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CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. The role We’re looking for a Drug Development Project Manager — someone who understands how discovery turns into development, and development turns into real therapies for patients. This is not a generic project management position; it’s about driving the scientific, technical and operational progress that determines whether a potential medicine succeeds. You’ll be the connection between scientific strategy and operational delivery, coordinating complex, global programmes that draw on expertise from discovery, clinical, regulatory, CMC and commercial functions. Your focus will be keeping teams aligned, assessing scenarios and making decisions in a timely fashion. This ensures that every milestone moves us closer to patients who need new treatment options. Why this job This role sits along the central axis of some of CSL’s most strategically important development programmes — the kind of projects where coordination and clarity make the difference between momentum and delay. It’s an opportunity to work at the point where science, strategy and execution meet; to see the bigger picture while ensuring every moving part is in sync. For an experienced drug development project manager, this is the chance to apply your skills where they truly shape outcomes, not just track them. CSL is at an inflection point. We’re undergoing a massive transformation in R&D. It represents a tremendous opportunity to be involved, to work with key decision makers and have influence on project progression. We have exciting, new assets coming out of our research portfolio as well as an existing portfolio of medicines which we’re looking into further transforming to improve the quality of patients’ lives What you’ll do • Translate project strategy into executable plans with clear timelines, budgets and risk management., • Lead and motivate multidisciplinary teams across discovery, clinical, regulatory and CMC., • Anticipate challenges, evaluate scenarios and keep teams aligned on critical path activities., • Present concise updates and recommendations to senior stakeholders., • Coach and mentor colleagues in project management best practice and delivery discipline. What you’ll bring • Bachelor’s degree or equivalent in science, engineering or related discipline (advanced degree preferred)., • 7+ years in biotech or pharmaceutical R&D, including 5+ years managing cross-functional programmes., • Broad understanding of drug development, clinical, CMC and regulatory processes., • Demonstrated success in delivering projects on time, within budget and to agreed quality standards., • Excellent communication and influencing skills; ability to work effectively across cultures and time zones., • Strong proficiency in project management tools and methodologies (e.g. Microsoft Project, PMP certification advantageous). Join us if you want to combine scientific curiosity with disciplined delivery — helping shape the therapies that make a lasting difference for patients around the world. CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

Join our latest project! We’re supporting a specialist engineering test environment delivering RF regulatory and compliance testing and are now looking for an experienced RF Test Engineer to support conducted testing activities across a range of wireless and RF systems. This role will suit engineers with a strong background in RF testing and compliance, who are comfortable working independently in a structured lab environment and can take ownership of their testing activities. You’ll be working as part of a small, highly focused team, contributing to critical regulatory and performance validation work. Due to the nature of the projects, candidates must be eligible to work in the UK. You will need to be able to work on our client’s site in Slough. This is a 12 month contract. Key responsibilities include: • Performing conducted RF testing on wireless and RF systems, • Executing receiver performance tests including blocking, DFS (Dynamic Frequency Selection), and AFS testing, • Carrying out power-related RF measurements in line with industry standards, • Working to ETSI and regulatory compliance requirements, • Operating RF lab equipment such as spectrum analysers, signal generators, oscilloscopes, and network analysers, • Accurately documenting, analysing, and reporting test results Technical exposure will include: • Conducted RF measurement techniques (non-radiated testing environments), • Receiver performance and interference testing methodologies, • Wireless system validation and compliance processes, • Hands-on use of advanced RF lab instrumentation, • Working within structured certification or test house environments Essential Skills & Experience • Strong RF testing experience, • Proven experience within regulatory or compliance testing environments, • Hands-on experience with RF lab equipment (spectrum analysers, signal generators, oscilloscopes, network analysers), • Experience working in a test house or certification environment, • Ability to work independently and take ownership of deliverables If you think you are suitable, please apply below! Get in touch CMC provide expert engineering solutions on an international capacity for advanced engineering projects. Established in 2016, we set out our mission to be the best service-driven consulting business in global STEM markets, and after rapid growth in just a few years, we’re already delivering true expertise to major technology brands and leading companies around the world. As we expand our reach and take on new projects, we have assignments available for experienced engineering professionals to join our consultancy and deliver the expert solutions and high level of service we’re known for across multiple ventures. By partnering with CMC you get the chance to work with some of the world’s leading technology specialists. From our global offices we support you with each new project, providing a complete scope of work definition ahead of any engagement so you know exactly what’s required by the assignment before you land on-site. As projects are completed, we continue to support you by securing your next opportunity from our global network of leading technology companies. No terminology in this advert is intended to discriminate on the grounds of experience, and we confirm that we are happy to accept applications from persons of any experience for this role.

A successful biopharmaceutical company is looking for a lab-based Scientist to join its Injectable Formulation Development (IFD) team within CMC Development Sciences. This group plays a key role in supporting monoclonal antibody programmes across the full development lifecycle – from early toxicology through to Phase III clinical studies. The team is also focused on advancing formulation platforms to improve stability and performance of both established and novel antibody formats. The role You’ll be hands-on in the lab, contributing to formulation and analytical activities that underpin both non-clinical and clinical development. Working in a collaborative, cross-functional environment, you’ll support a range of projects in a fast-paced setting. Key responsibilities include: • Designing and performing experiments to support development studies, • Conducting protein and antibody analysis using techniques such as HPLC/UPLC, iCE, UV spectroscopy, DLS, CGE, rheology and particle analysis, • Supporting pre-formulation and formulation activities, including lab set-up and technical resourcing, • Writing protocols, reports and supporting documentation, • Interpreting and presenting data to internal stakeholders Candidate profile: • MSc or PhD in Biotechnology, Biochemistry, Biology or a related field, • At least 3 years’ laboratory experience in a relevant setting, • Strong experience in protein/antibody characterisation (e.g. HPLC/UPLC, iCE, UV, DLS, CGE, rheology, MFI), • Experience in formulation development and/or automation (advantageous) The role is offered on an initial 12-month contract with realistic potential for extension. Keywords: pharmaceutical, biopharmaceutical, protein, antibody, formulation, R&D, research, development, characterisation, HPLC, UPLC, chromatography, iCE, capillary electrophoresis, spectroscopy, DLS, rheology, London, Reading, Slough, VRS9406SE

Immunocore (NASDAQ: IMCR) is a pioneering, commercial-stage T cell receptor biotechnology company whose purpose is to develop and commercialize a new generation of transformative medicines which address unmet patient needs in oncology, infectious diseases and autoimmune disease. Our leaders in R&D are internationally recognised as some of the biotech industry's most successful drug developers. We are creating not just an environment where great minds can interact but an innovation powerhouse answering the big questions. Focused on delivering first-in-class biological therapies to patients, we have developed a highly innovative soluble TCR platform. Our ImmTAX molecules underpin a new generation of precision engineered drugs that harness the immune system to treat a broad spectrum of diseases with high unmet medical need, including oncology, infectious diseases and autoimmune diseases. At Immunocore, we recognize that our employees are our greatest asset. We value the unique contributions each person brings to our team. By embracing Science, Trust, Respect, Integrity, Diversity, and Entrepreneurship (STRIDE), we create an environment where collaboration thrives, ideas flourish, and transformative changes happen. STRIDE represents more than just letters; it embodies our shared identity and drives our mission. We are dedicated to developing breakthrough therapies that transform patients' lives, advancing medicine, and supporting one another in these pursuits. Immunocore is proud to be an equal opportunity employer. As such, we are committed to fostering an inclusive workplace where everyone feels valued, respected, and empowered. We encourage applications from individuals of all backgrounds, regardless of race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, or any other characteristic protected by law. To characterise the companies biotherapeutic recombinant T-cell receptor based and related molecules using a wide variety of protein characterisation and mass spectrometry methods. To contribute to the development of characterisation methods for the company's biopharmaceutical products, including peptide mapping (LC-MS/MS) and intact mass spectrometry analysis. KEY RESPONSIBILITIES • Supporting drug substance and drug product impurity characterisation and identification, • Performing protein sequence and post translational modification identification, including glycosylation analysis., • Supporting drug substance and drug product process development by performing characterisation of process intermediates, • Contribute to the Development of characterisation methods of ImmTAX and other products, including peptide mapping (LC-MS/MS) and intact mass analysis, • Designing and carrying out biochemical characterisation, chemical stability and comparability studies of biologics/drug products., • Contribute to writing study protocols and reports., • Independently testing and, increasingly, leading lines of investigation. Proposing new experiments based on emerging data and other related information. Providing support on technical aspects to others., • Priorities: establishing priorities for own work and team-based projects; making decisions on prioritisation based on the overall goals of the team, department and project, using direct evidence and personal experience as guidance., • Technical Knowledge: sharing knowledge with the wider team and, across departments representing the department. May also act as a mentor to other colleagues, sharing scientific knowledge. Providing analysis of new techniques and theories from outside the Company to advance the way the company works; sharing these with leaders across the department., • Laboratory records: ensuring that all records and information are up to date, on time and recorded to the correct standard. Supporting and encouraging others to achieve this., • Laboratory equipment: providing technical guidance to others within the team on how to use equipment most effectively., • Reporting: communicating and presenting research findings at meetings with colleagues, senior management and partners., • Adhere to safe working practices in laboratories according to Immunocore EHS policies. PERSON SPECIFICATION Experience & knowledge Essential • Experience in development of HPLC based peptide mapping methods and mass spectrometric characterisation of recombinant proteins or antibodies., • Experience of glycosylation analysis of recombinant proteins or antibodies., • Independently coordinated extensive testing of protein biomolecules., • Experienced in the characterisation of proteins expressed in both microbial and mammalian systems., • Understanding of expected post-translational modifications in biological systems., • Worked in a bench-based biopharmaceutical laboratory environment., • Experienced in assay development, • Familiar with biopharmaceutical stability study principles and interpretation thereof, • Worked and contributed actively in a diverse team environment, • Proposed and driven changes in working practices that have improved efficiency, supported teams through adoption and change, • Presented detailed scientific findings and papers to internal and external audiences Desirable • Experience of glycosylation analysis of recombinant proteins or antibodies, • Experience with late stage/commercial biopharmaceutical assay development and characterisation, • Familiar with the principles of Good Manufacturing Practise (GMP), • Presented at external conferences, • Led a small project team, formally or informally, through a change in practice including project management, • Understanding of analytical requirements to support materials for use in clinical trials Education & qualifications • Essential: BSc. Or MSc. in biochemistry, biotechnology or related discipline, • Desirable: PhD in related discipline

Talentmark are recruiting for a Scientist (Antibody Formulation Development) to join a global pharmaceutical company on a contract basis initially for 12 months. Salary: Up to £22.40 per hour PAYE or £30.81 per hour Umbrella (Inside IR35) Scientist (Antibody Formulation Development) Role: Perform laboratory-based experiments and analytical studies to support non-clinical and clinical development. Support pre-formulation and formulation activities, including lab set-up and technical resource coordination. Develop and optimise injectable formulations for monoclonal antibodies across the development lifecycle. Author formulation protocols, reports, and supporting documentation. Analyse and interpret data relating to biochemical and physical stability of antibody-derived molecules. Collaborate cross-functionally with CMC, development, and other project teams.Your Background: MSc or PhD in Biotechnology, Biochemistry, Biology, or a related discipline. At least 3 years’ laboratory experience within biopharmaceutical development. Strong experience in protein/antibody analysis techniques such as HPLC/UPLC, iCE, UV spectroscopy, DLS, CGE, rheology, or particle analysis. Experience in formulation development and/or lab automation is advantageous. Strong data analysis skills with the ability to interpret complex datasets.Company: Our client is a global biopharmaceutical company focused on creating value for people li...

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, were building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. The role Were looking for a Drug Development Project Manager someone who understands how discovery turns into development, and development turns into real therapies for patients. This is not a generic project management position; its about driving the scientific, technical and operational progress that determines whether a potential medicine succeeds. Youll be the connection between scientific strategy and operational delivery, coordinating complex, global programmes that draw on expertise from discovery, clinical, regulatory, CMC and commercial functions. Your focus will be keeping teams aligned, assessing scenarios and making decisions in a timely fashion. This ensures that every milestone moves us closer to patients who need new treatment options. Why this job This role sits along the central axis of some of CSLs most strategically important development programmes the kind of projects where coordination and clarity make the difference between momentum and delay. Its an opportunity to work at the point where science, strategy and execution meet; to see the bigger picture while ensuring every moving part is in sync. For an experienced drug development project manager, this is the chance to apply your skills where they truly shape outcomes, not just track them. CSL is at an inflection point. Were undergoing a massive transformation in R&D. It represents a tremendous opportunity to be involved, to work with key decision makers and have influence on project progression. We have exciting, new assets coming out of our research portfolio as well as an existing portfolio of medicines which were looking into further transforming to improve the quality of patients lives What youll do • Translate project strategy into executable plans with clear timelines, budgets and risk management., • Lead and motivate multidisciplinary teams across discovery, clinical, regulatory and CMC., • Anticipate challenges, evaluate scenarios and keep teams aligned on critical path activities., • Present concise updates and recommendations to senior stakeholders., • Bachelors degree or equivalent in science, engineering or related discipline (advanced degree preferred)., • 7+ years in biotech or pharmaceutical R&D, including 5+ years managing cross-functional programmes., • Broad understanding of drug development, clinical, CMC and regulatory processes., • Demonstrated success in delivering projects on time, within budget and to agreed quality standards., • Excellent communication and influencing skills; ability to work effectively across cultures and time zones. CSL Behring operates one of the worlds largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit and CSL Plasma at . Our Benefits For more information on CSL benefits visit How CSL Supports Your Well-being | CSL. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit . JBRP1_UKTJ

Senior Technical Writer – CMC (Consultant). An experienced CMC Technical Writer is required to support late-stage drug development programmes, working on complex submission documentation within a fast‑paced development environment. Scientist to CMC Technical Writer.

Extensive experience in CMC strategy and a minimum of ten years of experience in CMC development and regulatory compliance. Provide innovative drug development plans, data gap analyses and international regulatory strategies from a CMC perspective for complex products within the changing regulatory

Principal / Senior Regulatory Affairs CMC Consultant. As a Principal or Senior Regulatory Affairs CMC Consultant, you will play a key leadership role, providing high-level regulatory and technical guidance for complex therapeutics. Provide strategic, technical, and regulatory CMC advice to clients,

Strong understanding of CMC regulatory frameworks, quality systems, and manufacturing processes. If you are a detail‑driven Regulatory CMC specialist who thrives in a flexible freelance environment, we would love to hear from you. Regulatory CMC Technical Writer.

To act as the CMC Regulatory Lead on CMC Teams, representing the CMC Regulatory viewpoint and expertise on the CMC Team;. As a key member of the Regulatory Affairs CMC team, the candidate will have responsibility for developing CMC regulatory strategy for the clinical portfolio from a Regulatory CMC

A leading biotech organization is seeking a Senior Director, CMC Lead to spearhead their gene therapy programmes in Greater London. In this pivotal role, you will shape global CMC strategy, guiding complex development programmes from early stages to commercial readiness. Candidates should have a PhD

Minimum 10 years of experience in CMC within the pharmaceutical industry and CMC regulatory technical writing. Senior CMC Regulatory Technical Writer. You will play a key role in translating complex CMC scientific and technical data into clear, concise, and compliant regulatory documentation (Module

A clinical-stage biopharmaceutical firm in the United Kingdom is seeking a Director, Regulatory Affairs CMC. This leadership role involves developing global CMC regulatory strategies for innovative therapies aimed at cancer treatment.

The Financial Risk Manager will understand all existing and new products offered by CMC Markets, with particular reference to how they are captured and reported by the Financial Risk Management team. When dealing with all customers, clients or colleagues ensure that we provide a clear, fair and cons

A global pharmaceutical company seeks a CMC Regulatory Manager to lead post-approval regulatory strategies and ensure compliance for life-saving medicines.

Knowledge of the markets and products that CMC is operational in. CMC Markets is an equal opportunities employer and positively encourages applications from suitably qualified and eligible candidates regardless of gender, sexual orientation, marital or civil partner status, gender reassignment, race

This role involves authoring complex CMC submission documentation within a fast-paced environment.

A leading financial technology firm in the UK is seeking an experienced Cloud Telephony & Contact Centre Engineer for a 12-month FTC contract.The role involves supporting a cloud-based contact centre migration and enhancing capabilities to improve customer and agent experiences.Ideal candidates will

ZS’s CMC team partners with leading biopharmaceutical companies to accelerate and optimize drug development through science‑driven, data‑enabled strategies that enhance efficiency, quality, and speed to market. As a Manager in our CMC team, you will be at the forefront of driving innovation ac

A financial services company in Greater London is seeking a Financial Risk Manager to support the Risk team in delivering the Futures & Options project.The role involves developing and monitoring risk metrics, reporting on financial risks, and participating in group projects.The ideal candidate will

A biopharmaceutical solutions organization is seeking a Regulatory CMC Consultant to support global regulatory strategies for cell and gene therapy products.

CMC Markets has pioneered the development of online trading in markets around the world to become a world leading spread betting and CFD provider. CMC Markets is an equal opportunities employer and positively encourages applications from suitably qualified and eligible candidates regardless of gende

The ideal candidate will have significant experience across the product lifecycle, particularly with CMC regulatory submissions.

Suitable candidates must have the right to work in the UK and a strong background in CMC and MSAT.

A prominent financial services firm in Greater London is seeking a Security Platform Engineering Manager to lead a team focused on building reusable security capabilities for cloud infrastructure.You will define the strategic direction of security platform engineering while ensuring that security co

CMC Consulting are excited to be partnering exclusively with a leading International Business Consultancy at an exciting time of transformation and growth.

A leading global pharmaceutical firm is seeking a Regulatory Affairs Manager to oversee post-approval regulatory strategies and manage compliance for high-quality medicines.The role involves evaluating manufacturing changes, drafting regulatory documents, and collaborating with cross-functional team

An established industry player is seeking a commercially focused qualified accountant to join their dynamic team.In this role, you will play a crucial part in driving margin and revenue growth by delivering comprehensive sales and margin performance reporting.Collaborating closely with the Director

A consulting firm in Milton Keynes seeks an experienced Interim Finance Manager for a 3-6 month hybrid working contract.The role focuses on day-to-day finance functions during a period of transition, requiring expertise in statutory accounting, VAT returns, and management reporting.Ideal candidates

A leading financial technology company seeks a Security Platform Engineering Manager to enhance its Platform Engineering capabilities.This role involves defining and operating reusable security capabilities for customer-facing services.The ideal candidate will have deep expertise in securing cloud n

For similar opportunities and the latest updates from CMC Consulting please follow our company page: .

A leading trading firm in the United Kingdom is seeking an experienced Information Security Manager to shape global security governance and risk frameworks.This senior role focuses on strategic oversight and regulatory alignment, requiring strong leadership and collaboration with teams across region

Roald Dahl Neonatal CMC Nurse Specialist. Homerton Neonatal Unit, in partnership with Roald Dahl's Marvellous Children Charity, is establishing a pioneering Band 8a Neonatal Nurse Specialist role to lead care for neonates with complex medical needs (CMC) across North East London. Lead and influence

For similar opportunities and the latest updates from CMC Consulting please follow our company page: . Direct message the job poster from CMC Consulting Ltd. CMC Consulting are partnered with a rapidly expanding multi-site leisure company who are recruiting a Management Accountant to supp

Quantitative Researcher - Principal Specialist page is loaded## Quantitative Researcher - Principal Specialistlocations: Londontime type: Full timeposted on: Posted 3 Days Agojob requisition id: CMC4556Since launching in 1989, CMC Markets (CMC) has become one of the world's leading online fi

Group Accountant – First Move from Practice.This role offers an excellent first move into industry for an ACA‑qualified (or recently qualified) accountant seeking exposure to commercial finance within a multi‑entity organisation.The position provides hands‑on involvement in core financial ac

A leading financial trading platform in the UK is looking for a Quantitative Researcher - Principal Specialist.This role involves mentoring existing team members, developing pricing models for complex products, and collaborating with various teams to optimize risk management strategies.Qualified can

A leading healthcare company seeks a Senior CMC Regulatory Technical Writer to translate complex scientific data into clear regulatory documentation. The ideal candidate will have a minimum of 10 years of experience in CMC within the pharmaceutical industry and have excellent writing and organizatio

CMC Consulting is committed to equal opportunities.

CMC Partners, part of the G&E Group, is a specialist Executive Search and Consulting firm working across the. At CMC Partners, you’ll benefit from:.

A fast-growing SME in Finance based in Dacorum is looking for a proactive finance professional to join their expanding team.Key responsibilities include preparing and maintaining accounts, reconciling journals, and managing balance sheets.The ideal candidate should have 2-3 years of relevant finance

Interim Finance Manager - Milton Keynes.My client is a high-performing business seeking an experienced Interim Finance Manager to take ownership of the day-to-day finance function during a key period of transition and growth.This is a hands-on role requiring a strong blend of technical accounting ex

A leading healthcare organization in Greater London seeks a Band 8a Neonatal Nurse Specialist to provide expert clinical leadership for neonates with complex medical needs.The role involves acting as a primary resource for families, leading education and quality initiatives, and ensuring smooth tran

A leading financial technology company in Greater London is seeking an experienced ML Ops Engineer / Data Engineer to enhance the reliability of machine-learning systems.The role involves building robust data pipelines, deploying models, and ensuring operational clarity.Ideal candidates will have 3�

A leading International Business Consultancy in the UK seeks a skilled Tax Manager to enhance tax operations as part of its transformation journey.The role involves managing tax audits, preparing consolidated tax provisions, and ensuring compliance with corporate income tax globally.Ideal candidates

A leading executive search firm in Greater London is seeking ambitious professionals to join as Executive Search Consultants.This role involves delivering impactful recruitment projects, managing processes from briefing to placement, and collaborating with senior decision-makers.Ideal candidates wil