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The Opportunity: Reporting to the Head of Risk Management, Aggregate Reports & Pharmacovigilance, as the Senior Manager, ICSR Quality, you will have Individual Case Safety Reports (ICSRs) accountability and you will be responsible for the oversight and control of the operational management and activities performed by the Global Case Management Pharmacovigilance vendor(s) for CSL Behring, CSL Seqirus, CSL Vifor and CSL Plasma products. This is a hybrid role, which offers a combination of an onsite and remote work schedule. #LI-hybrid The Role: • Oversight of Global Case Management Pharmacovigilance vendor(s) as it relates to , governance, financials, contracts, quality and training, and resourcing., • Ensure consistency and monitor quality and compliance of end-to-end case processing and other outsourced activities performed by the case management vendor., • Oversee case management vendor(s) to manage and resolve emerging issues., • Develop and/or maintain/ update existing documents for relevant vendor responsibilities., • Contributes ICSR quality strategy., • Responsible for Global ICSR Reconciliation activities., • Support audit/inspections and contribute to CAPAs specific to case quality or vendor/resource management, as required. Your Skills & Abilities: • BS/BA, RN, Pharmacist, or equivalent., • Minimum of 8 years of Clinical Trial and Post-marketing Pharmacovigilance (PV) experience., • Global pharmacovigilance database knowledge is required along with proficient knowledge of global and local regulatory rules and regulations., • Experience working with third parties (e.g., contract service providers) and relationship management. 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 ___.

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 ___.

Senior Manager, R&D Outsourcing (M/F/X) Maidenhead, S.E. England or Zurich, Switzlerland The Senior Manager, R&D Outsourcing is responsible for managing the full contracting lifecycle for strategic outsourced R&D services and projects across assigned therapeutic and functional areas. This includes drafting, reviewing, and negotiating scopes of work, budgets, and contracts with external service providers to support CSL’s global clinical and portfolio development needs. This individual contributor role partners closely with Business Strategy Leads, Project Owners, Legal, Finance, and Procurement to ensure timely contract execution, cost control, and compliance with CSL’s policies and standards. Outsourcing Execution * Manage vendor identification, RFI/RFP processes, proposal reviews, and budget and contract negotiations for strategic outsourced R&D services (e.g., MSAs, Work Orders, Change Orders, rate cards). * Draft, review, and finalize contracts to ensure timely execution and compliance with CSL policies. * Coordinate with project teams and stakeholders to align contract deliverables with operational needs. Contract Oversight and Compliance * Track contractual obligations and ensure vendors meet agreed terms, budgets, and timelines. * Support resolution of contract or performance issues in collaboration with Legal, Finance, and project stakeholders. * Maintain organized and up-to-date contract documentation in line with internal requirements and industry regulations. Financial and Operational Support * Review vendor proposals and budgets for accuracy and alignment with scope. * Monitor ongoing vendor spending versus approved budgets; highlight variances as needed. * Support financial forecasting and reporting by providing timely contract and spend data. Cross-Functional Collaboration * Partner with Business Strategy Leads, Project Owners, Legal, Finance, and Procurement to ensure smooth contract operations. * Communicate contract requirements and processes clearly to internal stakeholders. * Serve as a resource for questions on contract terms, templates, and procedures Process Improvement and Reporting * Identify opportunities to improve contracting efficiency, consistency, and compliance. * Contribute to tracking and reporting of outsourcing metrics and performance indicators. * Participate in cross-functional initiatives to enhance vendor management practices. Required: * Bachelor’s degree in Business, Finance, Life Sciences, or a related field. * Minimum 7 years of experience managing end-to-end contracting with R&D service providers (e.g., CROs). * Proven ability to draft, review, and negotiate budgets and contracts. * Working knowledge of clinical trial operations and vendor cost structures. * Strong attention to detail, organizational skills, and ability to manage multiple priorities. * Excellent communication and collaboration skills across functional teams. * 60% approx. onsite in either Maidenhead or Zurich * Ability to travel including internationally up to 20% Preferred: * Experience supporting outsourcing in global or matrixed R&D organizations. * Familiarity with contract lifecycle management software or financial systems. * Understanding of basic financial principles (e.g., budget tracking, forecasting). What we offer * Hybrid working models. * Extensive management/leadership programs. * Global and diverse environment with modern workspaces. * Our benefit plan offers our employees a vast number of options such as medical plan, life insurance and retirement plan. * Find Inclusion and Belonging at all sites and with every colleague. Come as you are. Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable. 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 ___.

Scientist – Injectable Formulation Development (Biologics) Location: EU-based (right to work required) About the Opportunity Our client, a leading global biopharmaceutical organisation, is seeking a talented laboratory-based scientist to join their Injectable Formulation Development team. This group plays a pivotal role in advancing biologics programmes, providing robust formulations to support the full development lifecycle—from early toxicology studies through to late‑stage clinical trials. The team is also committed to innovating new formulation technologies to enhance the stability of both conventional and next‑generation antibody formats. This is an excellent opportunity to contribute to high‑impact therapeutic development within a collaborative, cross‑functional environment. Key Responsibilities • Conduct analytical experiments and enabling studies to support non‑clinical and clinical development., • Contribute to pre‑formulation and formulation activities, including lab set‑up and maintenance of technical resources., • Prepare scientific documentation such as protocols and reports, drawing on a strong understanding of biochemical and biophysical degradation pathways in antibody‑based molecules., • Present experimental findings to project teams and stakeholders. Skills & Experience • Master’s degree (or equivalent) or PhD in Biotechnology, Biochemistry, Biology, or a related discipline., • Minimum of 3 years’ hands‑on laboratory experience., • Strong technical expertise in protein/antibody analytical methods such as HPLC/UPLC, iCE, UV spectroscopy, DLS, CGE, rheology, and sub‑visible particle analysis., • Experience in formulation development and/or laboratory automation is advantageous., • High level of numeracy with the ability to critically interpret data., • Strong organisational and communication skills, with the ability to thrive in a dynamic environment with shifting priorities., • Proven ability to work effectively within a team.

Cell Line Development Scientist: Antibody Therapeutics Long-term Contract Location: Slough (Onsite) We are supporting a leading global biopharmaceutical organisation in the search for a Cell Line Development Scientist to join their Antibody & Novel Therapeutics team on a 12-month contract. This role sits within a specialist group responsible for the engineering and development of stable mammalian cell lines used in the manufacturing of therapeutic antibodies and biologics. The successful candidate will contribute to host cell engineering, cell line optimisation, and expression system development to support the production of next-generation biologics. Key Responsibilities • Establish and develop host cell lines suitable for therapeutic manufacturing, • Generate and optimise stable mammalian cell lines for protein expression, • Apply genome engineering technologies such as CRISPR for cell line development, • Analyse expression and engineering data to support optimisation strategies, • Work closely with molecular biology and engineering teams to drive successful outcomes, • Maintain clear and accurate scientific documentation in line with GMP standards, • Communicate progress, challenges and opportunities across multidisciplinary teams Requirements • BSc (minimum) in Cell Biology, Molecular Biology, Biotechnology or related discipline, • Industry experience generating stable mammalian cell lines for protein or antibody expression, • Hands-on experience with cell culture and cell line engineering techniques, • Experience with CRISPR or other genome engineering technologies, • Strong molecular biology experience including cloning, plasmid construction and ddPCR, • Experience with flow cytometry / FACS and single-cell cloning systems, • Strong documentation, reporting and scientific communication skills, • Experience using electronic lab notebooks and molecular biology software tools

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

An exciting opportunity for a Research Scientist to join a leading pharmaceutical company specialising in antibody formulation development. Based in a collaborative and innovative environment, this role offers the chance to contribute to cutting-edge therapies aimed at improving the lives of people living with severe diseases. The position is initially a 12-month temporary contract with potential for extension, supporting key stages of monoclonal antibody development. Our client is committed to breakthrough research and rigorous scientific excellence. As part of their dynamic team, you will play a pivotal role in supporting pivotal clinical studies and enhancing formulation technologies that advance therapeutic solutions. KEY DUTIES AND RESPONSIBILITIES Your duties as the Research Scientist will be varied however the key duties and responsibilities are as follows: • As the Research Scientist, you will support the development and optimisation of antibody formulations, executing experiments to enhance stability and efficacy across different development stages., • As the Research Scientist, you will conduct protein/antibody analysis using techniques such as HPLC/UPLC, iCE, UV spectroscopy, DLS, CGE, rheology, and sub-visible particle analysis., • As the Research Scientist, you will support laboratory setup, manage technical resources, and contribute to the creation of protocols, reports, and documentation based on biochemical and physical degradation analysis., • As the Research Scientist, you will present experimental results clearly to cross-functional teams to inform decision-making., • As the Research Scientist, you will work within a fast-paced environment, collaborating across departments to ensure project goals are met efficiently. ROLE REQUIREMENTS To be successful in your application to this exciting role as the Scientist we are looking to identify the following on your profile and past history: • A Degree or higher level in Biotechnology, Biochemistry, Biology or similar, with a proven minimum of 3 years of laboratory experience and application of emerging technologies., • Experience in protein/antibody analysis techniques such as HPLC/UPLC, iCE, UV spectroscopy, DLS, CGE, rheology, and sub-visible particle analysis; experience in formulation development and automation is advantageous., • Excellent communication and organisational skills, with the ability to adapt to a rapidly changing environment., • Highly self-motivated team player capable of managing multiple priorities effectively. Key Words: Antibody / Monoclonal Antibodies (mAbs) / Biologics / Biopharmaceuticals / Protein Analysis / Protein Characterisation / Antibody Stability / Formulation Development / Pre-formulation / Injectable Formulations / Drug Product Development / CMC / Development Sciences / Biochemistry / Biotechnology / Analytical Development / Bioanalysis / Biophysical Characterisation / Stability Studies / Degradation Pathways / Aggregation / Particle Analysis / Sub-visible Particle Analysis / Rheology / MFI / Excipient Screening / Buffer Optimisation / HPLC / UPLC / SEC-HPLC / iCE / CGE / UV Spectroscopy / DLS / Chromatography / Spectroscopy / Method Development / Data Analysis / Laboratory Scientist / Research Scientist / Wet Lab / GLP / GMP / Pharmaceutical Industry / Clinical Development / Preclinical / Phase I–III / Drug Development / Automation / High-Throughput / Protocol Writing / Technical Documentation / Scientific Reports / Data Presentation / Cross-functional Collaboration / Stakeholder Communication / Experimental Design "Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career."

Cell Culture / Expression Scientist – Antibody Cell Line Sciences Location: Slough (Fully Onsite) Rate: £22.40 per hour (PAYE) / £30.81 per hour (Umbrella) Contract: 12 Months (Ajax) Schedule: Weekend working required – maximum 1 in 4 weekends Overview We are seeking a highly skilled Cell Culture / Expression Scientist to join the Antibody Cell Line Sciences sub-team, part of the Antibody and Novel Therapeutics Group. The successful candidate will contribute to host cell line establishment, engineering, and the generation of stable mammalian cell lines to support the development and manufacturing of UCB therapeutics. Primary Purpose / Regulatory Responsibilities • Establish and develop a toolbox of host cell lines for therapeutic manufacturing., • Ensure host systems are suitable for expressing diverse molecule types and compliant with GMP manufacturing requirements, supported by rigorous documentation., • Communicate scientific progress clearly across teams, highlighting issues, risks, and opportunities, and proposing practical solutions., • Apply multiple host-engineering and genome-editing techniques in close collaboration with engineering and molecular biology groups., • Contribute strong lab-based scientific expertise to support successful project outcomes. Key Responsibilities • Generate and optimize stable mammalian cell lines for protein expression., • Conduct cell line engineering using technologies such as CRISPR-mediated editing., • Analyse expression and engineering data to drive decision-making and project progression., • Perform essential molecular biology techniques (e.g., ddPCR, cloning, plasmid construction)., • Execute flow cytometry/FACS, single-cell cloning, and related workflows., • Maintain meticulous documentation, including electronic lab notebooks (eLNs)., • Contribute to scientific reports and cross-functional updates., • Use relevant lab and IT systems, including Office tools, SnapGene/Geneious, and literature/patent search tools. Required Skills & Experience • BSc minimum in a relevant scientific discipline., • Industry experience generating stable cell lines for antibody or novel biologic expression., • Proficiency in genome-engineering technologies, particularly CRISPR., • Strong data analysis skills with the ability to draw clear scientific conclusions., • Competence in key molecular biology methods (ddPCR, cloning)., • Hands-on experience with flow cytometry/FACS and single-cell cloning platforms., • Excellent written and verbal communication skills., • Strong scientific writing ability, including preparation of structured technical reports., • High standards of accuracy in documentation and record‑keeping., • Working knowledge of lab and IT platforms including eLNs, molecular biology software, and search tools.

A leading food wholesaler is seeking experienced butchers to manage their butchery departments.You will develop customer relationships, ensure high service standards, and maintain stock quality.The position provides the flexibility of running a department with a focus on meat protein knowledge and c

CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. 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 a

A leading pharmaceutical company in Slough is seeking an analytical testing professional to perform quality assessments on therapeutic proteins.

A leading life sciences company in Slough is seeking an Associate Principal Scientist in Protein Chemistry to drive analytical innovation and manage high-value scientific projects.

CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. 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 a

Associate Principal Scientist – Protein Chemistry. As Associate Principal Scientist in Protein Chemistry, you will drive analytical innovation and lead high-value scientific projects within our Protein & Process Analytics R&D team. Provide oversight and execute scientific activities, including stu

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 living with severe diseases in immunology and neurology now and into the future. Location: This role is based at our client’s site in Slough. Apply: For more information, or to apply for this Scientist (Antibody Formulation Development) role please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (phone number removed). It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check

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. Coach and mentor colleagues in project management best practice and delivery discipline. What youll bring 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. 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. About CSL Behring 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 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 . TPBN1_UKTJ

Job title: R&D Scientist Location: Slough Contract Length: 12 months Working Hours: 37.5 hours/week Pay Rate: £17.96/hour About the Role We are currently looking for a Scientist to join our clients' Protein Chemistry group within R&D Protein and Process Analytics department. This team is responsible for delivering high-value technical innovation, both via specialist analytical projects and as part of wider collaborative project teams. As a Scientist, you will be responsible for planning and execution of scientific/ experimental work for target projects, including elements of laboratory work, scientific writing and review, testing of new technologies, method development and optimization. This position requires experience in analytical separation and characterization of biotherapeutics proteins, and with analysis of relevant protein CQAs/ PTMs, as charge/ size variant analysis, purity and glycosylation profile. Key Responsibilities: Planning and execution of scientific activities for target projects, including elements of laboratory work, scientific writing and review, testing of new technologies and method development Performing a range of analysis using mainly liquid chromatography and capillary electrophoresis for characterisation of proteins and their relevant CQAs Analysis and interpretation of complex data and presentation to internal stakeholders Execution and reporting analytical studies, and communication with the project team Key requirements: BSc or MSc in life sciences or equivalent. Preferred area of study: Biochemistry/ Biology/ Biotechnology Previous practical industry and/or academic experience in an analytical laboratory, with focus on protein analysis Knowledge and practical expertise in chromatography (RP, HILIC, SEC, IEX), capillary electrophoresis (CE-SDS, icIEF) and other relevant techniques for protein analysis Research focused, with a keen interest in innovation within the biologics area A good general background in established analytical methods in the industry, and understanding of the state of the art technologies and their applications in the area of analytical characterization of biotherapeutics Good communication and interpersonal skills Proven ability to deliver innovative solutions to scientific challengesGuidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy

Talentmark are recruiting for a Scientist to join a global pharmaceutical company on a contract basis initially for 12-months. Salary: £22.40 per hour PAYE or £30.81 per hour via umbrella. Scientist (Antibody Cell Line Sciences) Role: Establish and develop host cell line systems to support the manufacturing of therapeutic antibodies and novel biologics. Generate and optimize stable mammalian cell lines for protein expression using advanced cell engineering and genome engineering techniques. Apply laboratory-based scientific expertise to support the development of manufacturing-ready host systems while ensuring compliance with GMP requirements. Work with molecular biology and engineering teams to support the development of robust cell line platforms. Carry out laboratory techniques including ddPCR, cloning, plasmid construction, flow cytometry/FACS and single-cell cloning.Your Background: BSc degree in a relevant life sciences discipline. Industry experience in cell culture and the generation of stable mammalian cell lines for antibody or biologics expression. Experience with genome engineering technologies such as CRISPR-based cell engineering. Strong knowledge of molecular biology techniques including cloning, ddPCR and plasmid construction. Hands-on experience with flow cytometry/FACS and single-cell cloning systems. Experience working with laboratory and IT systems such as electronic lab notebooks, Office tools and molecular biology software such as SnapGene or Geneious. Ability to work occasional weekend shifts (approximately 1 in 4), with time off in lieu provided.Company: Our client is a global biopharmaceutical company focused on creating value for people living with severe diseases in immunology and neurology now and into the future. Location: This role is based at our client’s site in Slough, with a future relocation to Windlesham, Surrey anticipated in the coming years. Apply: For more information, or to apply for this Scientist role please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (phone number removed). It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check

Your new company You'll be joining a well-established global biopharmaceutical organisation advancing next‑generation antibody and therapeutic technologies. You'll be part of an innovative team focused on developing high‑quality, manufacturable mammalian cell lines. Your new role You'll be joining an experienced team who drive a lot of the mammalian cell line development behind the company's entire portfolio, where you will contribute to the creation and optimisation of stable host cell lines to support therapeutic manufacturing. This is initially a 12 month contract that is likely to extend to at least 18 months and potentially run for 2 years. The role will mainly involve working regular hours Monday-Friday but there may be occasional weekend work. Key responsibilities include: Establishing, developing, and optimising stable mammalian cell lines for protein and antibody expression Working extensively with CHO cells, while applying experience with other mammalian lines where relevant Ensuring host systems meet manufacturing and molecule‑format requirements, with documentation aligned to high‑quality standards Applying and supporting cell engineering methods (e.g., CRISPR/Cas9) where needed Analysing expression and engineering data to support decision‑making Maintaining high‑quality documentation, reports, and records Collaborating across molecular biology and engineering teams to drive successful outcomes Communicating progress, challenges, and solutions to multidisciplinary stakeholders What you'll need to succeed A strong candidate will bring hands‑on experience with cell line development for manufacturing and a keen eye for scientific detail and also have: Strong experience of generating stable mammalian cell lines, ideally for antibody production Strong preference for candidates with CHO cell experience; experience with other cell lines (eg HEK) also considered Experience with cell engineering technologies (e.g., CRISPR/Cas9) is beneficial but not essential Proficiency in molecular biology techniques such as cloning, ddPCR, and plasmid construction Hands‑on experience with flow cytometry / FACS and/or cloning workflows Excellent documentation, organisational, and scientific writing skills Strong communication abilities and experience working cross‑functionally Familiarity with lab IT systems and molecular biology software (e.g., SnapGene, Geneious) What you'll get in return You'll have the opportunity to impact the production of the company's therapeutics across a significant majority of their portfolio, working within a collaborative and friendly team with plenty of opportunities for professional development and training. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career. Keywords: CHO, Mammalian, Cell, Line, Development, Scientist, Expression, Antibody, Protein, Stable, Clonal, Engineering, CRISPR, Cas9, Genome, Cloning, Plasmid, ddPCR, Cytometry, FACS, Culture, Biotech, Fermentation, Molecular, Biology, Manufacturing, Host, Screening, Optimisation, Therapeutics, pharmaceutical, research

Your new company You'll be joining an experienced team in a leading biopharmaceutical organisation focused on advancing innovative antibody and protein therapeutics. You'll be part of a collaborative R&D environment dedicated to developing high‑quality formulations that support all stages of product development. Your new role This is initially a 12 month contract position that has the potential to extend. The role is fully based on site at the company's labs. As a Scientist in antibody formulation development, you will support non‑clinical and clinical programs by developing, analysing, and optimising formulations for monoclonal antibodies and novel therapeutic formats. Key responsibilities include: Performing analytical and formulation experiments to support toxicology and clinical studies Conducting protein/antibody analysis using methods such as HPLC/UPLC, iCE, UV spectroscopy, DLS, CGE, rheology, and sub‑visible particle analysis Supporting pre‑formulation and formulation laboratory activities, including setup and resource coordination Authoring protocols, reports, and technical documentation based on an understanding of protein degradation mechanisms Presenting findings to project teams and internal stakeholders Contributing to technology platform improvements, including automation where applicable What you'll need to succeed You should have: An MSc or PhD (or equivalent experience) in Biotechnology, Biochemistry, Biology, or a related discipline Strong hands-on lab experience with the analysis of large molecules (proteins, peptides, antibodies, etc) using a variety of techniques, preferably in an industry setting, eg a pharmaceutical company, biotech or CRO Direct experience with protein/antibody analytical methods (HPLC/UPLC, iCE, UV, DLS, CGE, rheology, MFI) Experience in formulation development and/or automation is an advantage Excellent communication, organisation, and teamwork abilities All candidates MUST have the right to work in the UK without visa sponsorship until at least April 2027. What you'll get in return You'll get a good daily rate as well as the chance to impact the company's projects all the way from preclinical through to late phase clinical studies while working with a highly collaborative and friendly team. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career. Keywords: Formulation, Antibody, Drug, Protein, Scientist, pharmaceutical, Biochemistry, Biotech, Biology, Biopharma, HPLC, UPLC, Spectroscopy, Rheology, DLS, CGE, MFI, Analytical, Stability, Research, R&D, Development, Laboratory, Automation, Therapeutics, Injectable, Characterisation, Assay, Data

Your new company You'll be joining a leading biopharmaceutical organisation advancing innovative medicines and technologies. You'll be part of a collaborative R&D environment focused on developing high‑quality, scalable processes. Your new role As an Associate Scientist in upstream process development, you will support the optimisation and scale‑up of microbial processes across lab‑ and pilot‑scale operations. This is initially a 12 month contract that may extend and there will be some out of hours/weekend work involved in this role. Key responsibilities include: Performing microbial process optimisation and development experiments from 250 mL to 200 L scale Operating bioreactor and fermenter systems to support upstream development Documenting experiments, writing protocols, and updating procedures Analysing data and presenting results to managers and internal teams Working independently and collaboratively to deliver team objectives Maintaining a safe and compliant laboratory environment Developing technical expertise in microbial fermentation and primary isolation Supporting cross‑functional teams in recombinant protein and plasmid production What you'll need to succeed You should have: A BSc/BEng (or equivalent experience) in Biology, Biotechnology, Biochemical Engineering, or a related field Experience with upstream lab‑ or pilot‑scale microbial processes and associated control systems, especially around fermentation or cultivation of microbes / cells Hands‑on laboratory experience, ideally with E. coli Understanding of E. coli physiology is preferred but work with other microbial organisms or even mammalian cell lines is also acceptable Excellent organisation and attention to detail Strong teamwork and communication skills Enthusiasm for developing new technical and soft skills The right to work in the UK without requiring visa sponsorship until at least April 2027 What you'll get in return The chance to build your skills and experience within a high performing and innovative biopharmaceutical company while working with a friendly and collaborative team. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. Keywords: Process, Optimisation, Development, Upstream, Microbial, Expression, Scientist, Fermentation, Bioprocess, Bioreactor, Pilot, Scale, Antibody, Research, Laboratory, e.coli, Biotechnology, Biology, Engineering, Plasmid, Protein, Recombinant, Data, Analysis, Protocols, Fermenter, Cultivation, Microbiology, Scaling, Isolation

Cell Culture / Expression Scientist - Antibody Cell Line Sciences Location: Slough (Fully Onsite) Rate: £22.40 (PAYE) / £30.81 (Umbrella) Contract: 12 Months (Ajax) Schedule: Weekend working required - maximum 1 in 4 weekends Overview We are seeking a highly skilled Cell Culture / Expression Scientist to join the Antibody Cell Line Sciences sub-team, part of the Antibody and Novel Therapeutics Group. The successful candidate will contribute to host cell line establishment, engineering, and the generation of stable mammalian cell lines to support the development and manufacturing of UCB therapeutics. Primary Purpose / Regulatory Responsibilities Establish and develop a toolbox of host cell lines for therapeutic manufacturing. Ensure host systems are suitable for expressing diverse molecule types and compliant with GMP manufacturing requirements, supported by rigorous documentation. Communicate scientific progress clearly across teams, highlighting issues, risks, and opportunities, and proposing practical solutions. Apply multiple host-engineering and genome-editing techniques in close collaboration with engineering and molecular biology groups. Contribute strong lab-based scientific expertise to support successful project outcomes. Key Responsibilities Generate and optimize stable mammalian cell lines for protein expression. Conduct cell line engineering using technologies such as CRISPR-mediated editing. Analyse expression and engineering data to drive decision-making and project progression. Perform essential molecular biology techniques (e.g., ddPCR, cloning, plasmid construction). Execute flow cytometry/FACS, single-cell cloning, and related workflows. Maintain meticulous documentation, including electronic lab notebooks (eLNs). Contribute to scientific reports and cross-functional updates. Use relevant lab and IT systems, including Office tools, SnapGene/Geneious, and literature/patent search tools. Required Skills & Experience BSc minimum in a relevant scientific discipline. Industry experience generating stable cell lines for antibody or novel biologic expression. Proficiency in genome-engineering technologies, particularly CRISPR. Strong data analysis skills with the ability to draw clear scientific conclusions. Competence in key molecular biology methods (ddPCR, cloning). Hands-on experience with flow cytometry/FACS and single-cell cloning platforms. Excellent written and verbal communication skills. Strong scientific writing ability, including preparation of structured technical reports. High standards of accuracy in documentation and record‑keeping. Working knowledge of lab and IT platforms including eLNs, molecular biology software, and search tools. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy

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