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Key responsibilities include: * Leading cross-functional project teams across CMC, non-clinical, regulatory and clinical functions * Building and maintaining integrated development plans * Managing timelines, milestones, risks and mitigation strategies * Supporting the preparation and su

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

As a Senior Specialist in Regulatory Affairs CMC, you are responsible for supporting the development and tracking of high-quality regulatory CMC and device documentation in alignment with MoonLake’s development programs, working closely with Technical Operations colleagues. As a Senior Specialist

A global biopharma company seeks an Associate Director of Drug Product Development in Cambridge.This role entails overseeing the development and manufacturing processes of drug products across various stages.Candidates need 10 years of experience in pharmaceutical product development, with strong le

If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. The Director of Drug Product Development is responsible for providing scientific and technical leadership for Jazz Pharmaceuticals’ Pharmaceutical Development programs at various stages of the development life-cycle including preformulation, formulation and process development, technical transfer and validation. The Director of Drug Product Development will oversee drug product aspects of development and manufacturing projects from pre-formulation and product feasibility through to clinical trial supply and technology transfer/commercialization. In addition, the Director of Drug Product Development will be expected to provide leadership of cross-functional CMC development teams. The Director of Drug Product Development will have extensive experience in pharmaceutical product development, demonstrated problem solving ability, module 3 authorship, development of robust manufacturing processes through designed experiments and data analysis, and excellent project management, teamwork and leadership skills. Essential Functions Leads the development of small molecule drug product formulations, appropriate to the phase of pharmaceutical development, with sufficient stability and robustness for clinical and/or commercial manufacturing. Responsible for specifying product and process requirements, including manufacturing equipment and methods, performance criteria, materials, test protocols, required analytical methodology, packaging (clinical and commercial); and in developing robust processes for pharmaceutical production. Directs projects and leads cross-functional teams with technical proficiency, scientific creativity, collaboration with others to achieve project goals on time and within budget. Create intellectual property covering Jazz Pharmaceuticals products and ensure freedom to operate in the development of new drug products Support the identification and selection of suitable drug product development and commercial manufacturing vendors (CMOs). Direct technical projects (internally and at CDMOs) including developing detailed technical work plans and managing performance of vendors. Work cooperatively with, or lead, internal and external teams as required. Author CMC sections of regulatory dossiers for products at all stages to enable acceptance by global regulators. Supports asset due diligence and new product introduction and integrations Apply current knowledge of cGMP and industry standards for process design and validation to manage vendors and contract development organizations. Assist other department team members in providing guidance / mentoring / reviewing documents / data in support of product development (e.g. clinical protocols, PK study results). Enhance and improve ways of working in Drug Product development, utilising knowledge of industry best practice Required Knowledge, Skills, and Abilities 10 – 15 years’ experience in drug product development in the pharmaceutical industry required. Direct experience with formulation development, process development, technical transfer and/or process validation. Demonstrated technical proficiency, engineering, collaboration with others, and independent thought. Strong track record in delivering achievements with meaningful impact in Pharmaceutical Development projects Demonstrated ability to lead cross-functional CMC Development teams Demonstrated troubleshooting and problem-solving skills including the use of designed experiments, statistical process control, Development/authorship of CMC regulatory filings for pharmaceutical products. Experience in defending processes, procedures and investigation during Regulatory Agency inspections desirable. Track record in generating intellectual property development. Broad exposure to multiple drug delivery technologies and knowledge of standard dosage forms. Excellent written and verbal communication skills, with demonstrated ability to communicate at executive leader level Current knowledge of quality systems and FDA and EU regulations as they relate to pharmaceutical development and validation. Proven project management skills for technical programs. Flexibility to travel on company business when required Required/Preferred Education and Licenses Master’s degree, PhD, or equivalent combination of education and work-related experience required. Description of Physical Demands Occasional mobility within office environment. Routinely sitting for extended periods of time. Constantly operating a computer, printer, telephone and other similar office machinery. Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. FOR US BASED CANDIDATES ONLY Jazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is: $(phone number removed) - $(phone number removed) Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis. At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here

If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. The Associate Director of Drug Product Development is responsible for providing scientific and technical leadership for Jazz Pharmaceuticals’ Pharmaceutical Development programs at various stages of the development life-cycle including preformulation, formulation and process development, technical transfer and validation. The Associate Director of Drug Product Development will oversee drug product aspects of development and manufacturing projects from pre-formulation and product feasibility through to clinical trial supply and technology transfer/commercialization. In addition, the Associate Director of Drug Product Development may provide leadership of cross-functional CMC development teams. The Associate Director of Drug Product Development will have broad experience in pharmaceutical product development, demonstrated problem solving ability, module 3 authorship, development of robust manufacturing processes through designed experiments and data analysis, and excellent project management, teamwork and leadership skills. Essential Functions Leads the development of small molecule drug product formulations, appropriate to the phase of pharmaceutical development, with sufficient stability and robustness for clinical and/or commercial manufacturing. Responsible for specifying product and process requirements, including manufacturing equipment and methods, performance criteria, materials, test protocols, required analytical methodology, packaging (clinical and commercial); and in developing robust processes for pharmaceutical production. Directs projects and leads cross-functional teams (as required) with technical proficiency, scientific creativity, collaboration with others to achieve project goals on time and within budget. Create intellectual property covering Jazz Pharmaceuticals products and ensure freedom to operate in the development of new drug products Support the identification and selection of suitable drug product development and commercial manufacturing vendors (CMOs). Direct technical projects (internally and at CDMOs) including developing detailed technical work plans and managing performance of vendors. Work cooperatively with, or lead, internal and external teams as required. Author CMC sections of regulatory dossiers for products at all stages to enable acceptance by global regulators. Supports asset due diligence and new product introduction and integrations Apply current knowledge of cGMP and industry standards for process design and validation to manage vendors and contract development organizations. Required Knowledge, Skills, and Abilities 10 years’ experience in drug product development in the pharmaceutical industry required. Direct experience with formulation development, process development, technical transfer and/or process validation. Demonstrated technical proficiency, engineering, collaboration with others, and independent thought. Strong teamwork skills. Demonstrated troubleshooting and problem-solving skills including the use of designed experiments, statistical process control, Development/authorship of CMC regulatory filings for pharmaceutical products. Broad exposure to multiple drug delivery technologies and knowledge of standard dosage forms preferred. Excellent written and verbal communication skills Current knowledge of quality systems and FDA and EU regulations as they relate to pharmaceutical development and validation. Experience in intellectual property development desirable. Proven project management skills for technical programs. Flexibility to travel on company business when required Required/Preferred Education and Licenses Advanced degree in Chemistry, Pharm. Sci., Engineering, or related field, or equivalent combination of education and work-related experience required. Description of Physical Demands Occasional mobility within office environment. Routinely sitting for extended periods of time. Constantly operating a computer, printer, telephone and other similar office machinery. Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. FOR US BASED CANDIDATES ONLY Jazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is: $(phone number removed) - $(phone number removed) Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis. At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here

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.

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

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.

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,

A financial services company in London seeks a mid-level Corporate Communications Specialist.This role focuses on shaping the company narrative, managing media relations, and executing internal communications.The ideal candidate has 4-6 years of experience in corporate communications or PR, strong m

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

ML Ops / Data Engineer page is loaded## ML Ops / Data Engineerlocations: Londontime type: Full timeposted on: Posted Yesterdayjob requisition id: CMC5104# ML Ops / Data EngineerRole OverviewWe’re hiring an ML Ops Engineer / Data Engineer to own the reliability, scalability, and

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 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

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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, colour, nationality, ethnic or national origin, religion or beli

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

Minimum 10 years of experience in CMC within the pharmaceutical industry and CMC regulatory technical writing. We are looking for a detail‑oriented and experienced regulatory technical writer with a solid background in CMC documentation. Senior CMC Regulatory Technical Writer.

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 support their Financial Controller during this exciting growth phase. For similar opportunities and the latest updates

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

A leading financial services firm in Greater London is seeking an experienced Senior Project Manager to lead large-scale change initiatives.This high-impact role requires overseeing complex, cross-functional programmes and managing the entire project lifecycle.The ideal candidate will possess strong

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

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

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

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

My client is a household name, branded multisite business, and they are now seeking a commercially focused qualified accountant to join them in a role where you will directly affect margin and revenue growth.Deliver comprehensive sales and margin performance reporting across locations, identifying k

Since launching in 1989, CMC Markets (CMC) has become one of the world's leading online financial trading businesses. CMC is listed on the London Stock Exchanges and serves retail and institutional clients through regulated offices and branches in 13 countries. CMC offers an award winning online and

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 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 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

A leading healthcare provider is seeking a skilled Roald Dahl Neonatal CMC Nurse Specialist to provide expert clinical leadership for neonates across North East London.

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

Homerton Neonatal Unit, in partnership with Roald Dahl's Marvellous Children's 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 care pathways, guidelines, and standards

A leading global professional services firm is seeking an experienced Associate Tax Director to manage a UK corporate tax team.Responsibilities include leading tax compliance for corporate clients, managing team performance, and driving operational excellence.Ideal candidates will be ICAEW, ACCA, or

CMC Markets requires a suitably skilled Liquidity Risk Manager responsible for the assisting with the implementation of an effective Liquidity Risk framework. When dealing with all customers, clients or colleagues ensure that we provide a clear, fair and consistent high-quality service that presents

A leading global professional services firm is seeking an experienced Associate Tax Director to support and lead a UK corporate tax team.The role involves managing a portfolio of complex clients, overseeing compliance and advisory matters, and contributing to the strategic direction of the departmen

Help shape a high‑ambition agenda: advance the global CMC brand, expand our multi‑asset experience, and meaningfully increase market visibility. CMC Markets is an equal opportunities employer and positively encourages applications from suitably qualified and eligible candidates regardless of gen

A global, media and entertainment business is seeking a Commercial Finance Analyst to support a key revenue-generating function within a fast-paced, international environment.This role offers strong exposure to senior stakeholders and the opportunity to work closely with commercial teams to drive pe

CMC Markets is powered by our people.

A global healthcare company is seeking a Regulatory CMC Specialist to enhance regulatory strategies and manage projects within the respiratory product portfolio. The ideal candidate possesses significant experience in CMC authoring and regulatory affairs for respiratory products.

A leading consulting firm is seeking a Group Accountant for their Midlands office.This position offers an excellent first move into industry for an ACA-qualified (or recently qualified) accountant.The role involves hands-on financial accounting, reporting, and compliance activities, alongside the op

A leading consulting firm is seeking an experienced Regulatory CMC Technical Writer for a fully remote freelance role. The successful candidate will prepare high-quality CMC documentation for global regulatory submissions and ensure alignment with regulatory guidelines.

CMC Markets is one of the world’s first ever fin-tech companies and was launched in 1989 to break down the barriers of financial trading and make trading accessible to everyone. Security Platform Engineering Manager page is loaded## Security Platform Engineering Managerlocations: Londontime type

A leading executive search firm in Greater London is seeking ambitious graduates to join as Executive Search Consultants.The role focuses on delivering high-impact recruitment projects and includes comprehensive training and development opportunities.Ideal candidates demonstrate strong commercial aw

A leading consultancy firm in the UK is seeking a Management Accountant to join a rapidly expanding leisure company.This role includes full responsibility for management accounts across allocated sites, monthly P&Ls, and business partnering with Site Managers to drive EBITDA improvements.Candidates