List Recruitment is supporting Phillips 66 with the recruitment of a number of roles in the North Lincolnshire and Jarrow areas. Phillips 66 & You Together we can fuel the future Phillips 66 has been operating in the UK for over 65 years and we are as excited about our future as we are proud of our past. We are committed to improving lives, and that is our promise to our employees and communities. We are sustained by the backgrounds and experiences of our diverse teams, which reflect who we are, the environment we create and how we work together. Our company is built on values of safety, honour and commitment. We call our cultural mindset Our Energy in Action, which we define through four simple, intuitive behaviors: We work for the greater good, create an environment of trust, seek different perspectives and achieve excellence. Our employees are the heart of our success, and there is a reason why we continue to attract great talent and it s not just the excellent benefits package, or the opportunities for personal growth, it s also the caring and committed culture of the organisation that makes everyone feel like they can bring their authentic self to work and be truly part of our team. Job Description The Shift Response Chemist will Primarily be a day-based role responsible for specialist and adhoc analysis ensuring it is carried out in a timely and accurate manner consistent with the enhancement of the Refinery operation whilst maintaining high levels of safety. Working on shift, as required, in the Shift Production Chemist role to cover increases in workload, holidays, sickness, or training. Core Responsibilities • Work safely adhering to the P66 safety culture • Ensure that all sample analysis is done quickly, accurately and efficiently and delays due to result availability are eliminated • Ensure all interested parties are informed of unusual or off specification results. • Conversant with analytical techniques • Be proficient in the use of PC software to analyse results • Cross train in different areas of the laboratory • Perform special analytical testing as directed by supervision • Provide additional testing capability during unit upsets and periods of high workload on shifts. Also to cover holidays, sickness, or training for shift personnel. • Give detailed handover to the oncoming shift • Communicate shift instrument problems to P66 leader • Occasional sample collection both on and off site Education Requirements/Key Skills • Full UK driving license • Knowledge of oil refinery laboratory testing • Good laboratory practise • Knowledge of laboratory sample handling requirements What are we looking for • Team player • Self-starter • Communication Skills • Prioritisation Skills • Flexible and adaptable to changing priorities Providing Energy. Improving Lives. The Humber Refinery is playing its part of the UK s decarbonisation efforts. As a part of the UK Government s net zero ambition, the Humber Refinery is on a journey to become the Refinery of the Future. With proposed plans for a number of projects including to implement a first-of-a-kind FCC carbon capture project, the Humber Refinery is part of Humber Zero, a world-scale concept to reduce UK industry carbon emissions, saving up to 8 million tonnes of CO2 by 2030 from the Immingham industrial area. On top of this, the Humber Refinery is the UK s only refiner producing Sustainable Aviation Fuel at scale. It is also the only European facility producing battery anode coke, which forms a critical component for lithium-ion batteries used in electrical vehicles and in consumer electronics. Our current production of battery anode coke is equivalent to placing 1.3 million EVs on the road every year, and we are developing multiple projects to expand this capability. We are on an exciting journey, are you ready to join us? Phillips 66 has more than 140 years of experience in providing the energy that enables people to dream bigger and go farther, faster. We are committed to improving lives, and that is our promise to our employees and our communities. We are sustained by the backgrounds and experiences of our diverse teams, which reflect who we are, the environment we create and how we work together. We have been recognized by the Human Rights Campaign, U.S. Department of Labor and the Military Times for our continued commitment to inclusive practices and policies in the hiring and retention of those in the LGBTQ+ community and military veterans. Our company is built on values of safety, honor and commitment. We call our cultural mindset Our Energy in Action, which we define through four simple, intuitive behaviors: We work for the greater good, create an environment of trust, seek different perspectives and achieve excellence. Learn more about Phillips 66 and how we are working to meet the world's energy needs today and tomorrow, by visiting phillips66 website. Phillips 66 is an Equal Opportunity Employer By applying for this role your details will be submitted to List Recruitment. List Recruitment acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. Our Candidate Privacy Policy (available on our website) explains how we will use your information.
Mar 01, 2026
Full time
List Recruitment is supporting Phillips 66 with the recruitment of a number of roles in the North Lincolnshire and Jarrow areas. Phillips 66 & You Together we can fuel the future Phillips 66 has been operating in the UK for over 65 years and we are as excited about our future as we are proud of our past. We are committed to improving lives, and that is our promise to our employees and communities. We are sustained by the backgrounds and experiences of our diverse teams, which reflect who we are, the environment we create and how we work together. Our company is built on values of safety, honour and commitment. We call our cultural mindset Our Energy in Action, which we define through four simple, intuitive behaviors: We work for the greater good, create an environment of trust, seek different perspectives and achieve excellence. Our employees are the heart of our success, and there is a reason why we continue to attract great talent and it s not just the excellent benefits package, or the opportunities for personal growth, it s also the caring and committed culture of the organisation that makes everyone feel like they can bring their authentic self to work and be truly part of our team. Job Description The Shift Response Chemist will Primarily be a day-based role responsible for specialist and adhoc analysis ensuring it is carried out in a timely and accurate manner consistent with the enhancement of the Refinery operation whilst maintaining high levels of safety. Working on shift, as required, in the Shift Production Chemist role to cover increases in workload, holidays, sickness, or training. Core Responsibilities • Work safely adhering to the P66 safety culture • Ensure that all sample analysis is done quickly, accurately and efficiently and delays due to result availability are eliminated • Ensure all interested parties are informed of unusual or off specification results. • Conversant with analytical techniques • Be proficient in the use of PC software to analyse results • Cross train in different areas of the laboratory • Perform special analytical testing as directed by supervision • Provide additional testing capability during unit upsets and periods of high workload on shifts. Also to cover holidays, sickness, or training for shift personnel. • Give detailed handover to the oncoming shift • Communicate shift instrument problems to P66 leader • Occasional sample collection both on and off site Education Requirements/Key Skills • Full UK driving license • Knowledge of oil refinery laboratory testing • Good laboratory practise • Knowledge of laboratory sample handling requirements What are we looking for • Team player • Self-starter • Communication Skills • Prioritisation Skills • Flexible and adaptable to changing priorities Providing Energy. Improving Lives. The Humber Refinery is playing its part of the UK s decarbonisation efforts. As a part of the UK Government s net zero ambition, the Humber Refinery is on a journey to become the Refinery of the Future. With proposed plans for a number of projects including to implement a first-of-a-kind FCC carbon capture project, the Humber Refinery is part of Humber Zero, a world-scale concept to reduce UK industry carbon emissions, saving up to 8 million tonnes of CO2 by 2030 from the Immingham industrial area. On top of this, the Humber Refinery is the UK s only refiner producing Sustainable Aviation Fuel at scale. It is also the only European facility producing battery anode coke, which forms a critical component for lithium-ion batteries used in electrical vehicles and in consumer electronics. Our current production of battery anode coke is equivalent to placing 1.3 million EVs on the road every year, and we are developing multiple projects to expand this capability. We are on an exciting journey, are you ready to join us? Phillips 66 has more than 140 years of experience in providing the energy that enables people to dream bigger and go farther, faster. We are committed to improving lives, and that is our promise to our employees and our communities. We are sustained by the backgrounds and experiences of our diverse teams, which reflect who we are, the environment we create and how we work together. We have been recognized by the Human Rights Campaign, U.S. Department of Labor and the Military Times for our continued commitment to inclusive practices and policies in the hiring and retention of those in the LGBTQ+ community and military veterans. Our company is built on values of safety, honor and commitment. We call our cultural mindset Our Energy in Action, which we define through four simple, intuitive behaviors: We work for the greater good, create an environment of trust, seek different perspectives and achieve excellence. Learn more about Phillips 66 and how we are working to meet the world's energy needs today and tomorrow, by visiting phillips66 website. Phillips 66 is an Equal Opportunity Employer By applying for this role your details will be submitted to List Recruitment. List Recruitment acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. Our Candidate Privacy Policy (available on our website) explains how we will use your information.
Job Title: Senior AI Scientist - Hit Discovery and Protein Sciences Location: Cambridge, UK Competitive salary and benefits Introduction to the role: Are you acuriousDataand AIScientist seeking a role where yourexpertisecan make an extraordinary impact? This is an opportunity to join a dynamic and enthusiastic environment and transform the way we discoverhitsand protein reagentsin drug discovery. Diverse Minds. Bold Disruptors. Meaningful Impactthrough Partnership. At AstraZenecawe'rededicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit.There'sno better place to make a difference to medicine,patientsand society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning,growthand development. Join a place built on innovation and creativity. We harness digital, data science & AI to fast-forward our research. Your scientific vision would ensure that new small moleculesand peptidesdiscovered usingyour skillsandinpartnershipwith our technical platformscan serve as the seeds for future medicines and make a real difference in our mission to help patients. You will be basedin early drug discovery R&DwithinData Sciences & Quantitative Biologydepartmentin Discovery Sciencesand will work closely with our colleagues in the Hit Discoveryand Protein Sciencesdepartments.To learn more about our department and culture watch this video: A Life-changing day - Meet our Quantitative Biology team at AstraZeneca. What you will do You will develop data science, computational and AI solutions to enable the discovery of hits (small molecules and peptides) and protein reagents enhancing the output from our hit and ledatageneration platforms. This will involve close collaboration with screening scientists, chemists, biologists, informaticians and statisticians. Wetruly believethat everyone hasan important rolein drug discoveryandeach individualbringsaunique set of competencies. Your curiosity and passion for personal development combined with support from colleagues and leaders, will ensure you maximise your potential and contribution, building from your current skills and experience. Essential requirements: Our team is a highly collaborative group of scientists, working in an evolving technical and scientific landscape. Therefore, you will be comfortable workingin a dynamic and team-focussedenvironment. Critical will be tohave effective communication skills and a proactive and delivery-focused approach. Aligned to Hit Discoveryand Protein Sciencesactivities, you will bring analytical skills,innovationand your strategic mindsetto this excitingand evolvingarea. A PhD or equivalent numbers of years in industry/academia in bioinformatics, cheminformatics, computer science, AI/ML, statistics or related computational and data science subject areas applied to chemistry, biology or medicine. Experience in data science, AI/ML and/or modelling methods applied to the analysis of highly multidimensional or unstructured datasets in molecular, drug discovery or biomedical contexts. Programming in Python, R and/or Shell, and experience with querying and integrating data from disparate sources (e.g. SQL, NoSQL, Graph or file-based approaches). Experience in developing computational workflows applied to the analysis of experimental or AI-generated data (e.g. Nextflow or Snakemake), knowledge of version control systems (e.g. Git and GitHub) and high-performance computing infrastructure. Experiencereporting data analysis results, drawing conclusions and defining recommended actions in interdisciplinary and collaborative environments. Desirables: Experience in AI/ML and/or physics-based mathematical modelling methods applied to peptides, small molecules and/or proteins. Experience in data analysis of high-throughput assays (peptides /small molecule screens, virtual or high content screening, chemical profiling, mass spectrometry, recombinant protein expression and/or omics). Experience in developing software and packages. Track record of publishing relevant research as preprints, peer-reviewed journals, conferences, and other scientific proceedings. Ability to collaborate and build consensus across cross-functional teams. Ability to identify opportunities and synergies across projects. Experience in communicating chemistry and protein concepts within a data science context. Why AstraZeneca There are many opportunities to develop yourself and your career. From our diverse portfolio and collaboration to our ground-breaking innovations -it's a place for lifelong learning. You'll be based in our Discovery Centre placed in the heart of the Cambridge Biomedical Campus - an open, welcoming and vibrant centre that will encourage us and our partners to push the boundaries of scientific innovation. Next Steps: Are you already imagining yourself joining our team? Good, because we can't wait to hear from you. Please apply via the link and one of our team members will be in touch as soon as possible. This is being actively recruited so early application is advised. Where can you find more? Follow AstraZeneca on LinkedIn Follow AstraZeneca on Facebook Follow AstraZeneca on Instagram
Feb 28, 2026
Full time
Job Title: Senior AI Scientist - Hit Discovery and Protein Sciences Location: Cambridge, UK Competitive salary and benefits Introduction to the role: Are you acuriousDataand AIScientist seeking a role where yourexpertisecan make an extraordinary impact? This is an opportunity to join a dynamic and enthusiastic environment and transform the way we discoverhitsand protein reagentsin drug discovery. Diverse Minds. Bold Disruptors. Meaningful Impactthrough Partnership. At AstraZenecawe'rededicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit.There'sno better place to make a difference to medicine,patientsand society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning,growthand development. Join a place built on innovation and creativity. We harness digital, data science & AI to fast-forward our research. Your scientific vision would ensure that new small moleculesand peptidesdiscovered usingyour skillsandinpartnershipwith our technical platformscan serve as the seeds for future medicines and make a real difference in our mission to help patients. You will be basedin early drug discovery R&DwithinData Sciences & Quantitative Biologydepartmentin Discovery Sciencesand will work closely with our colleagues in the Hit Discoveryand Protein Sciencesdepartments.To learn more about our department and culture watch this video: A Life-changing day - Meet our Quantitative Biology team at AstraZeneca. What you will do You will develop data science, computational and AI solutions to enable the discovery of hits (small molecules and peptides) and protein reagents enhancing the output from our hit and ledatageneration platforms. This will involve close collaboration with screening scientists, chemists, biologists, informaticians and statisticians. Wetruly believethat everyone hasan important rolein drug discoveryandeach individualbringsaunique set of competencies. Your curiosity and passion for personal development combined with support from colleagues and leaders, will ensure you maximise your potential and contribution, building from your current skills and experience. Essential requirements: Our team is a highly collaborative group of scientists, working in an evolving technical and scientific landscape. Therefore, you will be comfortable workingin a dynamic and team-focussedenvironment. Critical will be tohave effective communication skills and a proactive and delivery-focused approach. Aligned to Hit Discoveryand Protein Sciencesactivities, you will bring analytical skills,innovationand your strategic mindsetto this excitingand evolvingarea. A PhD or equivalent numbers of years in industry/academia in bioinformatics, cheminformatics, computer science, AI/ML, statistics or related computational and data science subject areas applied to chemistry, biology or medicine. Experience in data science, AI/ML and/or modelling methods applied to the analysis of highly multidimensional or unstructured datasets in molecular, drug discovery or biomedical contexts. Programming in Python, R and/or Shell, and experience with querying and integrating data from disparate sources (e.g. SQL, NoSQL, Graph or file-based approaches). Experience in developing computational workflows applied to the analysis of experimental or AI-generated data (e.g. Nextflow or Snakemake), knowledge of version control systems (e.g. Git and GitHub) and high-performance computing infrastructure. Experiencereporting data analysis results, drawing conclusions and defining recommended actions in interdisciplinary and collaborative environments. Desirables: Experience in AI/ML and/or physics-based mathematical modelling methods applied to peptides, small molecules and/or proteins. Experience in data analysis of high-throughput assays (peptides /small molecule screens, virtual or high content screening, chemical profiling, mass spectrometry, recombinant protein expression and/or omics). Experience in developing software and packages. Track record of publishing relevant research as preprints, peer-reviewed journals, conferences, and other scientific proceedings. Ability to collaborate and build consensus across cross-functional teams. Ability to identify opportunities and synergies across projects. Experience in communicating chemistry and protein concepts within a data science context. Why AstraZeneca There are many opportunities to develop yourself and your career. From our diverse portfolio and collaboration to our ground-breaking innovations -it's a place for lifelong learning. You'll be based in our Discovery Centre placed in the heart of the Cambridge Biomedical Campus - an open, welcoming and vibrant centre that will encourage us and our partners to push the boundaries of scientific innovation. Next Steps: Are you already imagining yourself joining our team? Good, because we can't wait to hear from you. Please apply via the link and one of our team members will be in touch as soon as possible. This is being actively recruited so early application is advised. Where can you find more? Follow AstraZeneca on LinkedIn Follow AstraZeneca on Facebook Follow AstraZeneca on Instagram
Process Chemist! Are you passionate about transforming innovative ideas into reality? Do you thrive in a dynamic environment where your expertise can drive significant improvements? If so, we invite you to become a vital part of our client's team as a Process Chemist! What You'll Do: Process Development & optimisation: Take the lead in planning and executing laboratory work aimed at developing and testing new and enhanced manufacturing processes. Ensure these processes meet our ambitious targets! Technical Expertise: Leverage your expert knowledge in process chemistry to guide our Process Development, Supply Chain, and project teams in crafting and executing effective development plans. Problem Solving: Be the go-to advisor! Support manufacturing and development personnel in troubleshooting process challenges and uncovering exciting opportunities for improvement. Safety & Compliance: Champion safety! Ensure all activities comply with site, company, and regulatory standards while continuously striving to enhance safe working practises. Data Management & Reporting: Keep meticulous records! Document experimental results and prepare technical reports that showcase your findings and insights. What They're Looking For: Experience: Significant experience in process development chemistry, with expertise in critical data analysis (statistics/experimental design), scale-up, and manufacturing support. Comprehensive knowledge and hands-on experience in laboratory and analytical work. Critical Capabilities: Problem Solving: You excel at analysing complex situations creatively, generating and implementing original solutions. Communication: Possess excellent verbal, written, and presentation skills tailored for diverse audiences. Networking: Proven ability to build and maintain internal and external networks, contributing positively to team success. Physico-chemical Awareness: Strong capability to apply physico-chemical concepts to process development, utilising specialised data analysis tools. Leadership & Personal Attributes: A strong execution and results orientation, combined with sound judgement and self-awareness. A continuous learning mindset, eager to share knowledge and grow in an open environment. Ability to establish trust and work effectively within a collaborative team. Education: An Honours Degree (or equivalent) in Chemistry is essential; a PhD is advantageous. We also value several years of experience in a Process Chemistry role. Why Join Us? Exciting Opportunities: Work on cutting-edge projects that make a real impact in the industry. Collaborative Environment: Be part of a supportive team that values your input and encourages professional growth.
Feb 28, 2026
Contractor
Process Chemist! Are you passionate about transforming innovative ideas into reality? Do you thrive in a dynamic environment where your expertise can drive significant improvements? If so, we invite you to become a vital part of our client's team as a Process Chemist! What You'll Do: Process Development & optimisation: Take the lead in planning and executing laboratory work aimed at developing and testing new and enhanced manufacturing processes. Ensure these processes meet our ambitious targets! Technical Expertise: Leverage your expert knowledge in process chemistry to guide our Process Development, Supply Chain, and project teams in crafting and executing effective development plans. Problem Solving: Be the go-to advisor! Support manufacturing and development personnel in troubleshooting process challenges and uncovering exciting opportunities for improvement. Safety & Compliance: Champion safety! Ensure all activities comply with site, company, and regulatory standards while continuously striving to enhance safe working practises. Data Management & Reporting: Keep meticulous records! Document experimental results and prepare technical reports that showcase your findings and insights. What They're Looking For: Experience: Significant experience in process development chemistry, with expertise in critical data analysis (statistics/experimental design), scale-up, and manufacturing support. Comprehensive knowledge and hands-on experience in laboratory and analytical work. Critical Capabilities: Problem Solving: You excel at analysing complex situations creatively, generating and implementing original solutions. Communication: Possess excellent verbal, written, and presentation skills tailored for diverse audiences. Networking: Proven ability to build and maintain internal and external networks, contributing positively to team success. Physico-chemical Awareness: Strong capability to apply physico-chemical concepts to process development, utilising specialised data analysis tools. Leadership & Personal Attributes: A strong execution and results orientation, combined with sound judgement and self-awareness. A continuous learning mindset, eager to share knowledge and grow in an open environment. Ability to establish trust and work effectively within a collaborative team. Education: An Honours Degree (or equivalent) in Chemistry is essential; a PhD is advantageous. We also value several years of experience in a Process Chemistry role. Why Join Us? Exciting Opportunities: Work on cutting-edge projects that make a real impact in the industry. Collaborative Environment: Be part of a supportive team that values your input and encourages professional growth.
Associate Director Chemical Developer Location: Macclesfield Competitive salary and Benefits Hybrid working 3 days a week in the office About us At AstraZeneca, we're united by a bold ambition: to push the boundaries of science and deliver life changing medicines to patients worldwide. As a global, science led biopharmaceutical company, we transform pioneering research into breakthrough treatments across oncology, cardiovascular, respiratory, and rare diseases. Here, your talent will contribute to innovations that truly matter-helping us reimagine healthcare and create a healthier future for all! Introduction to role Are you ready to lead world class small molecule chemistry development that turns bold science into reliable medicines for patients? In this role, you will set the technical direction for your team and elevate how we design, scale, and validate robust drug substance processes-reducing risk, shortening timelines, and enabling confident clinical supply and launch! Small molecule Active Pharmaceutical Ingredients (APIs) remain a powerful modality for tackling disease. The complexity of small molecule therapeutics continues to grow, necessitating innovative and efficient means for their synthesis and manufacture to meet volume, cost and sustainability goals. We are seeking a highly skilled and motivated leader to join the Chemistry function in AstraZeneca's Chemical Development department as Associate Director - Chemistry. You will be responsible for leading a team within the Chemistry function developing synthetic manufacturing processes and supporting regulatory documentation. Working closely with the Senior Director for Chemistry to deliver aspects of the Small Molecule development strategy and drive successful delivery of the projects portfolio through Phase 3 enabling clinical development to commercialisation. Do you thrive when you can mentor scientists, deliver strategic goals, and see tangible impact on medicines reaching patients faster? Accountabilities Lead a team of Synthetic Chemists to deliver the Chemistry contribution to small molecule drug substance projects, with responsibility for: Synthetic process development with associated scale up assessment, and control strategy development Technology transfer and support of clinical drug substance manufacture and process validation Delivery of CMC regulatory submissions for clinical and marketing - acting as reviewer Driving effective collaboration with other skill groups to deliver drug substance projects Line management of Synthetic Chemists, including: Coaching and mentoring to support professional development, including onboarding of new starters Performance management - goal setting and regular feed forward to drive impactful contributions Driving SHE and compliance for team Contribute to the Chemistry development strategy Lead improvement projects to enhance the capability and capacity of the Chemistry function to deliver their contribution to drug substance projects Drive uptake of improved standards and ways of working within the Chemistry function Essential Skills/Experience Degree or equivalent experience in Chemistry + demonstrated experience in synthetic drug substance process development Evidence of people leadership skills through previous responsibilities, including coaching and mentoring of scientists Track record of leading development and scale up of synthetic chemistry to deliver commercially viable manufacturing processes, including understanding of the contribution of analytical chemistry, chemical engineering, and particle science Good understanding of the drug development process, especially late stage development to support Phase 3 clinical studies and launch including control strategy development Proven experience in authoring module 3.2 regulatory submissions Desirable Skills/Experience Previous people management experience, including performance management and individual development Experience of reviewing module 3.2 regulatory submissions Evidence of driving the introduction of digital approaches and new synthetic manufacturing technology Good project management skills and the ability to drive multiple projects simultaneously within the team Experience of driving change and continuous improvement to improve overall efficiency with measurable impact at team level When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life changing medicines. In person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world! Why AstraZeneca Here, your leadership turns complex science into dependable supply for patients worldwide. You will work with pioneering chemistry, digital technologies, and lean principles, side by side with colleagues who put unexpected teams in the same room to crack tough problems. With a truly global network and strong investment in people and modern facilities, you will grow your impact and your career-learning from diverse teams, shaping standards across sites, and contributing to a more sustainable future. We value kindness alongside ambition, and we back decisive leaders who take ownership and deliver outcomes that matter. So, what's next? Complete your application before the below closing date. We welcome your application no later than 26th February 2026 Where can I find out more? Follow AstraZeneca on LinkedIn Follow AstraZeneca on Facebook Follow AstraZeneca on Instagram Date Posted 10-Feb-2026 Closing Date 26-Feb-2026 Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.
Feb 27, 2026
Full time
Associate Director Chemical Developer Location: Macclesfield Competitive salary and Benefits Hybrid working 3 days a week in the office About us At AstraZeneca, we're united by a bold ambition: to push the boundaries of science and deliver life changing medicines to patients worldwide. As a global, science led biopharmaceutical company, we transform pioneering research into breakthrough treatments across oncology, cardiovascular, respiratory, and rare diseases. Here, your talent will contribute to innovations that truly matter-helping us reimagine healthcare and create a healthier future for all! Introduction to role Are you ready to lead world class small molecule chemistry development that turns bold science into reliable medicines for patients? In this role, you will set the technical direction for your team and elevate how we design, scale, and validate robust drug substance processes-reducing risk, shortening timelines, and enabling confident clinical supply and launch! Small molecule Active Pharmaceutical Ingredients (APIs) remain a powerful modality for tackling disease. The complexity of small molecule therapeutics continues to grow, necessitating innovative and efficient means for their synthesis and manufacture to meet volume, cost and sustainability goals. We are seeking a highly skilled and motivated leader to join the Chemistry function in AstraZeneca's Chemical Development department as Associate Director - Chemistry. You will be responsible for leading a team within the Chemistry function developing synthetic manufacturing processes and supporting regulatory documentation. Working closely with the Senior Director for Chemistry to deliver aspects of the Small Molecule development strategy and drive successful delivery of the projects portfolio through Phase 3 enabling clinical development to commercialisation. Do you thrive when you can mentor scientists, deliver strategic goals, and see tangible impact on medicines reaching patients faster? Accountabilities Lead a team of Synthetic Chemists to deliver the Chemistry contribution to small molecule drug substance projects, with responsibility for: Synthetic process development with associated scale up assessment, and control strategy development Technology transfer and support of clinical drug substance manufacture and process validation Delivery of CMC regulatory submissions for clinical and marketing - acting as reviewer Driving effective collaboration with other skill groups to deliver drug substance projects Line management of Synthetic Chemists, including: Coaching and mentoring to support professional development, including onboarding of new starters Performance management - goal setting and regular feed forward to drive impactful contributions Driving SHE and compliance for team Contribute to the Chemistry development strategy Lead improvement projects to enhance the capability and capacity of the Chemistry function to deliver their contribution to drug substance projects Drive uptake of improved standards and ways of working within the Chemistry function Essential Skills/Experience Degree or equivalent experience in Chemistry + demonstrated experience in synthetic drug substance process development Evidence of people leadership skills through previous responsibilities, including coaching and mentoring of scientists Track record of leading development and scale up of synthetic chemistry to deliver commercially viable manufacturing processes, including understanding of the contribution of analytical chemistry, chemical engineering, and particle science Good understanding of the drug development process, especially late stage development to support Phase 3 clinical studies and launch including control strategy development Proven experience in authoring module 3.2 regulatory submissions Desirable Skills/Experience Previous people management experience, including performance management and individual development Experience of reviewing module 3.2 regulatory submissions Evidence of driving the introduction of digital approaches and new synthetic manufacturing technology Good project management skills and the ability to drive multiple projects simultaneously within the team Experience of driving change and continuous improvement to improve overall efficiency with measurable impact at team level When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life changing medicines. In person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world! Why AstraZeneca Here, your leadership turns complex science into dependable supply for patients worldwide. You will work with pioneering chemistry, digital technologies, and lean principles, side by side with colleagues who put unexpected teams in the same room to crack tough problems. With a truly global network and strong investment in people and modern facilities, you will grow your impact and your career-learning from diverse teams, shaping standards across sites, and contributing to a more sustainable future. We value kindness alongside ambition, and we back decisive leaders who take ownership and deliver outcomes that matter. So, what's next? Complete your application before the below closing date. We welcome your application no later than 26th February 2026 Where can I find out more? Follow AstraZeneca on LinkedIn Follow AstraZeneca on Facebook Follow AstraZeneca on Instagram Date Posted 10-Feb-2026 Closing Date 26-Feb-2026 Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.
Job Title: Laboratory Assistant Hours: Full Time, Monday to Friday, 8:00am - 5:00pm Location: Dukinfield Reports to: Laboratory Manager / Senior Technician Role Overview We are seeking a reliable and analytical Laboratory Assistant to support day-to-day laboratory operations. This role would suit a graduate (or equivalent) with a strong interest in science and laboratory work, or someone with relevant laboratory experience looking to develop their career further. The successful candidate will be detail-oriented, methodical, and comfortable working with data, samples, and testing procedures in a structured environment. Key Responsibilities Comply with all safety protocols; Ensure quality control of Raw Materials, Work in Progress Products and Finished-goods, performing necessary adjustments, according to existing Control Plans; Investigate if results are outside control parameters; Record all test results (relevant RM and In-Process testing) on appropriate database and perform all transactions in ERP system; Correctly label and store the retained samples, as well as their recycling and disposal; Ensure all equipments are in good working order and calibrated/verified as scheduled; Maintain good housekeeping and ensure the cleaning of lab materials and equipments; Record internal non conformances and actively work with Production and Logistics to identify the root causes; Ensure that all information for the customer (CoA) is available; Define and perform calibrations and verifications plan for Monitoring and Measuring Devices; Ensure weighing verifications as per legal and process requirements; Execute the orders of cleaning products and all supplies for QC Lab. Candidate Requirements Degree (or working towards) in a Science-related discipline (e.g., Chemistry, Biology, Biomedical Science, Environmental Science) or relevant laboratory experience Strong analytical and problem-solving skills High attention to detail and accuracy Comfortable working with data and technical information Good IT skills, including Microsoft Office Ability to follow strict procedures and work independently Strong organisational and time management skills Personal Attributes Analytical thinker with a methodical approach Eager to learn and develop within a laboratory environment Reliable and punctual Able to work both independently and as part of a team Committed to maintaining high standards of quality and safety
Feb 27, 2026
Contractor
Job Title: Laboratory Assistant Hours: Full Time, Monday to Friday, 8:00am - 5:00pm Location: Dukinfield Reports to: Laboratory Manager / Senior Technician Role Overview We are seeking a reliable and analytical Laboratory Assistant to support day-to-day laboratory operations. This role would suit a graduate (or equivalent) with a strong interest in science and laboratory work, or someone with relevant laboratory experience looking to develop their career further. The successful candidate will be detail-oriented, methodical, and comfortable working with data, samples, and testing procedures in a structured environment. Key Responsibilities Comply with all safety protocols; Ensure quality control of Raw Materials, Work in Progress Products and Finished-goods, performing necessary adjustments, according to existing Control Plans; Investigate if results are outside control parameters; Record all test results (relevant RM and In-Process testing) on appropriate database and perform all transactions in ERP system; Correctly label and store the retained samples, as well as their recycling and disposal; Ensure all equipments are in good working order and calibrated/verified as scheduled; Maintain good housekeeping and ensure the cleaning of lab materials and equipments; Record internal non conformances and actively work with Production and Logistics to identify the root causes; Ensure that all information for the customer (CoA) is available; Define and perform calibrations and verifications plan for Monitoring and Measuring Devices; Ensure weighing verifications as per legal and process requirements; Execute the orders of cleaning products and all supplies for QC Lab. Candidate Requirements Degree (or working towards) in a Science-related discipline (e.g., Chemistry, Biology, Biomedical Science, Environmental Science) or relevant laboratory experience Strong analytical and problem-solving skills High attention to detail and accuracy Comfortable working with data and technical information Good IT skills, including Microsoft Office Ability to follow strict procedures and work independently Strong organisational and time management skills Personal Attributes Analytical thinker with a methodical approach Eager to learn and develop within a laboratory environment Reliable and punctual Able to work both independently and as part of a team Committed to maintaining high standards of quality and safety
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.
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.
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.
Quality Control Laboratory Analyst GMP / GLP Kent Opportunity: Are you currently working in analytical quality control? Does your experience include hands on particle size analysis, analytical testing of Raw Materials, In-process, Release and Stability checks of drug products? Want to work for a large pharmaceutical company? Yes then this is the role for you! Your role as a Quality Control Analytical Laboratory Analyst GMP/GLP based in Kent will involve testing raw materials, finished products, in process controls and composite samples to GMP / GLP standards. Testing techniques may include, but is not limited to, routine particle size analysis (Malvern Mastersizers, Sympatec), cleaning verification (HPLC), identification testing (FTIR and Raman), method development and validation (including particle size and cleanability assessments), DSC, Light microscopy, SEM, Moisture content (Karl Fisher), method optimisation and trouble-shooting, technology transfer and pharmacopoeia analyses. You will also get involved in CAPA s, deviations and document control. The hours of work are: Early shift 6am - 2pm Monday-Friday for 3 weeks then it changes to Late shift 1.30pm - 10pm Monday-Thursday, 1.30pm - 7pm Friday for 3 weeks then it changes to Night shift 9pm - 7am Monday - Thursday for 3 weeks then back to the early shift. This is a 6 months contract which will be reviewed for a possible extension or go permanent but this is all dependent on the candidate and business performance. The PAYE rate is £17.18 per hour. Skills: To apply for the Quality Control Analytical Laboratory Analyst GMP / GLP role you will have the following skills: Degree or equivalent in a scientific subject. Experience in wet chemistry / analytical techniques ideally within the pharmaceutical or related industry. Need to be clean-shaven due to working in clean rooms. No make up, false eye lashes and nail varnish due to working in clean rooms. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit the Quality Start website. If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
Feb 23, 2026
Contractor
Quality Control Laboratory Analyst GMP / GLP Kent Opportunity: Are you currently working in analytical quality control? Does your experience include hands on particle size analysis, analytical testing of Raw Materials, In-process, Release and Stability checks of drug products? Want to work for a large pharmaceutical company? Yes then this is the role for you! Your role as a Quality Control Analytical Laboratory Analyst GMP/GLP based in Kent will involve testing raw materials, finished products, in process controls and composite samples to GMP / GLP standards. Testing techniques may include, but is not limited to, routine particle size analysis (Malvern Mastersizers, Sympatec), cleaning verification (HPLC), identification testing (FTIR and Raman), method development and validation (including particle size and cleanability assessments), DSC, Light microscopy, SEM, Moisture content (Karl Fisher), method optimisation and trouble-shooting, technology transfer and pharmacopoeia analyses. You will also get involved in CAPA s, deviations and document control. The hours of work are: Early shift 6am - 2pm Monday-Friday for 3 weeks then it changes to Late shift 1.30pm - 10pm Monday-Thursday, 1.30pm - 7pm Friday for 3 weeks then it changes to Night shift 9pm - 7am Monday - Thursday for 3 weeks then back to the early shift. This is a 6 months contract which will be reviewed for a possible extension or go permanent but this is all dependent on the candidate and business performance. The PAYE rate is £17.18 per hour. Skills: To apply for the Quality Control Analytical Laboratory Analyst GMP / GLP role you will have the following skills: Degree or equivalent in a scientific subject. Experience in wet chemistry / analytical techniques ideally within the pharmaceutical or related industry. Need to be clean-shaven due to working in clean rooms. No make up, false eye lashes and nail varnish due to working in clean rooms. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit the Quality Start website. If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
Quality Control Laboratory Analyst GMP / GLP Kent Opportunity: Are you currently working in analytical quality control? Does your experience include hands on particle size analysis, analytical testing of Raw Materials, In-process, Release and Stability checks of drug products? Want to work for a large pharmaceutical company? Yes then this is the role for you! Your role as a Quality Control Analytical Laboratory Analyst GMP/GLP based in Kent will involve testing raw materials, finished products, in process controls and composite samples to GMP / GLP standards. Testing techniques may include, but is not limited to, routine particle size analysis (Malvern Mastersizers, Sympatec), cleaning verification (HPLC), identification testing (FTIR and Raman), method development and validation (including particle size and cleanability assessments), DSC, Light microscopy, SEM, Moisture content (Karl Fisher), method optimisation and trouble-shooting, technology transfer and pharmacopoeia analyses. You will also get involved in CAPA s, deviations and document control. The hours of work are: Early shift 6am - 2pm Monday-Friday for 3 weeks then it changes to Late shift 1.30pm - 10pm Monday-Thursday, 1.30pm - 7pm Friday for 3 weeks then it changes to Night shift 9pm - 7am Monday - Thursday for 3 weeks then back to the early shift. This is a 6 months contract which will be reviewed for a possible extension or go permanent but this is all dependent on the candidate and business performance. The PAYE rate is £17.18 per hour. Skills: To apply for the Quality Control Analytical Laboratory Analyst GMP / GLP role you will have the following skills: Degree or equivalent in a scientific subject. Experience in wet chemistry / analytical techniques ideally within the pharmaceutical or related industry. Need to be clean-shaven due to working in clean rooms. No make up, false eye lashes and nail varnish due to working in clean rooms. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit the Quality Start website. If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
Feb 22, 2026
Contractor
Quality Control Laboratory Analyst GMP / GLP Kent Opportunity: Are you currently working in analytical quality control? Does your experience include hands on particle size analysis, analytical testing of Raw Materials, In-process, Release and Stability checks of drug products? Want to work for a large pharmaceutical company? Yes then this is the role for you! Your role as a Quality Control Analytical Laboratory Analyst GMP/GLP based in Kent will involve testing raw materials, finished products, in process controls and composite samples to GMP / GLP standards. Testing techniques may include, but is not limited to, routine particle size analysis (Malvern Mastersizers, Sympatec), cleaning verification (HPLC), identification testing (FTIR and Raman), method development and validation (including particle size and cleanability assessments), DSC, Light microscopy, SEM, Moisture content (Karl Fisher), method optimisation and trouble-shooting, technology transfer and pharmacopoeia analyses. You will also get involved in CAPA s, deviations and document control. The hours of work are: Early shift 6am - 2pm Monday-Friday for 3 weeks then it changes to Late shift 1.30pm - 10pm Monday-Thursday, 1.30pm - 7pm Friday for 3 weeks then it changes to Night shift 9pm - 7am Monday - Thursday for 3 weeks then back to the early shift. This is a 6 months contract which will be reviewed for a possible extension or go permanent but this is all dependent on the candidate and business performance. The PAYE rate is £17.18 per hour. Skills: To apply for the Quality Control Analytical Laboratory Analyst GMP / GLP role you will have the following skills: Degree or equivalent in a scientific subject. Experience in wet chemistry / analytical techniques ideally within the pharmaceutical or related industry. Need to be clean-shaven due to working in clean rooms. No make up, false eye lashes and nail varnish due to working in clean rooms. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit the Quality Start website. If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
Job Description QC Lab Manager Petersfield 8.15am - 4.30pm Monday - Friday JOB REQUIREMENTS & QUALIFICATIONS Minimum Education level: Batchelor s science degree or equivalent experience Five years laboratory experience, with at least three years in a supervisory position, preferably in microbiology, analytical chemistry or product evaluation laboratories in Quality Control for a global consumer goods or pharmaceutical company Experience in developing laboratory SOPs and revisions according to regulatory guidelines. Effective oral and written communication skills and ability to appropriately communicate information to cross functional stakeholders and suppliers Strong knowledge of GMP, ISO and safety guidelines Strong problem-solving skills Knowledge of statistical assessments of data Solid knowledge of all laboratory equipment (e.g., Viscometer, ACS Color Computer, Vitek, Analytical Instrumentation) Proficiency in Microsoft Office Suite, Electronic QMS, and SAP systems is preferred Flexible to support off-shift work when needed. POSITION SUMMARY Support the Senior Manager, in the QC Lab for a particular shift and/or lab function in planning, organizing, implementing and controlling the daily activities of the QC laboratory to ascertain that raw materials, mass and finished goods meet internal and external specifications. Responsible for overseeing lab testing processes with ability to troubleshoot instruments and issues. Conduct and supervise all OOS investigations and reject investigations. Manage QC lab equipment, qualification protocols and reports, and administration. Participate in continuous improvement projects regionally to drive efficiencies in the lab. KEY ROLES & RESPONSIBILITIES Management of QC Lab Testing for a shift or lab function Plan, organise, implement and control the daily activities of the QC laboratory to ascertain that both raw materials and assay of finished goods / mass meet internal and external specification. This includes management for lab workflow, sample analysis, sample retention, standards management, raw material qualification, TPM testing, outsourced testing, inventory management and document management Ensure execution of data integrity checks / verifications per procedures Provide QC expertise to plant hygiene program and lead corrective action based on findings. Ensure there is testing support in relation to the environmental monitoring program and any associated risk assessments Identify SOPs and support the Senior Manager, QC Lab in work instruction updates or creating new based on lab trends and CAPAs. Review SOPs and work instructions and provide to QC Lab Lead for approval. Review and trending of OOS, CAPAs and deviations related to their QC lab function Testing Data Review and Release -Data Reviewer role responsibilities Review routine supporting test data and results, including sample preparation records, chromatograms / graphs, logbooks, calculations, and data sheets. Enter results in SAP/LIMS. Release raw materials, non-OTC mass, and Cosmetic FGs in SAP Review non-routine supporting test data and results (i.e. micro testing for water systems, validation testing) Equipment Program Manage QC lab equipment budget, equipment purchases, installation and initiate change control as needed Develop lab equipment qualification (IQ/OQ/PQ) protocols and reports Manage specific area s equipment administration, including calibration, preventive maintenance, and troubleshooting as needed Compliance / Continuous Improvement within Lab Function Area Ensure all lab processes are adhering to relevant regulatory GMPs and global company policies & procedures Participate in internal audits to ensure regulatory readiness Work collaboratively with Planning, GBSC, QA Labs, Manufacturing, Validation, and Operations to drive continuous improvement. Monitor lab KPIs and drive improvements Ensure all customer complaints are investigated, improvements implemented and response made in a timely manner Support Plant and Global programmes to ensure compliance in key areas including Good Manufacturing Practices, Data Integrity, and the General Data Protection Regulation (GDPR). Personnel Management & Training Apply QC Lab objectives to their lab function area and conduct performance reviews against those objectives. Provide the coaching, mentorship and training necessary to support ongoing personal and professional development of QC lab staff (GMP and refresher training) Assist in the development and execution of quality training curriculum for the laboratory.
Feb 22, 2026
Full time
Job Description QC Lab Manager Petersfield 8.15am - 4.30pm Monday - Friday JOB REQUIREMENTS & QUALIFICATIONS Minimum Education level: Batchelor s science degree or equivalent experience Five years laboratory experience, with at least three years in a supervisory position, preferably in microbiology, analytical chemistry or product evaluation laboratories in Quality Control for a global consumer goods or pharmaceutical company Experience in developing laboratory SOPs and revisions according to regulatory guidelines. Effective oral and written communication skills and ability to appropriately communicate information to cross functional stakeholders and suppliers Strong knowledge of GMP, ISO and safety guidelines Strong problem-solving skills Knowledge of statistical assessments of data Solid knowledge of all laboratory equipment (e.g., Viscometer, ACS Color Computer, Vitek, Analytical Instrumentation) Proficiency in Microsoft Office Suite, Electronic QMS, and SAP systems is preferred Flexible to support off-shift work when needed. POSITION SUMMARY Support the Senior Manager, in the QC Lab for a particular shift and/or lab function in planning, organizing, implementing and controlling the daily activities of the QC laboratory to ascertain that raw materials, mass and finished goods meet internal and external specifications. Responsible for overseeing lab testing processes with ability to troubleshoot instruments and issues. Conduct and supervise all OOS investigations and reject investigations. Manage QC lab equipment, qualification protocols and reports, and administration. Participate in continuous improvement projects regionally to drive efficiencies in the lab. KEY ROLES & RESPONSIBILITIES Management of QC Lab Testing for a shift or lab function Plan, organise, implement and control the daily activities of the QC laboratory to ascertain that both raw materials and assay of finished goods / mass meet internal and external specification. This includes management for lab workflow, sample analysis, sample retention, standards management, raw material qualification, TPM testing, outsourced testing, inventory management and document management Ensure execution of data integrity checks / verifications per procedures Provide QC expertise to plant hygiene program and lead corrective action based on findings. Ensure there is testing support in relation to the environmental monitoring program and any associated risk assessments Identify SOPs and support the Senior Manager, QC Lab in work instruction updates or creating new based on lab trends and CAPAs. Review SOPs and work instructions and provide to QC Lab Lead for approval. Review and trending of OOS, CAPAs and deviations related to their QC lab function Testing Data Review and Release -Data Reviewer role responsibilities Review routine supporting test data and results, including sample preparation records, chromatograms / graphs, logbooks, calculations, and data sheets. Enter results in SAP/LIMS. Release raw materials, non-OTC mass, and Cosmetic FGs in SAP Review non-routine supporting test data and results (i.e. micro testing for water systems, validation testing) Equipment Program Manage QC lab equipment budget, equipment purchases, installation and initiate change control as needed Develop lab equipment qualification (IQ/OQ/PQ) protocols and reports Manage specific area s equipment administration, including calibration, preventive maintenance, and troubleshooting as needed Compliance / Continuous Improvement within Lab Function Area Ensure all lab processes are adhering to relevant regulatory GMPs and global company policies & procedures Participate in internal audits to ensure regulatory readiness Work collaboratively with Planning, GBSC, QA Labs, Manufacturing, Validation, and Operations to drive continuous improvement. Monitor lab KPIs and drive improvements Ensure all customer complaints are investigated, improvements implemented and response made in a timely manner Support Plant and Global programmes to ensure compliance in key areas including Good Manufacturing Practices, Data Integrity, and the General Data Protection Regulation (GDPR). Personnel Management & Training Apply QC Lab objectives to their lab function area and conduct performance reviews against those objectives. Provide the coaching, mentorship and training necessary to support ongoing personal and professional development of QC lab staff (GMP and refresher training) Assist in the development and execution of quality training curriculum for the laboratory.
Blue Arrow is recruiting a Quality Control (QC) Analyst to join our clients team based in the Llantrisant area. Salary : 27,000p.a / 14.79 per hour Hours: 4 days on, 4 days off, 10-hour shifts from 07:00 to 18:00 Contract: 6 month fixed term contract Role Overview As a QC Analyst, you will be responsible for conducting a variety of laboratory tests and analyses to ensure our products meet regulatory standards and client specifications. You will play a key role in monitoring production processes, identifying deviations, and implementing corrective actions to maintain the integrity and safety of our products. Main Responsibilities Perform routine and non-routine analyses of raw materials, in-process samples, and finished products using established analytical techniques (e.g., FPLC, UV-Vis, FTIR, titration, wet chemistry). Interpret and report analytical results accurately, maintaining detailed and organised records in compliance with Good Laboratory Practices (GLP) and company SOPs. Calibrate, operate, and maintain laboratory equipment, ensuring all instruments are functioning optimally and maintaining calibration logs as required. Participate in method development, method validation, and continuous improvement initiatives to optimise laboratory performance. Conduct investigations into non-conforming results and work collaboratively to determine root causes and implement effective corrective actions. Assist in the preparation and review of technical documents such as SOPs, test methods, specifications, and validation protocols. Support internal and external audits by providing necessary documentation, data, and explanations regarding laboratory practices and results. Ensure all laboratory activities are conducted in accordance with health, safety, and environmental regulations. Collaborate with cross-functional teams, including production, quality assurance, and research and development, to resolve quality issues and drive continuous improvement. Stay current with advances in analytical techniques, regulatory requirements, and industry best practices. Requirements Bachelor's degree in chemistry, Biochemistry, Pharmaceutical Science, Microbiology, Food Science, or a related scientific discipline. Familiarity with analytical instrumentation (e.g., HPLC, GC, UV-Vis, FTIR) and associated software. Strong understanding of GLP, GMP, or ISO standards as applicable to the industry. Excellent attention to detail, time management, and organisational skills. Strong communication abilities, both written and verbal, and ability to convey technical information clearly. Problem-solving skills and an investigative mindset. Ability to work independently as well as collaboratively in a fast-paced, team-oriented environment. Proficient in using standard office and laboratory software (e.g., Microsoft Office, LIMS). Desirable Skills Experience with method development and validation. Knowledge of statistical analysis and data interpretation. Familiarity with regulatory submissions and documentation (e.g., MHRA, FDA, EMA). Previous experience in root cause analysis and CAPA (Corrective and Preventive Action) processes. Additional language skills are an advantage. If you feel you would be suitable for the above role, please submit your CV for immediate response. Blue Arrow is proud to be a Disability Confident Employer and is committed to helping find great work opportunities for great people.
Feb 20, 2026
Seasonal
Blue Arrow is recruiting a Quality Control (QC) Analyst to join our clients team based in the Llantrisant area. Salary : 27,000p.a / 14.79 per hour Hours: 4 days on, 4 days off, 10-hour shifts from 07:00 to 18:00 Contract: 6 month fixed term contract Role Overview As a QC Analyst, you will be responsible for conducting a variety of laboratory tests and analyses to ensure our products meet regulatory standards and client specifications. You will play a key role in monitoring production processes, identifying deviations, and implementing corrective actions to maintain the integrity and safety of our products. Main Responsibilities Perform routine and non-routine analyses of raw materials, in-process samples, and finished products using established analytical techniques (e.g., FPLC, UV-Vis, FTIR, titration, wet chemistry). Interpret and report analytical results accurately, maintaining detailed and organised records in compliance with Good Laboratory Practices (GLP) and company SOPs. Calibrate, operate, and maintain laboratory equipment, ensuring all instruments are functioning optimally and maintaining calibration logs as required. Participate in method development, method validation, and continuous improvement initiatives to optimise laboratory performance. Conduct investigations into non-conforming results and work collaboratively to determine root causes and implement effective corrective actions. Assist in the preparation and review of technical documents such as SOPs, test methods, specifications, and validation protocols. Support internal and external audits by providing necessary documentation, data, and explanations regarding laboratory practices and results. Ensure all laboratory activities are conducted in accordance with health, safety, and environmental regulations. Collaborate with cross-functional teams, including production, quality assurance, and research and development, to resolve quality issues and drive continuous improvement. Stay current with advances in analytical techniques, regulatory requirements, and industry best practices. Requirements Bachelor's degree in chemistry, Biochemistry, Pharmaceutical Science, Microbiology, Food Science, or a related scientific discipline. Familiarity with analytical instrumentation (e.g., HPLC, GC, UV-Vis, FTIR) and associated software. Strong understanding of GLP, GMP, or ISO standards as applicable to the industry. Excellent attention to detail, time management, and organisational skills. Strong communication abilities, both written and verbal, and ability to convey technical information clearly. Problem-solving skills and an investigative mindset. Ability to work independently as well as collaboratively in a fast-paced, team-oriented environment. Proficient in using standard office and laboratory software (e.g., Microsoft Office, LIMS). Desirable Skills Experience with method development and validation. Knowledge of statistical analysis and data interpretation. Familiarity with regulatory submissions and documentation (e.g., MHRA, FDA, EMA). Previous experience in root cause analysis and CAPA (Corrective and Preventive Action) processes. Additional language skills are an advantage. If you feel you would be suitable for the above role, please submit your CV for immediate response. Blue Arrow is proud to be a Disability Confident Employer and is committed to helping find great work opportunities for great people.
Role:-QC Manager- Chemical Location:-Dudley- ability to work from home on an adhoc basis. Salary:-Attractive salary (DOE) Russell Taylor Group have a fantastic opportunity to join a Chemical Manufacturing organisation in the Midlands For this role you need some management experience but also a technical/analytical mindset within the chemical industry. The main responsibility with this role is overseeing the quality control processes within the chemical manufacturing facility, but also involves developing and implementing quality assurance policies and helping to support the QA manager. Key Responsibilities Provide leadership, direction and support across QC and QA functions Manage a team of 9 QC analysts and shift inspectors, ensuring all products meet regulatory standards and customer specifications Oversee the testing and analysis of raw materials, in-process samples and finished products Establish and maintain quality control procedures and protocols for chemical products Ensure compliance with industry standards, regulatory requirements and internal policies Maintain and improve ISO 9001 and associated quality systems Act as the prime contact for all site quality audits Help develop, implement and maintain the Quality Management System (QMS) Provide technical guidance to customers and manage product specification queries Provide training and development opportunities to the QC team Develop and promote a culture of continuous improvement Ensure accurate and timely reporting of test results and data analysis Investigate and resolve quality-related issues Prepare and present reports on quality performance metrics when required Contribute as an active member of the site management team About you Educated to degree level (or equivalent) in Chemistry, Chemical Engineering or a related field Minimum 5 years' industrial experience in analytical chemistry (GC, GCMS, HPLC) within a chemical manufacturing environment Previous senior-level experience within Quality Control in the chemical industry Proven management/leadership experience (essential) Strong knowledge of quality control methodologies and statistical analysis Familiarity with testing methods used within the chemical industry Thorough understanding of ISO requirements (ISO 9001 essential; GMP desirable) Proficient in quality management software and data analysis tools Excellent leadership, communication and interpersonal skills Detail-oriented with a strong analytical mindset Proactive problem solver Ability to work under pressure and meet deadlines Comfortable working as part of a small, hands-on management team Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or GDPR please get in touch with us here.
Feb 19, 2026
Full time
Role:-QC Manager- Chemical Location:-Dudley- ability to work from home on an adhoc basis. Salary:-Attractive salary (DOE) Russell Taylor Group have a fantastic opportunity to join a Chemical Manufacturing organisation in the Midlands For this role you need some management experience but also a technical/analytical mindset within the chemical industry. The main responsibility with this role is overseeing the quality control processes within the chemical manufacturing facility, but also involves developing and implementing quality assurance policies and helping to support the QA manager. Key Responsibilities Provide leadership, direction and support across QC and QA functions Manage a team of 9 QC analysts and shift inspectors, ensuring all products meet regulatory standards and customer specifications Oversee the testing and analysis of raw materials, in-process samples and finished products Establish and maintain quality control procedures and protocols for chemical products Ensure compliance with industry standards, regulatory requirements and internal policies Maintain and improve ISO 9001 and associated quality systems Act as the prime contact for all site quality audits Help develop, implement and maintain the Quality Management System (QMS) Provide technical guidance to customers and manage product specification queries Provide training and development opportunities to the QC team Develop and promote a culture of continuous improvement Ensure accurate and timely reporting of test results and data analysis Investigate and resolve quality-related issues Prepare and present reports on quality performance metrics when required Contribute as an active member of the site management team About you Educated to degree level (or equivalent) in Chemistry, Chemical Engineering or a related field Minimum 5 years' industrial experience in analytical chemistry (GC, GCMS, HPLC) within a chemical manufacturing environment Previous senior-level experience within Quality Control in the chemical industry Proven management/leadership experience (essential) Strong knowledge of quality control methodologies and statistical analysis Familiarity with testing methods used within the chemical industry Thorough understanding of ISO requirements (ISO 9001 essential; GMP desirable) Proficient in quality management software and data analysis tools Excellent leadership, communication and interpersonal skills Detail-oriented with a strong analytical mindset Proactive problem solver Ability to work under pressure and meet deadlines Comfortable working as part of a small, hands-on management team Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or GDPR please get in touch with us here.
Job Title: Sustainable Packaging Materials Scientist Location: Port Sunlight Research Lab JOB PURPOSE Unilever is committed to creating a waste free world through its ambitious Packaging Strategy - We are taking on the toughest challenges to make our vision a reality. We are re inventing our product packaging and materials to craft the sustainability journey towards our ambition of circular, waste free and net zero future. To achieve these goals, we need completely new packaging materials and technologies that are yet to be discovered. Our industry leading material science program strives to change our industry for good, transforming the traditional packaging sector into a next generation technical industry where entrepreneurial passion meets science backed innovations. We are looking for a creative, dedicated and ambitious individual with an innovative mindset who shares our passion for the challenge. The One Packaging R&D Centre aims to create a waste free, net zero packaging portfolio through a world class packaging materials capability with strong partnerships and ecosystems. The Centre will enable and accelerate the creation of novel packaging solutions to help meet Unilever's packaging ambitions and completely revolutionise our packaging with a particular focus on our flexibles portfolio. It is the place where future scientific leaders of the business are created. We are a high performing, diverse and inclusive team of dynamic entrepreneurial people with a strong scientific background, courage and curiosity, and passion for sustainability and delivery that will have a positive impact on the planet. RESPONSIBILITIES Support the selection, application, and optimisation of inks, coatings, and overprint varnishes on flexible substrates to meet performance and sustainability requirements. Assess and help interpret the physical, chemical, and surface properties of fibre based and film substrates to ensure compatibility with coatings and printing solutions. Contribute to coating and ink evaluation by applying established analytical and characterisation approaches to assess adhesion, barrier behaviour, durability, and overall performance. Provide day to day technical support to the team, including sample preparation, test execution, data collection, and basic troubleshooting. Support scale up activities from lab to pilot trials by preparing materials, assisting with trial execution, resolving routine issues, and documenting processing conditions. Contribute to experimental design and project planning, helping to generate data driven insights, hypotheses, and recommendations that advance program objectives and support claims or IP development. Maintain high quality documentation, contribute to SOP creation, ensure reliable testing practices, and help prepare data packages for internal reviews, sustainability claims, or IP filings. Engage with external partners and suppliers to gather information or samples and support the evaluation of new technologies, while fostering strong relationships across the internal R&D community. Plan and execute work with increasing autonomy, collaborating with program leaders to deliver activities aligned with project milestones. Work with digital experts and use digital tools to support material selection, data interpretation, and process optimisation. ALL ABOUT YOU We are looking for someone that shares our passion for innovation, applied material science and sustainability, and the drive to take our paper packaging portfolio to the next level. Our Packaging strategy is not just about understanding and developing new materials - it's about making smart decisions on how, when, and where to use them. You will be part of a multi disciplinary project team ethos where everybody contributes to achieving the same goal. What you will bring A higher education qualification in Materials Science, Polymer Chemistry, Chemical Engineering, Packaging Science, Printing & Coating Technology, Paper Technology, or a closely related discipline. Experience in industrially relevant materials development and/or characterisation. Working knowledge of coatings, inks, and overprint varnishes for fibre based and/or film substrates, with the ability to build deeper understanding of how application methods and substrate interactions influence performance, is highly desirable. Practical experience working with coatings, inks, or overprint varnishes in a laboratory environment, and familiarity with fundamental characterisation approaches used to assess performance, is highly desirable. Experience supporting scale up or pilot activities, including sample preparation, troubleshooting minor issues, and documenting processing conditions. Competent in the use of laboratory equipment and data analysis, with a proactive, problem solving approach and strong analytical skills for interpreting data and identifying business relevant insights. Demonstrated ability to collaborate effectively with cross functional teams and to build constructive working relationships with internal and external partners to support project delivery. Strong communication and presentation skills, with the ability to explain technical findings clearly to a range of audiences. Must be creative, highly passionate, willing to think big and inspire both the team, stakeholders and customers. NOTES Not only do we offer a competitive salary and pension scheme, we also offer an annual bonus, subsidised gym membership, a discounted staff shop and shares. You'll have the opportunity to work directly with our renowned and exciting brands in a flexible and hybrid working environment. Whilst the role is advertised on a full time basis, we would be happy to discuss possible flexible working options and what this may look like for you. We are a key advocate of wellbeing and offer a variety of support for our people including hubs, programmes and development opportunities. We strive to achieve a family friendly and inclusive workplace and to, above all, create possibilities for all. Diversity at Unilever Diversity at Unilever is about inclusion, embracing differences, creating possibilities and growing together for better business performance. We embrace diversity in our workforce. This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity. We are also more than happy to provide reasonable adjustments during our application and interview process to enable you to be present your best self. To find out more, including about our Employee Resource Groups, please refer to Equity, Diversity & Inclusion at Unilever.
Feb 16, 2026
Full time
Job Title: Sustainable Packaging Materials Scientist Location: Port Sunlight Research Lab JOB PURPOSE Unilever is committed to creating a waste free world through its ambitious Packaging Strategy - We are taking on the toughest challenges to make our vision a reality. We are re inventing our product packaging and materials to craft the sustainability journey towards our ambition of circular, waste free and net zero future. To achieve these goals, we need completely new packaging materials and technologies that are yet to be discovered. Our industry leading material science program strives to change our industry for good, transforming the traditional packaging sector into a next generation technical industry where entrepreneurial passion meets science backed innovations. We are looking for a creative, dedicated and ambitious individual with an innovative mindset who shares our passion for the challenge. The One Packaging R&D Centre aims to create a waste free, net zero packaging portfolio through a world class packaging materials capability with strong partnerships and ecosystems. The Centre will enable and accelerate the creation of novel packaging solutions to help meet Unilever's packaging ambitions and completely revolutionise our packaging with a particular focus on our flexibles portfolio. It is the place where future scientific leaders of the business are created. We are a high performing, diverse and inclusive team of dynamic entrepreneurial people with a strong scientific background, courage and curiosity, and passion for sustainability and delivery that will have a positive impact on the planet. RESPONSIBILITIES Support the selection, application, and optimisation of inks, coatings, and overprint varnishes on flexible substrates to meet performance and sustainability requirements. Assess and help interpret the physical, chemical, and surface properties of fibre based and film substrates to ensure compatibility with coatings and printing solutions. Contribute to coating and ink evaluation by applying established analytical and characterisation approaches to assess adhesion, barrier behaviour, durability, and overall performance. Provide day to day technical support to the team, including sample preparation, test execution, data collection, and basic troubleshooting. Support scale up activities from lab to pilot trials by preparing materials, assisting with trial execution, resolving routine issues, and documenting processing conditions. Contribute to experimental design and project planning, helping to generate data driven insights, hypotheses, and recommendations that advance program objectives and support claims or IP development. Maintain high quality documentation, contribute to SOP creation, ensure reliable testing practices, and help prepare data packages for internal reviews, sustainability claims, or IP filings. Engage with external partners and suppliers to gather information or samples and support the evaluation of new technologies, while fostering strong relationships across the internal R&D community. Plan and execute work with increasing autonomy, collaborating with program leaders to deliver activities aligned with project milestones. Work with digital experts and use digital tools to support material selection, data interpretation, and process optimisation. ALL ABOUT YOU We are looking for someone that shares our passion for innovation, applied material science and sustainability, and the drive to take our paper packaging portfolio to the next level. Our Packaging strategy is not just about understanding and developing new materials - it's about making smart decisions on how, when, and where to use them. You will be part of a multi disciplinary project team ethos where everybody contributes to achieving the same goal. What you will bring A higher education qualification in Materials Science, Polymer Chemistry, Chemical Engineering, Packaging Science, Printing & Coating Technology, Paper Technology, or a closely related discipline. Experience in industrially relevant materials development and/or characterisation. Working knowledge of coatings, inks, and overprint varnishes for fibre based and/or film substrates, with the ability to build deeper understanding of how application methods and substrate interactions influence performance, is highly desirable. Practical experience working with coatings, inks, or overprint varnishes in a laboratory environment, and familiarity with fundamental characterisation approaches used to assess performance, is highly desirable. Experience supporting scale up or pilot activities, including sample preparation, troubleshooting minor issues, and documenting processing conditions. Competent in the use of laboratory equipment and data analysis, with a proactive, problem solving approach and strong analytical skills for interpreting data and identifying business relevant insights. Demonstrated ability to collaborate effectively with cross functional teams and to build constructive working relationships with internal and external partners to support project delivery. Strong communication and presentation skills, with the ability to explain technical findings clearly to a range of audiences. Must be creative, highly passionate, willing to think big and inspire both the team, stakeholders and customers. NOTES Not only do we offer a competitive salary and pension scheme, we also offer an annual bonus, subsidised gym membership, a discounted staff shop and shares. You'll have the opportunity to work directly with our renowned and exciting brands in a flexible and hybrid working environment. Whilst the role is advertised on a full time basis, we would be happy to discuss possible flexible working options and what this may look like for you. We are a key advocate of wellbeing and offer a variety of support for our people including hubs, programmes and development opportunities. We strive to achieve a family friendly and inclusive workplace and to, above all, create possibilities for all. Diversity at Unilever Diversity at Unilever is about inclusion, embracing differences, creating possibilities and growing together for better business performance. We embrace diversity in our workforce. This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity. We are also more than happy to provide reasonable adjustments during our application and interview process to enable you to be present your best self. To find out more, including about our Employee Resource Groups, please refer to Equity, Diversity & Inclusion at Unilever.
Technical Assessor - Waste Management and Environmental Services Location: Wolverhampton, UK Salary: circa. 33,000pa (DOE) Are you experienced in the waste management or environmental services industry? Are you looking to start or develop your career with an accredited and renowned waste management company? My client is offering a fantastic package for a Hazardous Waste and Recycling Technical Assessor to join their team based in Wolverhampton. The right candidate will possess a degree in Chemistry or equivalent and ideally have worked previously for a UK based Waste and Recycling Management Company. Package Benefits: 23 days Holiday Allowance + Bank Holidays Company Pension Private Health Care Scheme On-site parking Excellent and on-going training programme Opportunity for growth and development within the company Key Responsibilities: Review and classify hazardous and non-hazardous waste streams using chemical data, site information, and relevant legislation (e.g., EWC/LoW codes). Assess analytical results, risk assessments, method statements, waste profiles, and safety data to determine appropriate disposal or treatment pathways. Keep up to date with UK and EU environmental regulations (e.g., Environmental Permitting Regulations, ADR, CLP) and ensure assessments reflect legal obligations. Produce clear technical reports, audit records, waste acceptance criteria, and recommendations for clients or internal teams. Work with operations, health & safety, logistics, and laboratory teams to resolve technical issues and approve waste movements. Contribute to process improvements, technical standards, and quality assurance systems. Requirements: Bachelor's degree in Chemistry, Environmental Science or similar, is essential. Previous experience working in the waste management industry. Knowledge and understanding of the waste management process for hazardous materials. Excellent experience in Customer Service. Full right to live and work in the UK. WR Logistics are the recruitment partner for all vacancies in the logistics industry. We recruit in the UK & USA for permanent jobs. WR is acting as an Employment Agency in relation to this vacancy.
Feb 15, 2026
Full time
Technical Assessor - Waste Management and Environmental Services Location: Wolverhampton, UK Salary: circa. 33,000pa (DOE) Are you experienced in the waste management or environmental services industry? Are you looking to start or develop your career with an accredited and renowned waste management company? My client is offering a fantastic package for a Hazardous Waste and Recycling Technical Assessor to join their team based in Wolverhampton. The right candidate will possess a degree in Chemistry or equivalent and ideally have worked previously for a UK based Waste and Recycling Management Company. Package Benefits: 23 days Holiday Allowance + Bank Holidays Company Pension Private Health Care Scheme On-site parking Excellent and on-going training programme Opportunity for growth and development within the company Key Responsibilities: Review and classify hazardous and non-hazardous waste streams using chemical data, site information, and relevant legislation (e.g., EWC/LoW codes). Assess analytical results, risk assessments, method statements, waste profiles, and safety data to determine appropriate disposal or treatment pathways. Keep up to date with UK and EU environmental regulations (e.g., Environmental Permitting Regulations, ADR, CLP) and ensure assessments reflect legal obligations. Produce clear technical reports, audit records, waste acceptance criteria, and recommendations for clients or internal teams. Work with operations, health & safety, logistics, and laboratory teams to resolve technical issues and approve waste movements. Contribute to process improvements, technical standards, and quality assurance systems. Requirements: Bachelor's degree in Chemistry, Environmental Science or similar, is essential. Previous experience working in the waste management industry. Knowledge and understanding of the waste management process for hazardous materials. Excellent experience in Customer Service. Full right to live and work in the UK. WR Logistics are the recruitment partner for all vacancies in the logistics industry. We recruit in the UK & USA for permanent jobs. WR is acting as an Employment Agency in relation to this vacancy.
Overview Are you a talented Chemist or a recent Graduate looking for an exciting opportunity to join a world-class analytical team? Look no further than Smithers MDT! Our Medical Device Testing (MDT) division has invested heavily in new instrumentation and additional Chemists to increase capacity and broaden our expertise. We're expanding our Chemistry Department and seeking a new Analyst to join our team. Responsibilities As an Analyst at Smithers MDT, you'll be responsible for conducting a wide range of analyses using chromatographic techniques such as HP-LC, LC-MS, and GC-MS. We welcome applicants from diverse backgrounds, but it's essential that you have a degree in a relevant subject or possess relevant industrial experience. Opportunity and Benefits In addition, you'll have the opportunity to work with a team of world-class Chemists and develop your career within a growing and dynamic industry. As a global employer, we offer a generous benefits package, including: Private healthcare Pension scheme 25 days annual leave plus Bank Holidays Flexible working hours with a midday finish on Fridays Equal Opportunity Smithers MDT is an equal opportunities employer.
Feb 10, 2026
Full time
Overview Are you a talented Chemist or a recent Graduate looking for an exciting opportunity to join a world-class analytical team? Look no further than Smithers MDT! Our Medical Device Testing (MDT) division has invested heavily in new instrumentation and additional Chemists to increase capacity and broaden our expertise. We're expanding our Chemistry Department and seeking a new Analyst to join our team. Responsibilities As an Analyst at Smithers MDT, you'll be responsible for conducting a wide range of analyses using chromatographic techniques such as HP-LC, LC-MS, and GC-MS. We welcome applicants from diverse backgrounds, but it's essential that you have a degree in a relevant subject or possess relevant industrial experience. Opportunity and Benefits In addition, you'll have the opportunity to work with a team of world-class Chemists and develop your career within a growing and dynamic industry. As a global employer, we offer a generous benefits package, including: Private healthcare Pension scheme 25 days annual leave plus Bank Holidays Flexible working hours with a midday finish on Fridays Equal Opportunity Smithers MDT is an equal opportunities employer.
Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . on X, Facebook, Instagram, YouTube, LinkedIn and TikTok. Job Description AbbVie is searching for an in-house Associate General Counsel for our Patent Prosecution group, part of AbbVie's Intellectual Property, Transactions, and Innovation legal team. This position will support AbbVie's pharmaceutical products and be based in our offices in North Chicago, IL, Waltham, MA, South San Francisco, CA, or Irvine, CA with a hybrid work model (onsite 3+ days/week). Acting individually and in cross-functional teams, the Associate General Counsel will develop and implement intellectual property strategies for AbbVie's products and product candidates. Responsibilities: Maximize AbbVie's competitive position through creation and implementation of intellectual property strategies Provide legal advice and counsel to cross-functional R&D and business teams on a variety of IP-related matters Draft, file, and prosecute strategically useful patent applications worldwide both directly and through management of outside counsel Challenge and defend patents in IPR, opposition, interference, and other post-grant proceedings Conduct prior art searches, analyze third-party patent positions, and conduct due diligence to support business development activities Qualifications Requirements: JD degree from an accredited law school, state bar admission enabling in-house practice (specific state not required), and registration to practice before the USPTO 8+ years of experience practicing patent law as an attorney or patent agent at a law firm and/or life sciences company, including substantial U.S. and foreign patent prosecution Experience with India, China, and emerging markets a plus Technical background relevant for pharmaceutical patent prosecution, such as: Experience with small molecule and/or biological pharmaceutical discovery & development, and/or Technical degree in relevant field, such as molecular biology, biotechnology, biochemistry, biology, chemistry, chemical engineering, or biomedical engineering Strong legal, analytical, communication, collaboration, and people skills Demonstrated ability to manage complex projects to meet deadlines Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: What AbbVie Has to Offer Our work can-and does-have a tangible, lasting impact on millions of people. But it's not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.
Feb 08, 2026
Full time
Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . on X, Facebook, Instagram, YouTube, LinkedIn and TikTok. Job Description AbbVie is searching for an in-house Associate General Counsel for our Patent Prosecution group, part of AbbVie's Intellectual Property, Transactions, and Innovation legal team. This position will support AbbVie's pharmaceutical products and be based in our offices in North Chicago, IL, Waltham, MA, South San Francisco, CA, or Irvine, CA with a hybrid work model (onsite 3+ days/week). Acting individually and in cross-functional teams, the Associate General Counsel will develop and implement intellectual property strategies for AbbVie's products and product candidates. Responsibilities: Maximize AbbVie's competitive position through creation and implementation of intellectual property strategies Provide legal advice and counsel to cross-functional R&D and business teams on a variety of IP-related matters Draft, file, and prosecute strategically useful patent applications worldwide both directly and through management of outside counsel Challenge and defend patents in IPR, opposition, interference, and other post-grant proceedings Conduct prior art searches, analyze third-party patent positions, and conduct due diligence to support business development activities Qualifications Requirements: JD degree from an accredited law school, state bar admission enabling in-house practice (specific state not required), and registration to practice before the USPTO 8+ years of experience practicing patent law as an attorney or patent agent at a law firm and/or life sciences company, including substantial U.S. and foreign patent prosecution Experience with India, China, and emerging markets a plus Technical background relevant for pharmaceutical patent prosecution, such as: Experience with small molecule and/or biological pharmaceutical discovery & development, and/or Technical degree in relevant field, such as molecular biology, biotechnology, biochemistry, biology, chemistry, chemical engineering, or biomedical engineering Strong legal, analytical, communication, collaboration, and people skills Demonstrated ability to manage complex projects to meet deadlines Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: What AbbVie Has to Offer Our work can-and does-have a tangible, lasting impact on millions of people. But it's not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.
We are seeking an experienced Waste Classification Lead to join our clients technical team and play a key role in delivering compliant, high-quality soil assessment and waste classification services. This is a senior technical position combining leadership, regulatory expertise, and client-facing responsibilities within a fast-paced commercial environment. The Role As Waste Classification Lead, you will be responsible for overseeing soil classification activities from enquiry through to reporting, ensuring compliance with current waste regulations and company KPIs. You will work closely with the Commercial Director, manage technical staff, and act as a trusted expert for both internal teams and external clients. Key Responsibilities Lead the preparation of tenders alongside the Commercial Director for soil testing and assessment projects Manage and coordinate soil sampling visits to assess quality and chemical composition of waste soils Classify soils in line with prevailing regulatory guidance (including WM3) using client-provided or company analytical data Lead and support a team producing standardised waste classification reports for internal and external use Ensure all enquiries are assessed and results issued to the Commercial Manager within 24 hours, in line with company KPIs Communicate technical assessments clearly to both technical and non-technical clients and colleagues Maintain accurate and detailed records of assessments, findings, and decisions within the company database Personal Attributes & Qualifications HND in Chemistry (or higher), with a strong understanding of soil field testing methods (e.g. XRF, UV fluorescence) and third-party laboratory analysis Extensive experience with WM3, HazWaste Online, and hazardous waste regulations for external reporting Strong understanding of the regulatory framework for compliant soil disposal Highly organised with excellent administrative skills and attention to detail Confident communicator with the ability to engage a wide range of stakeholders Intelligent, well-rounded, and approachable personality Strong commitment to quality, compliance, and the overall success of the business Why Join Us? Key leadership role within a growing technical and commercial team Varied workload combining technical expertise, client interaction, and strategic input Excellent salary and bonus scheme as well as package including healthcare and pension. To be considered for this role, please send a cv or call (phone number removed) quoting reference M9628
Feb 05, 2026
Full time
We are seeking an experienced Waste Classification Lead to join our clients technical team and play a key role in delivering compliant, high-quality soil assessment and waste classification services. This is a senior technical position combining leadership, regulatory expertise, and client-facing responsibilities within a fast-paced commercial environment. The Role As Waste Classification Lead, you will be responsible for overseeing soil classification activities from enquiry through to reporting, ensuring compliance with current waste regulations and company KPIs. You will work closely with the Commercial Director, manage technical staff, and act as a trusted expert for both internal teams and external clients. Key Responsibilities Lead the preparation of tenders alongside the Commercial Director for soil testing and assessment projects Manage and coordinate soil sampling visits to assess quality and chemical composition of waste soils Classify soils in line with prevailing regulatory guidance (including WM3) using client-provided or company analytical data Lead and support a team producing standardised waste classification reports for internal and external use Ensure all enquiries are assessed and results issued to the Commercial Manager within 24 hours, in line with company KPIs Communicate technical assessments clearly to both technical and non-technical clients and colleagues Maintain accurate and detailed records of assessments, findings, and decisions within the company database Personal Attributes & Qualifications HND in Chemistry (or higher), with a strong understanding of soil field testing methods (e.g. XRF, UV fluorescence) and third-party laboratory analysis Extensive experience with WM3, HazWaste Online, and hazardous waste regulations for external reporting Strong understanding of the regulatory framework for compliant soil disposal Highly organised with excellent administrative skills and attention to detail Confident communicator with the ability to engage a wide range of stakeholders Intelligent, well-rounded, and approachable personality Strong commitment to quality, compliance, and the overall success of the business Why Join Us? Key leadership role within a growing technical and commercial team Varied workload combining technical expertise, client interaction, and strategic input Excellent salary and bonus scheme as well as package including healthcare and pension. To be considered for this role, please send a cv or call (phone number removed) quoting reference M9628
