The Role At Notpla, we're at the forefront of sustainable innovation, creating natural alternatives to single-use plastic packaging that are carefully engineered to help build a healthier planet. Founded on the belief that nature knows best, we're an innovative, action-oriented scale-up developing and manufacturing uncompromisingly natural packaging solutions from seaweed and plants. As a Laboratory Technician you will support our R&D team in developing and testing innovative natural polymer materials. This role is perfect for someone eager to learn, with an interest in material science, chemistry or engineering. You will gain hands-on experience in a lab environment, working with cutting-edge materials and processes while developing key analytical and technical skills. This is an exciting time to join Notpla - we're on the brink of a record-breaking year for revenue and on track for major growth in the next 18-24 months. To support this, we have just secured a £20 million Series A+ fundraise, enabling us to scale our growth and environmental impact faster than ever. Beyond offering meaningful roles and a vibrant working environment, Notpla provides competitive compensation, including EMI Share Options, a zero-carbon pension scheme, discounts with local businesses, and subsidised social activities. Our office-first hybrid working policy lets you work in the way that maximises your productivity while maintaining a dynamic and collaborative atmosphere. We're a social business with regular clubs and events, and we're proud of how our diverse, mission-driven community works together to make plastic disappear. Led by strong values, all Notpla employees are encouraged to take ownership of their domain, enjoying a high degree of autonomy. Our aim is to build an inspiring culture reflected in our working policies, environment, and people. As a Laboratory Technician you will be trained in advanced lab techniques and analytical tools and gain hands-on experience working with natural polymer materials and extrusion technologies. You will assist our R&D team while also receiving mentorship and support from experienced scientists and engineers. The role will have opportunities to work on innovative projects with real-world applications. In order to succeed in this role you will need a strong technical background in science-related subjects such as Chemistry, Physics, Biology or Engineering. You are a self starter with a strong work ethic, attention to detail, excellent time management and problem-solving skills. Proven track record of working safely and following protocols in a lab environment. Experience in running lab operations (e.g. raw material goods-in, 5S, health and safety) is a plus. Key Responsibilities Measure and analyse material properties, including barrier properties, rheology and contact angle measurements. Assist with preparation of lab and pilot scale batches of biomaterials for further testing. Assist in preparing and testing formulations in a laboratory setting. Maintain lab equipment, ensure safe working practices, and follow lab protocols. Accurately record and report experimental data in a useful format. Facilitate external testing where required.
Mar 13, 2026
Full time
The Role At Notpla, we're at the forefront of sustainable innovation, creating natural alternatives to single-use plastic packaging that are carefully engineered to help build a healthier planet. Founded on the belief that nature knows best, we're an innovative, action-oriented scale-up developing and manufacturing uncompromisingly natural packaging solutions from seaweed and plants. As a Laboratory Technician you will support our R&D team in developing and testing innovative natural polymer materials. This role is perfect for someone eager to learn, with an interest in material science, chemistry or engineering. You will gain hands-on experience in a lab environment, working with cutting-edge materials and processes while developing key analytical and technical skills. This is an exciting time to join Notpla - we're on the brink of a record-breaking year for revenue and on track for major growth in the next 18-24 months. To support this, we have just secured a £20 million Series A+ fundraise, enabling us to scale our growth and environmental impact faster than ever. Beyond offering meaningful roles and a vibrant working environment, Notpla provides competitive compensation, including EMI Share Options, a zero-carbon pension scheme, discounts with local businesses, and subsidised social activities. Our office-first hybrid working policy lets you work in the way that maximises your productivity while maintaining a dynamic and collaborative atmosphere. We're a social business with regular clubs and events, and we're proud of how our diverse, mission-driven community works together to make plastic disappear. Led by strong values, all Notpla employees are encouraged to take ownership of their domain, enjoying a high degree of autonomy. Our aim is to build an inspiring culture reflected in our working policies, environment, and people. As a Laboratory Technician you will be trained in advanced lab techniques and analytical tools and gain hands-on experience working with natural polymer materials and extrusion technologies. You will assist our R&D team while also receiving mentorship and support from experienced scientists and engineers. The role will have opportunities to work on innovative projects with real-world applications. In order to succeed in this role you will need a strong technical background in science-related subjects such as Chemistry, Physics, Biology or Engineering. You are a self starter with a strong work ethic, attention to detail, excellent time management and problem-solving skills. Proven track record of working safely and following protocols in a lab environment. Experience in running lab operations (e.g. raw material goods-in, 5S, health and safety) is a plus. Key Responsibilities Measure and analyse material properties, including barrier properties, rheology and contact angle measurements. Assist with preparation of lab and pilot scale batches of biomaterials for further testing. Assist in preparing and testing formulations in a laboratory setting. Maintain lab equipment, ensure safe working practices, and follow lab protocols. Accurately record and report experimental data in a useful format. Facilitate external testing where required.
Posted Thursday, February 26, 2026 at 6:00 AM Quotient Sciences: Molecule to Cure. Fast. Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and Clinical (CRO) services across the entire development pathway, including formulation development, clinical pharmacology, clinical trials, and commercial product manufacturing. Our proprietary and disruptive platform - "Translational Pharmaceutics " - integrates Drug Product Manufacturing and Clinical Testing to eliminate silos in the drug development process. This in turn reduces costs, improves outcomes, and significantly accelerates drug development times. Why join us: Because every day counts when bringing new medicines to patients. Our 1,000+ experts across the US, UK, and beyond are united by science, agility, and a culture that turns ideas into impact-fast. The Role This is an excellent opportunity to contribute to the development of innovative drug products that progress quickly into clinical manufacture. As part of our formulation development team, you will support both formulation and radiolabelling activities that underpin Quotient Sciences' integrated Translational Pharmaceutics offering. Working within a regulated environment, you will help design, prepare, characterise and transfer formulations and radiolabelling methods into GMP clinical manufacturing, ensuring each process is robust, compliant and ready for clinical delivery. Main Responsibilities Plan and conduct experiments in line with agreed schedules, ensuring accurate protocol development. Prepare and characterise formulations for pre clinical and clinical use. Support development and validation of radiolabelling methods for clinical studies. Transfer formulation and radiolabelling methods into GMP clinical manufacture, contributing to protocol design, validation criteria and operational parameters. Work in accordance with GMP, GxP guidance and all relevant regulations. Manage the safe storage, use and disposal of radioactive isotopes following PP SOPs and liaise with the Radiation Protection Supervisor or Deputy as required. Maintain clear, detailed and accurate laboratory records. Analyse results accurately and in line with protocols/SOPs. Write internal and external reports as needed. Communicate experimental progress to senior managers or internal project teams. Perform routine cleaning, housekeeping and general laboratory duties. Maintain confidentiality and carry out additional duties as reasonably required. Skills/Experience Required Degree in pharmacy, chemistry or a related scientific discipline. Experience in formulation development is desirable; knowledge of radioisotopes beneficial but not essential. Experience working to cGMP standards is an advantage. Strong attention to detail and high quality documentation skills. Ability to work safely, responsibly and collaboratively in a laboratory environment. Strong communication and organisational skills. Application Requirements When applying for a position with Quotient Sciences to be able to work in our organization you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined. Our Commitment to Diversity, Equity and Inclusion Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of acceptance for every person within our organization. As a global employer, we recognize the value in having an organization that is a true reflection and representation of our society today. Specifically we will not discriminate on the basis of race, color, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws. This applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.
Mar 12, 2026
Full time
Posted Thursday, February 26, 2026 at 6:00 AM Quotient Sciences: Molecule to Cure. Fast. Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and Clinical (CRO) services across the entire development pathway, including formulation development, clinical pharmacology, clinical trials, and commercial product manufacturing. Our proprietary and disruptive platform - "Translational Pharmaceutics " - integrates Drug Product Manufacturing and Clinical Testing to eliminate silos in the drug development process. This in turn reduces costs, improves outcomes, and significantly accelerates drug development times. Why join us: Because every day counts when bringing new medicines to patients. Our 1,000+ experts across the US, UK, and beyond are united by science, agility, and a culture that turns ideas into impact-fast. The Role This is an excellent opportunity to contribute to the development of innovative drug products that progress quickly into clinical manufacture. As part of our formulation development team, you will support both formulation and radiolabelling activities that underpin Quotient Sciences' integrated Translational Pharmaceutics offering. Working within a regulated environment, you will help design, prepare, characterise and transfer formulations and radiolabelling methods into GMP clinical manufacturing, ensuring each process is robust, compliant and ready for clinical delivery. Main Responsibilities Plan and conduct experiments in line with agreed schedules, ensuring accurate protocol development. Prepare and characterise formulations for pre clinical and clinical use. Support development and validation of radiolabelling methods for clinical studies. Transfer formulation and radiolabelling methods into GMP clinical manufacture, contributing to protocol design, validation criteria and operational parameters. Work in accordance with GMP, GxP guidance and all relevant regulations. Manage the safe storage, use and disposal of radioactive isotopes following PP SOPs and liaise with the Radiation Protection Supervisor or Deputy as required. Maintain clear, detailed and accurate laboratory records. Analyse results accurately and in line with protocols/SOPs. Write internal and external reports as needed. Communicate experimental progress to senior managers or internal project teams. Perform routine cleaning, housekeeping and general laboratory duties. Maintain confidentiality and carry out additional duties as reasonably required. Skills/Experience Required Degree in pharmacy, chemistry or a related scientific discipline. Experience in formulation development is desirable; knowledge of radioisotopes beneficial but not essential. Experience working to cGMP standards is an advantage. Strong attention to detail and high quality documentation skills. Ability to work safely, responsibly and collaboratively in a laboratory environment. Strong communication and organisational skills. Application Requirements When applying for a position with Quotient Sciences to be able to work in our organization you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined. Our Commitment to Diversity, Equity and Inclusion Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of acceptance for every person within our organization. As a global employer, we recognize the value in having an organization that is a true reflection and representation of our society today. Specifically we will not discriminate on the basis of race, color, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws. This applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.
A leading drug development and manufacturing company in the United Kingdom seeks a Formulation Development Scientist to support innovative drug product development. The successful candidate will plan experiments, prepare formulations for clinical use, and ensure GMP compliance in a collaborative lab environment. Ideal applicants will have a degree in pharmacy, chemistry or a related field, along with a desire to enhance their skills in formulation and radiolabelling methods. This position offers an impactful career in an organization committed to diversity and advancement.
Mar 12, 2026
Full time
A leading drug development and manufacturing company in the United Kingdom seeks a Formulation Development Scientist to support innovative drug product development. The successful candidate will plan experiments, prepare formulations for clinical use, and ensure GMP compliance in a collaborative lab environment. Ideal applicants will have a degree in pharmacy, chemistry or a related field, along with a desire to enhance their skills in formulation and radiolabelling methods. This position offers an impactful career in an organization committed to diversity and advancement.
Vacancies Scientist - Formulation Development Job Introduction Why Dechra? Thank you for checking out our vacancy, we're delighted you want to learn more about joining Dechra. Dechra is a growing, global specialist within the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing and sales of high quality products exclusively for veterinarians worldwide. Here at Dechra, our values are embedded within our culture and thrive within our family of almost 3000 colleagues globally. From manufacturing to marketing, (D)edication, (E)njoyment, (C)ourage, (H)onesty, (R)elationships and (A)mbition are at the heart of our everyday operations and the way we do business. The Opportunity Dechra is an international specialist veterinary pharmaceuticals products business. Our expertise lies in the development, manufacture, sales and marketing of high quality products exclusively for veterinarians worldwide. The Scientist Formulation Development role contributes to the successful and timely development of novel and generic pharmaceutical products, via the development, preparation and selection of appropriate and physically/chemically stable formulations for a variety of dosage forms. The incumbent should have a high degree of independence in the conduct of laboratory scale research and development programmes. They will be responsible for drug product formulation development in support of (pre)clinical and stability studies, contribute to the design of the manufacturing process and support the scale of up for manufacturing of registration batches. The incumbent participates in execution of Dechra development projects and can participate in international cross-functional and cross-site project teams. Solid dosage forms (tablets) are the primary (but not exclusively) products developed and evaluated by the Skipton team. Role Responsibilities So, what will you be doing? This role has a broad and varied remit and the successful candidate will have responsibility for duties including: Development and characterisation of appropriate formulations(and their constituents e.g. API) and selection of packages to meet marketing, clinical and regulatory requirements (target product profile) Manufacture small (laboratory) scale formulation batches using processes that are appropriate for manufacturing on a commercial scale, for use in characterization, non-clinical and clinical testing (such as direct compression, wet granulation, fluid bed drying/granulation, tablet coating). Contribute to the to technology transfer (scale-up) to manufacturing site. Competent in the handling of tablet manufacturing equipment, such as blending, granulation and compression equipment and physical characterisation tools to analyse the formulations. Keeping up to date with advances in formulation and manufacturing technology. Applies key API and/or formulation physicochemical data to support development process and identify the root cause of potential R&D, stability and performance issues (eg.pKa, pH, solubility, disintegration, dissolution, particle size, HPLC assay, etc.) Actively contributes to planning, developing and implementation of scientifically well-designed experimental programs and demonstrates creativity and capability in pharmaceutical research and development (with support from senior colleagues as required). Adheres to departmental and Dechra EH&S requirements. Adheres to Dechra SOP and GMP requirements. Accurately and contemporaneously records experimental procedures, test results and observations and reviews data to meet corporate and regulatory requirements. Actively manages priorities and schedules experimental work etc to meet or exceed project milestones in collaboration with analytical and other CMC colleagues. Regularly communicates project progress, challenges and potential delays to stakeholders. As applicable, arranges/performs Preventative Maintenance (PM) and Performance Qualification (PQ) for equipment for which they are responsible. Authors and reviews technical documents, such as protocols, reports, batch records, and operating procedures. Assists in preparation of Chemistry, Manufacturing and Control (CMC) documents for Regulatory submission Actively manages working relationships through engagement with cross-functional and cross-site teams in the design and execution of studies e.g. technical services/manufacturing, clinical, regulatory, QA/QC etc. Reports project progress against technical and project objectives to Product Development Manager, CMC (CMC lead)and Pharmaceutical Development Manager (functional line management). The Candidate Here at Dechra we pride ourselves on being an inclusive employer. We know that individuals' unique background and experience can bring a wealth of variety and expertise to our global workforce. For this role, we're particularly keen to hear from those who have/are: Bachelor's Degree in a relevant field e.g. Chemistry, Pharmaceutical Sciences and Cosmetic Science. Hands on experience in formulation development in at least one dosage forms. At Scientist level, considerable past formulation experience is essential to role. However, applications are encouraged from candidates with limited practical experience in formulation as there is potential for you to be considered for a more junior role instead. Hands on experience in formulation development of a variety of dosage forms, some past tablet experience is essential to role . Good working knowledge of physical and chemical techniques used to characterise raw materials and finished products. Desirable Working knowledge of regulatory requirements, including FDA, EMEA, VICH/ICH regulations. Experience in some of the following; solids: direct compression, wet and dry granulation, liquids, suspensions. Master's Degree in a relevant field e.g. Chemistry, Pharmaceutical Sciences, Pharmacy For the more junior role, at least a year-sandwich placement in a commercial setting working in formulation development will be required. What we can offer you 30 days annual (inclusive of Bank Holidays) 9 day working fortnight (every 2nd Friday off) Holiday purchase scheme Healthcare Employee Assistance Program Life Assurance 8% Employer Pension Contribution Enhanced Family Leave Discounted Pet Food About the Company All applications received are reviewed by our internal talent acquisition team and we will get in touch if your skills and experience match what we're looking for. Should you not hear back from us within 28 days please don't be too disappointed - we may keep your CV on our database for any future vacancies which could be suitable, and we encourage you to keep an eye on our careers site. We value diversity within our global workforce and encourage an inclusive culture. Any questions or queries, please contact us at
Mar 12, 2026
Full time
Vacancies Scientist - Formulation Development Job Introduction Why Dechra? Thank you for checking out our vacancy, we're delighted you want to learn more about joining Dechra. Dechra is a growing, global specialist within the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing and sales of high quality products exclusively for veterinarians worldwide. Here at Dechra, our values are embedded within our culture and thrive within our family of almost 3000 colleagues globally. From manufacturing to marketing, (D)edication, (E)njoyment, (C)ourage, (H)onesty, (R)elationships and (A)mbition are at the heart of our everyday operations and the way we do business. The Opportunity Dechra is an international specialist veterinary pharmaceuticals products business. Our expertise lies in the development, manufacture, sales and marketing of high quality products exclusively for veterinarians worldwide. The Scientist Formulation Development role contributes to the successful and timely development of novel and generic pharmaceutical products, via the development, preparation and selection of appropriate and physically/chemically stable formulations for a variety of dosage forms. The incumbent should have a high degree of independence in the conduct of laboratory scale research and development programmes. They will be responsible for drug product formulation development in support of (pre)clinical and stability studies, contribute to the design of the manufacturing process and support the scale of up for manufacturing of registration batches. The incumbent participates in execution of Dechra development projects and can participate in international cross-functional and cross-site project teams. Solid dosage forms (tablets) are the primary (but not exclusively) products developed and evaluated by the Skipton team. Role Responsibilities So, what will you be doing? This role has a broad and varied remit and the successful candidate will have responsibility for duties including: Development and characterisation of appropriate formulations(and their constituents e.g. API) and selection of packages to meet marketing, clinical and regulatory requirements (target product profile) Manufacture small (laboratory) scale formulation batches using processes that are appropriate for manufacturing on a commercial scale, for use in characterization, non-clinical and clinical testing (such as direct compression, wet granulation, fluid bed drying/granulation, tablet coating). Contribute to the to technology transfer (scale-up) to manufacturing site. Competent in the handling of tablet manufacturing equipment, such as blending, granulation and compression equipment and physical characterisation tools to analyse the formulations. Keeping up to date with advances in formulation and manufacturing technology. Applies key API and/or formulation physicochemical data to support development process and identify the root cause of potential R&D, stability and performance issues (eg.pKa, pH, solubility, disintegration, dissolution, particle size, HPLC assay, etc.) Actively contributes to planning, developing and implementation of scientifically well-designed experimental programs and demonstrates creativity and capability in pharmaceutical research and development (with support from senior colleagues as required). Adheres to departmental and Dechra EH&S requirements. Adheres to Dechra SOP and GMP requirements. Accurately and contemporaneously records experimental procedures, test results and observations and reviews data to meet corporate and regulatory requirements. Actively manages priorities and schedules experimental work etc to meet or exceed project milestones in collaboration with analytical and other CMC colleagues. Regularly communicates project progress, challenges and potential delays to stakeholders. As applicable, arranges/performs Preventative Maintenance (PM) and Performance Qualification (PQ) for equipment for which they are responsible. Authors and reviews technical documents, such as protocols, reports, batch records, and operating procedures. Assists in preparation of Chemistry, Manufacturing and Control (CMC) documents for Regulatory submission Actively manages working relationships through engagement with cross-functional and cross-site teams in the design and execution of studies e.g. technical services/manufacturing, clinical, regulatory, QA/QC etc. Reports project progress against technical and project objectives to Product Development Manager, CMC (CMC lead)and Pharmaceutical Development Manager (functional line management). The Candidate Here at Dechra we pride ourselves on being an inclusive employer. We know that individuals' unique background and experience can bring a wealth of variety and expertise to our global workforce. For this role, we're particularly keen to hear from those who have/are: Bachelor's Degree in a relevant field e.g. Chemistry, Pharmaceutical Sciences and Cosmetic Science. Hands on experience in formulation development in at least one dosage forms. At Scientist level, considerable past formulation experience is essential to role. However, applications are encouraged from candidates with limited practical experience in formulation as there is potential for you to be considered for a more junior role instead. Hands on experience in formulation development of a variety of dosage forms, some past tablet experience is essential to role . Good working knowledge of physical and chemical techniques used to characterise raw materials and finished products. Desirable Working knowledge of regulatory requirements, including FDA, EMEA, VICH/ICH regulations. Experience in some of the following; solids: direct compression, wet and dry granulation, liquids, suspensions. Master's Degree in a relevant field e.g. Chemistry, Pharmaceutical Sciences, Pharmacy For the more junior role, at least a year-sandwich placement in a commercial setting working in formulation development will be required. What we can offer you 30 days annual (inclusive of Bank Holidays) 9 day working fortnight (every 2nd Friday off) Holiday purchase scheme Healthcare Employee Assistance Program Life Assurance 8% Employer Pension Contribution Enhanced Family Leave Discounted Pet Food About the Company All applications received are reviewed by our internal talent acquisition team and we will get in touch if your skills and experience match what we're looking for. Should you not hear back from us within 28 days please don't be too disappointed - we may keep your CV on our database for any future vacancies which could be suitable, and we encourage you to keep an eye on our careers site. We value diversity within our global workforce and encourage an inclusive culture. Any questions or queries, please contact us at
About Sava All the health information we need is within us. Just below the skin. SAVA is redefining the way people interact with their health by developing the most advanced biosensing technology science has to offer, capable of accessing bodily information in a painless, real-time and affordable way. The Role We are seeking an exceptional Senior Scientist to join our New Analyte Team within the Biosensing and In Vivo Performance Department. This role will be directly reporting into the New Analyte Team Lead. This role is critical to future sensor development, focusing on the development of novel enzymatic and non-enzymatic based sensing technologies which will help shape and define the future of this company. This is a highly practical hands on role which will require a meticulous and tenacious approach to work. We're looking for someone willing to own end to end sensor development cycles from upstream process development to downstream performance testing and characterisation. The ideal candidate will have demonstrated excellence in process science, chemistry, or biotechnology; solid understanding of designing and executing experiments to capture quantitative data, with the ability to translate findings into actionable product and performance improvements. A track record of taking initiative-identifying problems, proposing solutions, and seeing them through to completion without waiting to be directed. The determination and curiosity to push through setbacks and iterate toward breakthroughs. What You'll Do Work within the New Analyte Team to develop and characterise novel sensing blend formulations using defined Process tools and QC instrumentation. Collaborate with the Synthesis, Process, and Biomaterials teams to learn, optimise and implement material and process changes for improved sensor performance. Build upon and develop existing protocols to further the understanding of various aspects of materials and processes used in sensor manufacturing and performance characterisation. Develop explorative trials, including DoE trials, that investigate material and process parameters to optimise sensor performance. Carry out performance testing of new sensing formulations. Generate, analyse and report data to the team and wider company, verbally and in writing. Research and implement novel test methods and experimental procedures support characterisation. Liaise with internal and external stakeholders to coordinate projects, manage deadlines and requirements in parallel to advancing device development. Support internal and external collaborations with vendors and research groups. What We're Looking For BSc degree or above, and at least 2-4 years lab experience in a relevant discipline (e.g., chemistry, process science, materials science). Experience in a lab/industry working with process development and characterisation. Hands on experience in a biotechnology, process chemistry or synthetic chemistry laboratory setting, either through university research projects, industry positions, and/or internships. A multidisciplinary background is highly advantageous. The candidate will be expected to work cross functionally with teams including Biosensing, Synthetic Chemistry, Manufacturing, Data and Engineering, which may include: process characterisation, new material investigation, medical device manufacture, sterilisation, in vitro testing, enzyme stability and activity, microscopy (Keyence experience), operation of precision dispensing systems. Bonus Points For Experience working in a start up environment. Working knowledge of electrochemical testing using Palmsense hardware/software. Working knowledge of Precision Dispensing equipment. Why Sava? This is a high ownership, high responsibility role in a company that's building something complex, meaningful, and fast. The expectations are high, the learning curve is steep, and the work is often messy - but the impact is real. We don't have room for egos or passengers. What we do have is a team of thoughtful, driven, and mission aligned people who are committed to building something better-and doing it with urgency and integrity.
Mar 11, 2026
Full time
About Sava All the health information we need is within us. Just below the skin. SAVA is redefining the way people interact with their health by developing the most advanced biosensing technology science has to offer, capable of accessing bodily information in a painless, real-time and affordable way. The Role We are seeking an exceptional Senior Scientist to join our New Analyte Team within the Biosensing and In Vivo Performance Department. This role will be directly reporting into the New Analyte Team Lead. This role is critical to future sensor development, focusing on the development of novel enzymatic and non-enzymatic based sensing technologies which will help shape and define the future of this company. This is a highly practical hands on role which will require a meticulous and tenacious approach to work. We're looking for someone willing to own end to end sensor development cycles from upstream process development to downstream performance testing and characterisation. The ideal candidate will have demonstrated excellence in process science, chemistry, or biotechnology; solid understanding of designing and executing experiments to capture quantitative data, with the ability to translate findings into actionable product and performance improvements. A track record of taking initiative-identifying problems, proposing solutions, and seeing them through to completion without waiting to be directed. The determination and curiosity to push through setbacks and iterate toward breakthroughs. What You'll Do Work within the New Analyte Team to develop and characterise novel sensing blend formulations using defined Process tools and QC instrumentation. Collaborate with the Synthesis, Process, and Biomaterials teams to learn, optimise and implement material and process changes for improved sensor performance. Build upon and develop existing protocols to further the understanding of various aspects of materials and processes used in sensor manufacturing and performance characterisation. Develop explorative trials, including DoE trials, that investigate material and process parameters to optimise sensor performance. Carry out performance testing of new sensing formulations. Generate, analyse and report data to the team and wider company, verbally and in writing. Research and implement novel test methods and experimental procedures support characterisation. Liaise with internal and external stakeholders to coordinate projects, manage deadlines and requirements in parallel to advancing device development. Support internal and external collaborations with vendors and research groups. What We're Looking For BSc degree or above, and at least 2-4 years lab experience in a relevant discipline (e.g., chemistry, process science, materials science). Experience in a lab/industry working with process development and characterisation. Hands on experience in a biotechnology, process chemistry or synthetic chemistry laboratory setting, either through university research projects, industry positions, and/or internships. A multidisciplinary background is highly advantageous. The candidate will be expected to work cross functionally with teams including Biosensing, Synthetic Chemistry, Manufacturing, Data and Engineering, which may include: process characterisation, new material investigation, medical device manufacture, sterilisation, in vitro testing, enzyme stability and activity, microscopy (Keyence experience), operation of precision dispensing systems. Bonus Points For Experience working in a start up environment. Working knowledge of electrochemical testing using Palmsense hardware/software. Working knowledge of Precision Dispensing equipment. Why Sava? This is a high ownership, high responsibility role in a company that's building something complex, meaningful, and fast. The expectations are high, the learning curve is steep, and the work is often messy - but the impact is real. We don't have room for egos or passengers. What we do have is a team of thoughtful, driven, and mission aligned people who are committed to building something better-and doing it with urgency and integrity.
1100 Mylan Pharmaceuticals Inc.
Stone Cross, Sussex
Analytical Scientist page is loaded Analytical Scientistlocations: Sandwich, England, United Kingdomtime type: Tiempo completoposted on: Publicado hace 2 díasjob requisition id: RMylan Pharma UK LimitedEn VIATRIS, vemos la atención médica no como es, sino como debería de ser. Actuamos con valentía y estamos en una posición única para ser una fuente de estabilidad en un mundo de necesidades de atención médica en constante evolución.Viatris ayuda a las personas de todo el mundo a vivir de manera más saludable en cada etapa de la vida.Lo hacemos a través de:Acceso - suministrando medicamentos de confianza y de alta calidad independientemente de la geografía o las circunstancias;Liderazgo - promoviendo operaciones sostenibles y soluciones innovadoras para mejorar la salud del paciente;Colaboración - aprovechando nuestra experiencia común para conectar a las personas con productos y servicios.Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment.For those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place to work. This is a place to make a difference in the world. The Role & What You Will Be Doing Every day, we rise to the challenge to make a difference and here's how the Analytical Scientist role will make an impact: Working within our Materials Science team, carry out all analytical activities required to deliver new respiratory products to clinical studies and commercialization Plan and execute experiments to generate scientific understanding in development of analytical methods, formulations and processes. Perform analyses related to clinical supplies, stability, and process scale up. Process data, interpret results and report experimental outcomes to project development team. Troubleshoot instrumentation and investigate aberrant sample results. Maintain laboratory documentation in accordance with cGMP documentation practices. Contribute to project delivery by carrying out other tasks (e.g. laboratory housekeeping, ordering, shipping samples) as required. Adherence to all applicable policies and procedures, including those relating to EHS, GMP, GCP, Quality and Compliance, consistent with the role and any associated responsibilities, including people management where applicable. Perform other duties as assigned consistent with the grade of the role About Your Skills & Experience For this role, we're looking for a candidate who has an effective combination of the following qualifications, skills and experiences: Relevant Bachelor of Science Degree (for example Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics) or equivalent, or substantial practical work experience. Good understanding of basic principles of physical, organic and analytical chemistry. Familiar with basic concepts of calculations used in analytical chemistry. Has a good understanding and practical experience of analytical chemistry in product development, including modern laboratory techniques for API, excipient, and drug product testing, e.g., particle sizing, FT-IR, SEM and thermal analysis techniques. Able to work autonomously to deliver individual tasks; able to organise tasks allocated by supervisor and plan own work to consistently achieve output of high quality results in a timely manner. Able to work collaboratively within a team environment. Good understanding of laboratory safety and best practice. Good IT skills (including Microsoft Excel, Word, PowerPoint). Effective verbal and written communication skills. Enthusiasm to work in a laboratory based role.At Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you're excited about this role but your past experience doesn't fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or other roles. Benefits at Viatris At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. Some of our benefits include the following on top of a competitive salary: Focus on career progression with growth and development opportunities Emphasis on Health & Wellness programmes 100% paid medical insurance and Employee Assistance Programme Life cover Excellent employer-matched pension scheme with Viatris contributing up to 11% 2 paid volunteer days per year Diversity & Inclusion at Viatris At Viatris, diversity and inclusion are essential to our mission. The diversity we foster in all aspects of our business can be one of our greatest strengths in redefining healthcare not as it is, but as it should be. If you would like to know more about what diversity, equity and inclusion means to us, please visit Sustainability at Viatris Corporate social responsibility is fundamental to the Viatris mission. We work to advance responsible and sustainable operations and leverage our collective expertise to empower people to live healthier at every stage of life, recognizing that our actions affect the stakeholders and communities we serve. To learn more about our efforts, please visitEn Viatris, ofrecemos salarios competitivos, beneficios y un entorno inclusivo donde puede usar sus experiencias, perspectivas y habilidades para ayudar a generar un impacto en la vida de los demás.Viatris es una compañía global del cuidado de la salud creada en 2020 a través de la combinación de Mylan y Upjohn, una división legada de Pfizer. Al integrar las fortalezas de estas dos compañías, incluida nuestra fuerza laboral global de aprox. 45,000, nuestro objetivo es proporcionar acceso mejorado a medicamentos de calidad asequibles a pacientes de todo el mundo, independientemente de dónde vivan o de las circunstancias. Creemos en el cuidado de la salud como debe ser: empoderamos a las personas de todo el mundo para que vivan de manera más saludable en cada etapa de la vida. Debido a nuestra creencia firme de que un acceso mejorado permite una mejor salud, aprovechamos nuestra experiencia científica y de manufactura inmejorable, al igual que las capacidades comerciales comprobadas, para ofrecer a los pacientes medicamentos de calidad en el momento y en el lugar que los necesiten.
Mar 11, 2026
Full time
Analytical Scientist page is loaded Analytical Scientistlocations: Sandwich, England, United Kingdomtime type: Tiempo completoposted on: Publicado hace 2 díasjob requisition id: RMylan Pharma UK LimitedEn VIATRIS, vemos la atención médica no como es, sino como debería de ser. Actuamos con valentía y estamos en una posición única para ser una fuente de estabilidad en un mundo de necesidades de atención médica en constante evolución.Viatris ayuda a las personas de todo el mundo a vivir de manera más saludable en cada etapa de la vida.Lo hacemos a través de:Acceso - suministrando medicamentos de confianza y de alta calidad independientemente de la geografía o las circunstancias;Liderazgo - promoviendo operaciones sostenibles y soluciones innovadoras para mejorar la salud del paciente;Colaboración - aprovechando nuestra experiencia común para conectar a las personas con productos y servicios.Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment.For those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place to work. This is a place to make a difference in the world. The Role & What You Will Be Doing Every day, we rise to the challenge to make a difference and here's how the Analytical Scientist role will make an impact: Working within our Materials Science team, carry out all analytical activities required to deliver new respiratory products to clinical studies and commercialization Plan and execute experiments to generate scientific understanding in development of analytical methods, formulations and processes. Perform analyses related to clinical supplies, stability, and process scale up. Process data, interpret results and report experimental outcomes to project development team. Troubleshoot instrumentation and investigate aberrant sample results. Maintain laboratory documentation in accordance with cGMP documentation practices. Contribute to project delivery by carrying out other tasks (e.g. laboratory housekeeping, ordering, shipping samples) as required. Adherence to all applicable policies and procedures, including those relating to EHS, GMP, GCP, Quality and Compliance, consistent with the role and any associated responsibilities, including people management where applicable. Perform other duties as assigned consistent with the grade of the role About Your Skills & Experience For this role, we're looking for a candidate who has an effective combination of the following qualifications, skills and experiences: Relevant Bachelor of Science Degree (for example Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics) or equivalent, or substantial practical work experience. Good understanding of basic principles of physical, organic and analytical chemistry. Familiar with basic concepts of calculations used in analytical chemistry. Has a good understanding and practical experience of analytical chemistry in product development, including modern laboratory techniques for API, excipient, and drug product testing, e.g., particle sizing, FT-IR, SEM and thermal analysis techniques. Able to work autonomously to deliver individual tasks; able to organise tasks allocated by supervisor and plan own work to consistently achieve output of high quality results in a timely manner. Able to work collaboratively within a team environment. Good understanding of laboratory safety and best practice. Good IT skills (including Microsoft Excel, Word, PowerPoint). Effective verbal and written communication skills. Enthusiasm to work in a laboratory based role.At Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you're excited about this role but your past experience doesn't fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or other roles. Benefits at Viatris At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. Some of our benefits include the following on top of a competitive salary: Focus on career progression with growth and development opportunities Emphasis on Health & Wellness programmes 100% paid medical insurance and Employee Assistance Programme Life cover Excellent employer-matched pension scheme with Viatris contributing up to 11% 2 paid volunteer days per year Diversity & Inclusion at Viatris At Viatris, diversity and inclusion are essential to our mission. The diversity we foster in all aspects of our business can be one of our greatest strengths in redefining healthcare not as it is, but as it should be. If you would like to know more about what diversity, equity and inclusion means to us, please visit Sustainability at Viatris Corporate social responsibility is fundamental to the Viatris mission. We work to advance responsible and sustainable operations and leverage our collective expertise to empower people to live healthier at every stage of life, recognizing that our actions affect the stakeholders and communities we serve. To learn more about our efforts, please visitEn Viatris, ofrecemos salarios competitivos, beneficios y un entorno inclusivo donde puede usar sus experiencias, perspectivas y habilidades para ayudar a generar un impacto en la vida de los demás.Viatris es una compañía global del cuidado de la salud creada en 2020 a través de la combinación de Mylan y Upjohn, una división legada de Pfizer. Al integrar las fortalezas de estas dos compañías, incluida nuestra fuerza laboral global de aprox. 45,000, nuestro objetivo es proporcionar acceso mejorado a medicamentos de calidad asequibles a pacientes de todo el mundo, independientemente de dónde vivan o de las circunstancias. Creemos en el cuidado de la salud como debe ser: empoderamos a las personas de todo el mundo para que vivan de manera más saludable en cada etapa de la vida. Debido a nuestra creencia firme de que un acceso mejorado permite una mejor salud, aprovechamos nuestra experiencia científica y de manufactura inmejorable, al igual que las capacidades comerciales comprobadas, para ofrecer a los pacientes medicamentos de calidad en el momento y en el lugar que los necesiten.
Senior Development Chemist page is loaded Senior Development Chemistlocations: Folkestone, Kent, United Kingdomtime type: Full timeposted on: Posted 2 Days Agojob requisition id: R6A collective energy and ambition. A place where you can make a real difference.We're a company that genuinely cares about our people, our products, our consumers and the environment.Our unique, informal culture champions courage, determination and collaboration. Knowing we have an open and supportive team means each of us has the freedom to take responsibility and ownership. We have a shared passion to work hard, innovate and push boundaries.United by the belief that when we strive for growth, anything is possible. While we might not be the largest company in our industry, we believe we can have the biggest impact because: Together We Have the Power to Win. Based at our R&D Facility in Folkestone, Kent this role offers a unique opportunity to work with cutting-edge technologies and collaborate with diverse teams both internally and externally. Key Responsibilities: Lead and manage a portfolio of projects across multiple brands, focusing on post-launch maintenance and business continuity. Drive product development activities, including the qualification of alternative manufacturing sites and raw material sources. Collaborate with R&D process and manufacturing teams to understand and qualify process changes. Develop and ensure relevant test methods are in place for product and process changes. Plan and execute testing studies, coordinating with external partners when necessary. Prepare and review critical documentation, including development plans and validation reports. Facilitate the design transfer activities ensuring successful product transitions to manufacturing plants. Foster strong working relationships with internal functions such as supply chain, procurement, and quality, as well as external partners. Provide operational support to maintain ongoing product manufacture and contribute to quality improvement projects. Manage project budgets and communicate progress to project teams and PMO regularly. Stay informed about relevant regulations, including the EU Cosmetics Directive and Medical Device Regulation.The ideal candidate will hold a master's degree in sciences or a related field and have substantial industry experience in the development of healthcare or personal care products, encompassing formulation, process, testing, and regulatory knowledge. 3+ years in healthcare/ personal care product development or technical services including post launch changes. Demonstrates regulatory and quality fluency, with familiarity in EU Cosmetics Regulation (EC 1223/2009) and ISO 22716 (GMP), and the ability to quickly learn company procedures; exposure to MDR/ISO 13485 V&V and design transfer for device-adjacent products is advantageous, with a willingness to upskill as needed.You will possess excellent communication and influencing skills, allowing you to build effective cross-functional project teams and forge strong working relationships. A self-motivated individual, you will demonstrate the ability to plan ahead, use initiative, and proactively address challenges. Proficiency in MS Word and Excel is essential, with the capability to present information clearly and effectively. The ideal candidate will also have a proven track record of innovative problem-solving and a proactive approach to driving solutions. Working hours are 39 per week: Monday - Thursday 8-4:30pm and Friday 8-3.30pm. In return we offer a competitive package, including 24 days annual leave, a pension matched up to 9% contributions .For more information on our company, our brands and our culture visit us at When applying for a role and sending your cv, you understand that the Company will hold your personal data in relation to your prospective employment and will process that data for legitimate business reasons within the requirements of UK data protection laws currently in effect and as they become applicable, including the Data Protection Act 1998, the General Data Protection Regulation (Regulation (EU) 2016/679 and any successor legislation. .
Mar 11, 2026
Full time
Senior Development Chemist page is loaded Senior Development Chemistlocations: Folkestone, Kent, United Kingdomtime type: Full timeposted on: Posted 2 Days Agojob requisition id: R6A collective energy and ambition. A place where you can make a real difference.We're a company that genuinely cares about our people, our products, our consumers and the environment.Our unique, informal culture champions courage, determination and collaboration. Knowing we have an open and supportive team means each of us has the freedom to take responsibility and ownership. We have a shared passion to work hard, innovate and push boundaries.United by the belief that when we strive for growth, anything is possible. While we might not be the largest company in our industry, we believe we can have the biggest impact because: Together We Have the Power to Win. Based at our R&D Facility in Folkestone, Kent this role offers a unique opportunity to work with cutting-edge technologies and collaborate with diverse teams both internally and externally. Key Responsibilities: Lead and manage a portfolio of projects across multiple brands, focusing on post-launch maintenance and business continuity. Drive product development activities, including the qualification of alternative manufacturing sites and raw material sources. Collaborate with R&D process and manufacturing teams to understand and qualify process changes. Develop and ensure relevant test methods are in place for product and process changes. Plan and execute testing studies, coordinating with external partners when necessary. Prepare and review critical documentation, including development plans and validation reports. Facilitate the design transfer activities ensuring successful product transitions to manufacturing plants. Foster strong working relationships with internal functions such as supply chain, procurement, and quality, as well as external partners. Provide operational support to maintain ongoing product manufacture and contribute to quality improvement projects. Manage project budgets and communicate progress to project teams and PMO regularly. Stay informed about relevant regulations, including the EU Cosmetics Directive and Medical Device Regulation.The ideal candidate will hold a master's degree in sciences or a related field and have substantial industry experience in the development of healthcare or personal care products, encompassing formulation, process, testing, and regulatory knowledge. 3+ years in healthcare/ personal care product development or technical services including post launch changes. Demonstrates regulatory and quality fluency, with familiarity in EU Cosmetics Regulation (EC 1223/2009) and ISO 22716 (GMP), and the ability to quickly learn company procedures; exposure to MDR/ISO 13485 V&V and design transfer for device-adjacent products is advantageous, with a willingness to upskill as needed.You will possess excellent communication and influencing skills, allowing you to build effective cross-functional project teams and forge strong working relationships. A self-motivated individual, you will demonstrate the ability to plan ahead, use initiative, and proactively address challenges. Proficiency in MS Word and Excel is essential, with the capability to present information clearly and effectively. The ideal candidate will also have a proven track record of innovative problem-solving and a proactive approach to driving solutions. Working hours are 39 per week: Monday - Thursday 8-4:30pm and Friday 8-3.30pm. In return we offer a competitive package, including 24 days annual leave, a pension matched up to 9% contributions .For more information on our company, our brands and our culture visit us at When applying for a role and sending your cv, you understand that the Company will hold your personal data in relation to your prospective employment and will process that data for legitimate business reasons within the requirements of UK data protection laws currently in effect and as they become applicable, including the Data Protection Act 1998, the General Data Protection Regulation (Regulation (EU) 2016/679 and any successor legislation. .
Senior R&D Formulation Chemist Are you ready to shape the next generation of advanced manufacturing? Join Photocentric Ltd, a globally recognised leader in 3D printing innovation with offices in the UK and the USA. From our headquarters in Peterborough, we develop and export cutting-edge 3D printing technologies and manufacture our own resins that are transforming how products are designed and made across many industries. As we continue to expand, we are seeking an experienced Senior R&D Chemist with a strong background in formulation / polymer chemistry to join our chemistry team. This is a fantastic opportunity for a talented Formulation Chemist to use your experience and knowledge to drive projects through the development process from early stage research through to manufacturing and production. Key Responsibilities of the Senior R&D Formulation Chemist will include: Lead assigned R&D projects, showing tangible progress month after month, working closely with other company departments, external partners, and customers Perform cutting edge, challenging research by designing, formulating, and testing 3D printable resins for specific applications Manage and carry out multiple development projects to support various grants Communicate with customers/collaborators to understand application needs and translate them into technical targets and programmes of work Record all results in a systematic manner, and prepare reports about test results Stay at the forefront of developments in 3D printing materials, polymer science, and formulation chemistry, proposing new ideas and research directions Maintain close awareness of scientific literature, polymer science, raw materials, new technologies trends, and competitors' innovation required to create exciting and relevant product innovations. Comply with company policies and procedures and lead by example in all areas Actively participate in the process of continuous improvement of the Company's Product Safety and Quality Management System, products, and processes. Opportunity to mentor and manage a small team Required Education, Skills, and Qualifications of our Senior R&D Formulation Chemist: Proven experience in formulation chemistry, ideally within polymer or coating industry Experience in chemical synthesis preferred Excellent research profile in the area of polymer and/or formulation chemistry Industry experience is preferred Ability to take an objective view of technical problems and address them with creativity and innovation. Excellent organisational skills with the ability to prioritise work and meet deadlines Demonstrated experience in preparing technical concise reports, discuss findings, and provide recommendations on next steps. Confidence written and verbal communication to varying audiences with differing scientific and technological background. If you're excited by the idea of manufacturing in orbit and want to be part of a project that's changing how things are made in space and become our Senior R&D Formulation Chemist, please click 'apply' now! We'd love to hear from you.
Mar 11, 2026
Full time
Senior R&D Formulation Chemist Are you ready to shape the next generation of advanced manufacturing? Join Photocentric Ltd, a globally recognised leader in 3D printing innovation with offices in the UK and the USA. From our headquarters in Peterborough, we develop and export cutting-edge 3D printing technologies and manufacture our own resins that are transforming how products are designed and made across many industries. As we continue to expand, we are seeking an experienced Senior R&D Chemist with a strong background in formulation / polymer chemistry to join our chemistry team. This is a fantastic opportunity for a talented Formulation Chemist to use your experience and knowledge to drive projects through the development process from early stage research through to manufacturing and production. Key Responsibilities of the Senior R&D Formulation Chemist will include: Lead assigned R&D projects, showing tangible progress month after month, working closely with other company departments, external partners, and customers Perform cutting edge, challenging research by designing, formulating, and testing 3D printable resins for specific applications Manage and carry out multiple development projects to support various grants Communicate with customers/collaborators to understand application needs and translate them into technical targets and programmes of work Record all results in a systematic manner, and prepare reports about test results Stay at the forefront of developments in 3D printing materials, polymer science, and formulation chemistry, proposing new ideas and research directions Maintain close awareness of scientific literature, polymer science, raw materials, new technologies trends, and competitors' innovation required to create exciting and relevant product innovations. Comply with company policies and procedures and lead by example in all areas Actively participate in the process of continuous improvement of the Company's Product Safety and Quality Management System, products, and processes. Opportunity to mentor and manage a small team Required Education, Skills, and Qualifications of our Senior R&D Formulation Chemist: Proven experience in formulation chemistry, ideally within polymer or coating industry Experience in chemical synthesis preferred Excellent research profile in the area of polymer and/or formulation chemistry Industry experience is preferred Ability to take an objective view of technical problems and address them with creativity and innovation. Excellent organisational skills with the ability to prioritise work and meet deadlines Demonstrated experience in preparing technical concise reports, discuss findings, and provide recommendations on next steps. Confidence written and verbal communication to varying audiences with differing scientific and technological background. If you're excited by the idea of manufacturing in orbit and want to be part of a project that's changing how things are made in space and become our Senior R&D Formulation Chemist, please click 'apply' now! We'd love to hear from you.
Analytical Scientist page is loaded Analytical Scientistlocations: Sandwich, England, United Kingdomtime type: Praca na pełny etatposted on: Opublikowano 2 dni temujob requisition id: RMylan Pharma UK LimitedW Viatris postrzegamy opiekę zdrowotną taką, jaką być powinna, a nie taką jaka jest. Działamy odważnie i mamy wyjątkowe uwarunkowania, dzięki czemu stanowimy źródło stabilności w świecie zmieniających się potrzeb zdrowotnych. Viatris umożliwia ludziom na całym świecie zdrowsze życie na każdym jego etapie Osiągamy to poprzez (via): Dostęp - dostarczanie pacjentom wysokiej jakości leków, cieszących się powszechnym zaufaniem, w czasie i miejscu, w jakim ich potrzebują; Przywództwo - podejmowanie zrównoważonych działań i opracowywanie innowacyjnych rozwiązań w celu poprawy zdrowia pacjentów; oraz Partnerstwo - wykorzystanie wspólnej wiedzy w celu dostarczenia naszych produktów i usług.Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment.For those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place to work. This is a place to make a difference in the world. The Role & What You Will Be Doing Every day, we rise to the challenge to make a difference and here's how the Analytical Scientist role will make an impact: Working within our Materials Science team, carry out all analytical activities required to deliver new respiratory products to clinical studies and commercialization Plan and execute experiments to generate scientific understanding in development of analytical methods, formulations and processes. Perform analyses related to clinical supplies, stability, and process scale up. Process data, interpret results and report experimental outcomes to project development team. Troubleshoot instrumentation and investigate aberrant sample results. Maintain laboratory documentation in accordance with cGMP documentation practices. Contribute to project delivery by carrying out other tasks (e.g. laboratory housekeeping, ordering, shipping samples) as required. Adherence to all applicable policies and procedures, including those relating to EHS, GMP, GCP, Quality and Compliance, consistent with the role and any associated responsibilities, including people management where applicable. Perform other duties as assigned consistent with the grade of the role About Your Skills & Experience For this role, we're looking for a candidate who has an effective combination of the following qualifications, skills and experiences: Relevant Bachelor of Science Degree (for example Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics) or equivalent, or substantial practical work experience. Good understanding of basic principles of physical, organic and analytical chemistry. Familiar with basic concepts of calculations used in analytical chemistry. Has a good understanding and practical experience of analytical chemistry in product development, including modern laboratory techniques for API, excipient, and drug product testing, e.g., particle sizing, FT-IR, SEM and thermal analysis techniques. Able to work autonomously to deliver individual tasks; able to organise tasks allocated by supervisor and plan own work to consistently achieve output of high quality results in a timely manner. Able to work collaboratively within a team environment. Good understanding of laboratory safety and best practice. Good IT skills (including Microsoft Excel, Word, PowerPoint). Effective verbal and written communication skills. Enthusiasm to work in a laboratory based role.At Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you're excited about this role but your past experience doesn't fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or other roles. Benefits at Viatris At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. Some of our benefits include the following on top of a competitive salary: Focus on career progression with growth and development opportunities Emphasis on Health & Wellness programmes 100% paid medical insurance and Employee Assistance Programme Life cover Excellent employer-matched pension scheme with Viatris contributing up to 11% 2 paid volunteer days per year Diversity & Inclusion at Viatris At Viatris, diversity and inclusion are essential to our mission. The diversity we foster in all aspects of our business can be one of our greatest strengths in redefining healthcare not as it is, but as it should be. If you would like to know more about what diversity, equity and inclusion means to us, please visit Sustainability at Viatris Corporate social responsibility is fundamental to the Viatris mission. We work to advance responsible and sustainable operations and leverage our collective expertise to empower people to live healthier at every stage of life, recognizing that our actions affect the stakeholders and communities we serve. To learn more about our efforts, please visitW Viatris stawiamy sobie za cel by zaoferować Ci konkurencyjne wynagrodzenie, świetne benefity i wspierające środowisko pracy, gdzie będziesz mógł rozwijać swoje doświadczenie, umiejętności i osiągać nowe cele, mając wpływ na zdrowie innych.
Mar 11, 2026
Full time
Analytical Scientist page is loaded Analytical Scientistlocations: Sandwich, England, United Kingdomtime type: Praca na pełny etatposted on: Opublikowano 2 dni temujob requisition id: RMylan Pharma UK LimitedW Viatris postrzegamy opiekę zdrowotną taką, jaką być powinna, a nie taką jaka jest. Działamy odważnie i mamy wyjątkowe uwarunkowania, dzięki czemu stanowimy źródło stabilności w świecie zmieniających się potrzeb zdrowotnych. Viatris umożliwia ludziom na całym świecie zdrowsze życie na każdym jego etapie Osiągamy to poprzez (via): Dostęp - dostarczanie pacjentom wysokiej jakości leków, cieszących się powszechnym zaufaniem, w czasie i miejscu, w jakim ich potrzebują; Przywództwo - podejmowanie zrównoważonych działań i opracowywanie innowacyjnych rozwiązań w celu poprawy zdrowia pacjentów; oraz Partnerstwo - wykorzystanie wspólnej wiedzy w celu dostarczenia naszych produktów i usług.Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment.For those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place to work. This is a place to make a difference in the world. The Role & What You Will Be Doing Every day, we rise to the challenge to make a difference and here's how the Analytical Scientist role will make an impact: Working within our Materials Science team, carry out all analytical activities required to deliver new respiratory products to clinical studies and commercialization Plan and execute experiments to generate scientific understanding in development of analytical methods, formulations and processes. Perform analyses related to clinical supplies, stability, and process scale up. Process data, interpret results and report experimental outcomes to project development team. Troubleshoot instrumentation and investigate aberrant sample results. Maintain laboratory documentation in accordance with cGMP documentation practices. Contribute to project delivery by carrying out other tasks (e.g. laboratory housekeeping, ordering, shipping samples) as required. Adherence to all applicable policies and procedures, including those relating to EHS, GMP, GCP, Quality and Compliance, consistent with the role and any associated responsibilities, including people management where applicable. Perform other duties as assigned consistent with the grade of the role About Your Skills & Experience For this role, we're looking for a candidate who has an effective combination of the following qualifications, skills and experiences: Relevant Bachelor of Science Degree (for example Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics) or equivalent, or substantial practical work experience. Good understanding of basic principles of physical, organic and analytical chemistry. Familiar with basic concepts of calculations used in analytical chemistry. Has a good understanding and practical experience of analytical chemistry in product development, including modern laboratory techniques for API, excipient, and drug product testing, e.g., particle sizing, FT-IR, SEM and thermal analysis techniques. Able to work autonomously to deliver individual tasks; able to organise tasks allocated by supervisor and plan own work to consistently achieve output of high quality results in a timely manner. Able to work collaboratively within a team environment. Good understanding of laboratory safety and best practice. Good IT skills (including Microsoft Excel, Word, PowerPoint). Effective verbal and written communication skills. Enthusiasm to work in a laboratory based role.At Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you're excited about this role but your past experience doesn't fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or other roles. Benefits at Viatris At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. Some of our benefits include the following on top of a competitive salary: Focus on career progression with growth and development opportunities Emphasis on Health & Wellness programmes 100% paid medical insurance and Employee Assistance Programme Life cover Excellent employer-matched pension scheme with Viatris contributing up to 11% 2 paid volunteer days per year Diversity & Inclusion at Viatris At Viatris, diversity and inclusion are essential to our mission. The diversity we foster in all aspects of our business can be one of our greatest strengths in redefining healthcare not as it is, but as it should be. If you would like to know more about what diversity, equity and inclusion means to us, please visit Sustainability at Viatris Corporate social responsibility is fundamental to the Viatris mission. We work to advance responsible and sustainable operations and leverage our collective expertise to empower people to live healthier at every stage of life, recognizing that our actions affect the stakeholders and communities we serve. To learn more about our efforts, please visitW Viatris stawiamy sobie za cel by zaoferować Ci konkurencyjne wynagrodzenie, świetne benefity i wspierające środowisko pracy, gdzie będziesz mógł rozwijać swoje doświadczenie, umiejętności i osiągać nowe cele, mając wpływ na zdrowie innych.
We have several vacancies at different levels for R&D Scientists. We encourage applications from candidates with all levels of relevant experience in this field and will match candidates accordingly to roles based on experience. The job description below is an example of a mid-level role - other roles are available requiring less or more experience. Company Overview At FlexMedical Solutions, we help our customers bring their ideas to life and create a healthier tomorrow, by providing contract design, development, and manufacturing services to medical device OEMs. We focus on the disposable component of the medical device and have significant expertise with point of care (POC) in vitro diagnostic (IVD) tests. Our in-house capabilities range from screen printing and laser ablation of electrodes for biosensors to final device assembly, including the formulation and deposition of chemistries. Our modern facility is based in Livingston, central Scotland, less than 20 minutes from Edinburgh airport and 40 minutes from Glasgow. Further growth means that we are now developing our capabilities in product development. With a mixture of UK and international clients, we are a forward-looking organisation with an exciting future. Role Description As a qualified scientist you will bring hands-on, technical expertise to the company. Having gained experience in the laboratory, you will understand in-vitro diagnostics and may have some specific experience in electrochemical and other common assay detection methods. With an interest in how products work chemically, mechanically, and electrically it is probable that your work experience goes beyond the lab. As a contract business, we work on multiple projects simultaneously. This brings a lot of variety and requires people who are both willing and able to develop new products and processes in unison with our design control process. Your time will be spent working on some of our customer specific contracts (developing and manufacturing diagnostic products on their behalf) and working on internal development programmes. Working for a scale-up organisation will provide you with a fantastic opportunity to make your mark and implement your ideas. Key Responsibilities Reporting to the Technical Lead/CSO, you will: - Design and build reagents / formulate customer solutions to their requirements. Develop and execute electrochemical methods for external customer requirements, and internal development programmes. Develop reagent deposition methods and sensor build processes, to ensure rapid, consistent, and precise sensor production for development programmes. Work with clients to devise and execute experimental designs (DoE's) and create summary reports for discussion. Author, oversee and execute protocols and write reports. Develop product and process technical documents to successfully introduce new products and processes into manufacturing. Communicate effectively with sub-contractors, suppliers, and clients. Provide scientific input into product and process designs ensuring optimal performance and client satisfaction. Produce characterisation reports for customer products and development reports for projects, aligned with FMS design Quality Management System. Stay informed of latest developments and trends in your field e.g. current trends and methods in IVD development through routine review of current scientific literature. Skills, Knowledge, and Experience required As a minimum, you will hold a degree level qualification in a relevant scientific subject. You will have demonstrable, relevant experience gained in a regulated environment. However, consideration will be given where relevant academic experience can be demonstrated in lieu of industry experience. Competent using routine and complex laboratory equipment. Experienced in designing and building reagents and formulations from first principles. Significant experience in electrochemical methods or other test measurement systems. Experience of designing experimentation to resolve technical uncertainty through scientific rigor and root cause analysis. Experience in IVD product development and familiar with Design Control concept. Able to perform statistical analysis on data to drive decision making. Understand Good Manufacturing and Good Laboratory Practices (GxP). Experience of working to ISO13485 and / or 21 CFR Part 820, and familiar with product and process validation. A Green/Black Belt qualification in Six Sigma / process excellence is highly advantageous. Competent in the use of modern manufacturing equipment (e.g. lasers, dispensing, lamination assembly). Understand Design for Manufacture (DFM) methodology. Experienced using statistical tools such as Minitab and understand Design of Experiments methodology. Experienced in reagent chemistry as applied in IVD products. Experienced in surface chemistry: modification and analysis. Experience in microfluidic devices. People management experience would be advantageous. FlexMedical Solutions is a young, vibrant organisation operating in a highly regulated industry. It is a changing environment that requires you to be very flexible and willing to learn and grow with the company. It is essential that you communicate with your team and contribute to the company's success. As a provider of sub-contract services, working for FlexMedical Solutions will bring a great deal of variety and excitement to your working day. Initiative will be rewarded and personal development is guaranteed. Apply Now Please send your CV and a covering letter, outlining your suitability for the post:
Mar 11, 2026
Full time
We have several vacancies at different levels for R&D Scientists. We encourage applications from candidates with all levels of relevant experience in this field and will match candidates accordingly to roles based on experience. The job description below is an example of a mid-level role - other roles are available requiring less or more experience. Company Overview At FlexMedical Solutions, we help our customers bring their ideas to life and create a healthier tomorrow, by providing contract design, development, and manufacturing services to medical device OEMs. We focus on the disposable component of the medical device and have significant expertise with point of care (POC) in vitro diagnostic (IVD) tests. Our in-house capabilities range from screen printing and laser ablation of electrodes for biosensors to final device assembly, including the formulation and deposition of chemistries. Our modern facility is based in Livingston, central Scotland, less than 20 minutes from Edinburgh airport and 40 minutes from Glasgow. Further growth means that we are now developing our capabilities in product development. With a mixture of UK and international clients, we are a forward-looking organisation with an exciting future. Role Description As a qualified scientist you will bring hands-on, technical expertise to the company. Having gained experience in the laboratory, you will understand in-vitro diagnostics and may have some specific experience in electrochemical and other common assay detection methods. With an interest in how products work chemically, mechanically, and electrically it is probable that your work experience goes beyond the lab. As a contract business, we work on multiple projects simultaneously. This brings a lot of variety and requires people who are both willing and able to develop new products and processes in unison with our design control process. Your time will be spent working on some of our customer specific contracts (developing and manufacturing diagnostic products on their behalf) and working on internal development programmes. Working for a scale-up organisation will provide you with a fantastic opportunity to make your mark and implement your ideas. Key Responsibilities Reporting to the Technical Lead/CSO, you will: - Design and build reagents / formulate customer solutions to their requirements. Develop and execute electrochemical methods for external customer requirements, and internal development programmes. Develop reagent deposition methods and sensor build processes, to ensure rapid, consistent, and precise sensor production for development programmes. Work with clients to devise and execute experimental designs (DoE's) and create summary reports for discussion. Author, oversee and execute protocols and write reports. Develop product and process technical documents to successfully introduce new products and processes into manufacturing. Communicate effectively with sub-contractors, suppliers, and clients. Provide scientific input into product and process designs ensuring optimal performance and client satisfaction. Produce characterisation reports for customer products and development reports for projects, aligned with FMS design Quality Management System. Stay informed of latest developments and trends in your field e.g. current trends and methods in IVD development through routine review of current scientific literature. Skills, Knowledge, and Experience required As a minimum, you will hold a degree level qualification in a relevant scientific subject. You will have demonstrable, relevant experience gained in a regulated environment. However, consideration will be given where relevant academic experience can be demonstrated in lieu of industry experience. Competent using routine and complex laboratory equipment. Experienced in designing and building reagents and formulations from first principles. Significant experience in electrochemical methods or other test measurement systems. Experience of designing experimentation to resolve technical uncertainty through scientific rigor and root cause analysis. Experience in IVD product development and familiar with Design Control concept. Able to perform statistical analysis on data to drive decision making. Understand Good Manufacturing and Good Laboratory Practices (GxP). Experience of working to ISO13485 and / or 21 CFR Part 820, and familiar with product and process validation. A Green/Black Belt qualification in Six Sigma / process excellence is highly advantageous. Competent in the use of modern manufacturing equipment (e.g. lasers, dispensing, lamination assembly). Understand Design for Manufacture (DFM) methodology. Experienced using statistical tools such as Minitab and understand Design of Experiments methodology. Experienced in reagent chemistry as applied in IVD products. Experienced in surface chemistry: modification and analysis. Experience in microfluidic devices. People management experience would be advantageous. FlexMedical Solutions is a young, vibrant organisation operating in a highly regulated industry. It is a changing environment that requires you to be very flexible and willing to learn and grow with the company. It is essential that you communicate with your team and contribute to the company's success. As a provider of sub-contract services, working for FlexMedical Solutions will bring a great deal of variety and excitement to your working day. Initiative will be rewarded and personal development is guaranteed. Apply Now Please send your CV and a covering letter, outlining your suitability for the post:
A leading 3D printing innovation firm in the UK is looking for a Senior R&D Formulation Chemist to join their team. This position involves leading R&D projects, designing and testing innovative materials, and enhancing product quality and safety. Candidates should have proven formulation chemistry expertise, ideally within the polymer or coating industry, along with excellent organizational and communication skills. Join us in reshaping advanced manufacturing and explore cutting-edge technologies in this pivotal role.
Mar 09, 2026
Full time
A leading 3D printing innovation firm in the UK is looking for a Senior R&D Formulation Chemist to join their team. This position involves leading R&D projects, designing and testing innovative materials, and enhancing product quality and safety. Candidates should have proven formulation chemistry expertise, ideally within the polymer or coating industry, along with excellent organizational and communication skills. Join us in reshaping advanced manufacturing and explore cutting-edge technologies in this pivotal role.
Manpower are currently seeking an interim Laboratory Technician, to work with our global FMCG client Unilever, renowned for brands such as Dove, Sure, Persil, and Simple, and become an integral part of their fast-paced FMCG environment. The position is based in Port Sunlight Village, Wirral easily accessible by train and car. This is a full-time temporary role to last till 19th September 2026, requiring 37.5 hours per week, Monday to Friday. Compensation for this role is competitive, paying up to 34,672 per annum, pro rata, depending upon experience. The role involves hybrid working (time split between the workplace and remote working) this is subject to change and based on business requirements. As standard it is 60% of their working hours in the office. JOB DESCRIPTION Support the Hair & Skin Care Category Innovation Programme, specifically in the development and formulation of new products and in the re-development of existing products to meet regulatory requirements. This specifically involves working in the laboratory on formulations of Hair Care & Skin Care products, e.g. shampoos, conditioners, creams & lotions. Design, plan and execute own work plans (with support from workstream leader), ensuring compliance with COSHH, GLP and SOP requirements. Prepare and characterise products, including measuring rheological properties, physical/sensory evaluations and storage stability tests etc. Data analysis & communication: statistical analysis of data and clear communication of results and recommendations, via presentations and formal written reports. Formulation data entry on SAP PLM for formulations, INCI lists and other technical information. Use of digital IT systems to enable local R&D, regulatory and safety teams to process formulations. Effective collaboration within cross-functional teams. Develop technical mastery of hair care formulations; technologies, hair science and measurement understanding. Establish networks with relevant external collaborators, e.g. suppliers, industry associations or equivalent, to understand information on product/consumer trend. Use understanding of formulation technologies to contribute ideas for new product activations with marketing and trade. KEY REQUIREMENTS Degree in science or equivalent previous experience, preferably chemistry, but science background needed. Some experience in Personal Care Research Product Development or working in a laboratory. A rigorous approach and attention to detail. Ability to work to tight deadlines using dynamic problem-solving skills. Excellent communication and interpersonal skills. Additional Information Port Sunlight working environment: Staff shop discounted products Free tea, coffee & ice cream Working in carefully restored listed building, in modern and bright working environment Free parking onsite 5 mins walk to train station serving Liverpool & Chester 20-minute drive from Liverpool city centre/30-minutes' drive from Chester Disabled parking In the heart of picturesque Port Sunlight village There are also several site clubs available to join covering a range of topics including Book Club, Running, Choir, Pool, Genealogy and much more. The site has three catering outlets which provide a range of hot and cold food and drinks daily. In addition there are a range of vending machines and cold water dispensers around the site accessible throughout the day.
Mar 07, 2026
Seasonal
Manpower are currently seeking an interim Laboratory Technician, to work with our global FMCG client Unilever, renowned for brands such as Dove, Sure, Persil, and Simple, and become an integral part of their fast-paced FMCG environment. The position is based in Port Sunlight Village, Wirral easily accessible by train and car. This is a full-time temporary role to last till 19th September 2026, requiring 37.5 hours per week, Monday to Friday. Compensation for this role is competitive, paying up to 34,672 per annum, pro rata, depending upon experience. The role involves hybrid working (time split between the workplace and remote working) this is subject to change and based on business requirements. As standard it is 60% of their working hours in the office. JOB DESCRIPTION Support the Hair & Skin Care Category Innovation Programme, specifically in the development and formulation of new products and in the re-development of existing products to meet regulatory requirements. This specifically involves working in the laboratory on formulations of Hair Care & Skin Care products, e.g. shampoos, conditioners, creams & lotions. Design, plan and execute own work plans (with support from workstream leader), ensuring compliance with COSHH, GLP and SOP requirements. Prepare and characterise products, including measuring rheological properties, physical/sensory evaluations and storage stability tests etc. Data analysis & communication: statistical analysis of data and clear communication of results and recommendations, via presentations and formal written reports. Formulation data entry on SAP PLM for formulations, INCI lists and other technical information. Use of digital IT systems to enable local R&D, regulatory and safety teams to process formulations. Effective collaboration within cross-functional teams. Develop technical mastery of hair care formulations; technologies, hair science and measurement understanding. Establish networks with relevant external collaborators, e.g. suppliers, industry associations or equivalent, to understand information on product/consumer trend. Use understanding of formulation technologies to contribute ideas for new product activations with marketing and trade. KEY REQUIREMENTS Degree in science or equivalent previous experience, preferably chemistry, but science background needed. Some experience in Personal Care Research Product Development or working in a laboratory. A rigorous approach and attention to detail. Ability to work to tight deadlines using dynamic problem-solving skills. Excellent communication and interpersonal skills. Additional Information Port Sunlight working environment: Staff shop discounted products Free tea, coffee & ice cream Working in carefully restored listed building, in modern and bright working environment Free parking onsite 5 mins walk to train station serving Liverpool & Chester 20-minute drive from Liverpool city centre/30-minutes' drive from Chester Disabled parking In the heart of picturesque Port Sunlight village There are also several site clubs available to join covering a range of topics including Book Club, Running, Choir, Pool, Genealogy and much more. The site has three catering outlets which provide a range of hot and cold food and drinks daily. In addition there are a range of vending machines and cold water dispensers around the site accessible throughout the day.
Senior R&D Formulation Chemist Are you ready to shape the next generation of advanced manufacturing? Join Photocentric Ltd, a globally recognised leader in 3D printing innovation with offices in the UK and the USA. From our headquarters in Peterborough, we develop and export cutting-edge 3D printing technologies and manufacture our own resins that are transforming how products are designed and mad click apply for full job details
Mar 07, 2026
Full time
Senior R&D Formulation Chemist Are you ready to shape the next generation of advanced manufacturing? Join Photocentric Ltd, a globally recognised leader in 3D printing innovation with offices in the UK and the USA. From our headquarters in Peterborough, we develop and export cutting-edge 3D printing technologies and manufacture our own resins that are transforming how products are designed and mad click apply for full job details
An exciting opportunity has arisen for a Materials Scientist to join a established chemical manufacturing company that is investing heavily in its future. This role offers excellent progression and development opportunities, a competitive salary of £40,000-£45,000, and a strong benefits package. As a full-time, permanent position based at their Accrington site, and is an ideal next step for a Materials Scientist looking to contribute to innovation within a growing business. The company is committed to long-term investment, making it a great environment for a candidate seeking technical challenge. Roles & Responsibilities Conduct laboratory work to synthesise and characterise inorganic compounds and related structures as part of your development as a Material Scientist Improve testing protocols, including equipment procurement and training colleagues in new methods Test the performance of polymeric and coating systems containing inorganic additives Engage with customers and prospective clients to understand their requirements and develop technical solutions that meet their needs Develop and refine structure property relationships for polymers and coatings incorporating inorganic materials Support the development of new materials and products, progressing formulations from laboratory scale to pilot-plant scale Assist with scaling up new or improved products to pilot and full manufacturing scale Qualifications and Experience Required Master's degree or PhD in Chemistry or Materials Science Working knowledge of materials characterisation, polymer testing, or synthetic chemistry applied in industry is highly desirable Confidence in working autonomously and managing third-party contract and technical customer relationships is advantageous If you like the sound of the Materials Scientist position and would like to be considered, please follow the apply process and submit your most up-to-date CV. Kate Wadsworth is overseeing this role and can provide more information after a successful application, or you can contact our office for support.
Mar 06, 2026
Full time
An exciting opportunity has arisen for a Materials Scientist to join a established chemical manufacturing company that is investing heavily in its future. This role offers excellent progression and development opportunities, a competitive salary of £40,000-£45,000, and a strong benefits package. As a full-time, permanent position based at their Accrington site, and is an ideal next step for a Materials Scientist looking to contribute to innovation within a growing business. The company is committed to long-term investment, making it a great environment for a candidate seeking technical challenge. Roles & Responsibilities Conduct laboratory work to synthesise and characterise inorganic compounds and related structures as part of your development as a Material Scientist Improve testing protocols, including equipment procurement and training colleagues in new methods Test the performance of polymeric and coating systems containing inorganic additives Engage with customers and prospective clients to understand their requirements and develop technical solutions that meet their needs Develop and refine structure property relationships for polymers and coatings incorporating inorganic materials Support the development of new materials and products, progressing formulations from laboratory scale to pilot-plant scale Assist with scaling up new or improved products to pilot and full manufacturing scale Qualifications and Experience Required Master's degree or PhD in Chemistry or Materials Science Working knowledge of materials characterisation, polymer testing, or synthetic chemistry applied in industry is highly desirable Confidence in working autonomously and managing third-party contract and technical customer relationships is advantageous If you like the sound of the Materials Scientist position and would like to be considered, please follow the apply process and submit your most up-to-date CV. Kate Wadsworth is overseeing this role and can provide more information after a successful application, or you can contact our office for support.
Are you a personal care formulator with some post graduate experience and looking for your next role? Do you like working in a small, collaborative technical team? Is liaising with 3rd parties, suppliers and manufacturers one of your strengths? Perhaps this Development Chemist role is the next opportunity for you? Working with brands and manufacturers, our very well established client is responsible for the design and development of beauty products and is seeking an experienced formulator with confident communication skills to join their team. What you will do: Develop innovative formulations in response to client briefs and performance criteria. Reformulate existing products to meet updated regulations, enhance efficacy, and optimise cost. Liaise with contract manufacturers and suppliers to ensure product quality, timelines, and compliance. Partner with fragrance houses to create bespoke fragrances and manage regulatory documentation. Coordinate and remotely manage product testing programmes, including user trials and clinical studies. Oversee and review product artwork for technical and regulatory accuracy. Collaborate with production to resolve scale-up and process challenges, ensuring batch consistency. Mentor junior chemists and technicians, fostering skill development and technical growth. Contribute to cross-functional project teams, aligning product development with overall business goals. What you will need: Proven experience in formulation development, particularly in bath & body and skincare. Strong technical understanding of raw materials, with experience sourcing from Far East and European suppliers (desirable). Analytical and creative problem solving skills for formulation and process troubleshooting. Solid project management experience and familiarity with the NPD process. Excellent communication, organisation, and planning abilities.
Feb 27, 2026
Full time
Are you a personal care formulator with some post graduate experience and looking for your next role? Do you like working in a small, collaborative technical team? Is liaising with 3rd parties, suppliers and manufacturers one of your strengths? Perhaps this Development Chemist role is the next opportunity for you? Working with brands and manufacturers, our very well established client is responsible for the design and development of beauty products and is seeking an experienced formulator with confident communication skills to join their team. What you will do: Develop innovative formulations in response to client briefs and performance criteria. Reformulate existing products to meet updated regulations, enhance efficacy, and optimise cost. Liaise with contract manufacturers and suppliers to ensure product quality, timelines, and compliance. Partner with fragrance houses to create bespoke fragrances and manage regulatory documentation. Coordinate and remotely manage product testing programmes, including user trials and clinical studies. Oversee and review product artwork for technical and regulatory accuracy. Collaborate with production to resolve scale-up and process challenges, ensuring batch consistency. Mentor junior chemists and technicians, fostering skill development and technical growth. Contribute to cross-functional project teams, aligning product development with overall business goals. What you will need: Proven experience in formulation development, particularly in bath & body and skincare. Strong technical understanding of raw materials, with experience sourcing from Far East and European suppliers (desirable). Analytical and creative problem solving skills for formulation and process troubleshooting. Solid project management experience and familiarity with the NPD process. Excellent communication, organisation, and planning abilities.
Quality Systems Specialist - Chester - Chemicals - Contract Our client is an innovative chemicals manufacturer specialising in industrial formulations and coatings across a wide range of industries. At present they are seeking a Quality Systems Specialist on a contract basis to support their quality and compliance function. Candidates will ideally have a science background preferably in Chemistry (formulation and GC experience would be advantageous) but will be primarily experienced in managing QMS systems and lifecycle management software solutions such as Product Vision software or similar. Candidate will be required to demonstrate statistical analysis required for method development and maintain computer efficiency and proficiency in using software programs such as Color eye, Electronic Bench Record (EBR), Excel, Lotus Notes, PowerPoint, Product Vision, QAD, MS Office packages. Problem solving abilities, technical creativity and cross functional team work will be essential for this role.
Feb 27, 2026
Contractor
Quality Systems Specialist - Chester - Chemicals - Contract Our client is an innovative chemicals manufacturer specialising in industrial formulations and coatings across a wide range of industries. At present they are seeking a Quality Systems Specialist on a contract basis to support their quality and compliance function. Candidates will ideally have a science background preferably in Chemistry (formulation and GC experience would be advantageous) but will be primarily experienced in managing QMS systems and lifecycle management software solutions such as Product Vision software or similar. Candidate will be required to demonstrate statistical analysis required for method development and maintain computer efficiency and proficiency in using software programs such as Color eye, Electronic Bench Record (EBR), Excel, Lotus Notes, PowerPoint, Product Vision, QAD, MS Office packages. Problem solving abilities, technical creativity and cross functional team work will be essential for this role.
Are you an experienced chemist who loves turning complex ideas into real, innovative products? Do you enjoy designing experiments, developing new materials and pushing the boundaries of polymer chemistry? Ready to play a key role in driving new product development within a fast-moving R&D environment? If this role sounds like your next move, click apply to explore this further! The Opportunity One of our key clients who are a leading chemicals manufacturer is seeking an R&D Development Chemist to support the creation and improvement of their high-performance polymer materials. Working as part of a collaborative research team, you ll contribute to new product pipelines, laboratory experimentation and the advancement of next-generation technologies. This role would suit candidates working as a Polymer Chemist, Research Chemist, Development Scientist, Materials Chemist, R&D Scientist, Formulation Chemist, Polymer Technologist, Product Development Chemist, Laboratory Scientist or Process Development Chemist. Your duties and responsibilities will be Supporting safe laboratory operations, ensuring procedures, documentation and practices meet internal and regulatory standards. Leading elements of product development projects, planning and carrying out experiments focused on polymer synthesis and material innovation. Producing and interpreting experimental data, documenting findings and providing clear recommendations through technical reports. Working with colleagues across R&D, technical, production and commercial teams to progress development projects and share technical insight. Keeping informed of new polymer technologies and identifying opportunities for improved processes, novel materials or new applications. You will have the following qualifications & experience: A degree or higher qualification in Chemistry, Polymer Chemistry or Chemical Engineering. Industrial laboratory experience, ideally involving polymer development, synthesis or advanced material testing. Strong understanding of analytical techniques, physical testing and polymer characterisation. Confident applying safe working practices, including risk assessments and chemical safety systems. Familiarity with structured experimentation, data analysis and project based working. It s great if you also have the following Experience working with polyurethane chemistry or related polymer systems Working knowledge of REACH, COSHH and chemical regulatory compliance Millbank Holdings Ltd is an equal opportunities employer committed to creating an inclusive and diverse workforce. We welcome applications from all suitably qualified individuals, regardless of background, and encourage candidates from underrepresented groups to apply. We are proud to be a member of the Disability Confident Scheme, and we are committed to ensuring an accessible and supportive recruitment process for everyone. If you require any adjustments at any stage, please let us know and we ll do our best to accommodate. Millbank operates as both an Employment Agency and an Employment Business.
Feb 27, 2026
Full time
Are you an experienced chemist who loves turning complex ideas into real, innovative products? Do you enjoy designing experiments, developing new materials and pushing the boundaries of polymer chemistry? Ready to play a key role in driving new product development within a fast-moving R&D environment? If this role sounds like your next move, click apply to explore this further! The Opportunity One of our key clients who are a leading chemicals manufacturer is seeking an R&D Development Chemist to support the creation and improvement of their high-performance polymer materials. Working as part of a collaborative research team, you ll contribute to new product pipelines, laboratory experimentation and the advancement of next-generation technologies. This role would suit candidates working as a Polymer Chemist, Research Chemist, Development Scientist, Materials Chemist, R&D Scientist, Formulation Chemist, Polymer Technologist, Product Development Chemist, Laboratory Scientist or Process Development Chemist. Your duties and responsibilities will be Supporting safe laboratory operations, ensuring procedures, documentation and practices meet internal and regulatory standards. Leading elements of product development projects, planning and carrying out experiments focused on polymer synthesis and material innovation. Producing and interpreting experimental data, documenting findings and providing clear recommendations through technical reports. Working with colleagues across R&D, technical, production and commercial teams to progress development projects and share technical insight. Keeping informed of new polymer technologies and identifying opportunities for improved processes, novel materials or new applications. You will have the following qualifications & experience: A degree or higher qualification in Chemistry, Polymer Chemistry or Chemical Engineering. Industrial laboratory experience, ideally involving polymer development, synthesis or advanced material testing. Strong understanding of analytical techniques, physical testing and polymer characterisation. Confident applying safe working practices, including risk assessments and chemical safety systems. Familiarity with structured experimentation, data analysis and project based working. It s great if you also have the following Experience working with polyurethane chemistry or related polymer systems Working knowledge of REACH, COSHH and chemical regulatory compliance Millbank Holdings Ltd is an equal opportunities employer committed to creating an inclusive and diverse workforce. We welcome applications from all suitably qualified individuals, regardless of background, and encourage candidates from underrepresented groups to apply. We are proud to be a member of the Disability Confident Scheme, and we are committed to ensuring an accessible and supportive recruitment process for everyone. If you require any adjustments at any stage, please let us know and we ll do our best to accommodate. Millbank operates as both an Employment Agency and an Employment Business.
An exciting opportunity has arisen for a Material Scientist to join a established chemical manufacturing company that is investing heavily in its future. This role offers excellent progression and development opportunities, a competitive salary of 40,000- 45,000, and a strong benefits package. As a full-time, permanent position based at their Accrington site, and is an ideal next step for a Material Scientist looking to contribute to innovation within a growing business. The company is committed to long-term investment, making it a great environment for a candidate seeking technical challenge. Roles & Responsibilities for Material Scientist: Conduct laboratory work to synthesise and characterise inorganic compounds and related structures as part of your development as a Material Scientist Improve testing protocols, including equipment procurement and training colleagues in new methods. Test the performance of polymeric and coating systems containing inorganic additives Engage with customers and prospective clients to understand their requirements and develop technical solutions that meet their needs. Develop and refine structure property relationships for polymers and coatings incorporating inorganic materials. Support the development of new materials and products, progressing formulations from laboratory scale to pilot-plant scale. Assist with scaling up new or improved products to pilot and full manufacturing scale. Qualifications and Experience Required for Material Scientist: Master's degree or PhD in Chemistry or Materials Science. Working knowledge of materials characterisation, polymer testing, or synthetic chemistry applied in industry is highly desirable. Confidence in working autonomously and managing third-party contract and technical customer relationships is advantageous. If you like the sound of the Material Scientist position and would like to be considered, please follow the apply process and submit your most up-to-date CV. Kate Wadsworth is overseeing this role and can provide more information after a successful application, or you can contact our office for support.
Feb 27, 2026
Full time
An exciting opportunity has arisen for a Material Scientist to join a established chemical manufacturing company that is investing heavily in its future. This role offers excellent progression and development opportunities, a competitive salary of 40,000- 45,000, and a strong benefits package. As a full-time, permanent position based at their Accrington site, and is an ideal next step for a Material Scientist looking to contribute to innovation within a growing business. The company is committed to long-term investment, making it a great environment for a candidate seeking technical challenge. Roles & Responsibilities for Material Scientist: Conduct laboratory work to synthesise and characterise inorganic compounds and related structures as part of your development as a Material Scientist Improve testing protocols, including equipment procurement and training colleagues in new methods. Test the performance of polymeric and coating systems containing inorganic additives Engage with customers and prospective clients to understand their requirements and develop technical solutions that meet their needs. Develop and refine structure property relationships for polymers and coatings incorporating inorganic materials. Support the development of new materials and products, progressing formulations from laboratory scale to pilot-plant scale. Assist with scaling up new or improved products to pilot and full manufacturing scale. Qualifications and Experience Required for Material Scientist: Master's degree or PhD in Chemistry or Materials Science. Working knowledge of materials characterisation, polymer testing, or synthetic chemistry applied in industry is highly desirable. Confidence in working autonomously and managing third-party contract and technical customer relationships is advantageous. If you like the sound of the Material Scientist position and would like to be considered, please follow the apply process and submit your most up-to-date CV. Kate Wadsworth is overseeing this role and can provide more information after a successful application, or you can contact our office for support.
The Associate Director of Drug Product Development is responsible for providing scientific and technical leadership for Jazz Pharmaceuticals' Pharmaceutical Development programs at various stages of the development life cycle including preformulation, formulation and process development, technical transfer and validation. The Associate Director of Drug Product Development will oversee drug product aspects of development and manufacturing projects from pre formulation and product feasibility through to clinical trial supply and technology transfer/commercialization. In addition, the Associate Director of Drug Product Development may provide leadership of cross functional CMC development teams. The Associate Director of Drug Product Development will have broad experience in pharmaceutical product development, demonstrated problem solving ability, module 3 authorship, development of robust manufacturing processes through designed experiments and data analysis, and excellent project management, teamwork and leadership skills. Essential Functions Leads the development of small molecule drug product formulations, appropriate to the phase of pharmaceutical development, with sufficient stability and robustness for clinical and/or commercial manufacturing. Responsible for specifying product and process requirements, including manufacturing equipment and methods, performance criteria, materials, test protocols, required analytical methodology, packaging (clinical and commercial), and in developing robust processes for pharmaceutical production. Directs projects and leads cross functional teams (as required) with technical proficiency, scientific creativity, collaboration with others to achieve project goals on time and within budget. Create intellectual property covering Jazz Pharmaceuticals products and ensure freedom to operate in the development of new drug products. Support the identification and selection of suitable drug product development and commercial manufacturing vendors (CMOs). Direct technical projects (internally and at CDMOs) including developing detailed technical work plans and managing performance of vendors. Work cooperatively with, or lead, internal and external teams as required. Author CMC sections of regulatory dossiers for products at all stages to enable acceptance by global regulators. Supports asset due diligence and new product introduction and integrations. Apply current knowledge of cGMP and industry standards for process design and validation to manage vendors and contract development organizations. Required Knowledge, Skills, and Abilities Demonstrated technical proficiency, engineering, collaboration with others, and independent thought. Strong teamwork skills. Demonstrated troubleshooting and problem solving skills including the use of designed experiments, statistical process control. Development/authorship of CMC regulatory filings for pharmaceutical products. Broad exposure to multiple drug delivery technologies and knowledge of standard dosage forms preferred. Excellent written and verbal communication skills. Current knowledge of quality systems and FDA and EU regulations as they relate to pharmaceutical development and validation. Experience in intellectual property development desirable. Proven project management skills for technical programs. Flexibility to travel on company business when required. Required/Preferred Education and Licenses Advanced degree in Chemistry, Pharm. Sci., Engineering, or related field, or equivalent combination of education and work related experience required. Description of Physical Demands Occasional mobility within office environment. Routinely sitting for extended periods of time. Constantly operating a computer, printer, telephone and other similar office machinery.
Feb 27, 2026
Full time
The Associate Director of Drug Product Development is responsible for providing scientific and technical leadership for Jazz Pharmaceuticals' Pharmaceutical Development programs at various stages of the development life cycle including preformulation, formulation and process development, technical transfer and validation. The Associate Director of Drug Product Development will oversee drug product aspects of development and manufacturing projects from pre formulation and product feasibility through to clinical trial supply and technology transfer/commercialization. In addition, the Associate Director of Drug Product Development may provide leadership of cross functional CMC development teams. The Associate Director of Drug Product Development will have broad experience in pharmaceutical product development, demonstrated problem solving ability, module 3 authorship, development of robust manufacturing processes through designed experiments and data analysis, and excellent project management, teamwork and leadership skills. Essential Functions Leads the development of small molecule drug product formulations, appropriate to the phase of pharmaceutical development, with sufficient stability and robustness for clinical and/or commercial manufacturing. Responsible for specifying product and process requirements, including manufacturing equipment and methods, performance criteria, materials, test protocols, required analytical methodology, packaging (clinical and commercial), and in developing robust processes for pharmaceutical production. Directs projects and leads cross functional teams (as required) with technical proficiency, scientific creativity, collaboration with others to achieve project goals on time and within budget. Create intellectual property covering Jazz Pharmaceuticals products and ensure freedom to operate in the development of new drug products. Support the identification and selection of suitable drug product development and commercial manufacturing vendors (CMOs). Direct technical projects (internally and at CDMOs) including developing detailed technical work plans and managing performance of vendors. Work cooperatively with, or lead, internal and external teams as required. Author CMC sections of regulatory dossiers for products at all stages to enable acceptance by global regulators. Supports asset due diligence and new product introduction and integrations. Apply current knowledge of cGMP and industry standards for process design and validation to manage vendors and contract development organizations. Required Knowledge, Skills, and Abilities Demonstrated technical proficiency, engineering, collaboration with others, and independent thought. Strong teamwork skills. Demonstrated troubleshooting and problem solving skills including the use of designed experiments, statistical process control. Development/authorship of CMC regulatory filings for pharmaceutical products. Broad exposure to multiple drug delivery technologies and knowledge of standard dosage forms preferred. Excellent written and verbal communication skills. Current knowledge of quality systems and FDA and EU regulations as they relate to pharmaceutical development and validation. Experience in intellectual property development desirable. Proven project management skills for technical programs. Flexibility to travel on company business when required. Required/Preferred Education and Licenses Advanced degree in Chemistry, Pharm. Sci., Engineering, or related field, or equivalent combination of education and work related experience required. Description of Physical Demands Occasional mobility within office environment. Routinely sitting for extended periods of time. Constantly operating a computer, printer, telephone and other similar office machinery.
The Role At Notpla, we're at the forefront of sustainable innovation, creating natural alternatives to single-use plastic packaging that are carefully engineered to help build a healthier planet. Founded on the belief that nature knows best, we're an innovative, action-oriented scale-up developing and manufacturing uncompromisingly natural packaging solutions from seaweed and plants. As a Senior Material Scientist, you'll spearhead scientific and technological breakthroughs, playing a pivotal role in developing natural polymer technologies to replace plastic. This role will suit someone with a background in Materials Science, Polymer Chemistry, or Chemical Engineering, with hands-on experience working with natural materials such as biopolyesters, rubbers, resins, seaweed, and/or processes such as PET recycling or polymer extrusion. This is an exciting time to join Notpla - we're on the brink of a record-breaking year for revenue and on track for major growth in the next 18-24 months. To support this, we have just secured a £20 million Series A+ fundraise, enabling us to scale our growth and environmental impact faster than ever. Beyond offering meaningful roles and a vibrant working environment, Notpla provides competitive compensation, including EMI Share Options, a zero-carbon pension scheme, discounts with local businesses, and subsidised social activities. Our office-first hybrid working policy lets you work in the way that maximises your productivity while maintaining a dynamic and collaborative atmosphere. We're a social business with regular clubs and events, and we're proud of how our diverse, mission-driven community works together to make plastic disappear. Led by strong values, all Notpla employees are encouraged to take ownership of their domain, enjoying a high degree of autonomy. Our aim is to build an inspiring culture reflected in our working policies, environment, and people. As a Senior Material Scientist, you'll balance fast-paced feasibility initiatives with in-depth polymer and process development. Your work will be highly hands-on and collaborative, engaging with cross-disciplinary teams and international partners. You'll tackle complex materials challenges, coordinate trials, scout novel natural polymer opportunities, and engage with a network of scientific experts and labs to bring innovation to life. Within the Innovation Team, you'll thrive in a setting that embraces ambiguity and agile ways of working. You'll collaborate closely with colleagues from diverse backgrounds - such as design, engineering, and business - to develop new materials and products. A true innovator, you'll explore the unknown, constantly learning and pushing the boundaries of science rooted in nature. Key Responsibilities Play a central scientific role in Notpla's in a large funded consortium project, executing and coordinating polymer chemistry activities across the consortium. Pioneer new approaches to polymer synthesis from abundant natural materials. Conduct feasibility studies and fast-paced discovery projects to address material science and packaging challenges. Collaborate closely with cross-disciplinary teams - including designers, engineers, seaweed specialists, and business development managers - to solve complex problems. Identify, source, and test natural materials; develop formulations that meet performance, sustainability, and cost targets. Design and execute experiments, analyse data, and present findings to drive decision-making and project progress. Stay up to date with the latest scientific and industry advancements, integrating new knowledge into projects. Contribute to the development of intellectual property, including patents and trade secrets. Provide technical input for grant and client proposals to secure funding. Lead in-depth development projects to advance the understanding of seaweed and biomaterials for packaging applications. Characterise polymer structures, reactions, and material behaviour, and conduct performance, shelf-life, and compatibility studies. Represent Notpla to external partners, academic institutions, and commercial labs; coordinate third-party testing as needed. Develop technical strategies and approaches to solve key challenges. Mentor colleagues (scientists, designers, engineers) to help develop their technical skills and support their project work. Plan and manage your own workload effectively. Salary £38,000 - £45,000 + EMI Share Options
Feb 18, 2026
Full time
The Role At Notpla, we're at the forefront of sustainable innovation, creating natural alternatives to single-use plastic packaging that are carefully engineered to help build a healthier planet. Founded on the belief that nature knows best, we're an innovative, action-oriented scale-up developing and manufacturing uncompromisingly natural packaging solutions from seaweed and plants. As a Senior Material Scientist, you'll spearhead scientific and technological breakthroughs, playing a pivotal role in developing natural polymer technologies to replace plastic. This role will suit someone with a background in Materials Science, Polymer Chemistry, or Chemical Engineering, with hands-on experience working with natural materials such as biopolyesters, rubbers, resins, seaweed, and/or processes such as PET recycling or polymer extrusion. This is an exciting time to join Notpla - we're on the brink of a record-breaking year for revenue and on track for major growth in the next 18-24 months. To support this, we have just secured a £20 million Series A+ fundraise, enabling us to scale our growth and environmental impact faster than ever. Beyond offering meaningful roles and a vibrant working environment, Notpla provides competitive compensation, including EMI Share Options, a zero-carbon pension scheme, discounts with local businesses, and subsidised social activities. Our office-first hybrid working policy lets you work in the way that maximises your productivity while maintaining a dynamic and collaborative atmosphere. We're a social business with regular clubs and events, and we're proud of how our diverse, mission-driven community works together to make plastic disappear. Led by strong values, all Notpla employees are encouraged to take ownership of their domain, enjoying a high degree of autonomy. Our aim is to build an inspiring culture reflected in our working policies, environment, and people. As a Senior Material Scientist, you'll balance fast-paced feasibility initiatives with in-depth polymer and process development. Your work will be highly hands-on and collaborative, engaging with cross-disciplinary teams and international partners. You'll tackle complex materials challenges, coordinate trials, scout novel natural polymer opportunities, and engage with a network of scientific experts and labs to bring innovation to life. Within the Innovation Team, you'll thrive in a setting that embraces ambiguity and agile ways of working. You'll collaborate closely with colleagues from diverse backgrounds - such as design, engineering, and business - to develop new materials and products. A true innovator, you'll explore the unknown, constantly learning and pushing the boundaries of science rooted in nature. Key Responsibilities Play a central scientific role in Notpla's in a large funded consortium project, executing and coordinating polymer chemistry activities across the consortium. Pioneer new approaches to polymer synthesis from abundant natural materials. Conduct feasibility studies and fast-paced discovery projects to address material science and packaging challenges. Collaborate closely with cross-disciplinary teams - including designers, engineers, seaweed specialists, and business development managers - to solve complex problems. Identify, source, and test natural materials; develop formulations that meet performance, sustainability, and cost targets. Design and execute experiments, analyse data, and present findings to drive decision-making and project progress. Stay up to date with the latest scientific and industry advancements, integrating new knowledge into projects. Contribute to the development of intellectual property, including patents and trade secrets. Provide technical input for grant and client proposals to secure funding. Lead in-depth development projects to advance the understanding of seaweed and biomaterials for packaging applications. Characterise polymer structures, reactions, and material behaviour, and conduct performance, shelf-life, and compatibility studies. Represent Notpla to external partners, academic institutions, and commercial labs; coordinate third-party testing as needed. Develop technical strategies and approaches to solve key challenges. Mentor colleagues (scientists, designers, engineers) to help develop their technical skills and support their project work. Plan and manage your own workload effectively. Salary £38,000 - £45,000 + EMI Share Options
