digital design environment (piping and / or MEP)., • Project experience within PM Group’s core sectors (e.g. Pharma, Mission Critical, or Advanced Manufacturing)., • Proven experience in multi-disciplinary project delivery environments., • An accomplished leader with the ability to build and motivate a team., • Self-driven, results-oriented with a positive outlook and a clear focus on high quality., • Self-starter, decision maker with strong work ethic., • Flexibility to travel both inside and outside the UK as required., • Critically assesses own performance and performance of others., • Customer focused with a demonstrable ability to communicate effectively with clients, including good presentation skills., • A willingness to take responsibility, identify and manage project issues to a satisfactory conclusion.

Overview PM Group is a leading International engineering, architecture, project and construction management firm. With a network of offices in Europe, Asia and the US and a multi-discipline team of 3,500 people, we deliver complex, capital projects in the life sciences, food and beverages, mission critical/ICT, advanced manufacturing, energy and environmental sectors. We have an exciting new opportunity to join the business at a senior level as Technical Director of Electrical Enigneering who wil be the central voice for Electrical Engineering Design and to develop and lead this discipline within PM Group. It is an exciting opportunity to contribute strategically to the future shaping of PM Group. This is a full time, recoverable, technical role within our design service. You will work with the Director of Engineering, the other Discipline Technical Directors and other Heads of Services to determine how we efficiently and consistently deliver design services across the Group. This is a group wide role, covering all 20 design offices.You will contribute significantly to the companies improved performance, to the delivery of safe assets to our customers and to the creation of a work environment that is conducive to enabling a safe, healthy and motivated workforce. This is a senior appointment, reporting to the Director of Engineering, with responsibility for leadership, governance, troubleshooting and for defining the ways of working in Electrical Engineering Design. We offer a flexible working environment, providing a hybrid working arrangement with the option to work from home up to two days a week for this role. This key role and can be based out of one of our offices in Ireland, UK. Poland or Belgium. Interested applicants should submit their CV Responsibilities 1.1 PM Group Strategy for Electrcial Engieering As the Technical Director you will lead the development of the discipline in support of PM Group’s strategy and local Business Unit plans. Key aspects include; 1. Develop a strategy for Electrical Engineering across the Group i.e. to forecast and plan the required capability and capacity., 2. Support the Business Units with strengthening and growing their departments i.e. department profiling, team competency gaps and associated training needs etc., 3. Develop targeted SME areas within Electrcial Engineering e.g. sustainability., 4. Work with Architecture and the Engineering Disciplines to align and develop cross functional competencies targeted at key sectors and technologies., 5. Define, for our core sectors, the range of design activities and deliverables required to deliver the projects safely and efficiently. 1.2 Digitalisation of Business Processes / ways of working 1. Define and implement a strategy for continuous improvement of Electrical Engineering, 2. Develop and improve the Electrical Engineering Service Delivery Platform (SDP) as part of our Quality management System (QMS)., 3. Create a Group wide standardized way of working for Electrical Engineering taking into account the specific requirements in local code and industry norms, 4. Ensure the integration of key considerations such as digitally enabled lean design DeLPD, sector specific approaches and our design office locations., 5. Business transformation projects are an investment cost (i.e. unsold) and their own time is managed by the Technical Director. 1.3 Governance of Design Delivery 1. Support / input to key Sales Proposals as requested by the Director of Engineering., 2. Work with the Director of Engineering to establish a ‘watch list’ of key projects based on the extent of design challenge and technical integrity risk., 3. Influence the early stages of design on key projects., 4. Chair Single Discipline Design Reviews (SDDRs) on key projects., 5. Review Project Basis of Safety documents as required by the Director of Engineering., 6. Input to end of Concept / BoD ‘go, no go’ reviews for high risk challenging projects. 1.4 Troubleshooting 1. Be a ‘first responder’ for critical issues regarding Electrcial Engineering design across the Group., 2. Meet with senior members of both our own and the customer’s team., 3. Agree corrective actions / way forward., 4. Act as Technical Sponsor for the corrective actions., 5. Keep PM Group management updated on correction action progress. Qualifications • Passion for Electrical Engineering, • Safe asset focus, • Bachelor degree, • Relevant industry experience with some working at senior management level, • Have good working knowledge of Pharma, Med Tech and Data Center industries, • Member of a recognized Engineering professional body. (Institution of Electrcial and Electronic Engineering for example)., • Strong technical, commercial, analytical and problem-solving skills., • Excellent communication and interpersonal abilities., • Ability to collaborate effectively with cross-functional teams, • Good communication & people skills, • Self-starter and decision maker Our benefits include: • Flexible working arrangements, including a hybrid working policy, • An employee-owned share scheme . All employees have the opportunity to invest in the company, every one contributing to the success of the company. Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future. PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know.

Company Description Turner & Townsend is a global professional services company with over 22,000 people in more than 60 countries. Working with our clients across real estate, infrastructure, energy and natural resources, we transform together delivering outcomes that improve people’s lives. Working in partnership makes it possible to deliver the world’s most impactful projects and programmes as we turn challenge into opportunity and complexity into success. Our capabilities include programme, project, cost, asset and commercial management, controls and performance, procurement and supply chain, net zero and digital solutions. We are majority-owned by CBRE Group, Inc., the world’s largest commercial real estate services and investment firm, with our partners holding a significant minority interest. Turner & Townsend and CBRE work together to provide clients with the premier programme, project and cost management offering in markets around the world. Please visit our website: Job Description We are currently recruiting for a Project Planner to undertake duties within our Project Controls team, supporting major construction projects across the Life Sciences / Pharma / Data Centre sectors. The Project Planner will work as part of our Project Controls team on high profile construction projects throughout the UK and Europe, providing performance reporting and analysis support. This may be part of a large team or as the key day to day contact point with the client. Key activities include: • Identify trends and root causes of deviations against the baseline using lead and lag indicators, recommend remedial actions to drive best value for the client., • Lead the evaluation of the projects time, cost, and quality targets, applying governance controls as necessary to enable the successful delivery of the project., • Cooperate with a remote team of cost managers responsible for reaching an agreed, market tested cost baseline and ensuring the client is receiving value for money., • Guide and influence the general contractor, ensuring they are progressing in line with the schedule and within agreed cash flow parameters., • Act as the key point of contact to the client overcoming delivery and commercial issues whilst preparing formal and ad hoc reports focussing on time, cost and quality targets., • Control costs with your knowledge of conceptual estimating, funding stage gates, basic contingency principals, procurement principals., • Create and/or work within a cost report, summarizing financials in a executive level dashboard., • Understand change management principals, lead agreed change management process and workflow, providing a platform for adding/tracking/monitoring/approving change., • Coordinate and lead planning sessions and workshops with clients and vendors to compile the master project/programme schedule, agreeing baselines and a critical path., • Understand procurement principals, collate lead times from vendors and client into the master schedule communicate the prioritisation of ordering materials and equipment to meet scheduled install dates., • Work closely with the client to define vendor schedule requirements., • Actively participate in project team risk evaluations, incorporating the defined risks into Monte Carlo to output quantitative impacts to the overall project cost and schedule., • Work closely with the project team to stay informed on status of project changes, incorporating and communicating these to the project team to allow for approvals in the change management process., • Previous experience working in a project controls environment within the life sciences, pharmaceutical or data centre sectors is required, as is experience in at least one of the following: Programme Controls Management, Earned Value (EVM), Change & Risk Management, Planning, Project Controls and or PMO., • Applicants will ideally be degree educated, with previous industry & sector experience being essential., • Previous experience of the following tools (or one of) is also required: Oracle Primavera, MS Project, Excel, PRISM (Cost Management System) Our inspired people share our vision and mission. We provide a great place to work, where each person has the opportunity and voice to affect change. We want our people to succeed both in work and life. To support this we promote a healthy, productive and flexible working environment that respects work-life balance. Turner & Townsend is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees and actively encourage applications from all sectors of the community. Please find out more about us at SOX control responsibilities may be part of this role, which are to be adhered to where applicable. Join our social media conversations for more information about Turner & Townsend and our exciting future projects: Twitter Instagram LinkedIn It is strictly against Turner & Townsend policy for candidates to pay any fee in relation to our recruitment process. No recruitment agency working with Turner & Townsend will ask candidates to pay a fee at any time. Any unsolicited resumes/CVs submitted through our website or to Turner & Townsend personal e-mail accounts, are considered property of Turner & Townsend and are not subject to payment of agency fees. In order to be an authorised Recruitment Agency/Search Firm for Turner & Townsend, there must be a formal written agreement in place and the agency must be invited, by the Recruitment Team, to submit candidates for review. SOX control responsibilities may be part of this role, which are to be adhered to where applicable. Join our social media conversations for more information about Turner & Townsend and our exciting future projects: Twitter Instagram LinkedIn It is strictly against Turner & Townsend policy for candidates to pay any fee in relation to our recruitment process. No recruitment agency working with Turner & Townsend will ask candidates to pay a fee at any time. Any unsolicited resumes/CVs submitted through our website or to Turner & Townsend personal e-mail accounts, are considered property of Turner & Townsend and are not subject to payment of agency fees. In order to be an authorised Recruitment Agency/Search Firm for Turner & Townsend, there must be a formal written agreement in place and the agency must be invited, by the Recruitment Team, to submit candidates for review.

Associate Director, AI Data Scientist.AI/ML/GenAI solutions that will transform clinical trial execution and digital healthcare.This is a highly visible, strategic role with the opportunity to impact patient recruitment, real-world data generation, and next-generation digital tools across global R&D

Reference Code: 86134-en_GBContract Type: PermanentProfessional Communities: SaaS Solutions As an SAP S/4HANA QM and PP Consultant, you will work as part of a great team shaping and delivering the latest processes and solutions to a wide and varied set of clients, across many different industry sectors. As an S/4HANA QM and PP consultant, you will oversee the end-to-end design and implementation of SAP solutions for customer and, fulfil the customer's requirements, deliver workshops with a view to configuring and understanding business processes. Working alongside Capgemini’s team of specialists in our Supply Chain Management Capability in delivering innovative projects to our existing and new clients, you will also have opportunities to develop our pipeline for future projects. This role is a unique chance to work on today’s SAP platform e.g. S/4HANA and driving forward with latest technologies (GenAI, Digital twin, automation), helping Clients to renew their enterprise as they move through their transformation journeys. You will be working on single or multiple project lifecycles, at any or all stages, from shaping the transformation roadmap, through agile delivery to post go live support. Your knowledge of the core Quality Management and Manufacturing area of SAP and the integration into other areas of Supply Chain will allow you to shape, build and deliver solutions in your functional area as well as contribute to the growth of the SAP SCM Capability. As part of the role, you will have access to enhance your consulting, functional and technical skills, through Capgemini learning and development, and the latest industry recognised certifications. About our UK SAP Practice Team: Capgemini UK is a leading SAP Integration Partner, helping our clients navigate through complex SAP transformations. Capgemini UK has 1000 + SAP practitioners across UK & India and are ranked #1 for SAP S/4HANA® certifications in UK and globally. We work closely with our clients to transform their business together using the latest SAP products and architecture, a deep knowledge of industries and markets, and innovative delivery methodologies. Hybrid working: The places that you work from day to day will vary according to your role, your needs, and those of the business; it will be a blend of Company offices, client sites, and your home; noting that you will be unable to work at home 100% of the time. If you are successfully offered this position, you will go through a series of pre-employment checks, including: Identity, nationality (single or dual) or immigration status, employment history going back 3 continuous years, and unspent criminal record check (known as Disclosure and Barring Service) • Using your experience, problem solving and drive to improve abilities to provide functional consulting (Including workshop delivery, business process knowledge, configuration), within SAP S/4HANA Quality Management and Manufacturing projects to drive value and benefits to our customers., • The Influential leadership with vision to engage with customers and deliver against business requirements to ensure the innovative and high-quality solutions integrated into core SAP and non-SAP solutions., • You must have deep expertise in business processes and transformation along with the capabilities of building awareness and really targeting development in SAP S/4HANA Quality Management and Manufacturing configuration and design elements to meet the customer requirements., • You will lead and mentor the team by following best practices for delivering the project business process documentation, make key decisions within the workstreams on best practices, process improvements, implementation plans etc. to meet the business requirements., • Performing leadership by providing thoughts to the Project teams, internal colleagues, and customers to bring innovations into Supply Chain strategy, specifically in the Quality Management and Manufacturing solutions space, road maps., • Training, supporting and mentoring team members, including junior talent to learn from your experiences and expertise., • Develop skills to provide thought leadership to our clients and internal customers with your knowledge of available solutions both within the SAP portfolio, and the supporting products recognised within the industries. You can bring your whole self to work. At Capgemini building an inclusive future is part of everyday life and will be part of your working reality. We have built a representative and welcoming environment, for everyone. ↵ • Consulting experience in SAP S/4HANA Quality Management and Manufacturing., • Multiple end-to-end design and implementation programmes within SAP S/4HANA Quality Management and Manufacturing., • Must have experience in conceptualize the functional and cross functional analysis and the modelling of business processes in relation to the project demand., • You must have a depth of consulting SAP S/4HANA Quality Management integration across one or more additional SAP Supply Chain business process like procurement, warehouse, Production, Sales and distribution, plant maintenance., • Deep knowledge of Industry’s QA and QC processes alongside all QM elements in one or more of the following sectors is an advantage: Aerospace and Defence, Consumer Products, Pharma or Discrete Manufacturing., • Leadership experience across small to medium sized teams, both onshore and offshore, • Commitment, flexibility, thought leadership and a hunger to develop your career within the SAP SCM team and the wider Capgemini Group. To be successfully appointed to this role, it is a requirement to obtain Security Check (SC) clearance. To obtain SC clearance, the successful applicant must have resided continuously within the United Kingdom for the last 5 years, along with other criteria and requirements. Throughout the recruitment process, you will be asked questions about your security clearance eligibility such as, but not limited to, country of residence and nationality. Some posts are restricted to sole UK Nationals for security reasons; therefore, you may be asked about your citizenship in the application process. You will be encouraged to have a positive work-life balance. Our hybrid-first way of working means we embed hybrid working in all that we do and make flexible working arrangements the day-to-day reality for our people. All UK employees are eligible to request flexible working arrangements You will reimagine what’s possible: creating value for the world’s leading organisations through technology to build a sustainable, more inclusive future. You will work with a range of clients all with a unique set of business, technological and societal ambitions, which will make a real impact across the UK. Capgemini. Get The Future You Want. Growing clients’ businesses while building a more sustainable, more inclusive future is a tough ask. When you join Capgemini, you’ll join a thriving company and become part of a collective of free-thinkers, entrepreneurs and industry experts. We find new ways technology can help us reimagine what’s possible. It’s why, together, we seek out opportunities that will transform the world’s leading businesses, and it’s how you’ll gain the experiences and connections you need to shape your future. By learning from each other every day, sharing knowledge, and always pushing yourself to do better, you’ll build the skills you want. You’ll use your skills to help our clients leverage technology to innovate and grow their business. So, it might not always be easy, but making the world a better place rarely is. Capgemini is a global business and technology transformation partner, helping organisations to accelerate their dual transition to a digital and sustainable world, while creating tangible impact for enterprises and society. It is a responsible and diverse group of 340,000 team members in more than 50 countries. With its strong over 55-year heritage, Capgemini is trusted by its clients to unlock the value of technology to address the entire breadth of their business needs. It delivers end-to-end services and solutions leveraging strengths from strategy and design to engineering, all fuelled by its market leading capabilities in AI, generative AI, cloud and data, combined with its deep industry expertise and partner ecosystem. The Group reported 2024 global revenues of €22.1 billion. Get The Future You Want |

Location: Manchester, United Kingdom. Hybrid remote/onsite, flexible approx. 2 days per week in office. We will consider fully remote applicants however spending time in the office is an advantage. Employment Type: Full-Time About Us: Factorytalk is a leading provider of cutting-edge digital solutions including Manufacturing Execution System (MES) solutions for the Life Sciences industry. We are a leading partner of Tulip Interfaces having deployed Tulip successfully for top 10 Pharma to more than 30 sites worldwide. We are committed to delivering innovative technology solutions that enhance productivity, ensure regulatory compliance, and drive digital transformation for our clients. Position Overview: We are seeking a highly skilled and experienced Senior Solution Consultant to join our dynamic Tulip team. The successful candidate will play a key role in developing and delivering MES solutions on the Tulip platform for life sciences clients, including pharmaceuticals, biotechnology, and medical devices. They may also work across other use cases outside of MES as needed. This role involves collaborating with cross-functional teams to define requirements, design solutions, and support implementation to ensure successful project delivery. Key Responsibilities: • Engage with clients to understand business processes and identify MES requirements specific to the Life Sciences industry., • Design and architect MES solutions to address complex manufacturing and regulatory challenges., • Define integration approaches and design between MES and other systems such as ERP, devices, and machines., • Lead requirements gathering workshops and create detailed functional and technical specifications., • Collaborate with project managers, developers, and stakeholders to ensure seamless solution delivery., • Provide technical leadership and mentorship to junior consultants., • Support pre-sales activities including product demonstrations, proposal preparation, and solution design., • Stay up-to-date with industry trends, regulatory requirements, and emerging technologies., • Conduct training sessions and workshops to educate clients and internal teams. Qualifications & Experience: • Bachelor’s or Master’s degree in Engineering, Computer Science, Life Sciences, or related field., • Minimum of 5 years of experience in MES implementation, preferably within the Life Sciences industry., • Strong knowledge of MES platforms such as Siemens Opcenter, Werum PAS-X, Rockwell PharmaSuite, etc., • Knowledge and experience of Tulip, or other low/no-code tools, is an advantage but not essential as extensive technical training will be provided., • Proven experience in leading complex MES projects from concept to deployment., • Knowledge and understanding of Pharma and Biotech industry & processes., • Familiarity with GMP, FDA 21 CFR Part 11, GAMP5, and other relevant regulatory requirements., • Excellent problem-solving, communication, and interpersonal skills., • Ability to travel as required to client sites. What We Offer: • Competitive salary and benefits package., • Opportunities for professional growth and development., • A collaborative and innovative work environment. How to Apply: Please submit your resume and cover letter to with the subject line "Senior Solution Consultant, MES Life Sciences Application." Factorytalk is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development, and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital, and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. We are seeking a dynamic Operations Strategy Lead to support the development of high-quality clinical trial proposals. In this role, you will lead the design, coordination, and delivery of operational strategies that respond to Request for Proposals (RFPs) from our biopharma clients. Your work will directly contribute to increasing our win rate and supporting business growth across key therapeutic areas. This role will support our IRCCD team (Infectious and Respiratory and Critical Care Disease) with a focus in the Respiratory area including COPD, Asthma, IPF, PH ILD. This is available in the EMEA region (please see separate advert for North America and LATAM regions). A day in the life: Lead the operational strategy component for assigned clinical trial proposals, ensuring alignment with client needs and internal capabilities. Collaborate with Therapeutic Unit representatives, feasibility teams, clinical operations, and finance to develop competitive, feasible study delivery plans. Participate in proposal kickoff meetings to gather client requirements and ensure strategic considerations are integrated throughout the proposal process. Translate the commercial win strategy into a clear operational approach, identifying delivery assumptions, risks, and mitigation strategies. Manage timelines and deliverables for the operational sections of proposals, coordinating input from cross-functional teams. Contribute to bid defense preparations, including development of key operational messages and supporting materials. Mentor and provide guidance to junior team members involved in proposal delivery. Capture lessons learned and contribute to continuous improvement of operational strategy processes and tools. Qualifications: Bachelor's degree in life sciences, healthcare, or a related field; advanced degree a plus. Minimum of 5 years of experience in clinical research or clinical trial operations, with at least 2 years in proposal strategy, feasibility, or project management. Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions. Knowledge, Skills, Abilities: Strong understanding of clinical trial lifecycle, operational planning, and proposal development. Excellent collaboration and communication skills with the ability to work cross-functionally in a matrixed environment. Detail-oriented with strong organizational skills and the ability to manage multiple deadlines. Comfortable working in a fast-paced, client-facing environment. Previous experience supporting RFPs, bid defenses, or business development activities. Familiarity with multiple therapeutic areas and global clinical operations. Experience working in CRO, biotech, or pharma settings. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation, and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds, and perspectives are valued. #J-18808-Ljbffr

Our Principal Biostatisticians provide statistical and development support and influence for client trials, offering expertise in processes, clinical development plans, concept sheets, and protocols. They may also oversee work supported by other vendors. Responsibilities include: Providing statistical leadership and expertise in clinical development plans, concept sheets, and protocols; representing Cytel on sponsor Product Development Teams. Having experience in Oncology, preferably in hematology and late-phase studies, with prior experience in registrational studies, acting as an independent statistician, participating in study meetings, and discussing statistical analysis plans and health authority questions. Leading statistical teams on clinical development projects, ensuring timely and aligned statistical outputs, and coordinating statistical aspects across trials. Contributing to study protocols, case report forms, data management plans, statistical analysis plans, and performing analyses. Reviewing study reports, regulatory submission sections, and leading electronic data submissions to authorities. Familiarity with ADAM and SDTM, capable of hands-on work to derive outputs or summary statistics quickly. Managing biostatisticians and statistical programmers in lead roles, focusing on strategy, deliverables, and processes. Innovating with statistical methodologies, developing or adapting techniques suitable for each project, and contributing to the company's visibility and expertise. Developing sourcing strategies for projects and fostering collaboration with sponsor teams and management. An experienced Principal Biostatistician with a passion for clinical development, adept at advanced statistical methods, will lead late-phase Oncology studies, motivate teams, and drive clinical progress. Minimum education required is a Ph.D. or MS in Statistics, Biostatistics, or a related discipline. Minimum work requirements include: At least 6 years of biostatistics experience in pharma/biotech clinical development. At least 3 years in a lead biostatistician role. Knowledge of international regulatory guidelines, experience with FDA interactions, and data submission. Fluency in English; French or German is a plus. Proficiency in SAS and CDISC; R experience is advantageous. Skills required include effective teamwork, customer focus, excellent communication, organization, time management, creativity, leadership, and mentorship abilities. Working embedded within a pharmaceutical client, you'll be at the forefront of innovation, working autonomously in a dynamic environment dedicated to advancing patient treatment. #J-18808-Ljbffr

Business Development Manager Pharma and Bio-Pharma Process Equipment/ Components/ Solutions/ Systems Valves, Pumps, Actuators, Components, Piping, Compressors Complex technical solution selling Basic salary £60,000 - £70,000 (negotiable experience dependent) Bonus Scheme OTE £80K + Car Allowance + Executive Benefits Package UK and some European UK Based Position - open on where you live Oxford, Northampton, Bristol, Coventry, Luton, London, Reading, Swindon, Southampton, Leeds, Manchester, Birmingham, Nottingham, Bristol etc. Mercury Hampton is working exclusively with this client. Our client is a well-established global leader in process equipment and components; they partner with most of the major process manufacturing companies across the world. They have an enviable reputation for customer service, innovation and help their customers to become more efficient, reliable, reduce downtime ensuring their process is optimised to the highest standards and levels of sustainability. Due to continued growth and success, they are now looking to hire a dynamic process equipment sales professional to target the Bio and Pharma sector across the UK. Mercury Hampton Ltd has been exclusively retained on this important position. You will take responsibility for managing and growing the Pharma and Bio-Pharma market segment across the UK, this is a sector specialist role. You will be working with existing Bio and Pharma clients, but the main emphasis will be new business, hunting down new project opportunities and opening up new customers. This is a strategic role, involving researching pharma and bio-pharma customers and devising a strategy in conjunction with senior management to win and grow this segment. You will be working for an outstanding brand with some powerful case studies, world class products, technical support and reputation for innovation and great customer service to help you achieve success. You will follow up on all leads and enquiries and take responsibility for managing the full sales process from prospecting, initial contact, tendering, technical support and follow up meetings when required. This will include regular customer site visits, understanding the customer requirements with a view to closing and winning the business. There will be full support and back up to ensure you are successful including marketing, internal sales, and product training in the USA and Europe. Moreover, often this companys products are already specified; you will need to work with the OEMs, EPCs and end users to refine, instil confidence and get the sale. The Candidate: The successful candidate will have an outstanding proven track record in selling, penetrating and winning business in the Pharma and BioPharma market in the UK Sold process equipment Flow related components systems beneficial, valves, pumps, piping, actuators, compressors, pneumatics etc. Sold to OEMs, EPCs, engineering Houses and Pharma End Users Engineering Background/ Qualification desireable Outstanding new business and key account management skills, comfortable building long term relationships Energetic, Dynamic, Self-starter, Personable, can-do attitude Strategic, understand how to map out a sector, self-generation and new business sales long term relationship building sales Ability / experience of accurate forecasting and budgeting Pipeline management and closing skills A strong strategic thinker, strong commercial acumen and emotional intelligence You will have an eye for upselling / cross selling opportunities and navigating and networking corporate businesses You will have excellent communication skills and able to communicate and sell to a wide variety of levels. Please click on the apply button or contact Mercury Hampton directly. We aim to respond to all successful applicants within two working days. TPBN1_UKTJ

Senior CSA Project Manager Manchester £85,000 - £115,000 + Travel Allowance + Stay Away Expensed + Discretionary Bonus + Pension + Holidays + Private Medical Insurance + Package + Technical Progression + 'Immediate Start' Take on the role of a Senior CSA Project Manager with a rapidly growing contractor in the thriving data centre / pharmaceutical / manufacturing and mission-critical construction sector. This role offers a clear path to progression into senior management. In this role, you will be reporting directly to the project director and form part of the leadership team which includes both operational and client engagement. You will oversee the full lifecycle of CSA works, from design coordination and technical tender assessments to subcontractor management and project execution. Your responsibilities will span procurement, programme and budget control, quality assurance, and client engagement. You will lead technical teams, manage daily activities across contractors and vendors, and ensure full compliance with project delivery standards across mission critical projects. Candidates can be based anywhere in the UK, but mobility is essential, as projects are located across the country. While this is a static role, you will be assigned to a single project for its extended duration, meaning you must be prepared to travel or stay away as required. The projects are spread across various locations in the UK, with additional opportunities to work abroad! Your Role as a Senior CSA Project Manager Will Include: Establish risk and opportunity management procedures and exercises including an early warning system which identifies potential risks or changes Responsible for handover of Project to operations team, including the resolution of all defects Liaise with clients where applicable and manage both their needs and expectations Responsible for creating and managing project budgets As a Senior CSA Project Manager, You Will Have: Strong CSA (civil, structural & architectural) construction background Demonstrated success delivering complex commercial, industrial, logistics, pharmaceutical or mission critical projects Background in leading high-value construction projects within structured, fast-paced environments Familiarity with full project lifecycle, from design coordination to commissioning and handover Keywords: senior project manager, project delivery, CSA, civil, structural, architectural, mission-critical, data centres, design management, tender evaluation, procurement, value engineering, subcontractor management, technical leadership, construction management, budget control, project scheduling, quality assurance, client liaison, project lifecycle, risk management, commercial evaluation, Senior PM, tier one contractor, CSA contractor, Derby, Nottingham, Leicester, Lincoln, Sheffield, Leeds, Bradford, Wakefield, Huddersfield, York, Doncaster, Hull, Rotherham, Barnsley, Halifax, Scunthorpe, Manchester, Liverpool, Preston, Salford, Bolton, Warrington, London, Blackburn, Blackpool, Burnley, Oldham, Rochdale, Stockport, St Helens, Wigan, Newcastle upon Tyne, Sunderland, Durham, Middlesbrough, Gateshead, Hartlepool, Stockton-on-Tees, Darlington, South Shields, Washington, project manager, construction manager, project lead, Engineering Project Manager, construction, mission-critical, data centres, pharma, logistics, industrial build projects TPBN1_UKTJ

Medical Science Liaison - PHD, bolton, greater manchester. Planet Pharma are partnered with a Medical Device client who is seeking to hire a Medical Science Liaison in the UK to be responsible for building relationships within the medical and scientific community, sharing medical and scientific info

Our practice focuses on projects like brand strategy, positioning, value proposition, disease area and portfolio strategy, lifecycle management, new product planning, competitor strategy, workshop facilitation, and strategic customer research. Prior experience in consulting, strategic research, or b

Planet Pharma are partnered with a leading Pharmaceutical client who is seeking to hire a Statistical Science Lead (Director level) to support drug development programs and individual studies within assigned projects. Statistical Science Lead, Director, bolton, greater manchester.

Operations Director - Commercial Consultancy - Rail. Associate Director - Commercial Consultancy - Rail. Associate Director, Commercial (Pharma Market Research).

To be considered for the role of Head of Regulatory Affairs, you will have:. Minimum 5 years experience in Regulatory Affairs, ideally gained in a generic, specialty or pharma distribution. Senior International Consultant - Regulatory Affairs and Executive Search.

We are seeking a Media Relations and Content Manager to play a key role in extending BioPhorum’s reputation as thought leaders within the biopharmaceutical industry. Beyond pharma, BioPhorum has also built relationships with other types of life science organisations, including those that provide s

Tulip is the leading Frontline Operations Platform, a cutting-edge no-code software platform recognised by The World Economic Forum, Gartner, Forester, Forbes and more. Openness to working in new ways with a flexible and creative mindset is key, as for most Pharma IT professionals this will be more

Do you want to be part of building and shaping the successful pharma brands of the future?.Are you passionate about using advanced primary market research methods to uncover why patients, healthcare professionals, and other stakeholders make the decisions they do?.Do you want to work across a mix of

As an Associate Director in Primary Market Research, you will take a leadership role in overseeing large-scale, high impact quantitative and qualitative research projects. More than 80% of our employees hold advanced life sciences degrees, and our teams deliver an impressive depth of therapeutic, cl

Senior Buyer (1 year initial FTC). Experience in a Buyer role within food, pharma, FMCG, or chemical production. MCIPS Level 4 qualified (or working towards it) – we’re open to experienced buyers ready to take this next step.

Commission + Team Bonus + Car Allowance + Full Expenses.New business hunters, who can also expand their customer relationships.Must have 3+ years of sales experience in B2B sales into the manufacturing sector (ideally FMCG, food, beverage or Pharma).Oliver Carol Recruitment have been exclusively bri

Senior Business Development Manager (f/m/d) for Pharma PPC / PDC and Channels. Senior Business Development Manager (f/m/d) for Pharma PPC / PDC and Channels. Senior Business Development Manager (f/m/d) for Pharma PPC / PDC and Channels.

Pharma Mechanical Fitter / Assembly Engineer. We are delighted that due to our continued growth, we have a vacancy for two Mechanical Fitters / Assembly Engineers within our Pharma Assembly Team.

Medical Science Liaison - MSc, Manchester. Planet Pharma is partnered with a Medical Device client seeking to hire a Medical Science Liaison in the UK.

Statistical Science Lead/Director - Remote in UK - Global Leasing Pharma!. Partnered with a global pharmaceutical innovator focused on transforming lives through breakthrough science and patient-

Industry experience in any of the following: Energy, Utilities, Mining and Infrastructure; Financial Services; Healthcare and Pharma; Industrial Manufacturing and Services; Retail, Consumer and Leisure; Real Estate; or Technology, Media and Telecommunications. This is an exciting opportunity for you

Statistical Science Lead/Director - Remote in UK - Global Leasing Pharma!. Partnered with a global pharmaceutical innovator focused on transforming lives through breakthrough science and patient-centric solution

Industry experience in any of the following: Energy, Utilities, Mining and Infrastructure; Financial Services; Healthcare and Pharma; Industrial Manufacturing and Services; Retail, Consumer and Leisure; Real Estate; or Technology, Media and Telecommunications. Transaction Services - Financial Due Di

Clinical Pharmacology Lead - AD/Director, bolton, greater manchester. Planet Pharma is seeking a Clinical Pharmacology Lead (AD/Director Level) – Neuroscience Focus to drive strategy and execution across neuroscience programs from candidate nomination through Phase 4. PhD or MD with strong experie

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Medical Science Liaison - MSc, Bolton, Greater Manchester. Planet Pharma is partnered with a Medical Device client seeking to hire a Medical Science Liaison in the UK. The role involves building relationships within the medical and scientific community, sharing medical and scientific information abo

Social network you want to login/join with:.Location: UK, France, or Germany (Flexible).Are you a PhD-level statistician with experience in pharma and Health Technology Assessment (HTA)? Looking to apply your expertise to improve patient access on a global scale? This could be your next move.Join a

Clinical Pharmacology Lead - AD/Director, manchester. Planet Pharma is seeking a Clinical Pharmacology Lead (AD/Director Level) – Neuroscience Focus to drive strategy and execution across neuroscience programs from candidate nomination through Phase 4. Lead clinical pharmacology strategy across al

Tulip is the leading Frontline Operations Platform, a cutting-edge no-code software platform recognised by The World Economic Forum, Gartner, Forester, Forbes and more. Openness to working in new ways with a flexible and creative mindset is key, as for most Pharma IT professionals this will be more

PhD or MSc in Biostatistics, Statistics or a closely related field. Associate Director, Statistics, bolton, greater manchester. Associate Director, Statistics | Global Pharma | UK | Home Based |.

Prescient is a global biopharma strategy consultancy working with leading companies across the product lifecycle, specializing in brand positioning, disease area and portfolio strategy, and strategic customer research. Are you passionate about understanding customer and patient behavior to shape suc

Packaging Operator – Pharmaceutical Industry. Pharmaceuticals / GMP Manufacturing.

At Planet Pharma, we connect top talent with impactful roles that drive innovation in life sciences — and this is one of them.

Proven track record in CMC-regulatory affairs within the pharmaceutical industr.

At Planet Pharma, we connect top talent with impactful roles that drive innovation in life sciences — and this is one of them.

Information Security Compliance Analyst.Are you passionate about cybersecurity, compliance, and driving risk management strategies? We’re seeking an experienced.Information Security Compliance Analyst.EMEA-wide Information Security Management System.This role plays a critical part in maintaini

Associate Director / Director, Clinical Pharmacology & Pharmacometrics. Associate Director / Director – Clinical Pharmacology & Pharmacometrics. Lead clinical pharmacology and PK/PD studies from Phase 1–4.

Within this role you will work with a global portfolio includes best-in-class, iconic brand-name products as well as global key brands, generics (including branded and complex generics) and other offerings across a wide range of therapeutic areas.Our client is committed to helping create healthier c

Planet Pharma are partnered with a leading Pharmaceutical client who is seeking to hire a Statistical Science Lead (Director level) to support drug development programs and individual studies within assigned projects. Planet Pharma is an American parented Employment Business/Agency that provides glo

Job Opportunity: Supply Chain Coordinator.We are seeking a proactive and detail-oriented.This is a development role, ideal for someone with initial experience in supply chain or customer service environments who is eager to grow into managing their own portfolio of products.The successful candidate

Senior Research Executive - Pharma. Are you currently an RE or SRE with experience in the pharmaceutical sector, looking to join a friendly, independently-owned research agency where your research career will be nurtured through peer support and robust continuous professional development?.

Planet Pharma is seeking a talented and motivated Biostatistician to support the design, analysis, and reporting of clinical trials and observational studies. PhD with some experience, or Master’s degree in Biostatistics with substantial experience in biomedical research, pharmaceutical, CRO, acad

Planet Pharma is seeking a highly skilled regulatory affairs candidate with strong Chemistry, Manufacturing, and Controls (CMC) experience, particularly in preparing documentation for both Clinical Trial Applications (CTAs) and Marketing Authorization Applications (MAAs). Deliver high-quality CMC re

Job Opportunity: Market Access Specialist (UK).Healthcare & Life Sciences Sector.Are you passionate about improving healthcare access and ensuring innovative treatments reach patients faster?.This role plays a pivotal part in shaping value-based strategies and driving commercial success across the U

Proven track record in CMC-regulatory affairs within the pharmaceutical industry.

Join a highly successful business and leading Life Science Consultancy, delivering high quality solutions to make their clients’ businesses safer, more quality focused, compliant and ultimately more sustainable and successful.Reporting to the Practice Leader you will play a crucial role in the con

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 extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissio

Dispensing of radiopharmaceutical products into vials. This is a fantastic opportunity for you to gain experience and full training in Radiopharmaceutical manufacturing to further your scientific career. Are you looking for a varied role in Pharmaceutical Production? Do you have a degree in a Scient

At Planet Pharma, we connect top talent with impactful roles that drive innovation in life sciences — and this is one of them.

Happy just to follow or would you rather innovate and lead? Your chance to join arguably the most innovative, forward thinking and flexible global CRO.Do you want to help to deliver creative solutions that exceed client expectations?.Can you shine within an organization that embraces expertise, tale

Planet Pharma is seeking a Clinical Pharmacology Lead (AD/Director Level) – Neuroscience Focus to drive strategy and execution across neuroscience programs from candidate nomination through Phase 4. Lead clinical pharmacology strategy across all development phases. Present and publish clinical pha

How will you make an impact at Envision Pharma Group?.

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Packaging Operator – Pharmaceutical Industry. Pharmaceuticals / GMP Manufacturing.

Vice President, Project Management, Europe, AsiaPacific & Africa.Join one of the world’s leading Global Clinical Research Organisations, with over 30 years’ experience and 7,000 staff globally, operating in over 80 countries.Reporting to the Executive Vice President Operations, you will be respo

Senior Research Executive - Pharma. Are you currently an RE or SRE with experience in the pharmaceutical sector, looking to join a friendly, independently-owned research agency where your research career will be nurtured through peer support and robust continuous professional development?.

You will be responsible for growing and maintaining a portfolio of clients – predominately in the pharmaceutical sector. To create an account strategy to drive sales and relationships across the business for owned pharmaceutical SMM accounts.

Join a highly successful business and leading Life Science Consultancy, delivering high quality solutions to make their clients’ businesses safer, more quality focused, compliant and ultimately more sustainable and successful.Reporting to the Practice Leader you will play a crucial role in the con

Build a foundation for a rewarding career in pharmaceutical or life sciences supply chain operations.

Vice President, Global Clinical Trial Management.Are you a natural leader and able to inspire others? Do you have the drive, enthusiasm and talent to lead others? Does your ambition match that of our client?.Our client is a successful global CRO, a company that has enjoyed a sustained period of grow

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 extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissio

Sharing broad knowledge encompassing PKPD, DMPK, Bioanalysis, Biomarkers and Quantitative Pharmacology. This is a rare and exciting opportunity to play a key role in the vision and strategy of an innovative BioPharmaceutical Company, focused on making a positive impact on patients’ lives.

At Planet Pharma, we connect top talent with impactful roles that drive innovation in life sciences — and this is one of them.

Direct message the job poster from 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 extensive functional expertise including: Regula

Planet Pharma are partnered with a leading Pharmaceutical client who is seeking a candidate with a solid background in SAS programming a working knowledge of CDISC standards (SDTM, ADaM, and TLFs). Planet Pharma is an American parented Employment Business/Agency that provides global staffing service

Minimum 5 years of Life Science managed services or pharmaceutical industry experience required. How will you make an impact at Envision Pharma Group?.

Several years current experience selling SaaS offerings to the UK Pharma, Biotech or associated markets. Proven recent background managing big Pharma/Biotech accounts. Proven experience hunting for and winning new business for alternate revenue streams within existing big-pharma accounts.

For further information or a discussion in complete confidence, please contact Dr Grant Coren, Pharma-Search Ltd – grant@pharma-search. Our client is a leading Global Pharmaceutical Company committed to driving innovative research to help people to do more, feel better and live longer. This is a u

Our client is a global leading and highly innovative biopharmaceutical services company, one that has enjoyed many years of unprecedented success.

At a time where the costs of R&D are increasing and the number of compounds achieving regulatory approval is decreasing, the Pharmaceutical and Lifesciences industry faces many challenges. As Director, R&D Consulting within the Pharmaceutical and Lifesciences practice you will play a key role in fur

You will be responsible for working closely with both the commercial and operational teams to provide outstanding service to clients within the Pharma, Biotech and CRO sectors.

Bachelor’s or Master’s degree in Pharmaceutical Sciences, Engineering, Quality Assurance, or a related field. Strong knowledge of ISO 13485, EU MDR (2017/745), and US FDA regulations for medical devices and pharmaceutical manufacturing.

Critical to your success will be your ability to develop and expand new business opportunities within established accounts and prospective new clients within USA, particularly big Pharma, mid Pharma, BioPharma, Biotech and CRO client companies.

Pharmaceutical Sales (2 years minimum). Orion Pharma (UK) Ltd Customer Account Specialist. NSHI, together with Orion Pharma (UK) Ltd.

Advance Regulatory Consulting is a regulatory affairs consultancy that provides consultancy services to the pharmaceutical and biotechnology industries to enable the successful development and commercialisation of medicines globally. Research and identify high-potential prospects in the pharmaceutic

Associate Director Biostatistics | Global Pharma | UK | Home Based |. Global Pharma recognised for its commitment to innovation and patient impact, is expanding rapidly in the UK.

Direct message the job poster from 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 extensive functional expertise including: Regula

Senior Pricing & Contracting Manager - Pharma. We're recruiting for a Senior Pricing & Contracting Manager to join a globally respected, privately owned pharmaceutical company. Define and lead the Pricing & Contracting team strategy, including setting clear objectives and KPIs aligned with corporate

Director – Biostatistics – Pharma – UK – Remote / Hybrid. We are seeking an experienced and highly skilled Biostatistics Director to join a cross-functional team in a leading global pharmaceutical environment. Minimum 6 years of relevant experience with a PhD (9+ years with a Master’s degr

Extensive knowledge and experience of Quality Assurance, Quality Systems, GMP guidelines and an understanding of the manufacture and packaging of pharmaceutical products. Pharmaceutical Manufacturing and Biotechnology Research. Referrals increase your chances of interviewing at Planet Pharma by 2x.

Direct message the job poster from Envision Pharma Group. How will you make an impact at Envision Pharma Group?. Proven track record of leading high-impact, strategic value communication projects for pharma clients, driving organic growth.

Based in the headquarters of a global biopharmaceutical company, you will play a key role within the Neuroscience Biology Group.

Executive Director, Health Economics and Outcomes Research (HEOR), EU / USA.Your chance to join the most innovative, forward thinking and flexible global CRO.Do you wish to play a key role in shaping the direction of a first in class Late Phase business?.Do you bring a high level of credibility and

The Director, Strategic Accounts, Pharma Services, leads development efforts that best address customer needs while coordinating the involvement of all necessary teams. The Director, Strategic Accounts, Pharma Services, will be responsible for building out a customer base, working collaboratively an

Our client has maintained and strengthened its position as the world’s leading provider of biopharmaceutical development and commercial outsourcing services. Join the world’s largest provider of biopharmaceutical development services with a leadership role.

Global experience in Market Access and Pricing either in a major pharma company or consultancy.

Direct message the job poster from Planet Pharma. This opportunity allows you to step into a pivotal role within a global biopharmaceutical leader at the forefront of oncology innovation. Pharmaceutical Manufacturing and Biotechnology Research.

Critical to your success will be your ability to develop and expand new business opportunities within established and new clients within USA, particularly big Pharma, mid Pharma, BioPharma, Biotech and CROs. Our client is a knowledge-based, science-led business providing a wide range of innovative a

Our client is a leading Global Pharmaceutical Company committed to driving innovative research to help people to do more, feel better and live longer.

In Fine PHARMA : network of 2000 pharmacists in France. Evidence-based research is increasingly desired by pharmaceutical companies due to recent FDA and EMEA initiatives as well as changing requirements from health care payers (government and private insurers). An established senior level network w

Compliance Regulatory Lead (Must have Pharma) - Outside IR35 - £600 - Remote. Exalto Consulting is recruiting for a contract Compliance Regulatory Lead with experience in the pharmaceutical sector.

You will be responsible for leading a customer focused franchise, consisting of medical and operational staff with significant subject matter expertise.You will present and sell the organisation’s medical and scientific capabilities to clients, working in conjunction with the business development

How will you make an impact at Envision Pharma Group?.

In line with our ambition, we are partnering with innovative biopharma and pharmaceutical development companies to bring medicines to patients. ADVANZ PHARMA is a global pharmaceutical company with the purpose to improve patients' lives by providing the specialty, hospital, and rare disease medicine

Do you have the ability to lead and inspire others?.Do you have the courage, drive and talent to innovate?.Do you have the experience to design and implement a global strategy?.Do you have the desire to help lead a growing business?.Our client is a highly innovative business leader; a business that

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

Head of in vivo Experimental Biology, Singapore.Join a highly successful business and the market leader to help continue the growth of their focused and ambitious product development pipeline.Reporting to the General Manager (Singapore) you will play a crucial role in the continued development, mana

Our client is a leading Global Pharmaceutical Company committed to continuing development in order to ensure that they maintain the broadest and most innovative portfolio of any company. Extensive knowledge and experience within clinical research in the pharmaceutical industry, ideally within. This

Join a highly successful business and market leader to help continue the growth of their focused and ambitious product development pipeline.Reporting to the Vice President Biological Systems Research (BSR) you will play a crucial role in the strategic leadership within BSR, creating and executing a

Based in the headquarters of a global biopharmaceutical company, you will play a key role within the Neuroscience Discovery Medicine Group.

Exec VP, Clinical Development & General Manager.Happy just to follow or would you rather innovate and lead? Your chance to join arguably the most innovative, forward thinking and flexible global CRO.Do you want to help to deliver creative solutions that exceed client expectations?.Can you shine with

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We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Statistical Science Lead/Director - Remote in UK - Global Leasing Pharma!*, bedford. Statistical Science

The Operations Manager supports the client in the specialty channel partner selection process, provides patient journey recommendations and understands the standard levels of services (core and enhanced) offered by specialty pharmacies, specialty distributors, data aggregators and other alternative

Business Development Director – Pharma & Healthcare. We’re supporting a well-established, specialist business in the search for a commercially focused Business Development Director to lead growth across the Pharma and Healthcare sectors in the UK, Europe and North America. You’ll need a strong

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

Designing, implementing, and overseeing network infrastructures.Configuring, supervising, and enhancing firewalls, VPNs, IDS/IPS, and other security measures.Investigating and mitigating network and security incidents.Maintaining the reliability, efficiency, and protection of the network.Offering ex

The role will allow you to take on key areas or responsibility, fostering relationships with key decision makers, across all service lines, within Pharmaceutical and Biotechnology companies. Blue chip pharmaceutical clients. Emerging and developing medium and small pharmaceutical clients.

Do you have experience of production and process validation? Are you looking for a new challenge with a leading Pharmaceutical Manufacturer?. A manufacturer of specialist pharmaceuticals is currently seeking a Validation Specialist to join the production team at their site in Guildford. Educated to

Critical to your success will be your ability to develop and expand new business opportunities within prospective new clients within DACH, particularly with mid Pharma, BioPharma, Biotech and MedTech client companies.

Critical to your success will be your ability to develop and expand new business opportunities within established accounts and prospective new clients within Europe and North & South America, particularly within big Pharma, mid Pharma, BioPharma, Biotech and CRO client companies. Ideally you will ha

Experience with AI/ML or GenAI applications in pharma commercial data ecosystems. Build strong, trust-based relationships by demonstrating deep understanding of pharma commercial operations and data ecosystems. Stay current with emerging technologies in pharma data management and analytics (Snowflak

Referrals increase your chances of interviewing at eXmoor Pharma by 2x. Direct message the job poster from eXmoor Pharma. Head of HR at eXmoor Pharma Concepts Ltd.

Extensive experience in pharmaceutical and/or healthcare industry. D in Life Science, MBA, Medical, or Pharmacy). Demonstrable Diagnostic / Medical Device / Pharma marketing experience within Oncology.

Critical to your success will be your ability to develop and expand new business opportunities within established accounts and prospective new clients within Europe, particularly with big Pharma, mid Pharma, BioPharma, Biotech and CRO client companies.

Phase 1–4), and analyze pharmacokinetic and pharmacodynamic data. Clinical Pharmacology & Pharmacometrics Director – Oncology & Neuroscience Focus. Are you ready to make a meaningful impact in the lives of patients with serious medical conditions? A leading global biopharma company is seeking an

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 extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissio

Critical to your success will be your ability to develop and expand new business opportunities within established accounts and prospective new clients within Europe, particularly with big Pharma, mid Pharma, BioPharma, Biotech and CRO client companies.

Dermatology Territory Manager - Toronto North York Ajax page is loaded.Dermatology Territory Manager - Toronto North York Ajax.Apply locations Thornhill posted on Posted 10 Days Ago job requisition id JR014627.Galderma is the emerging pure-play dermatology category leader, present in approximately 9

Client Dedicated Talent Acquisition Partner at Planet Pharma. Medical Equipment Manufacturing, Pharmaceutical Manufacturing, and Biotechnology Research. Referrals increase your chances of interviewing at Planet Pharma by 2x.

Senior Scientist – Antibody Discovery.Cambridge area | Biologics | Full-time | Permanent.Are you passionate about antibody discovery and ready to take the lead on exciting, high-impact biologics projects? We're looking for an experienced and driven.In this role, you'll play a key part in design

ITH Pharma specialises in the provision of Parenteral Nutrition, chemotherapy and CIVAS.

Vice President Scientific Affairs and Regulatory Engagement, Switzerland.You will be a key member of the senior executive leadership team within R&D, accountable for the scientific quality of product submission dossiers, and their successful approval by regulatory authorities.Under your guidance and

Pharmaceutical Manufacturing and Packaging and Containers Manufacturing. Business Development Manager - Pharma Syringes. Business Development Manager - Pharma Syringes.

Build a foundation for a rewarding career in pharmaceutical or life sciences supply chain operations.

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

Growth and investment remains firmly on the agenda and as such, we are looking to appoint an outstanding Business Development Manager – Life Sciences, Pharma and Data Centres to lead ongoing business growth within this progressive organisation. Reporting to the Head of Sales UKI and as such, part