762 jobs found

At Charles River, we are passionate about improving the quality of people's lives. When you join our global family, you will help create healthier lives for millions of patients and their families. Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career. As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving therapies to market faster through simpler, quicker, and more digitalized processes. Whether you are in lab operations, finance, IT, sales, or another area, when you work at Charles River, you will be the difference every day for patients across the globe. IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly. Job Summary We are seeking a Senior Associate Scientist Clinical Immunoassays within our Immunology, Bioanalysis & Biomarkers department located at Clear Water House on the Heriot Watt University Campus, Riccarton, Edinburgh. Please note this is a 12 month fixed term contract opportunity. This is a dynamic and fast-growing team of over 80 researchers which work to support our clients as they bring novel treatments to patients. The team is multifunctional using a wide variety of scientific techniques across the fields of Immunology, Immunochemistry, Cell Based Assays and Molecular Biology. Working as a scientist in our Clinical BioA team, you will be performing studies to support clinical trials for novel pharmaceuticals. The focus of this role will be on regulatory PK and immunogenicity studies using immunoassays. In this role you will demonstrate proficiency in the use of instrumentation and laboratory techniques; effectively apply your experience and knowledge to conduct method development and validation studies and troubleshoot method issues. You will contribute to the department by completing and project managing assigned projects on time, participating in process improvement initiatives and by communicating effectively with colleagues and customers. You will drive diversification and expansion of our capabilities in this space, collaborate with other teams locally and globally and drive the technical/scientific development of staff. You will travel occasionally to meet with sponsors and visit conferences. The following are the minimum requirements related to the Senior Associate Scientist position: • PhD with relevant experience or MSc/BSc with strong industry experience • Deep practical understanding of immunoassays • Understanding of preclinical and clinical phases of drug development • Understanding of large molecule PK and immunogenicity assays is desired • Excellent team spirit and people skills • Proven organizational and project management skills • Excellent communication skills Salary for this position is £33,272 per annum. IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV. About Safety Assessment Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities. About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 17,000 employees within 90 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 85% of the drugs approved by the FDA in 2019. For more information, please visit . 227911

Go back Northumbria Healthcare NHS Foundation Trust QC Validation Scientist The closing date is 21 May 2025 An exciting opportunity has arisen for a proactive and passionate Quality Control Validation Scientist to join the Medicines Manufacturing Centre (MMC)-a cutting-edge NHS pharmaceutical production facility based in Seaton Delaval, Northumberland. The MMC is in its final design stages, with facility construction planned through to September 2025. This is a fantastic opportunity to be part of a pioneering NHS manufacturing facility, supporting a leadership team committed to quality, innovation, and patient care. Please note we reserve the right to close this vacancy prior to the closing date once the required number of suitable applications have been received. All employees of the Medicine Manufacturing Centre (MMC) are currently employed by Northumbria Healthcare NHS Foundation Trust, under Agenda for Change Terms and Conditions. Should the service be transferred into alternative ownership, those employees with start dates prior to the transfer date will be protected under Transfer of Undertakings (Protection of Employment) Regulations 2006 (TUPE). Employees will transfer to the new employer on the same terms and conditions, which are protected, and their continuity of employment is preserved. Main duties of the job Oversee New Product Introduction processes from a QC perspective for products to be manufactured in the MMC, including: Analytical method validation (ICH Q2) Technology/method transfer QC stability testing (ICH Q1) Ongoing stability studies Sampling plans Lead the QC reference standards processes, including: Routine use and validation of working standards Management of reference and retention samples for finished products and raw materials Implement QC policies to ensure compliance with GMP, support management of contractors for outsourced QC Chemistry work, lead qualification, PPM, and servicing of QC chemistry equipment. Manage laboratory staff, lead training initiatives, and prepare QC documentation such as protocols, reports, SOPs, and stability plans. Perform assessments for the Pharmaceutical Quality System (PQS), including OOS investigations, RCA, QRA, and change control assessments. About us The MMC is a purpose-built NHS pharmaceutical production facility at the Northumbria Innovation and Manufacturing Hub, designed to meet the growing demand for high-quality, regionally manufactured medicines. Funded with £30 million from NHS England, it aims to support a sustainable supply chain for critical medicines, especially oncology and high-risk therapies, creating skilled jobs and fostering innovation. The facility will operate under a Manufacturer's Specials Licence and aims for WDA(H) compliance, ensuring adherence to MHRA, GMP, and GDP regulations from day one. Our core values focus on quality, patient safety, and staff wellbeing. We foster a culture of openness, learning, and continuous improvement, offering staff the opportunity to shape a modern NHS manufacturing unit. Working at the MMC means being part of a forward-thinking, supportive team dedicated to enabling clinical staff to spend more time with patients by delivering safe, ready-to-use medicines. Job responsibilities Perform QC data recording, trending, and statistical analysis for all QC chemistry data, ensuring accuracy and compliance. Oversee stability studies and ongoing stability testing programs, including investigational work and validations. Ensure analysis of raw materials, packaging components, and finished products aligns with approved QC worksheets and SOPs. Demonstrate compassionate and inclusive leadership by engaging, enabling, and empowering team members, promoting ownership of learning and quality improvement, and facilitating collaboration across departments. Person Specification Qualifications Masters degree in a relevant scientific discipline or equivalent experience. Eligible for registration with GPhC, HCPC, RSC, RSB, or RPS. Postgraduate qualification in Analytical Chemistry or Pharmaceutical Analysis. Postgraduate qualification in Quality Assurance or GMP. Experience Post-qualification experience with analytical techniques used in pharmaceutical QC. Knowledge of MHRA GMP guidelines and pharmacopeial requirements. Experience with analytical method validation (ICH Q2), stability studies (ICH Q1), and laboratory instrument maintenance (HPLC, FTIR, UV-VIS, pH meters, balances). Proficiency in data trending, statistical analysis, and laboratory safety standards (e.g., COSHH). Experience managing New Production Introduction from a QC perspective, GMP product formulation studies, and using Quality Management Systems. Experience with QC testing of sterile medicines, both chemistry and microbiology, aligned with pharmacopeial standards. Awareness of developments in pharmaceutical manufacturing and coaching/mentoring practices. Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975. A DBS check will be required to verify any criminal convictions. Northumbria Healthcare NHS Foundation Trust Full-time, flexible working, compressed hours

For 75 years, Charles River employees have worked together to assist in the discovery, development, and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales, or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about. IMPORTANT: To be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please ensure your work history and education are correctly added. Job Summary We are seeking a Scientific Associate in the Immunology, Bioanalysis & Biomarkers department at our site in Clearwater House, Riccarton, Edinburgh. This is a 12-month fixed-term contract. The Immunology, Bioanalysis, and Biomarker team comprises about 75 researchers supporting clients in bringing novel treatments across various therapeutic areas to patients. The team provides accurate and reliable data using techniques in Immunochemistry, Immunology, Cell-Based Assays, and Molecular Biology to meet regulatory standards. The successful candidate will develop, validate, and implement immunoassays for PK/TK and Biomarker assessments, including Safety, Pharmacodynamic, Surrogate, Predictive/Prognostic, Monitoring, and Susceptibility analyses. Key responsibilities include: Processing samples Operating advanced analytical equipment Recording and reporting data Applicants should have excellent organizational skills, attention to detail, and a good understanding of Immunology and Cell Biology or drug development, with a BSc or MSc degree in a relevant discipline. Requirements include: Strong teamwork and communication skills Interest in working with sophisticated laboratory equipment Knowledge of core laboratory techniques Ability to perform well under pressure Basic understanding of GLP and GCP The salary for this role is £27,163.48 per annum. The closing date is Wednesday, 27 May 2025. Initial training will be at Elphinstone, Tranent, with subsequent work at Clearwater House, Riccarton.

Job Details: Process Development Scientist, Downstream Full details of the job. Vacancy Name Vacancy Name Process Development Scientist, Downstream Vacancy No Vacancy No VN643 Employment Type Employment Type Full Time Location of role Location of role Oxford, UK Department Department CMC Key Responsibilities Key Responsibilities To conduct and design experimental investigations to drive the downstream process development of emerging drug candidates, supportive reagents and successful establishment of production processes for manufacturing and clinical development. Protein purification is core to this role, requiring knowledge and understanding of protein characteristics to implement robust column chromatography and separation techniques along with analytical assessments of purity, using methods such as SDS-PAGE and HPLC. The ability to work independently, as well as part of a team and to tight deadlines is essential. Robust record-keeping and strong communication skills are also required. The job also involves interaction and document/technical reviews with external CDMO partners to support successful GMP manufacturing and regulatory compliance. KEY RESPONSIBILITIES - ALL SCIENTISTS • Conducting experiments, observing, interpreting, and responding to results. • Following experimental protocols and writing reports • Planning experiments and carrying out priorities, with guidance from line manager or other team members • Maintaining and increasing technical knowledge in relevant fields through self-study, observation and attending relevant conferences or training courses. • Maintaining accurate records of all work by completing laboratory notebook on time, following company procedures. • Ensuring laboratory equipment is operated in accordance with safety and risk guidelines, acting promptly to report any faults or problems. • Operating in accordance with the Company's Health and Safety policies, especially within a laboratory environment. SPECIFIC RESPONSIBILITIES • Experiments: Independently running pre-established lines or areas of investigation, seeking guidance and support from colleagues and line managers as required and to confirm experimental direction. • Priorities: Planning and working to agreed experiment deadlines, schedules and objectives, alerting managers and colleagues to risks and deviations that may impact meeting the goals, so that these can be addressed. • Technical knowledge: Actively developing own knowledge, drawing on the experience of others and self-learning, practicing and sharing acquired skills that may benefit the team with colleagues and managers. • Laboratory records: Ensuring that all records and information are up to date, on time and recorded to the correct standard, seeking support when uncertain on how to complete these satisfactorily. • Laboratory equipment: Attending training on the use of technical instruments, using equipment appropriately, owning and maintaining assigned pieces of equipment. • Reporting: Presenting research, data and findings to colleagues at group/department team meetings. Regular reporting on progress of work verbally and in writing to line manager. Protocols and reports to be written and reviewed to meet the Immunocore Quality system. • Health & Safety: Compliance with all H&S requirements, attending appropriate training programmes. EXPERIENCE AND KNOWLEDGE Essential • Worked in a bench-based microbial or mammalian expression, biochemistry, molecular biology, analytical or bio-pharmaceutical laboratory environment gaining the following experience: - Aseptic techniques - Microbial manipulations, including transformation and culture - Recombinant protein expression - Protein purification techniques and operation of AKTA purification equipment - Protein characterisation, including SDS-PAGE - Competency in the use of general lab equipment and software • Recorded results in a concise and timely way and in compliance with agreed standards • Able to design experiments and interpret results with minimal guidance • Learnt about new practices based through observation, self-learning and an enquiring mind • Worked and contributed actively in a diverse team environment Desirable • Molecular biology skills • Biophysical characterisation of proteins • Analysing protein-protein interactions, using Biacore or Octet • Troubleshooting protein purification or recombinant protein expression • Mammalian expression • An awareness of cGMP and biopharmaceutical manufacturing requirements • DoE experience • Lab management and implementing/supporting best practice • Presented scientific findings and progress to internal and external audiences. • Worked in an industrial/biotechnology laboratory environment EDUCATION & QUALIFICATIONS • BSc. or MSc. Or PhD in protein or biochemical engineering, biochemistry, microbiology, molecular biology, or related discipline • Desirable: Relevant industrial or post-qualification academic experience About the Company About the Company 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.

At Charles River, we are passionate about improving the quality of people's lives. When you join our global family, you will help create healthier lives for millions of patients and their families. Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career. As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving therapies to market faster through simpler, quicker, and more digitalized processes. Whether you are in lab operations, finance, IT, sales, or another area, when you work at Charles River, you will be the difference every day for patients across the globe. IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly. Job Summary We are seeking a Senior Associate Scientist Clinical Immunoassays within our Immunology, Bioanalysis & Biomarkers department located at Clear Water House on the Heriot Watt University Campus, Riccarton, Edinburgh. Please note this is a 12 month fixed term contract opportunity. This is a dynamic and fast-growing team of over 80 researchers which work to support our clients as they bring novel treatments to patients. The team is multifunctional using a wide variety of scientific techniques across the fields of Immunology, Immunochemistry, Cell Based Assays and Molecular Biology. Working as a scientist in our Clinical BioA team, you will be performing studies to support clinical trials for novel pharmaceuticals. The focus of this role will be on regulatory PK and immunogenicity studies using immunoassays. In this role you will demonstrate proficiency in the use of instrumentation and laboratory techniques; effectively apply your experience and knowledge to conduct method development and validation studies and troubleshoot method issues. You will contribute to the department by completing and project managing assigned projects on time, participating in process improvement initiatives and by communicating effectively with colleagues and customers. You will drive diversification and expansion of our capabilities in this space, collaborate with other teams locally and globally and drive the technical/scientific development of staff. You will travel occasionally to meet with sponsors and visit conferences. The following are the minimum requirements related to the Senior Associate Scientist position: • PhD with relevant experience or MSc/BSc with strong industry experience • Deep practical understanding of immunoassays • Understanding of preclinical and clinical phases of drug development • Understanding of large molecule PK and immunogenicity assays is desired • Excellent team spirit and people skills • Proven organizational and project management skills • Excellent communication skills Salary for this position is £33,272 per annum. IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV. About Safety Assessment Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities. About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 17,000 employees within 90 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 85% of the drugs approved by the FDA in 2019. For more information, please visit . 227911

We're hiring for an exciting opportunity in the life sciences sector for a Scientist I/II to join a pioneering team advancing the next generation of mammalian cell expression systems. This role is ideal for candidates passionate about applying multi-omics approaches to gene target discovery, with a strong foundation in cell biology, molecular techniques, and omics-based data analysis. You'll contribute to projects shaping more efficient and cost-effective immunotherapeutic production processes. About the Role As a key member of a collaborative and multidisciplinary research team, you'll design and execute multi-omics workflows that fuel innovation in gene discovery and cell line engineering. Your expertise will drive characterisation efforts, contribute to hypothesis generation, and influence experimental designs involving CRISPR and ORF libraries. This is a hands-on lab role where your ability to optimise, interpret, and communicate scientific findings will be central to your success. Key Responsibilities Design and perform experiments to generate and analyse multi-omics datasets (transcriptomics, proteomics, metabolomics). Support gene/pathway discovery and development of predictive models using in silico tools. Develop and optimise high-throughput sample preparation protocols for omics applications. Conduct mammalian suspension cell culture, banking, nucleofection, and molecular assays (e.g. western blotting, FACS). Document research findings and contribute to scientific presentations and internal reporting. Maintain lab records, health and safety standards, and support shared lab responsibilities. Train team members to uphold data integrity and contribute to a culture of continuous improvement. About You You'll bring a mix of scientific expertise, curiosity, and collaborative spirit. Whether from an academic or industry background, you're excited to apply your omics and molecular biology skills to real-world bioprocess challenges. Required Qualifications and Experience: MSc with 5+ years of industry experience or PhD with 2+ years of industry experience in Biochemistry, Molecular Biology, or a related field. Hands-on experience with transcriptomic, proteomic, or metabolomic data generation and interpretation. Skilled in CRISPR/ORF library experiments and mammalian cell line development (e.g. CHO cells). Familiar with molecular biology techniques: FACS, qRT-PCR, Western Blot, ELISA. Comfortable working independently and collaboratively, with strong experimental planning and troubleshooting abilities. Knowledge of metabolic flux analysis (MFA). Experience applying Design of Experiments (DoE) methodologies. Skills and Attributes Innovative and analytical thinker Strong communication and documentation skills Organised and adaptable, with excellent time management Proactive, collaborative, and committed to continuous learning

In today's world, there is a continuous drive towards sustainability and reducing CO2, either through carbon capture or carbon upcycling. Our client has developed an innovative process to repurpose CO2 into high-performance polymeric materials for a variety of everyday products. Having successfully built the business through early research & development, they are now beginning the process of licensing this technology and process to established partners around the world! They now require an Analytical Lead Chemist to oversee and perform duties focused on the analytical characterization of starting materials, intermediates, and products; using a range of techniques e.g., HPLC, LC-MS, NMR, GPC. The Lead Chemist will be responsible for method development & validation, data analysis and reporting, training colleagues, and supervising the Analytical team's work. Additionally, you will collaborate with colleagues to drive process improvements and ensure the quality of work and materials produced is maintained. To be suitable for this role, you will have: At least 5 years' experience working in an analytical chemistry laboratory Developed and validated methods on chromatography instruments Knowledge and hands-on experience with HPLC, LC-MS, or GPC Experience analyzing polymers or theoretical knowledge of polymer chemistry Experience in polymer chemistry or polymer characterization would be extremely beneficial

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at . Job Function: Discovery & Pre-Clinical/Clinical Development Job Sub Function: Biotherapeutics R&D Job Category: Scientific/Technology All Job Posting Locations: Malvern, Pennsylvania, United States of America Job Description: Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at . Johnson & Johnson is hiring for a Senior Scientist, Biotherapeutics to join our team in Malvern, PA. We are the upstream process development group and are hiring a Sr Scientist in our team. In this position you will be contributing to cell culture process development within the therapeutic protein process development group in Malvern, PA. Key Responsibilities: Design and execution of experiments Analyze data and write/review reports. Lead and participate in development of control strategy Scale up the process from lab to pilot/manufacturing scale Evaluate facilities fit for the process, and perform tech transfer to manufacturing site Plan and manage process validation (laboratory and manufacturing-scale) Work in multi-disciplinary CMC team with representatives from analytical, manufacturing, quality and other functions. Lead process modeling for bioreactor scale up, tech transfer, and in support of process troubleshooting Lead and participate in scientific investigations and trouble-shoot process issues that arise during development, technology transfer, or scale-up Contribute to regulatory filings Participate in technology development Coordinate laboratory training initiatives Successful candidate will be working in a team environment as well as contributing individually to meet project and department objectives and timelines. Qualifications: Education: Minimum of a Bachelor's Degree in Biological Sciences or Cell Biology or Biochemistry or Chemical Engineering with 6 years of experience is required. MS Degree with 3 years OR PhD with 0-3 years of experience is preferred. Experience and Skills: Required: Hands-on experience with laboratory scale cell culture bioreactor equipment and instrumentation. Knowledge of large molecule drug substance (API) upstream manufacturing process development. Knowledge of cell culture media characterization and/or optimization. Familiarity with or hands-on experience with analytical methods typically used in the manufacture and characterization of recombinant proteins is preferred. It is required that the candidate be highly organized and capable of managing/pursuing multiple projects, and have good written and verbal communication skills. Experience maintaining written records of work in the form of laboratory notebooks (paper or electronic) is required. The ability to report data, present findings to management is required. Experience with team-based collaborations and direct/indirect management of staff is required. Occasional weekend work and domestic or international travel will be required. A pre-identified candidate for consideration has been identified. However, all applications will be considered. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center () or contact AskGS to be directed to your accommodation resource.

Press Tab to Move to Skip to Content Link The Company Sappi Biotech UK is part of the Sappi Group, a leading global provider of everyday materials made from woodfibre-based renewable resources and a diversified, innovative and trusted leader focused on sustainable processes and products. As part of the Group's ambition to construct biorefineries to convert pulping side-streams generated at our mills in South Africa, North America and Europe, the UK-based team are developing technologies to convert cellulose, sugars and lignin into high value products. More information can be found at: and Location Sappi Biotech UK, Wilton Centre, Redcar, North Yorkshire. Please note that the location has limited access via public transport. Position Description We are looking for a Senior Chemist to join a small and friendly team at the Wilton Centre. This is a permanent position and would suit anyone with a strong interest in innovation. In this position you will: • Design and lead technical development programmes and carry out high quality experimental work with a strong focus on safety. • Analyse, manage and interpret experimental data, record and report findings and provide recommendations for further activities. • Carry out analysis using a variety of techniques (HPLC, GC, GPC, FTIR), develop methods and use new techniques as required. • Carry out and develop tests to assess the performance of existing or newly developed products in relevant commercial application areas. • Work alone and in collaborative teams often involving scientists from other parts of the Sappi organisation. • Work at laboratory scale and small pilot scale (up to 20L). • Be involved in supplying data for process design of scale-up activities and support pilot plant activities at remote locations. • Provide technical support in discussions with external technology providers and our commercial teams. • Travel occasionally to Europe, South Africa and North America. Qualifications & Experience • Degree in chemistry (Masters or PhD) or analogous relevant experience in an industrial research laboratory. • Preferably 5 years minimum working experience. • Experience of using common laboratory analytical techniques. • Knowledge of lignins and lignocellulosic side-streams would be an advantage Profile • You are passionate about innovation. • You have excellent verbal and written communication and interpersonal skills. • You are self-motivated and well-organised. • You work effectively as part of a multi-disciplined team. • You are adaptable and versatile, happy to work in new areas or projects at short notice. Benefits In return for your expertise and innovation, we will provide you with; • a competitive salary • 25 days annual leave, excluding public holidays • Private health insurance • free parking ABOUT SAPPI Sappi isa leading global provider of everyday materials made from woodfibre-based renewable resources. As a diversified, innovative and trusted leader focused on sustainable processes and products, we are building a more circular economy by making what we should, not just what we can.

Press Tab to Move to Skip to Content Link The Company Sappi Biotech UK is part of the Sappi Group, a leading global provider of everyday materials made from woodfibre-based renewable resources and a diversified, innovative and trusted leader focused on sustainable processes and products. As part of the Group's ambition to construct biorefineries to convert pulping side-streams generated at our mills in South Africa, North America and Europe, the UK-based team are developing technologies to convert cellulose, sugars and lignin into high value products. More information can be found at: and Location Sappi Biotech UK, Wilton Centre, Redcar, North Yorkshire. Please note that the location has limited access via public transport. Position Description We are looking for a Senior Chemist to join a small and friendly team at the Wilton Centre. This is a permanent position and would suit anyone with a strong interest in innovation. In this position you will: • Design and lead technical development programmes and carry out high quality experimental work with a strong focus on safety. • Analyse, manage and interpret experimental data, record and report findings and provide recommendations for further activities. • Carry out analysis using a variety of techniques (HPLC, GC, GPC, FTIR), develop methods and use new techniques as required. • Carry out and develop tests to assess the performance of existing or newly developed products in relevant commercial application areas. • Work alone and in collaborative teams often involving scientists from other parts of the Sappi organisation. • Work at laboratory scale and small pilot scale (up to 20L). • Be involved in supplying data for process design of scale-up activities and support pilot plant activities at remote locations. • Provide technical support in discussions with external technology providers and our commercial teams. • Travel occasionally to Europe, South Africa and North America. Qualifications & Experience • Degree in chemistry (Masters or PhD) or analogous relevant experience in an industrial research laboratory. • Preferably 5 years minimum working experience. • Experience of using common laboratory analytical techniques. • Knowledge of lignins and lignocellulosic side-streams would be an advantage Profile • You are passionate about innovation. • You have excellent verbal and written communication and interpersonal skills. • You are self-motivated and well-organised. • You work effectively as part of a multi-disciplined team. • You are adaptable and versatile, happy to work in new areas or projects at short notice. Benefits In return for your expertise and innovation, we will provide you with; • a competitive salary • 25 days annual leave, excluding public holidays • Private health insurance • free parking ABOUT SAPPI Sappi isa leading global provider of everyday materials made from woodfibre-based renewable resources. As a diversified, innovative and trusted leader focused on sustainable processes and products, we are building a more circular economy by making what we should, not just what we can.

Oxford Nanopore Technologies is headquartered at the Oxford Science Park outside Oxford, UK, with satellite offices and a commercial presence in many global locations across the US, APAC and Europe. Oxford Nanopore employs from multiple subject areas including nanopore science, molecular biology and applications, informatics, engineering, electronics, manufacturing and commercialisation. The management team, led by CEO Dr Gordon Sanghera, has a track record of delivering disruptive technologies to the market. Oxford Nanopore's sequencing platform is the only technology that offers real-time analysis, in fully scalable formats from pocket to population scale, that can analyse native DNA or RNA and sequence any length of fragment to achieve short to ultra-long read lengths. Our goal is to enable the analysis of any living thing, by anyone, anywhere! We are looking for scientist with expertise in material science and experience of using ONT platforms to join the Chip Research team. This position will be focussed on the development and testing of future products, with a particular focus on current and voltage sensing platforms. The Details The role will primarily focus on cleanroom processing, with elements of wafer fabrication, materials science, and both wet and dry electrical testing. This position is part of a broader project aimed at implementing high-density sensing platforms. A graduate-level background (or equivalent) in Physics, Materials Science, Biomedical Engineering, Molecular Bioengineering, Chemistry, or a related field is required. Experience working with MEMS structures and nanofabrication is highly desirable. Strong knowledge of photolithography and micro/nanofabrication techniques is essential. Additionally, an understanding of surface properties in microfluidic systems-ideally supported by practical measurement experience-would be advantageous. What We're Looking For Essential Degree in Materials/ Engineering / Chemistry / Physics or related field (Masters preferable) or equivalent experience 2+ years experience in research / development environment Experience of working safely within a lab environment Experience of working with microfluidic devices Solid understanding of the fundamentals of surface science/material properties Hands-on experience of materials testing such as contact angle, microscopy SEM etc. Strong communication skills A Hands-on approach Desirable Experience with Python scripts and Spotfire analysis Cleanroom experience Role and Responsibilities Working under supervision and as part of a team, you will lead efforts to demonstrate new methods of array fabrication that can be transferred to emerging platforms, while also testing and evaluating the resulting structures. You will be responsible for exploring the potential of new materials, conducting material and surface analysis, performing characterisation, and contributing to design discussions. Additionally, you will test and assess the impact of implemented changes on platform performance, and be expected to report and present your findings. Duties include, but are not limited to: Design and fabrication of sensor related structures in a cleanroom environment to include photolithography processes Characterisation of materials and assembly processes using a range of techniques (contact angle, SEM, profilers, optical microscopy) Characterisation of surface and bulk properties of materials used for sensor manufacture The viability of new and novel materials for sensor layers upon new platforms Writing and editing electrical testing scripts Data analysis around relevant aspects of electrical testing Regular and timely communication between project team members to achieve optimal outcomes and performance Preparing technical reports, test procedures, process specifications and product documentation Providing input into experimental designs and method/protocol development We offer outstanding benefits to include an attractive bonus, generous pension contributions, private healthcare and an excellent starting salary. If you are looking to utilise your skills to really make a difference to humankind, then consider joining our team and apply today! Please note that no terminology in this advert is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Every candidate will be assessed only in accordance with their merits, qualifications and abilities to perform the duties of the job.

Job Title: Toxicology Safety Scientist Location: Colworth Science Park JOB PURPOSE At Unilever, we are committed to developing safe & sustainable products for our consumers. As a Toxicology Safety Scientist in our Safety, Environmental & Regulatory (SERS) team, you will provide scientific expertise to assure the safety of Unilever ingredients for consumers who use our products and the workers who make them. You will be joining a team of safety scientists, where you will be supported in your own development, while also being expected to help others grow in their roles. You will work as part of multidisciplinary teams (including biologists, bioinformaticians, computational chemists, and mathematical modellers), to apply novel, mechanistic approaches to safety assessment. You will also play a role in bringing robust, new science to our safety assessments, making sure that we meet both the current and future needs of Unilever. You will work alongside some of the industry's most respected scientists, learning new risk assessment approaches, growing as a professional and enjoying opportunities to publish and present. In addition, of course, you will have fantastic career opportunities within a successful global company that is focused on winning every day. The role is based in the dynamic environment of our SERS team at Colworth Science Park, Sharnbrook located near Bedford. RESPONSIBILITIES Assess human safety risks associated with ingredients with an emphasis on applying novel (non-animal) approaches. Deliver transparent, well documented, exposure-based risk assessments to enable robust decision-making. This will include clearly communicating the outcomes of these risk assessments, providing input to broader communication to maintain trust in the safe use of Unilever products. Contribute to the evolution of our approach to exposure-driven risk assessment including working with external groups. Build an understanding of the wider issues surrounding the use of ingredients and products. Be part of a team making an impact internally & externally on the way in which safety risk assessments are conducted and communicated now and in the future. Work closely with other SERS and Unilever scientists, as well as external collaborators, to provide expert scientific advice on new scientific approaches to non-animal safety assessment. Promote the acceptance and adoption of new scientific approaches external to Unilever through interactions with key opinion formers with international reputation and influence. ALL ABOUT YOU You'll need to be able to work effectively and with impact in cross-disciplinary teams and in multi-cultural environments, be flexible and willing to adapt within a fast-changing business environment. We would expect the successful candidate to have: A degree (BSc/MSc or equivalent) in Toxicology or a related discipline with relevant experience in commercial product safety or industrial/occupational health Experience of toxicology/consumer safety risk assessment and its application in an industrial context (FMCG, healthcare setting) Awareness of novel, non-animal approaches to safety assessment and their potential application for decision-making Excellent written & verbal communication skills including ability to convey scientific subject matter in a simple manner Evidence of a creative, problem-solving mindset Highly self-motivated, with a proven track record of collaborating effectively in interdisciplinary teams Ability to work with scientists from other disciplines as part of multidisciplinary teams. Strong team player, as both a leader and a team member Desirable Knowledge of different approaches to the risk assessment of carcinogens Post graduate experience or a higher degree/ qualification (e.g., PhD) Knowledge/Experience of product safety regulations Project leadership experience Understanding of computational approaches applied to consumer safety risk assessment/Toxicology NOTES About Unilever Unilever is one of the world's leading suppliers of Food, Home and Personal Care products with sales in over 190 countries and reaching 2 billion consumers a day. Unilever has more than 400 brands found in homes around the world, including Dove, Tresemme, Lynx, Lifebuoy, Shea Moisture, Persil, Domestos, Ben & Jerry's, Magnum, Marmite, The Vegetarian Butcher, Graze and Pot Noodle. Faced with the challenge of climate change and the need for human development, we want to move towards a world where everyone can live well and within the natural limits of the planet. That's why our purpose is 'to make sustainable living commonplace' What We Offer Not only do we offer a competitive salary and pension scheme, we also offer an annual bonus, subsidised gym membership, a discounted staff shop and shares. You'll have the opportunity to work directly with our renowned and exciting brands in a flexible and hybrid working environment. Whilst the role is advertised on a full-time basis, we would be happy to discuss possible flexible working options and what this may look like for you. We are a key advocate of wellbeing and offer a variety of support for our people including hubs, programmes and development opportunities. We strive to achieve a family-friendly and inclusive workplace and to, above all, create possibilities for all. Diversity at Unilever is about inclusion, embracing differences, creating possibilities and growing together for better business performance. We embrace diversity in our workforce. This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity. We are also more than happy to provide reasonable adjustments during our application and interview process to enable you to be present your best self. To find out more, including about our Employee Resource Groups, please click here Equity, Diversity & Inclusion at Unilever Unilever . Recruitment Fraud Cyber criminals advertise fake job adverts with prestigious employers as a way of stealing information or even defrauding individuals out of money. In the most sophisticated cases, they will set up fake websites, which have a similar address to companies like Unilever. They even conduct fake telephone interviews and then offer candidates a role with the proviso they pay a fee for background checks or to cover work visa costs. These types of attacks are becoming more common as more people are looking for employment in the economic climate. How is Unilever tackling this? Many of Unilever's recruitment sites publish a warning to candidates about recruitment fraud. The Cyber Security team also proactively scan for signs of people setting up fake Unilever sites and act to close them down. What can I do? If you become aware of potential recruitment fraud, spot fake Unilever recruitment adverts or fake LinkedIn profiles, report them via Una Live Chat. Unilever does not accept responsibility or liability for any candidates who are financially impacted by recruitment fraud. Your vigilance is key!

At Elanco (NYSE: ELAN) it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. We're driven by our vision of 'Food and Companionship Enriching Life' and our approach to sustainability the Elanco Healthy Purpose to advance the health of animals, people, the planet and our enterprise. At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights. Making animals' lives better makes life better join our team today! Job description: There is an exciting opportunity to join a dynamic process development team responsible for development and scale up of new biopharmaceutical and vaccine products. The Biopharma technical development team works collaboratively with an inclusive culture to deliver innovation for Elanco. This is a Global Lead Scientist role responsible for developing process for biopharma projects in R&D pipelines with an emphasis on downstream purification processes. The individual is expected to provide overarching technical and scientific expertise for process development and commercialization activities of new drug substances. This position is expected to be a senior technical expert for R&D Elanco globally and will work collaboratively with management and global project groups in line with site, functional and corporate business goals. The individual will be expected to lead downstream process development, scale up, technical transfers, process implementation, and material delivery activities for IVP or CT supply and registration. Additionally, the role will support process validation-related activities. The role is focused on ensuring that a robust manufacturing process is developed according to quality by design and 'end in mind' principles. The role is expected to be hands on but will provide technical direction, coaching and mentoring to scientists. Key Responsibilities: Provide technical leadership for downstream development (protein purification) from early through late phase large molecule projects, ensuring phase appropriate technical development and collaborating closely with relevant functions. Provide technical leadership/expertise for delivery of process development projects based in the laboratories and pilot plant areas. Ensure a sound laboratory/pilot plant program in alignment with global requirements, establishment of robust control strategies and successful product launch. Provide oversight for technical transfers and scale up into Speke pilot plant for delivery of pivotal materials. Ensure that project work is carried out with necessary scientific rigor across the team for quality data output. Responsible for ensuring use of sound statistical data methodology to design and execute experimental work as part of routine day-to-day projects. Lead Quality by Design and applying principles for development of control strategy and design space through experimentation. Support successful commercialization of new products strategically and tactically by partnering across functions. Provide leadership for technical transfers, process implementation, and material delivery activities for pivotal Investigational Product (IVP or CT) supply, registration, and validation batches internally or with external partners. Participate in the evaluation of new business opportunities through the processes of due diligence, product reviews, and cost modelling. Serve as a technical resource across Elanco and apply technical expertise to scientific problems to support across the network. Responsible for coaching and mentoring development scientists. Ensure delivery of high-quality technical reports, provide technical review for team development reports. Foster a collaborative culture, develop internal and external links. Highlight new technologies, build future capabilities, and influence strategy. Qualifications & experience: Preferred advanced degree in a scientific discipline (biochemistry, biotechnology/biologics or related discipline). Or degree with significant industrial experience. 10+ years of relevant experience in development/commercialization activities for pharmaceutical or vaccine products, or other relevant experience. Demonstrated success in the development and commercialization of new pharmaceutical or vaccine technologies (e.g. API, drug product, drug substance development; analytical method transfer; and/or packaging). Experience in regulated environments and working under Good Manufacturing Practices. Good knowledge and understanding of protein chemistry. Understanding of potential CQAs, process and product related impurities and stability needs. Strong problem-solving skills, including strategic and creative thinking. Strong interpersonal skills with demonstrated ability to collaborate with and influence teams. Ability to handle multiple priorities and deal with ambiguity. Strong presentation skills and scientific/technical writing skills. Ability to work in interdisciplinary teams, influence diverse groups and effectively manage relationships. Demonstrated ability to mentor and develop coworkers with a diverse background. Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status

Are you ready to make a groundbreaking impact in the world of biotechnology? Join a growing company that's shaping the future of healthcare and science. Hobson Prior is seeking an MSAT Senior Scientist I (DSP) or MSAT Scientist II (DSP) to focus on developing processes for manufacturing gene therapies. You will work on improving and scaling up production methods, ensuring they are efficient and reliable. This position involves working closely with a team while also taking initiative to drive projects forward. Please note that to be considered for this role you must have the right to work in this location. Responsibilities: Develop methods for purifying and preparing gene therapy products. Scale up lab processes for larger production. Lead and document experiments. Guide and support junior team members. Continuously improve processes for consistency and reliability. Assist in implementing new methods and solving production issues. Innovate and explore new technologies and tools. Use data analysis to enhance process understanding and find improvements. Key Skills and Requirements: Background in chemical or biochemical engineering or biochemistry. Experience in developing and scaling up production processes. Knowledge of purification techniques like chromatography and filtration. Familiarity with large-scale manufacturing standards. Ability to use statistical and modeling software. Strong analytical and problem-solving skills. Effective communication and teamwork abilities. Innovative thinking and adaptability to change. For more information, please contact Jessica Taylor . If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data -