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The Opportunity With Every Community, Stantec Redefines What’s Possible. Application Deadline: Recruitment is ongoing. Please apply as soon as possible as the advert may close once we have sufficient applicants. Your Role We are looking for a Graduate Structural Engineer to be based in Oxford, joining our 2026 Graduate Programme. As a Stantec graduate, you will collaborate with your team and wider cohort, developing your structural engineering expertise within an exciting and creative interdisciplinary environment. In this role, you'll join our large and supportive structures team based in the Oxford office. The team works closely with a number of key clients to deliver successful building projects, from initial concept all the way through to completion (i.e. construction). You'll gain experience across various project scales and sectors, including education, regeneration, refurbishment, healthcare, logistics, technology and commercial. As a Graduate Structural Engineer, you'll support senior staff with a range of tasks, including concept and preliminary designs, calculations, reviewing drawings, producing sketches, detailed designs, site visits and inspections and report writing. You will also learn to use a wide range of software, including Tekla, STAADPro and more. You will join a supportive and successful team with exciting career opportunities, gain great client exposure and professional development and work in an innovative and collaborative environment. Take a look at our Buildings business line here:- Buildings | Stantec , and review some of the projects you could be working on:- Buildings Projects | Stantec About You At Stantec, we value your potential over past experience. Along with your Bachelor’s degree in Civil or Structural Engineering and a keen interest in the buildings industry, we’d love to receive your application if you are:- • An adapter: you’re able to remain calm in new and changing situations, comfortably switching between a variety of dynamic and exciting tasks., • A Perseverer: you stay composed in the face of setbacks, approaching challenges with confidence and determination., • A Collaborator: you work effectively with lots of different people, considering other’s perspectives to shape better outcomes., • A Problem-Solver: you love to give your thoughts based on what you see, being unafraid to challenge conventional thinking. Please note, we ask our graduates to come into the office 4 days per week, to ensure that you receive sufficient time with your team and receive the appropriate level of support. What We Can Offer You • A competitive salary, • Private medical insurance, • A range of benefits, including holiday buy and sell, group income protection and life assurance, • Permanent employment contract to demonstrate our commitment to your long-term career at Stantec, • Professional progression plan, supporting you to gain professional chartership, • A supportive and collaborative team environment and Early Careers peer group and wider ERG network (see more on our ERGs here: Stantec Employee Resource Groups ) Applicants must have an unconditional right to live and work in the UK for an indefinite period without limitation. Please take a look at our Graduate FAQs ( Graduate Application FAQs ) if you have any questions. We look forward to receiving your application! #NextGen #StantecCareers #UKGraduate About Stantec The Stantec community unites more than 34,000 employees working in over 450 locations across 6 continents. We have been working with our clients and communities in the UK for over 150 years. We plan, design, deliver and manage the development and infrastructure needed to support the creation of sustainable, healthy and prosperous communities. Our teams provide effective and relevant solutions, translating our clients’ vision into valued consents, deliverable plans for projects and programmes, and efficient designs for delivery, based on technical excellence and deep market insights. We deal with today’s challenges, but also keep a fairer, better tomorrow in sight, looking at how we deliver clean growth, support radical changes in our economy and meet the needs of future communities. Stantec provides equal employment opportunities to all qualified employees and applicants for future and current employment and prohibit discrimination on the grounds of race, colour, religion, sex, national origin, age, marital status, genetic information, disability, sexual orientation, gender identity or gender expression. We prohibit discrimination in decisions concerning recruitment, hiring, referral, promotion, compensation, fringe benefits, job training, terminations or any other condition of employment. Stantec is in compliance with laws and regulations and ensures equitable opportunities in all aspects of employment. Building an inspired, inclusive work environment that attracts, supports, and develops world-class talent is a crucial key to our success. If you are excited by this role but worry that your experience doesn’t exactly align, we encourage you to apply. At Stantec we want you to perform your best at every stage of the recruitment process and are committed to ensuring it is accessible to all. If you need any support or require adjustments to be made then please contact [email protected] and we will talk to you about how we can support you.

We are looking for a highly motivated Imaging Biomarker Scientist to join our Translational Science team. This role sits at the intersection of medical imaging, data science and biomedical research and is ideal for someone who enjoys hands-on data handling, scientific interpretation and contributing to high-quality clinical evidence. It’s an excellent opportunity for someone with strong coding, biomedical statistics, and bioinformatics experience who wants to grow within a multidisciplinary translational research environment About the Role You will work with clinical datasets from our research collaborations, apply advanced medical statistics, and help evaluate the performance of our imaging metrics as biomarkers across a range of disease areas. Day to day duties include: • Performing data analyses on clinical data acquired with Perspectum’s core technologies., • Contributing to, and authoring, scientific publications including abstracts, posters and manuscripts., • Providing analysis and statistical support for regulatory submissions and clinical science publications, • Analysing and interpreting data, and reporting findings to internal and external stakeholders, • Working closely with our Data Science, Medical Affairs and wider Translational Science team About You We are looking for an individual who excels in a collaborative environment, has excellent communication and adapts well to changing priorities. You will be able to demonstrate your: • Strong coding experience in Python or R, • Experience handling biomedical, bioinformatic or imaging datasets., • Good understanding of statistical and research methods relevant to clinical or biomedical research., • Ability to analyse and interpret data and communicate findings clearly. A PhD in a related discipline (eg Biomedical Science, Biostatistics or similar) would be highly beneficial, however we would also welcome applications from those with a Masters in a similar field. Any experience in the following would also be advantageous however is not essential: • Experience with medical imaging data or imaging biomarkers., • Prior authorship or contribution to peer-reviewed publications., • Experience writing conference abstracts or contributing to scientific dissemination., • Familiarity with clinical research in areas such as liver disease, metabolic disease, oncology, or inflammatory conditions. Why Join Us? This is a fantastic opportunity to work in a collaborative environment where you can see how your work directly translates into meaningful clinical practice. At Perspectum, we are committed to fostering diversity, equity, and inclusion. We prioritise hiring based on merit, skills, and qualifications, valuing individuals for their unique contributions while ensuring a culture that respects and celebrates differences. If you require any reasonable adjustments as part of your application process, please let our Talent Team know.

Salary £58,340 - £68,574 per annum, pro rata - Civil service grade 7 Location Hybrid role based at our scientific campus in Chilton, Oxfordshire Job overview UKHSA’s Radiation, Chemical, Climate and Environment (RCCE) Hazards Directorate provides advice, research and services to protect the public from exposure to chemicals and poisons, ionising and non-ionising radiation, and other environmental hazards. RCCE provides a specialist assessment and advice function within UKHSA’s overall response as a Category 1 responder to radiation and chemical emergencies. RCCE has an extensive and diverse research function part of which is carried out in the context of NIHR Health Protection Research Units. The Radiation Dosimetry Department provides authoritative public health information and advice about exposures to lasers and optical radiation, electromagnetic fields, and ionising radiation used for medical diagnostic imaging. In addition, the department provides the secretariat to the Committee on Medical Aspects of Radiation in the Environment (COMARE). The work of the Department encompasses the provision and maintenance of calibration facilities, research programmes of physical measurement and theoretical dosimetry, health hazard exposure assessments, and the development of standards. It includes the provision of training courses, and liaison and collaborative input to national and international bodies concerned with setting and promulgating standards for protection. The Electromagnetic Fields (EMF) Dosimetry Group's role is to assess exposure characteristics of emerging and established EMF technologies, including mobiles phones, base stations and power lines. The group acts as the national contact point for UKHSA’s advice on the public health aspects of exposures to EMFs, input to regulations; research on health impacts and environmental monitoring of exposures to EMFs; training and input to the international and national guidance and standards on exposure to EMFs; development of methodology of public and occupational exposure assessments, and measurement infrastructure; support to the EMF capabilities of the Operational Services Department. The EMFD Group has two laboratories at Chilton in Oxfordshire; one primarily used for EMF exposure investigations and maintenance of measurement equipment, and the other for dielectric properties research. The Group carries a heavy burden of correspondence, with high-level requests and short deadlines arriving on a daily basis. Main duties of the job We are currently looking for a Principal Radiation Protection Scientist - Electromagnetic Field Dosimetry whose main duties will include: • To initiate, plan, lead and execute specialist research or equivalent advisory projects related to the assessment of exposure to electromagnetic fields, including experimental and numerical dosimetry and managing the work of others as necessary., • To provide the lead in writing and maintaining elements of published UKHSA advice on exposure to electromagnetic fields, including webpages., • To prepare scientific review material for UKHSA publications, including consultancy input and secretariat support for advisory and other high-level committees, e.g. the Committee on Medical Aspects of Radiation in the Environment (COMARE)., • To prepare and disseminate advice in response to Nationally Significant Infrastructure Projects (NSIPs), enquiries from public officials, members of the public, industry and other stakeholders., • To assist the Group Leader in conducting general management duties, for example in carrying out health and safety risk assessments, quality assurance audits and preparing proposals for new business opportunities., • To manage and maintain numerical simulation platforms, perform required updates and upgrades if necessary., • To manage and develop specialist measurement facilities and equipment related to experimental dosimetry, ensuring health and safety procedures are adhered to and supervising others in the use of equipment., • To prepare authoritative scientific reports and papers for publication., • To prepare and deliver scientific presentations at national and international conferences and for training courses and represent UKHSA at local, national and international meetings., • To provide support in UKHSA emergency plans, typically at the level of operations support manager of one of the RCCE emergency cells., • There will be an occasional need to work irregular hours. There will also be a requirement to travel within the UK and occasionally overseas. Essential Criteria • Qualification to PhD level in an appropriate scientific or public health/health protection discipline or equivalent experience., • Post-doctoral experience sufficient to undertake experimental and numerical EMF dosimetry research with minimal input from line management., • Theoretical and practical knowledge within the area of experimental dosimetry, sufficient to be acknowledged nationally and internationally., • Experience in scientific project management and co-ordinating collaborative work with UKHSA and non-UKHSA scientists., • Extensive experience in publishing scientific reports and peer-reviewed papers., • Experience in giving presentations at national /international scientific meetings and conferences., • Ability to interpret and explain the relevance of empirical findings in a wider multidisciplinary context for discussion at meetings, conferences and publication in the peer-reviewed literature., • Experience in planning and execution of complex scientific projects, identifying and managing risks appropriately., • Confident and proficient in the use of scientific data analysis software., • Working knowledge of Information Governance i.e. freedom of information and data protection., • Able to manipulate equipment and perform experiments in the EMF laboratory., • Able to operate a DSE workstation., • Able to load/unload measurement equipment from vehicles when performing surveys., • Current full UK driving licence and ability to drive vehicles to off-site locations., • An understanding of and commitment to equality of opportunity and good working relationships. Desirable Criteria • Theoretical and practical knowledge within the area of numerical dosimetry, sufficient to be acknowledged nationally and internationally., • Experience in the appropriate use of specialised EMF measurement equipment, including network analysers, spectrum analysers and field probes., • Experience in the use of specialised EMF numerical simulation platforms, including device and process design and interactions with anatomical phantoms., • Experience in planning and execution of complex scientific projects, identifying and managing risks appropriately., • Comprehensive understanding of the health and safety aspects of running an experimental dosimetry laboratory., • An understanding of risk management in the context of health and safety legislation., • Broad knowledge of a wide range of Health protection/Public health related topics., • Training/experience in emergency response. For all job details, please click 'apply' whereby you will be redirected to the role on HealthJobsUK.

This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job—you will find purpose and pride. Your Role at Baxter This is where your creativity addresses challenges The Senior QS Associate will be responsible for leading and supporting initiatives to ensure the continuous compliance of the UK Compounding business to cGMP and “Specials” manufacturing requirements, local procedural requirements, and Baxter Corporate policies. This role will focus on providing quality systems support across the UK compounding network. Reports into the UK Compounding Quality System Manager. You are creative, thorough, and a heads-down do-er. You embrace a challenge and truly apply the collaborative powers of your team to produce great results. You are motivated by work that is never the same from one day to the next. As a Senior QS Associate, you are unafraid of navigating through necessary internal processes to facilitate a product you deeply believe in. You can absorb and act on complex procedures and data and train your team or peers if needed. You take pride in getting things done quickly without sacrificing safety or quality. Your Team at Baxter Within Quality, every role makes a difference. Products that Baxter makes are shipped worldwide for patients in need. Whether it's building a new process from scratch or facing a never-before-seen production hurdle, individuals within Quality are given the trust and opportunity to bring creativity to the table. Regardless of your specific role with a product, it is sure to touch a portion of our global operation. The mission of Baxter is to save and sustain lives. This mission is embedded into everything we do. This means if there is a decision to be made where quantity and quality are at odds, we will always choose quality. Our patients come first, always. What You'll Be Doing • Ensure compliance with applicable GMP, GDP, MHRA, and other relevant regulatory standards., • Lead the development, implementation, and continuous improvement of the Quality Management System (QMS) in alignment with corporate and regulatory requirements. Stability and Temperature Excursion Management • Review Baxter stability studies, product SmPCs, and relevant scientific literature to define compounded product stability data., • Assess and document temperature excursion incidents within the Quality System., • Own and lead Temperature Excursion Evaluation Tasks, ensuring timely and thorough investigation., • Review and approve temperature excursion documentation and provide product disposition assessments., • Support the management of stability records in the Pharmacy electronic systems Merlin and Mercury, • Raise significant excursions through the nonconformance process, • Ensure regulatory reporting of issues to local Regulatory Authorities as required Field Actions and Recalls • Lead and coordinate field actions and product recalls in accordance with Baxter procedure., • Ensure effective communication and documentation throughout the recall process., • Liaise with internal and external partners such as MoH, Baxter Compounding Units, Baxter Commercial and Medical Affairs teams, Baxter Homecare, etc., • Collaborate with cross-functional teams to assess impact and implement corrective actions., • Lead and raise significant quality issues within the Global Compounding Organization for the purposes of Senior Management and other Compounding sites awareness Audit Management • Lead and support Internal, Corporate and external/Regulatory, audits, • Support site’s audit readiness activities., • Lead and support in the annual internal audit program as required., • Track and trend relevant unit audit findings. Other duties you will also be involved in as part of the role: Introduction of New Drugs and Components Change Control Process Corrective & Preventive Action Processes Documentation Quality Management Review (QMR) Communication and Training What You'll Bring • English minimum equivalent to RQF Grade 2, EQF Grade 3 or SCQF Grade 5, • At least 2 years’ experience in the pharmaceutical or medical device industry., • Proven knowledge of Quality System processes., • Bachelor’s degree or higher in Pharmaceutical, Biotechnology, Chemistry or Microbiology, • Minimum of 2 years' experience in quality team facilitation, project management, process improvement, or quality data analysis role., • Experience of coordinating and supporting Document Control, Internal Audit, CAPA, Non-conformance, and Complaints processes., • Experience of problem-solving using Root Cause Analysis techniques such as GEMBA, 5 Whys, Cause and Effect., • Working knowledge and hands-on experience of software tools to lead Quality Systems processes such as TrackWise., • Report and documentation writing skills., • Risk management tools and methods., • Excellent verbal and written communication skills. What are some of the benefits of working at Baxter? • Competitive total compensation package, • Professional development opportunities, • High importance placed on work life balance #IND-UKOPS #IND-UKCOM Equal Employment Opportunity Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the ___ here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our ___.

🌍 Molecular Imaging Account Manager – Europe We are seeking a Molecular Imaging Account Manager to spearhead the launch of our client’s European sales activity. This is a pivotal role, responsible for building the foundation of a commercial team across Europe and driving growth in the molecular imaging and radiopharmaceuticals space. The successful candidate will combine strategic leadership with hands-on account management, ensuring both commercial excellence and strong customer partnerships. This is a rare opportunity to join at the ground level of a European expansion and make a lasting impact. Key Responsibilities • Lead the launch of European sales operations in molecular imaging., • Develop and execute commercial strategies across multiple countries., • Manage P&L responsibilities and national tenders/contracts with healthcare providers., • Act as the primary point of contact for customers, distributors, and supply chain partners., • Collaborate with internal teams (QA, RA, R&D, logistics, production) to introduce new PET tracers and radiopharmaceuticals to market., • Build and nurture relationships with clinicians, technicians, and hospital management to understand needs and deliver solutions., • Deliver product presentations and represent the company at domestic and international congresses., • Share best practices and contribute to the growth of a collaborative European team. We are looking for candidates with: • Proven commercial experience in contrast media, radiopharmaceuticals, or molecular imaging., • Strong background in account management and tender/contract negotiations., • Experience working with PET tracers, radiopharmaceutical supply chains, or related modalities., • Ability to engage with healthcare professionals at all levels, from clinicians to hospital management., • Track record of delivering technical/medical presentations and representing products at congresses., • Leadership qualities, with experience in training, mentoring, or team-building., • Flexibility to travel extensively across Europe. Why Join? • Be at the forefront of a European market launch in a cutting-edge field., • Shape the future of a growing team and contribute to strategic expansion., • Work closely with international leadership while enjoying autonomy in your region. About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

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. The primary purpose of this role is to serve as a recognized technical leader in formulation development, leveraging extensive experience and expert knowledge to drive innovation and contribute to the company's scientific strategy. The incumbent is expected to advocate for process, platform, and technology improvements, and apply advanced knowledge of scientific principles and the drug development process to solve extremely complex problems. The individual will exercise independent judgment in developing methods and techniques, consistently making the right calls to achieve results. This position will be responsible for conducting and designing experimental investigations to support a low & high dose parenteral bio-pharmaceutical in the development and management of integrated formulation strategies supporting Immunocore's bio-pharmaceutical platforms. The formulation role will be a hands on role, primarily focussed on lab work designing and performing experimental work. It will also cover drug delivery approaches, investigate novel technologies such as LNP, Pegylation and other delivery systems applicable to biologicals. The role will also cover early stressing studies, formulation excipient screening, CMC process support, drug substance and drug product through to compatibility with final patient delivery systems. Support and direct IUS studies and progress the clinical programmes. Support and respond to main stake holders for example Clinical and Regulatory teams in the delivery of the clinical strategies. To work in close collaboration with the Head of Formulation, CMC teams and related functions to input into the formulation related sections for regulatory filings, development reports and other development related documents. Advanced people management skills are essential, including managing changing priorities while maintaining team motivation. They will create a safe environment for learning from mistakes, establish clear career paths, and hold career development conversations. The individual will engage in difficult conversations where appropriate, inspire action, and show employees how they contribute to higher goals. Key Responsibilities: • Conducting experiments, observing, interpreting and responding to results., • Maintaining and increasing technical knowledge in relevant fields through self-study, observation, attending relevant conferences and training courses., • Maintaining accurate records of all work by completing laboratory notebooks on time, following Company procedures, • Ensuring that laboratory equipment is operated in accordance with safety and risk guidelines; acting promptly to report any faults or problems to the relevant member of staff., • 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 both internally and externally. May also act as a mentor or manager to other colleagues, especially new hires, sharing scientific and company knowledge. Increasingly providing analysis of new techniques and theories from outside the Company to advance the way the company works; sharing these with leaders across the Company., • 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; making recommendations regarding acquisition of new pieces of equipment., • Health & Safety: championing and helping others to understand H&S within the company, providing ad-hoc training as required., • Reporting: communicating and presenting research findings at meetings with colleagues, senior management and partners. Experience and Knowledge: Essential • Background in recombinant protein or antibody formulation, Drug delivery of biologics. analytical development or protein characterisation, with proven industry experience and exposure to formulation strategies., • Experience in design of formulation studies, including the utilisation of design of experiments principles., • Strong expertise in electrophoretic or chromatographic assays and general biochemical lab techniques. Desirable • Experience of process development for production of biologics and conjugation of biomolecules, • Experience with lyophilisation development of Biotherapeutics, • Familiar with biopharmaceutical stability study principles, • Familiarity with novel drug delivery formats, • proactive in ensuring high quality of their work and seeking additional responsibilities to help meeting the goals of the team, • Presented detailed scientific findings and papers to internal and external audiences Essential Qualifications: • Essential: PhD In bio-manufacturing, protein engineering, biochemistry, molecular biology or related discipline, • Industrial company experience delivering formulations through drug development phases, • Normally requires a PhD in a scientific discipline and a minimum of 8+ years related experience; may include post-doctoral experience.

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