Talent STEM is supporting a leading UK waste and resource management organisation in the search for a Waste Management Chemist to join its Waste Treatment Division based in Sheffield. This is an excellent opportunity for a chemistry professional to apply their technical expertise in a practical, customer-focused environment. The successful candidate will support the safe handling, transportation, and disposal of hazardous and non-hazardous waste, ensuring compliance with environmental and safety legislation. Please note: This opportunity is open to both recent Chemistry or Chemical Engineering graduates and experienced Waste Chemists. The role may involve early start times (as early as 4:00am or 5:00am) and, in addition to the duties listed above, may include visiting client sites to collect hazardous waste. The role As a Waste Management Chemist, you will provide technical and operational support to customers and internal teams across the Waste Treatment Division. You ll be responsible for advising on waste classification, segregation, and labelling, as well as supporting transport and documentation processes. Key responsibilities: - Visit customer sites to support the safe and compliant management of hazardous and non-hazardous waste - Ensure waste is correctly listed, labelled, and transported in accordance with current regulations - Prepare transport documentation, waste labels, and data for invoicing - Work closely with operations, logistics, and commercial teams to deliver technical support - Assess sales enquiries and provide input on waste characterisation and handling requirements - Build and maintain strong relationships with customers and colleagues - Promote safe working practices and adherence to company procedures and policies About you You ll be a proactive, detail-oriented individual with a strong background in chemistry and a commitment to environmental compliance and safety. Essential requirements: - Degree in Chemistry or a related discipline - Full, clean UK driving licence (licence to drive a 7.5T vehicle or under advantageous) - Strong organisational and communication skills - Ability to work both independently and as part of a small, supportive team - Flexible approach to working hours and willingness to provide cover at short notice Desirable: - Experience in a waste assessment role - Previous experience in a waste management, laboratory, or environmental services role What s on offer - Competitive salary and discretionary bonus scheme - 25 days annual leave plus bank holidays - Pension and life insurance - Ongoing training, competency development, and clear career progression - Flexible benefits including high street discounts, cycle-to-work scheme, and gym membership options The company Our client is one of the UK s most respected names in waste and resource management, operating a nationwide network of facilities dedicated to reducing landfill and maximising resource recovery. With a strong commitment to sustainability and innovation, they play a vital role in helping businesses reduce their environmental impact and contribute to a circular economy. How to apply If you re a chemistry professional looking to apply your technical expertise in an environmental setting, we d love to hear from you. Apply today with your CV to Talent STEM.
Dec 06, 2025
Full time
Talent STEM is supporting a leading UK waste and resource management organisation in the search for a Waste Management Chemist to join its Waste Treatment Division based in Sheffield. This is an excellent opportunity for a chemistry professional to apply their technical expertise in a practical, customer-focused environment. The successful candidate will support the safe handling, transportation, and disposal of hazardous and non-hazardous waste, ensuring compliance with environmental and safety legislation. Please note: This opportunity is open to both recent Chemistry or Chemical Engineering graduates and experienced Waste Chemists. The role may involve early start times (as early as 4:00am or 5:00am) and, in addition to the duties listed above, may include visiting client sites to collect hazardous waste. The role As a Waste Management Chemist, you will provide technical and operational support to customers and internal teams across the Waste Treatment Division. You ll be responsible for advising on waste classification, segregation, and labelling, as well as supporting transport and documentation processes. Key responsibilities: - Visit customer sites to support the safe and compliant management of hazardous and non-hazardous waste - Ensure waste is correctly listed, labelled, and transported in accordance with current regulations - Prepare transport documentation, waste labels, and data for invoicing - Work closely with operations, logistics, and commercial teams to deliver technical support - Assess sales enquiries and provide input on waste characterisation and handling requirements - Build and maintain strong relationships with customers and colleagues - Promote safe working practices and adherence to company procedures and policies About you You ll be a proactive, detail-oriented individual with a strong background in chemistry and a commitment to environmental compliance and safety. Essential requirements: - Degree in Chemistry or a related discipline - Full, clean UK driving licence (licence to drive a 7.5T vehicle or under advantageous) - Strong organisational and communication skills - Ability to work both independently and as part of a small, supportive team - Flexible approach to working hours and willingness to provide cover at short notice Desirable: - Experience in a waste assessment role - Previous experience in a waste management, laboratory, or environmental services role What s on offer - Competitive salary and discretionary bonus scheme - 25 days annual leave plus bank holidays - Pension and life insurance - Ongoing training, competency development, and clear career progression - Flexible benefits including high street discounts, cycle-to-work scheme, and gym membership options The company Our client is one of the UK s most respected names in waste and resource management, operating a nationwide network of facilities dedicated to reducing landfill and maximising resource recovery. With a strong commitment to sustainability and innovation, they play a vital role in helping businesses reduce their environmental impact and contribute to a circular economy. How to apply If you re a chemistry professional looking to apply your technical expertise in an environmental setting, we d love to hear from you. Apply today with your CV to Talent STEM.
Reporting to the Director of Quality Control, the QC Microbiology Manager provides strategic managerial direction and technical leadership for the Quality Control laboratory operations, ensuring samples are tested to GMP standards in a timely and efficient manner, to meet the needs of the business. Duties include financial tracking, reporting and management of a significant budget, ensuring compliance with company policies, and managing and developing staff. Manages Quality Control activities to ensure compliance with company standards, GMP and regulatory guidelines Ensures all testing (routine, project, investigational, validation) is completed in accordance with scheduled timelines and to relevant specifications/criteria Ensures teams engagement and collaboration through Site Management System (SMS), including Tier meetings, escalation processes and continuous improvement Oversees activities related to transfer/implementation of analytical methods/equipment Ensure handling of investigations is completed on time, and to the required standards. Providing technical guidance and decision making when required. To include management of out of specification (OOS) and deviation investigations, change controls, regulatory actions and closure of assigned corrective/preventative actions. Approves GMP-related data, to support batch release Ensures departmental standard operating procedures (SOP) are in place, up to date and relevant Engages and collaborates with enterprise initiatives and forums to share best practices and deliver improvements. Has oversight of department training, ensuring department is achieving necessary training KPIs Responsible for the operational management of the QC laboratories within remit of role, ensuring appropriate standards of cGMP, HSE, housekeeping and discipline are applied in the department in accordance with relevant regulations. Provides strong leadership and organisational planning skills. Responsible for mentoring and development of staff technically and professionally. Supports efforts across multiple areas to accomplish goals, providing guidance and influencing the organisation Provides strategic direction and in depth technical expertise, to include determining future resource needs, outsourcing and insourcing assessments, continuous improvement potential, and technical needs to be operationally excellent. Develops and cascades functional deliverables in alignment with the site objectives, providing clear vision of goals and tangible results Provides clear and effective communication (written and oral) to staff and external stakeholders. Interfaces across management levels and departments Acts as lead presenter during regulatory inspections for areas of responsibility Develops and delivers to schedule and budget. Responsible for budgeting, monitoring, forecasting, and reporting cost and schedule Provides strong leadership on safety and creates a positive safety culture. Ensuring safety is always on the front line Requires comprehensive understanding of concepts, theories and principles within own discipline and knowledge of others. Applies in-depth understanding of how own discipline integrates within the function. Identifies and resolves complex technical, operational and organisational problems Supports supervisors in understanding the development needs of direct reports, assisting them in accessing appropriate assessment tools and providing insight and guidance. Assists in constructing and executing compelling development plans for direct reports, shaping developmental roles and assignments to balance individual and business function needs Provides in depth, one-on-one coaching to enable team members to achieve performance goals and maximise their potential Sets stretching objectives and goals, creating an organised plan for distributing the workload across multiple teams in the function Ensures that employees within the function have the necessary skills and resources to succeed in tasks, resolving skill gaps by providing training and guidance Brings out the best in people by recognising and rewarding initiative, supporting decisions taken by others to guide work across the function Qualifications Bachelor degree in a relevant scientific discipline (biology, microbiology, chemistry, etc.); advanced degree a plus Knowledge in Lean Principles/Continuous Improvement or a similar discipline Capabilities 5+ years' experience in microbiological and biological, chemical or biochemical analytics in a biologics/pharmaceutical GMP environment 4+ management/demonstrated leadership experience Knowledge of test methods, method validation, regulatory guidelines that apply to our industry Knowledge/demonstration of exposure to external regulatory health authority inspections/audits Please be advised this is a 12 Month Fixed Term Contract, internal candidates are invited to apply aligned to Secondment principles Our Benefits CSL Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives. Learn more about some of the benefits you can participate in when you join CSL Seqirus. About CSL Seqirus CSL Seqirus is part ofCSL. As one of the largest influenza vaccine providers in the world, CSL Seqirusis a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. With state-of-the-art production facilities in the U.S., the U.K. and Australia, CSL Seqirus utilizes egg, cell and adjuvant technologies to offer a broad portfolio of differentiated influenza vaccines in more than 20 countries around the world. We want Seqirus to reflect the world around us At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. Learn more Inclusion and Belonging CSL. Do work that matters at CSL Seqirus! Watch our On the Front Line video to learn more about CSL Seqirus JBRP1_UKTJ
Dec 06, 2025
Full time
Reporting to the Director of Quality Control, the QC Microbiology Manager provides strategic managerial direction and technical leadership for the Quality Control laboratory operations, ensuring samples are tested to GMP standards in a timely and efficient manner, to meet the needs of the business. Duties include financial tracking, reporting and management of a significant budget, ensuring compliance with company policies, and managing and developing staff. Manages Quality Control activities to ensure compliance with company standards, GMP and regulatory guidelines Ensures all testing (routine, project, investigational, validation) is completed in accordance with scheduled timelines and to relevant specifications/criteria Ensures teams engagement and collaboration through Site Management System (SMS), including Tier meetings, escalation processes and continuous improvement Oversees activities related to transfer/implementation of analytical methods/equipment Ensure handling of investigations is completed on time, and to the required standards. Providing technical guidance and decision making when required. To include management of out of specification (OOS) and deviation investigations, change controls, regulatory actions and closure of assigned corrective/preventative actions. Approves GMP-related data, to support batch release Ensures departmental standard operating procedures (SOP) are in place, up to date and relevant Engages and collaborates with enterprise initiatives and forums to share best practices and deliver improvements. Has oversight of department training, ensuring department is achieving necessary training KPIs Responsible for the operational management of the QC laboratories within remit of role, ensuring appropriate standards of cGMP, HSE, housekeeping and discipline are applied in the department in accordance with relevant regulations. Provides strong leadership and organisational planning skills. Responsible for mentoring and development of staff technically and professionally. Supports efforts across multiple areas to accomplish goals, providing guidance and influencing the organisation Provides strategic direction and in depth technical expertise, to include determining future resource needs, outsourcing and insourcing assessments, continuous improvement potential, and technical needs to be operationally excellent. Develops and cascades functional deliverables in alignment with the site objectives, providing clear vision of goals and tangible results Provides clear and effective communication (written and oral) to staff and external stakeholders. Interfaces across management levels and departments Acts as lead presenter during regulatory inspections for areas of responsibility Develops and delivers to schedule and budget. Responsible for budgeting, monitoring, forecasting, and reporting cost and schedule Provides strong leadership on safety and creates a positive safety culture. Ensuring safety is always on the front line Requires comprehensive understanding of concepts, theories and principles within own discipline and knowledge of others. Applies in-depth understanding of how own discipline integrates within the function. Identifies and resolves complex technical, operational and organisational problems Supports supervisors in understanding the development needs of direct reports, assisting them in accessing appropriate assessment tools and providing insight and guidance. Assists in constructing and executing compelling development plans for direct reports, shaping developmental roles and assignments to balance individual and business function needs Provides in depth, one-on-one coaching to enable team members to achieve performance goals and maximise their potential Sets stretching objectives and goals, creating an organised plan for distributing the workload across multiple teams in the function Ensures that employees within the function have the necessary skills and resources to succeed in tasks, resolving skill gaps by providing training and guidance Brings out the best in people by recognising and rewarding initiative, supporting decisions taken by others to guide work across the function Qualifications Bachelor degree in a relevant scientific discipline (biology, microbiology, chemistry, etc.); advanced degree a plus Knowledge in Lean Principles/Continuous Improvement or a similar discipline Capabilities 5+ years' experience in microbiological and biological, chemical or biochemical analytics in a biologics/pharmaceutical GMP environment 4+ management/demonstrated leadership experience Knowledge of test methods, method validation, regulatory guidelines that apply to our industry Knowledge/demonstration of exposure to external regulatory health authority inspections/audits Please be advised this is a 12 Month Fixed Term Contract, internal candidates are invited to apply aligned to Secondment principles Our Benefits CSL Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives. Learn more about some of the benefits you can participate in when you join CSL Seqirus. About CSL Seqirus CSL Seqirus is part ofCSL. As one of the largest influenza vaccine providers in the world, CSL Seqirusis a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. With state-of-the-art production facilities in the U.S., the U.K. and Australia, CSL Seqirus utilizes egg, cell and adjuvant technologies to offer a broad portfolio of differentiated influenza vaccines in more than 20 countries around the world. We want Seqirus to reflect the world around us At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. Learn more Inclusion and Belonging CSL. Do work that matters at CSL Seqirus! Watch our On the Front Line video to learn more about CSL Seqirus JBRP1_UKTJ
Principal Technical Safety Consultants (CFD-FLACS) Background Risktec Solutions is an established, independent and specialist risk management consulting and training company, and is part of the TV Rheinland Group. We help clients to manage health, safety, security, environmental and business risk in sectors where the impact of loss is significant. Our people are high calibre professionals, with a strong focus on meeting clients expectations and we have offices across the UK and in the Netherlands, Dubai, Muscat, Houston and Calgary. Further information is available at . Risktec has a number of vacancies across the company and in particular we are looking for experienced risk and safety consultants to be based in our London office to support clients in the following sectors: oil and gas (offshore and onshore) carbon capture and storage chemical manufacturing, handling and storage hydrogen generation and distribution onshore and offshore wind energy. Role Description The successful candidate will be part of an energetic, expanding team, and will be expected to work effectively and collaboratively with colleagues on multiple projects in a supportive, progressive environment. This permanent position would be based preferably at our London office, but our other office locations will also be considered. The role would involve occasional travel to UK and world-wide locations to meet project requirements. Key Skills Applicants should have a relevant science or engineering degree, and possess strong analytical thinking, numerical, written and verbal communication skills. The candidate must have a minimum of 5 years of relevant experience in some or all of the following: Proven experience in Computational Fluid Dynamics (CFD) simulation, ideally in the context of technical safety for industries (e.g., oil and gas, chemical processing, clean energy, etc.). Experience in the use of software packages such as FLACS-CFD, ANSYS Fluent / CFX, DNV KFX, or FDS to analyse fluid flow, dispersion, explosion, and fire dynamics. Strong understanding of fluid dynamics, thermodynamics, combustion chemistry and explosion science in process safety. Ability to work with complex models and large datasets, performing detailed analysis using programming languages and tools, and troubleshooting simulation issues. Support and guide junior engineers or team members where required, providing leadership on both technical and project delivery aspects. Excellent communication skills both written and verbal, with experience in writing technical reports and presenting findings to a wide range of stakeholders. Project planning and management able to lead technical safety projects from initiation through to completion, ensuring adherence to scope, budget, and timelines. Expertise in developing technical proposals, with a proven ability to translate client needs into innovative and cost-effective solutions, delivering high-quality technical outcomes within reasonable budget constraints. Experience in the following areas is also desirable: QRA and other technical safety studies (BRA, EERA, ESSA, FERA, Facility Siting Studies, etc.). Fire and Gas Mapping. Experience in the use of other software consequence modelling packages such as SAFETI, PHAST, FRED, SHEPHERD, Reliability / Availability Workbench. Reliability, Availability and Maintainability (RAM) studies. Functional Safety. Solid understanding of HPC and cloud computing environments, with experience in leveraging these platforms for complex simulations. Experience in handling large-scale CFD projects using HPC and cloud computing. Familiarity with industry regulations and safety standards such as ATEX, DSEAR, API, or other relevant safety standards would be an advantage. Marketing experience to promote technical services to potential clients. Experience in developing marketing materials, client outreach, or business development efforts will be an advantage. Ability to identify and develop business opportunities and contribute to the companys strategic growth through client relationship management and proposal development. Experience in financial management of projects, including budget forecasting and cost control. Our Offer We have an established competence framework, with regular appraisals and a defined pathway for progression. In addition, a competitive package of salary and benefits is offered for permanent staff, including: 33 days annual leave (including public holidays); Flexible working; Company-wide, inclusive profit share scheme; Private medical insurance; Life insurance; Up to 7.5% contribution into a pension scheme; Payment of subscription fees for membership of one professional body. JBRP1_UKTJ
Dec 05, 2025
Full time
Principal Technical Safety Consultants (CFD-FLACS) Background Risktec Solutions is an established, independent and specialist risk management consulting and training company, and is part of the TV Rheinland Group. We help clients to manage health, safety, security, environmental and business risk in sectors where the impact of loss is significant. Our people are high calibre professionals, with a strong focus on meeting clients expectations and we have offices across the UK and in the Netherlands, Dubai, Muscat, Houston and Calgary. Further information is available at . Risktec has a number of vacancies across the company and in particular we are looking for experienced risk and safety consultants to be based in our London office to support clients in the following sectors: oil and gas (offshore and onshore) carbon capture and storage chemical manufacturing, handling and storage hydrogen generation and distribution onshore and offshore wind energy. Role Description The successful candidate will be part of an energetic, expanding team, and will be expected to work effectively and collaboratively with colleagues on multiple projects in a supportive, progressive environment. This permanent position would be based preferably at our London office, but our other office locations will also be considered. The role would involve occasional travel to UK and world-wide locations to meet project requirements. Key Skills Applicants should have a relevant science or engineering degree, and possess strong analytical thinking, numerical, written and verbal communication skills. The candidate must have a minimum of 5 years of relevant experience in some or all of the following: Proven experience in Computational Fluid Dynamics (CFD) simulation, ideally in the context of technical safety for industries (e.g., oil and gas, chemical processing, clean energy, etc.). Experience in the use of software packages such as FLACS-CFD, ANSYS Fluent / CFX, DNV KFX, or FDS to analyse fluid flow, dispersion, explosion, and fire dynamics. Strong understanding of fluid dynamics, thermodynamics, combustion chemistry and explosion science in process safety. Ability to work with complex models and large datasets, performing detailed analysis using programming languages and tools, and troubleshooting simulation issues. Support and guide junior engineers or team members where required, providing leadership on both technical and project delivery aspects. Excellent communication skills both written and verbal, with experience in writing technical reports and presenting findings to a wide range of stakeholders. Project planning and management able to lead technical safety projects from initiation through to completion, ensuring adherence to scope, budget, and timelines. Expertise in developing technical proposals, with a proven ability to translate client needs into innovative and cost-effective solutions, delivering high-quality technical outcomes within reasonable budget constraints. Experience in the following areas is also desirable: QRA and other technical safety studies (BRA, EERA, ESSA, FERA, Facility Siting Studies, etc.). Fire and Gas Mapping. Experience in the use of other software consequence modelling packages such as SAFETI, PHAST, FRED, SHEPHERD, Reliability / Availability Workbench. Reliability, Availability and Maintainability (RAM) studies. Functional Safety. Solid understanding of HPC and cloud computing environments, with experience in leveraging these platforms for complex simulations. Experience in handling large-scale CFD projects using HPC and cloud computing. Familiarity with industry regulations and safety standards such as ATEX, DSEAR, API, or other relevant safety standards would be an advantage. Marketing experience to promote technical services to potential clients. Experience in developing marketing materials, client outreach, or business development efforts will be an advantage. Ability to identify and develop business opportunities and contribute to the companys strategic growth through client relationship management and proposal development. Experience in financial management of projects, including budget forecasting and cost control. Our Offer We have an established competence framework, with regular appraisals and a defined pathway for progression. In addition, a competitive package of salary and benefits is offered for permanent staff, including: 33 days annual leave (including public holidays); Flexible working; Company-wide, inclusive profit share scheme; Private medical insurance; Life insurance; Up to 7.5% contribution into a pension scheme; Payment of subscription fees for membership of one professional body. JBRP1_UKTJ
Are you a recent graduate with a passion for communications and a year of hands on B2B PR experience? We're looking for a B2B PR Account Executive to join a growing team and help shape the narrative for some of the most innovative organisations in science, technology, and engineering. As an Account Executive, you'll play a pivotal role in delivering impactful PR campaigns for clients across the STEM sector. You'll combine your scientific knowledge with creative storytelling to translate complex ideas into clear, compelling messages and help amplify the voices of innovators shaping the future. Key Responsibilities Support the planning and execution of B2B PR campaigns across STEM industries Draft press releases, thought leadership articles, and client communications Build and maintain relationships with journalists, analysts, and industry stakeholders Monitor media coverage and report on campaign performance Collaborate with senior team members to deliver strategic client outcomes Provide client relations support to global clients with big budgets About You • Degree Educated - a science-related discipline preferable. e.g., biology, chemistry, physics, engineering, or similar but flexible for the right experience • Minimum 12 months' experience in B2B Agency PR or communications • Strong writing skills with the ability to simplify technical concepts • Detail-oriented, proactive, and eager to learn in a fast-paced environment • Passionate about STEM innovation and its impact on business and society If you're ready to take your PR skills to the next level, apply today for an immediate interview. At Fourteen People, we are committed to offering equal opportunities to all candidates regardless of race, religion, gender, sexuality, disability, age or any other protected characteristics. We understand there is still much to be done as we partner with our clients to create and improve robust recruitment processes that will improve diversity equity and inclusion in the workplace. Fourteen People Ltd is acting as an Employment Agency in relation to this vacancy .
Dec 05, 2025
Full time
Are you a recent graduate with a passion for communications and a year of hands on B2B PR experience? We're looking for a B2B PR Account Executive to join a growing team and help shape the narrative for some of the most innovative organisations in science, technology, and engineering. As an Account Executive, you'll play a pivotal role in delivering impactful PR campaigns for clients across the STEM sector. You'll combine your scientific knowledge with creative storytelling to translate complex ideas into clear, compelling messages and help amplify the voices of innovators shaping the future. Key Responsibilities Support the planning and execution of B2B PR campaigns across STEM industries Draft press releases, thought leadership articles, and client communications Build and maintain relationships with journalists, analysts, and industry stakeholders Monitor media coverage and report on campaign performance Collaborate with senior team members to deliver strategic client outcomes Provide client relations support to global clients with big budgets About You • Degree Educated - a science-related discipline preferable. e.g., biology, chemistry, physics, engineering, or similar but flexible for the right experience • Minimum 12 months' experience in B2B Agency PR or communications • Strong writing skills with the ability to simplify technical concepts • Detail-oriented, proactive, and eager to learn in a fast-paced environment • Passionate about STEM innovation and its impact on business and society If you're ready to take your PR skills to the next level, apply today for an immediate interview. At Fourteen People, we are committed to offering equal opportunities to all candidates regardless of race, religion, gender, sexuality, disability, age or any other protected characteristics. We understand there is still much to be done as we partner with our clients to create and improve robust recruitment processes that will improve diversity equity and inclusion in the workplace. Fourteen People Ltd is acting as an Employment Agency in relation to this vacancy .
OPPORTUNITY FOR AN EXPERIENCED HAZARDOUS WASTE SITE CHEMIST OR A CHEMISTRY GRADUATE TO DEVELOP A CAREER WITH A LEADING WASTE MANAGEMENT COMPANY TITLE: Site Chemist / Chemistry Graduate - Hazardous Waste SALARY: Graduate - 30,300 up to 38,000 with EXTENSIVE hazardous waste SECTOR experience LOCATION: Walsall Area ROLE: Site Chemist / Chemistry Graduate - Hazardous Waste THIS ROLE IS PRIMARILY SITE-BASED AND WOULD SUIT A HANDS-ON INDIVIDUAL WHO ENJOYS WORKING OUTDOORS, AS 75% OF THE WORK WILL BE CONDUCTED ON-SITE WITH ONLY LIMITED LAB WORK. FLT Operation (training given) You will work in a hazardous waste management processing yard, where you will be responsible for unloading and testing incoming materials for pH, flammability, and compatibility for bulking. You will ensure that all goods are correctly labelled and complete all relevant paperwork. Additionally, you will ensure compliance with safety, environmental, and company policies. EXPERIENCE: Site Chemist / Chemistry Graduate - Hazardous Waste Due to the location a driving licence is essential. Ideally you could be an experienced Site Chemist, Process Chemist, Technical Assessor, Transfer Station Chemist, Laboratory Technician, Industrial Chemist, Shift Chemist, or Reception Chemist with a HNC or above You may be a Chemistry or Biochemistry Graduate looking for your first role. HNC Minimum Any forklift experience or yard or warehouse experience a plus, but full training given. You will demonstrate willingness to work outside and may have interests that demonstrate that e.g. playing outdoor sports, Duke of Edinburgh, previous jobs, outdoor enthusiast
Dec 05, 2025
Full time
OPPORTUNITY FOR AN EXPERIENCED HAZARDOUS WASTE SITE CHEMIST OR A CHEMISTRY GRADUATE TO DEVELOP A CAREER WITH A LEADING WASTE MANAGEMENT COMPANY TITLE: Site Chemist / Chemistry Graduate - Hazardous Waste SALARY: Graduate - 30,300 up to 38,000 with EXTENSIVE hazardous waste SECTOR experience LOCATION: Walsall Area ROLE: Site Chemist / Chemistry Graduate - Hazardous Waste THIS ROLE IS PRIMARILY SITE-BASED AND WOULD SUIT A HANDS-ON INDIVIDUAL WHO ENJOYS WORKING OUTDOORS, AS 75% OF THE WORK WILL BE CONDUCTED ON-SITE WITH ONLY LIMITED LAB WORK. FLT Operation (training given) You will work in a hazardous waste management processing yard, where you will be responsible for unloading and testing incoming materials for pH, flammability, and compatibility for bulking. You will ensure that all goods are correctly labelled and complete all relevant paperwork. Additionally, you will ensure compliance with safety, environmental, and company policies. EXPERIENCE: Site Chemist / Chemistry Graduate - Hazardous Waste Due to the location a driving licence is essential. Ideally you could be an experienced Site Chemist, Process Chemist, Technical Assessor, Transfer Station Chemist, Laboratory Technician, Industrial Chemist, Shift Chemist, or Reception Chemist with a HNC or above You may be a Chemistry or Biochemistry Graduate looking for your first role. HNC Minimum Any forklift experience or yard or warehouse experience a plus, but full training given. You will demonstrate willingness to work outside and may have interests that demonstrate that e.g. playing outdoor sports, Duke of Edinburgh, previous jobs, outdoor enthusiast
Starting salary £23,500 + plus benefits and welcome bonus Office based in Aldermaston, nr Reading, Berkshire. We are offering a rewarding and exciting one-year placement as an Undergraduate Materials & Systems Modeller at AWE - a role where you will make a genuine contribution to keeping the UK safe and secure. Entry Requirements We are interested in applications from candidates working towards a degree in: Mathematics (with modelling experience), Physics, Computer Science Materials Science, Chemistry students who can demonstrate strong maths or programming skills. Before starting with the business, you will need to be able to provide evidence that you have attained a minimum of a 2:2 in your degree so far by August 2026. You must be able to Join AWE in August 2026. We recruit on a rolling basis which means as soon as our positions have been filled, we will close. What to Expect on the Programme This role desk and lab based, so you can expect to work across these environments. Materials and Analytical Science at AWE supports the life cycle of warhead components and technologies to ensure the reliability of the UK's strategic deterrent and national security mission.A nuclear warhead contains a vast range of materials including metals, ceramics, inorganic salts, rubbers, foams, adhesives, high explosives and radioactive substances.Materials and Analytical Science is critical to understanding and predicting the behaviour of these types of materials under various conditions. As an undergraduate student within the Modelling Team in Materials and Analytical Science, you will get the opportunity to work in an exciting part of AWE through projects which may include working on a range of models and codes, utilising several coding languages, helping deliver our mission. Most importantly we are looking for enthusiastic individuals keen to get involved and work on interesting research and tasks. The Modelling Team work on the full model development lifecycle. Some of the projects you may get to work on include: Working with other Materials and Analytical Scientists to characterise material ageing processes, proposing approaches to model the observed trends Using a variety of statistical techniques to analyse experimental data Writing, developing and running codes written in a range of languages (e.g. MATLAB, Mathematica, OpenFOAM and R) Utilising computational techniques for parameter optimization Verifying and validating codes by identifying suitable test cases, determining analytical solutions where appropriate Benefits: £23,500 salary Holiday entitlement of 270 hours of leave annually including bank holidays Excellent work/life balance and a vibrant and welcoming grad social scene 9-day working fortnight - so every other Friday off A salary-sacrifice benefit scheme A welcome payment Potential to secure a Graduate role for when you finish university, subject to availability Access to savings on a wide range of everyday spending across retail, hospitality and leisure Access to our Employee Assistance Programme Access to our Occupational Health Services Application Process: Our process is designed to be simple, fair and transparent: Online Application Opens 15th September. Explore the option and apply for one pathway that best suits your interests and goals. Online Tests If shortlisted, youll complete numerical, verbal, logical and cognitive assessments. Practice materials will be available to ensure you know what to expect. Virtual Assessment Centre Successful candidates will be invited to virtual ACs running NovDec 2025, with pre-assessment webinars to guide you. You must be a British National, able to start in August 2026, and eligible for security clearance. Applications close on Friday 24th October, but will close earlier if we receive enough applications, so apply early. Support & Inclusion: We welcome diverse applicants and strive to create a workplace where differences are recognised and celebrated. We encourage requests for reasonable adjustments if required, to ensure you feel able to perform your best. Any information you share will be used only to support you through the process in line with GDPR. Why AWE?: Build leadership skills, self-awareness, and teamwork. Join a vibrant early careers community with events, ERGs and networking opportunities. Benefit from continual support: a line manager, pathway lead, and buddy to guide your journey. Who Were Looking For: Curious, problem-solvers with integrity, resilience, and a collaborative mindset. Youll thrive if youre eager to grow and ready to apply your skills to real-world challenges. JBRP1_UKTJ
Dec 05, 2025
Full time
Starting salary £23,500 + plus benefits and welcome bonus Office based in Aldermaston, nr Reading, Berkshire. We are offering a rewarding and exciting one-year placement as an Undergraduate Materials & Systems Modeller at AWE - a role where you will make a genuine contribution to keeping the UK safe and secure. Entry Requirements We are interested in applications from candidates working towards a degree in: Mathematics (with modelling experience), Physics, Computer Science Materials Science, Chemistry students who can demonstrate strong maths or programming skills. Before starting with the business, you will need to be able to provide evidence that you have attained a minimum of a 2:2 in your degree so far by August 2026. You must be able to Join AWE in August 2026. We recruit on a rolling basis which means as soon as our positions have been filled, we will close. What to Expect on the Programme This role desk and lab based, so you can expect to work across these environments. Materials and Analytical Science at AWE supports the life cycle of warhead components and technologies to ensure the reliability of the UK's strategic deterrent and national security mission.A nuclear warhead contains a vast range of materials including metals, ceramics, inorganic salts, rubbers, foams, adhesives, high explosives and radioactive substances.Materials and Analytical Science is critical to understanding and predicting the behaviour of these types of materials under various conditions. As an undergraduate student within the Modelling Team in Materials and Analytical Science, you will get the opportunity to work in an exciting part of AWE through projects which may include working on a range of models and codes, utilising several coding languages, helping deliver our mission. Most importantly we are looking for enthusiastic individuals keen to get involved and work on interesting research and tasks. The Modelling Team work on the full model development lifecycle. Some of the projects you may get to work on include: Working with other Materials and Analytical Scientists to characterise material ageing processes, proposing approaches to model the observed trends Using a variety of statistical techniques to analyse experimental data Writing, developing and running codes written in a range of languages (e.g. MATLAB, Mathematica, OpenFOAM and R) Utilising computational techniques for parameter optimization Verifying and validating codes by identifying suitable test cases, determining analytical solutions where appropriate Benefits: £23,500 salary Holiday entitlement of 270 hours of leave annually including bank holidays Excellent work/life balance and a vibrant and welcoming grad social scene 9-day working fortnight - so every other Friday off A salary-sacrifice benefit scheme A welcome payment Potential to secure a Graduate role for when you finish university, subject to availability Access to savings on a wide range of everyday spending across retail, hospitality and leisure Access to our Employee Assistance Programme Access to our Occupational Health Services Application Process: Our process is designed to be simple, fair and transparent: Online Application Opens 15th September. Explore the option and apply for one pathway that best suits your interests and goals. Online Tests If shortlisted, youll complete numerical, verbal, logical and cognitive assessments. Practice materials will be available to ensure you know what to expect. Virtual Assessment Centre Successful candidates will be invited to virtual ACs running NovDec 2025, with pre-assessment webinars to guide you. You must be a British National, able to start in August 2026, and eligible for security clearance. Applications close on Friday 24th October, but will close earlier if we receive enough applications, so apply early. Support & Inclusion: We welcome diverse applicants and strive to create a workplace where differences are recognised and celebrated. We encourage requests for reasonable adjustments if required, to ensure you feel able to perform your best. Any information you share will be used only to support you through the process in line with GDPR. Why AWE?: Build leadership skills, self-awareness, and teamwork. Join a vibrant early careers community with events, ERGs and networking opportunities. Benefit from continual support: a line manager, pathway lead, and buddy to guide your journey. Who Were Looking For: Curious, problem-solvers with integrity, resilience, and a collaborative mindset. Youll thrive if youre eager to grow and ready to apply your skills to real-world challenges. JBRP1_UKTJ
Site Name: UK - County Durham - Barnard Castle Posted Date: Dec 2 2025 GSK Barnard Castle is a key secondary manufacturing site and has invested heavily in industry 4.0 state of the art, bespoke equipment to support sustained new product introductions and volume increases, and as a key supplier of some of GSK's blockbuster products, the site contributes revenues of $2Bn annually. We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work. Discover more about our company wide benefits and life at GSK on our webpage Life at GSK GSK The Sterility Assurance Facility Manager leads sterility assurance projects and has overall oversight of facilities within their areas of responsibility, ensuring compliance with regulatory requirements and industry standards. This role drives contamination control strategies (CCS), ensures the implementation of sterility assurance measures across site facilities, and collaborates with operations to ensure the consistent application of sterility assurance requirements. In this role you will Lead sterility assurance projects to ensure contamination control strategies (CCS) are effectively implemented and aligned with site objectives and regulatory requirements. Provide overall oversight of facility operations, ensuring compliance with sterility assurance standards and contamination control measures. Drive the implementation of sterility assurance programmes across facilities, collaborating with cross-functional teams site and above site teams to ensure consistency and effectiveness. Ensure facilities are maintained and operated in alignment with industry best practices, regulatory requirements, and contamination prevention principles. Collaborate with operations and quality teams to ensure contamination control measures are integrated effectively into manufacturing processes. Monitor performance metrics related to facility operations and contamination control, identifying areas for improvement and implementing corrective actions as needed. Act as the primary point of contact for sterility assurance within facilities, representing the team during audits, inspections, and internal reviews. Contribute to the harmonisation and continuous improvement of sterility assurance practices across the organisation, sharing knowledge and best practices. Develop and deliver training programmes, ensuring staff understand and consistently apply sterility assurance and contamination control measures. Support the strategic planning and execution of facility upgrades or projects to optimise contamination control systems and ensure regulatory compliance. Why you? Basic Qualifications & Skills: Bachelor's degree in Chemistry, Biochemistry, Microbiology, or a related field Significant experience in sterility assurance within the pharmaceutical, biotechnology, or related industry Strong knowledge of regulatory requirements around sterility assurance and sterile manufacturing (e.g., FDA, MHRA, EMA) and industry standards (e.g., cGMP, ISO). Excellent problem-solving skills and attention to detail. Strong leadership and project management abilities. Effective communication and interpersonal skills. Preferred Qualifications & Skills: An advanced degree in Chemistry, Biochemistry, Microbiology, or a related field provides advanced knowledge of the scientific principles and methodologies that are crucial for ensuring product quality in the pharmaceutical industry. Closing Date: Closing Date: 16th December 2025 (COB) Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the 'cover letter' of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on or . The helpline is available from 8.30am to 12.00 noon Monday to Friday, during bank holidays these times and days may vary.
Dec 05, 2025
Full time
Site Name: UK - County Durham - Barnard Castle Posted Date: Dec 2 2025 GSK Barnard Castle is a key secondary manufacturing site and has invested heavily in industry 4.0 state of the art, bespoke equipment to support sustained new product introductions and volume increases, and as a key supplier of some of GSK's blockbuster products, the site contributes revenues of $2Bn annually. We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work. Discover more about our company wide benefits and life at GSK on our webpage Life at GSK GSK The Sterility Assurance Facility Manager leads sterility assurance projects and has overall oversight of facilities within their areas of responsibility, ensuring compliance with regulatory requirements and industry standards. This role drives contamination control strategies (CCS), ensures the implementation of sterility assurance measures across site facilities, and collaborates with operations to ensure the consistent application of sterility assurance requirements. In this role you will Lead sterility assurance projects to ensure contamination control strategies (CCS) are effectively implemented and aligned with site objectives and regulatory requirements. Provide overall oversight of facility operations, ensuring compliance with sterility assurance standards and contamination control measures. Drive the implementation of sterility assurance programmes across facilities, collaborating with cross-functional teams site and above site teams to ensure consistency and effectiveness. Ensure facilities are maintained and operated in alignment with industry best practices, regulatory requirements, and contamination prevention principles. Collaborate with operations and quality teams to ensure contamination control measures are integrated effectively into manufacturing processes. Monitor performance metrics related to facility operations and contamination control, identifying areas for improvement and implementing corrective actions as needed. Act as the primary point of contact for sterility assurance within facilities, representing the team during audits, inspections, and internal reviews. Contribute to the harmonisation and continuous improvement of sterility assurance practices across the organisation, sharing knowledge and best practices. Develop and deliver training programmes, ensuring staff understand and consistently apply sterility assurance and contamination control measures. Support the strategic planning and execution of facility upgrades or projects to optimise contamination control systems and ensure regulatory compliance. Why you? Basic Qualifications & Skills: Bachelor's degree in Chemistry, Biochemistry, Microbiology, or a related field Significant experience in sterility assurance within the pharmaceutical, biotechnology, or related industry Strong knowledge of regulatory requirements around sterility assurance and sterile manufacturing (e.g., FDA, MHRA, EMA) and industry standards (e.g., cGMP, ISO). Excellent problem-solving skills and attention to detail. Strong leadership and project management abilities. Effective communication and interpersonal skills. Preferred Qualifications & Skills: An advanced degree in Chemistry, Biochemistry, Microbiology, or a related field provides advanced knowledge of the scientific principles and methodologies that are crucial for ensuring product quality in the pharmaceutical industry. Closing Date: Closing Date: 16th December 2025 (COB) Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the 'cover letter' of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on or . The helpline is available from 8.30am to 12.00 noon Monday to Friday, during bank holidays these times and days may vary.
Help us to make a world of difference Urenco is a global leader in the production of low carbon energy. We work at the cutting edge of the transition to a sustainable, net zero world. We're looking for a Delivery Manager (Environmental). Based at our Capenhurst Site, you'll be responsible for leading a team of Senior Analysts and Analysts providing an exemplar chemistry analytical service to the Capenhurst site and the wider Urenco Group. The Delivery Manager also plays a role in setting on-going Chemistry Services strategy to ensure all customer expectations are met. At Urenco we're committed to giving you opportunities to be your best. If you feel you meet some, but not all of what were looking for, please still apply. We believe in embracing the passion and potential of our people, and to achieve this we offer market leading training and development experiences. Along with the opportunity to be mentored and coached by some of the smartest minds in the industry. What you'll do: • Lead a team of Senior Analyst(s) and Analysts to ensure that an exemplar production analysis service is provided to UUK and UCP • Works with other senior members of the department to identify future services with responsibility and accountability for implementation alongside ensuring a culture of continuous improvement to introduce new analytical methods and improved working practices. • Through informal and formal means effectively communicates with customers to ensure that they receive a high quality and proactive production analysis service. • Review and approve results prior to reporting to the customer. • Carries out reviews working methods, processes and practices to ensure all work is carried out safely. • Carry out quality and method audits to programme and takes responsibility for the implementation of any remedial actions ensuring such actions are communicated to the team in order to maintain an efficient service across the department. • Responsible and accountable for radiological surveys and routine radiological monitoring • Act on behalf of the CS Manger in their absence What do you need to thrive in this role? • Extensive experience of working in a busy analytical chemistry laboratory or other laboratory environment • Experience of introducing and following procedures and practices within a working laboratory where the work requires high level of attention to detail. • Experience of working in a highly regulated environment with significant focus on health and safety • Effective leadership skills with the ability to set objectives, monitor completion and manage individual and collective performance whilst maintaining high levels of engagement within a team • Ability to work on own initiative and programme own work. • Ability to establish rapport with customers in order to understand their requirements and provide solutions that meet or exceed their needs. • Able to identify opportunities to improve the services of the department including ensuring such opportunities are realised and the benefits delivered. • Understanding of criticality control requirements and the handling of chemicals (COSHH) • Ideally you will have experience working in an accredited lab with knowledge of ISO17025, GLP, GMP or GxP. What can you expect from us? More than just a job, we offer a future. More than just a place to work, we provide an opportunity to prosper. As an employee of Urenco you will receive: • Annual leave starting at 25 days, which increases by one day for every two years of service up to a maximum of 30 days. In addition, you will accrue 13 additional days off to be used flexibly. There's also a newly added scheme for buying and selling holiday, up to 5 days. • A diverse range of family friendly policies. including access to Bright Horizons Back-Up Care, which provides UK employees with emergency care options when regular arrangements fall through. • A generous bonus scheme. • A defined contribution pension scheme with up to 16% employer's contribution. • Single private medical and dental cover. • Flexible benefits package, including life assurance and income protection. In addition, you'll have an opportunity to purchase additional benefits that suit your lifestyle and take advantage of tax and NI savings. • Education and training we take pride in helping people learn and develop by supporting, accelerating and directing your learning. As well as the completion of mandatory health and safety courses, training packages will be offered to meet your specific needs. Creating a diverse and inclusive workforce As a truly global company with a presence in the UK, USA, Germany, and the Netherlands, we know that our individual differences make us stronger. Putting people at the heart of our business, we strive to create an open and inclusive workplace that allows every voice to be heard and diversity to thrive. If you require any reasonable adjustments to the recruitment process, please let our talent acquisition team know. Because together, we are one Urenco. We are enriching the world. And enriching your future. JBRP1_UKTJ
Dec 05, 2025
Full time
Help us to make a world of difference Urenco is a global leader in the production of low carbon energy. We work at the cutting edge of the transition to a sustainable, net zero world. We're looking for a Delivery Manager (Environmental). Based at our Capenhurst Site, you'll be responsible for leading a team of Senior Analysts and Analysts providing an exemplar chemistry analytical service to the Capenhurst site and the wider Urenco Group. The Delivery Manager also plays a role in setting on-going Chemistry Services strategy to ensure all customer expectations are met. At Urenco we're committed to giving you opportunities to be your best. If you feel you meet some, but not all of what were looking for, please still apply. We believe in embracing the passion and potential of our people, and to achieve this we offer market leading training and development experiences. Along with the opportunity to be mentored and coached by some of the smartest minds in the industry. What you'll do: • Lead a team of Senior Analyst(s) and Analysts to ensure that an exemplar production analysis service is provided to UUK and UCP • Works with other senior members of the department to identify future services with responsibility and accountability for implementation alongside ensuring a culture of continuous improvement to introduce new analytical methods and improved working practices. • Through informal and formal means effectively communicates with customers to ensure that they receive a high quality and proactive production analysis service. • Review and approve results prior to reporting to the customer. • Carries out reviews working methods, processes and practices to ensure all work is carried out safely. • Carry out quality and method audits to programme and takes responsibility for the implementation of any remedial actions ensuring such actions are communicated to the team in order to maintain an efficient service across the department. • Responsible and accountable for radiological surveys and routine radiological monitoring • Act on behalf of the CS Manger in their absence What do you need to thrive in this role? • Extensive experience of working in a busy analytical chemistry laboratory or other laboratory environment • Experience of introducing and following procedures and practices within a working laboratory where the work requires high level of attention to detail. • Experience of working in a highly regulated environment with significant focus on health and safety • Effective leadership skills with the ability to set objectives, monitor completion and manage individual and collective performance whilst maintaining high levels of engagement within a team • Ability to work on own initiative and programme own work. • Ability to establish rapport with customers in order to understand their requirements and provide solutions that meet or exceed their needs. • Able to identify opportunities to improve the services of the department including ensuring such opportunities are realised and the benefits delivered. • Understanding of criticality control requirements and the handling of chemicals (COSHH) • Ideally you will have experience working in an accredited lab with knowledge of ISO17025, GLP, GMP or GxP. What can you expect from us? More than just a job, we offer a future. More than just a place to work, we provide an opportunity to prosper. As an employee of Urenco you will receive: • Annual leave starting at 25 days, which increases by one day for every two years of service up to a maximum of 30 days. In addition, you will accrue 13 additional days off to be used flexibly. There's also a newly added scheme for buying and selling holiday, up to 5 days. • A diverse range of family friendly policies. including access to Bright Horizons Back-Up Care, which provides UK employees with emergency care options when regular arrangements fall through. • A generous bonus scheme. • A defined contribution pension scheme with up to 16% employer's contribution. • Single private medical and dental cover. • Flexible benefits package, including life assurance and income protection. In addition, you'll have an opportunity to purchase additional benefits that suit your lifestyle and take advantage of tax and NI savings. • Education and training we take pride in helping people learn and develop by supporting, accelerating and directing your learning. As well as the completion of mandatory health and safety courses, training packages will be offered to meet your specific needs. Creating a diverse and inclusive workforce As a truly global company with a presence in the UK, USA, Germany, and the Netherlands, we know that our individual differences make us stronger. Putting people at the heart of our business, we strive to create an open and inclusive workplace that allows every voice to be heard and diversity to thrive. If you require any reasonable adjustments to the recruitment process, please let our talent acquisition team know. Because together, we are one Urenco. We are enriching the world. And enriching your future. JBRP1_UKTJ
Job Title: Senior Purification Scientist Location: Slough Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. Lonza Slough was the first multi-product licensed contract manufacturing facility to be licensed by the FDA, with its original Establishment License for the production of monoclonal antibodies first granted in 1985. What you will get An agile career and dynamic working culture An inclusive and ethical workplace Compensation programs that recognize high performance A variety of benefits depending on role and location Access to global learning and development opportunities Supportive leadership and collaborative teams Opportunities to make a real impact in life sciences The full list of our global benefits can be found at: What you will do Design and execute studies to support process development projects with clear goals and timelines Evaluate and compare purification technologies to optimize downstream processes Develop scalable chromatography and filtration techniques Conduct high-throughput screening of chromatography conditions Analyze complex datasets and draw meaningful conclusions Manage large process data sets and perform statistical analysis Collaborate with cross-functional teams to implement technologies What we are looking for BSc in Biotechnology, Chemistry, or Chemical Engineering Understanding of CDMO operations and GMP requirements Hands-on experience with protein purification techniques Ability to design and optimize purification workflows Experience with biologics such as monoclonal and bispecific antibodies Knowledge of scale-up strategies for manufacturing Strong data analysis skills and scientific reporting Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
Dec 05, 2025
Full time
Job Title: Senior Purification Scientist Location: Slough Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. Lonza Slough was the first multi-product licensed contract manufacturing facility to be licensed by the FDA, with its original Establishment License for the production of monoclonal antibodies first granted in 1985. What you will get An agile career and dynamic working culture An inclusive and ethical workplace Compensation programs that recognize high performance A variety of benefits depending on role and location Access to global learning and development opportunities Supportive leadership and collaborative teams Opportunities to make a real impact in life sciences The full list of our global benefits can be found at: What you will do Design and execute studies to support process development projects with clear goals and timelines Evaluate and compare purification technologies to optimize downstream processes Develop scalable chromatography and filtration techniques Conduct high-throughput screening of chromatography conditions Analyze complex datasets and draw meaningful conclusions Manage large process data sets and perform statistical analysis Collaborate with cross-functional teams to implement technologies What we are looking for BSc in Biotechnology, Chemistry, or Chemical Engineering Understanding of CDMO operations and GMP requirements Hands-on experience with protein purification techniques Ability to design and optimize purification workflows Experience with biologics such as monoclonal and bispecific antibodies Knowledge of scale-up strategies for manufacturing Strong data analysis skills and scientific reporting Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
OPPORTUNITY FOR AN EXPERIENCED HAZARDOUS WASTE SITE CHEMIST OR A CHEMISTRY GRADUATE TO DEVELOP A CAREER WITH A LEADING WASTE MANAGEMENT COMPANY TITLE: Chemistry Graduate / Site Chemist - Hazardous Waste SALARY: 26,500 with no SECTOR experience (negotiable with hazardous waste SECTOR experience) BENEFITS: Bonus up to 1,800 p.a., Death in Service x 2, 25 days holiday + 8 bank holidays, Birthday leave Volunteering Day, Discount Scheme LOCATION: Cannock area You may have had experience in the hazardous waste industry as a Site Chemist, Process Chemist, Technical Assessor, Transfer Station Chemist, Laboratory Technician, Industrial Chemist, Shift Chemist, or Reception Chemist ROLE: Chemistry Graduate / Site Chemist - Hazardous Waste Hands-On Work: 75% of the tasks are conducted outdoors in a hazardous waste processing yard. FLT Operations: Training will be provided for Forklift Truck operation if required Unloading and testing materials for pH, flammability, and compatibility for bulking, and ensuring they appropriately stored Labelling & Documentation: Ensuring all materials are correctly labelled and completing relevant paperwork. Safety & Compliance: Adhering to safety, environmental, and company policies. This role is ideal for someone who enjoys reasonably physical, outdoor work and is comfortable working in a safety-critical environment EXPERIENCE: Chemistry Graduate / Site Chemist - Hazardous Waste You MUST either have an HNC of above in Chemistry, other science degrees, such as Forensic Science, Biochemistry, Chemical Engineering, Environmental Science will not be considered unless 4 of the modules listed on your degree literally contain the word Chemistry (not Chemical), this is a baseline requirement to comply environmental permitting and is sadly non-negotiable Due to the location a driving licence is essential. You may have had experience in the hazardous waste industry as a Site Chemist, Process Chemist, Technical Assessor, Transfer Station Chemist, Laboratory Technician, Industrial Chemist, Shift Chemist, or Reception Chemist Any forklift experience, or yard or warehouse experience a plus, but full training given. You will demonstrate willingness to work outside and may have interests that demonstrate that e.g. playing outdoor sports, Duke of Edinburgh, previous jobs, outdoor enthusiast
Dec 05, 2025
Full time
OPPORTUNITY FOR AN EXPERIENCED HAZARDOUS WASTE SITE CHEMIST OR A CHEMISTRY GRADUATE TO DEVELOP A CAREER WITH A LEADING WASTE MANAGEMENT COMPANY TITLE: Chemistry Graduate / Site Chemist - Hazardous Waste SALARY: 26,500 with no SECTOR experience (negotiable with hazardous waste SECTOR experience) BENEFITS: Bonus up to 1,800 p.a., Death in Service x 2, 25 days holiday + 8 bank holidays, Birthday leave Volunteering Day, Discount Scheme LOCATION: Cannock area You may have had experience in the hazardous waste industry as a Site Chemist, Process Chemist, Technical Assessor, Transfer Station Chemist, Laboratory Technician, Industrial Chemist, Shift Chemist, or Reception Chemist ROLE: Chemistry Graduate / Site Chemist - Hazardous Waste Hands-On Work: 75% of the tasks are conducted outdoors in a hazardous waste processing yard. FLT Operations: Training will be provided for Forklift Truck operation if required Unloading and testing materials for pH, flammability, and compatibility for bulking, and ensuring they appropriately stored Labelling & Documentation: Ensuring all materials are correctly labelled and completing relevant paperwork. Safety & Compliance: Adhering to safety, environmental, and company policies. This role is ideal for someone who enjoys reasonably physical, outdoor work and is comfortable working in a safety-critical environment EXPERIENCE: Chemistry Graduate / Site Chemist - Hazardous Waste You MUST either have an HNC of above in Chemistry, other science degrees, such as Forensic Science, Biochemistry, Chemical Engineering, Environmental Science will not be considered unless 4 of the modules listed on your degree literally contain the word Chemistry (not Chemical), this is a baseline requirement to comply environmental permitting and is sadly non-negotiable Due to the location a driving licence is essential. You may have had experience in the hazardous waste industry as a Site Chemist, Process Chemist, Technical Assessor, Transfer Station Chemist, Laboratory Technician, Industrial Chemist, Shift Chemist, or Reception Chemist Any forklift experience, or yard or warehouse experience a plus, but full training given. You will demonstrate willingness to work outside and may have interests that demonstrate that e.g. playing outdoor sports, Duke of Edinburgh, previous jobs, outdoor enthusiast
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. The role: As an Associate Principal Scientist at Lonza AG, you will lead scientific breakthroughs and drive innovative research to enhance lives through outstanding investigations. Situated in Slough, UK, you will play a vital role in our Protein and Peptide Analytics (PPA) R&D team, applying your expertise in protein interaction measurements to advance our projects. Your responsibilities include independent and team-based research, guaranteeing precise analytical project delivery and supporting our top-tier scientific direction. Your work will not only advance our technical capabilities but also encourage and mentor junior scientists within the team. Your expertise in quantifying antigen interactions for biopharmaceutical using diverse analytical methods is crucial! Key responsibilities: Plan and complete scientific activities including study development, method creation, laboratory tasks, scientific evaluation, mentoring of junior scientists, project oversight, and technology exploration. Evaluate and develop innovative protein interaction workflows to support biologics process development and drive innovation. Perform a range of analyses using SPR, ELISA, and related methods for the characterisation of proteins and their relevant post-translational modifications (PTMs) and critical quality attributes (CQAs). Analyse and interpret complex data, presenting findings to internal collaborators to inform project decisions. Take charge of scientific leadership within the team, facilitating collaboration across the Bio R&D department to align alliances and impact. Act as a Protein Interaction Subject Matter Expert (SME) in multiple collaborative projects, guiding analytical discussions, translating data into project context, and supporting decision-making processes. Key requirements: Degree or equivalent experience in Life Sciences or a related field, with a preferred focus on Biochemistry, Biomanufacturing, or Biotechnology. Extensive practical experience in an analytical laboratory with a focus on protein analysis. Extensive hands-on experience in SPR and ELISA for protein characterization, including operation of Biacore systems and associated software, with a focus on applications in biopharmaceutical research and development is a must have. Attitude towards innovation in the biologics field, with a keen interest in research and excellent scientific writing abilities. Robust foundation in proven analytical methods within the industry, with knowledge of innovative technologies and their applications in biotherapeutic characterisation. Strong communication and interpersonal skills, able to influence collaborators in a scientific capacity and accomplish technical projects within a matrix organisation. Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Dec 05, 2025
Full time
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. The role: As an Associate Principal Scientist at Lonza AG, you will lead scientific breakthroughs and drive innovative research to enhance lives through outstanding investigations. Situated in Slough, UK, you will play a vital role in our Protein and Peptide Analytics (PPA) R&D team, applying your expertise in protein interaction measurements to advance our projects. Your responsibilities include independent and team-based research, guaranteeing precise analytical project delivery and supporting our top-tier scientific direction. Your work will not only advance our technical capabilities but also encourage and mentor junior scientists within the team. Your expertise in quantifying antigen interactions for biopharmaceutical using diverse analytical methods is crucial! Key responsibilities: Plan and complete scientific activities including study development, method creation, laboratory tasks, scientific evaluation, mentoring of junior scientists, project oversight, and technology exploration. Evaluate and develop innovative protein interaction workflows to support biologics process development and drive innovation. Perform a range of analyses using SPR, ELISA, and related methods for the characterisation of proteins and their relevant post-translational modifications (PTMs) and critical quality attributes (CQAs). Analyse and interpret complex data, presenting findings to internal collaborators to inform project decisions. Take charge of scientific leadership within the team, facilitating collaboration across the Bio R&D department to align alliances and impact. Act as a Protein Interaction Subject Matter Expert (SME) in multiple collaborative projects, guiding analytical discussions, translating data into project context, and supporting decision-making processes. Key requirements: Degree or equivalent experience in Life Sciences or a related field, with a preferred focus on Biochemistry, Biomanufacturing, or Biotechnology. Extensive practical experience in an analytical laboratory with a focus on protein analysis. Extensive hands-on experience in SPR and ELISA for protein characterization, including operation of Biacore systems and associated software, with a focus on applications in biopharmaceutical research and development is a must have. Attitude towards innovation in the biologics field, with a keen interest in research and excellent scientific writing abilities. Robust foundation in proven analytical methods within the industry, with knowledge of innovative technologies and their applications in biotherapeutic characterisation. Strong communication and interpersonal skills, able to influence collaborators in a scientific capacity and accomplish technical projects within a matrix organisation. Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Job Description We're currently looking for subject matter experts in Math, Physics, Engineering, Chemistry, and Biology who are interested in working on AI- and LLM-based projects, including data labelling, AI model evaluation, and related tasks on a work-from-home basis. This is a freelance opportunity, and we're looking for candidates who can dedicate 15 or more hours per week. Work will be available regularly, allowing you to maintain a predictable schedule. Job Responsibilities Data Labelling and Annotation: Apply domain knowledge to classify, annotate, and evaluate complex technical material. AI Model Evaluation: Critically assess AI/LLM outputs for scientific accuracy, logical rigor, correctness, and clarity. Quality Assurance: Verify the integrity of scientific reasoning and methodology in model outputs. Task and Dataset Development: Create, refine, and validate domain-specific tasks for training or benchmarking AI systems. Collaboration: Work with project managers, data scientists, and researchers to ensure accurate, high-quality deliverables. Qualifications and Prerequisites A Bachelor's, Master's, or PhD in one of the subject areas listed below. Candidates should be based in the United States, United Kingdom or Germany and preferably educated at accredited U.S, U.K, or German institutions, ideally with an academic background from a top global university. Math: Background in mathematics, statistics, computer science, or data science, with experience in mathematical modelling, statistical inference, numerical analysis, and problem-solving using discrete and computational methods. Physics: Background in engineering or the physical sciences (e.g., mechanical, aerospace, physics, or earth sciences), with proficiency in thermodynamics, fluid mechanics, heat transfer, dynamics, differential equations, and strong quantitative, logical, and computational reasoning. Chemistry: Background in chemical or biochemical engineering, with expertise in transport phenomena, thermodynamics, reaction engineering, unit operations, materials science, differential equations, and system-level problem solving across bioprocessing, materials, and kinetics. Biology: Background in biology or a related life science (e.g., molecular biology, biochemistry, microbiology), with experience in biological systems thinking, experimental design, data interpretation, and hypothesis-driven problem solving. Additional Information Please note that only candidates whose profiles are shortlisted will be contacted. About CACTUS Established in 2002, Cactus Communications () is a leading technology company that specializes in expert services and AI-driven products which improve how research gets funded, published, communicated, and discovered. Its flagship brand Editage offers a comprehensive suite of researcher solutions, including expert services and cutting edge AI products like Mind the Graph, Paperpal, and R Discovery. With offices in Princeton, London, Singapore, Beijing, Shanghai, Seoul, Tokyo, and Mumbai and a global workforce of over 3,000 experts, CACTUS is a pioneer in workplace best practices and has been consistently recognized as a great place to work. Awards and Recognition Employers of the Future, 2024 Excellence in Employer Branding (Gold), 2024 ISO 17100 certification for translation services, 2024 Future of Workplace Disruptor, 2023 Top 100 Companies for Remote Jobs (Ranked ), 2023 Three star "Eruboshi" certification, 2023 India's Best Workplaces for Women (Top 100), 2022 Quartz's Best Companies for Remote Workers, 2022 HR Asia's Best Companies to Work for in Asia, 2021
Dec 05, 2025
Full time
Job Description We're currently looking for subject matter experts in Math, Physics, Engineering, Chemistry, and Biology who are interested in working on AI- and LLM-based projects, including data labelling, AI model evaluation, and related tasks on a work-from-home basis. This is a freelance opportunity, and we're looking for candidates who can dedicate 15 or more hours per week. Work will be available regularly, allowing you to maintain a predictable schedule. Job Responsibilities Data Labelling and Annotation: Apply domain knowledge to classify, annotate, and evaluate complex technical material. AI Model Evaluation: Critically assess AI/LLM outputs for scientific accuracy, logical rigor, correctness, and clarity. Quality Assurance: Verify the integrity of scientific reasoning and methodology in model outputs. Task and Dataset Development: Create, refine, and validate domain-specific tasks for training or benchmarking AI systems. Collaboration: Work with project managers, data scientists, and researchers to ensure accurate, high-quality deliverables. Qualifications and Prerequisites A Bachelor's, Master's, or PhD in one of the subject areas listed below. Candidates should be based in the United States, United Kingdom or Germany and preferably educated at accredited U.S, U.K, or German institutions, ideally with an academic background from a top global university. Math: Background in mathematics, statistics, computer science, or data science, with experience in mathematical modelling, statistical inference, numerical analysis, and problem-solving using discrete and computational methods. Physics: Background in engineering or the physical sciences (e.g., mechanical, aerospace, physics, or earth sciences), with proficiency in thermodynamics, fluid mechanics, heat transfer, dynamics, differential equations, and strong quantitative, logical, and computational reasoning. Chemistry: Background in chemical or biochemical engineering, with expertise in transport phenomena, thermodynamics, reaction engineering, unit operations, materials science, differential equations, and system-level problem solving across bioprocessing, materials, and kinetics. Biology: Background in biology or a related life science (e.g., molecular biology, biochemistry, microbiology), with experience in biological systems thinking, experimental design, data interpretation, and hypothesis-driven problem solving. Additional Information Please note that only candidates whose profiles are shortlisted will be contacted. About CACTUS Established in 2002, Cactus Communications () is a leading technology company that specializes in expert services and AI-driven products which improve how research gets funded, published, communicated, and discovered. Its flagship brand Editage offers a comprehensive suite of researcher solutions, including expert services and cutting edge AI products like Mind the Graph, Paperpal, and R Discovery. With offices in Princeton, London, Singapore, Beijing, Shanghai, Seoul, Tokyo, and Mumbai and a global workforce of over 3,000 experts, CACTUS is a pioneer in workplace best practices and has been consistently recognized as a great place to work. Awards and Recognition Employers of the Future, 2024 Excellence in Employer Branding (Gold), 2024 ISO 17100 certification for translation services, 2024 Future of Workplace Disruptor, 2023 Top 100 Companies for Remote Jobs (Ranked ), 2023 Three star "Eruboshi" certification, 2023 India's Best Workplaces for Women (Top 100), 2022 Quartz's Best Companies for Remote Workers, 2022 HR Asia's Best Companies to Work for in Asia, 2021
Knauf stands for opportunity. We know that opportunity looks different to each person and we are proud that we see opportunity in everyone. This exciting role within Knauf Insulation could be the perfect next opportunity for you to build a unique career, in a values-led culture with a clear purpose of making tomorrow a home for all of us. Knauf Insulation is proud to be part of the Knauf Group, a global manufacturer of construction materials. Our division is approaching 50 years of heritage in manufacturing insulation, with a growing global reach in 40 countries and ambitious goals for the future. We are looking for passionate, ambitious people to join our 6,000-strong team and help us achieve these goals. We are all led by the same core values and believe in the powerful potential of large companies to have a positive impact on the world. The expansion of the Process Development Department means we are now looking for aProcess Development Technicianin St Helens (UK) and reporting to the Process Development Director. Can you say yes? Are you motivated to blend lab work with on-site trials to elevate raw materials and packaging performance? Can you turn testing results into clear recommendations and concise weekly reports that guide manufacturing decisions? Would you enjoy collaborating with Batch & Melting and Packaging teams, suppliers, and production sites to qualify new materials? Are you proactive in refining test methods, keeping equipment calibrated, and championing safety and qualitywith occasional travel? This Process Development Technician role drives materials and process excellence by evaluating inputs, conducting targeted testing, and turning data into clear recommendations that enhance product performance. In this role, youll collaborate across manufacturing and packaging teams to support development, qualification, and continuous improvement initiatives in both lab and on-site settings. Expect a mix of hands-on experimentation, supplier engagement, and practical reporting. What youll be doing: Support the Batch & Melting Group by assessing and reporting raw materials and product properties (e.g., composition, granulometry). Support the Packaging Team by evaluating packaging materials. Plan and execute laboratory and plant trials to support process development and material qualification across Fiberising, Binder, Forming, Curing, and Cold End. Manage, analyze, and report laboratory data (routine and new material analyses) from the Central Laboratory. Develop and maintain local supply specifications for batch raw materials used across GMW plants. Write, review, and maintain laboratory procedures and work instructions. Conduct supplier audits (onsite and laboratory-based) for raw materials and packaging, as required. Perform in-house and external product benchmarking. Propose and validate new test methods and ideas, primarily for Batch & Melting and Packaging development activities. This position might require some travel (national and international), up to 10% of working time. We are interested in you as a person; your attitude, behaviours and values. As long as you have the willingness to learn anything you need for the role that you don't already have, we'd love to speak to you. What wed love for you to have: Degree level qualification in a Physical Science or Engineering Discipline (Physics, Chemistry, Materials Science, Chemical Engineering, Mechanical Engineering, etc.). Be numerate and able to demonstrate solid scientific and technical credentials and experience. Good working knowledge of Microsoft Office: Outlook, Excel, Word and Power Point. Data manipulation and data reporting skills using Excel or other data visualisation tools. Being flexible with a positive attitude, and will be as at home working in a clean analytical scientific laboratory, as within a factory or construction industry location which might require undertaking physically challenging tasks in dirty, dusty and uncomfortable environments. Ability to display initiative, be autonomous and work conscientiously and productively Candidates must be able to demonstrate good practical tool-based skills, commensurate with typical laboratory environments. Fluent in English If you have experience in the following areas this is an added advantage: Knowledge of advanced statistical testing, and experience of statistical tools (such as Minitab, JMP etc.) Previous laboratory experience Existing experience with any of the specialised testing techniques described in the previous section understanding of continuous improvement techniques, particularly 5S and workplace standardisation. Knowledge of any other languages, particularly French We will provide: As this is a central, international position, the package and associated benefits will be those of the contract's host country. Our common criterion was to build a comprehensive salary package that stands out in the market. On top of that, a dedicated time for personal development and potential for leadership training will be provided. What happens next? We appreciate that your time is precious and applying for a new job can be a lengthy process - so we have committed to replying to your application within five working days. Our commitment to diversity and inclusion (D&I) reinforces our Knauf Insulation values of Making Tomorrow a Home for all of us. We are committed to creating a workplace where we all can thrive, whoever we are, and inspiring a culture of inclusion and innovation that will drive future business success. We do our best to make sure being at work feels like home. To learn more about our business and culture go here:People & Culture - Knauf Insulation UK JBRP1_UKTJ
Dec 05, 2025
Full time
Knauf stands for opportunity. We know that opportunity looks different to each person and we are proud that we see opportunity in everyone. This exciting role within Knauf Insulation could be the perfect next opportunity for you to build a unique career, in a values-led culture with a clear purpose of making tomorrow a home for all of us. Knauf Insulation is proud to be part of the Knauf Group, a global manufacturer of construction materials. Our division is approaching 50 years of heritage in manufacturing insulation, with a growing global reach in 40 countries and ambitious goals for the future. We are looking for passionate, ambitious people to join our 6,000-strong team and help us achieve these goals. We are all led by the same core values and believe in the powerful potential of large companies to have a positive impact on the world. The expansion of the Process Development Department means we are now looking for aProcess Development Technicianin St Helens (UK) and reporting to the Process Development Director. Can you say yes? Are you motivated to blend lab work with on-site trials to elevate raw materials and packaging performance? Can you turn testing results into clear recommendations and concise weekly reports that guide manufacturing decisions? Would you enjoy collaborating with Batch & Melting and Packaging teams, suppliers, and production sites to qualify new materials? Are you proactive in refining test methods, keeping equipment calibrated, and championing safety and qualitywith occasional travel? This Process Development Technician role drives materials and process excellence by evaluating inputs, conducting targeted testing, and turning data into clear recommendations that enhance product performance. In this role, youll collaborate across manufacturing and packaging teams to support development, qualification, and continuous improvement initiatives in both lab and on-site settings. Expect a mix of hands-on experimentation, supplier engagement, and practical reporting. What youll be doing: Support the Batch & Melting Group by assessing and reporting raw materials and product properties (e.g., composition, granulometry). Support the Packaging Team by evaluating packaging materials. Plan and execute laboratory and plant trials to support process development and material qualification across Fiberising, Binder, Forming, Curing, and Cold End. Manage, analyze, and report laboratory data (routine and new material analyses) from the Central Laboratory. Develop and maintain local supply specifications for batch raw materials used across GMW plants. Write, review, and maintain laboratory procedures and work instructions. Conduct supplier audits (onsite and laboratory-based) for raw materials and packaging, as required. Perform in-house and external product benchmarking. Propose and validate new test methods and ideas, primarily for Batch & Melting and Packaging development activities. This position might require some travel (national and international), up to 10% of working time. We are interested in you as a person; your attitude, behaviours and values. As long as you have the willingness to learn anything you need for the role that you don't already have, we'd love to speak to you. What wed love for you to have: Degree level qualification in a Physical Science or Engineering Discipline (Physics, Chemistry, Materials Science, Chemical Engineering, Mechanical Engineering, etc.). Be numerate and able to demonstrate solid scientific and technical credentials and experience. Good working knowledge of Microsoft Office: Outlook, Excel, Word and Power Point. Data manipulation and data reporting skills using Excel or other data visualisation tools. Being flexible with a positive attitude, and will be as at home working in a clean analytical scientific laboratory, as within a factory or construction industry location which might require undertaking physically challenging tasks in dirty, dusty and uncomfortable environments. Ability to display initiative, be autonomous and work conscientiously and productively Candidates must be able to demonstrate good practical tool-based skills, commensurate with typical laboratory environments. Fluent in English If you have experience in the following areas this is an added advantage: Knowledge of advanced statistical testing, and experience of statistical tools (such as Minitab, JMP etc.) Previous laboratory experience Existing experience with any of the specialised testing techniques described in the previous section understanding of continuous improvement techniques, particularly 5S and workplace standardisation. Knowledge of any other languages, particularly French We will provide: As this is a central, international position, the package and associated benefits will be those of the contract's host country. Our common criterion was to build a comprehensive salary package that stands out in the market. On top of that, a dedicated time for personal development and potential for leadership training will be provided. What happens next? We appreciate that your time is precious and applying for a new job can be a lengthy process - so we have committed to replying to your application within five working days. Our commitment to diversity and inclusion (D&I) reinforces our Knauf Insulation values of Making Tomorrow a Home for all of us. We are committed to creating a workplace where we all can thrive, whoever we are, and inspiring a culture of inclusion and innovation that will drive future business success. We do our best to make sure being at work feels like home. To learn more about our business and culture go here:People & Culture - Knauf Insulation UK JBRP1_UKTJ
If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases - often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. Job Role: We are looking for dynamic, creative, and talented computational chemist to join our expanding Discovery & Medicinal Chemistry Department. Reporting to the Director of Medicinal Chemistry, you will apply your expertise, leadership and guidance to discover and develop novel small-molecule therapeutic agents. You will be working within a patient-focused, science-driven, and multi-disciplinary biopharmaceutical environment, covering all stages of the drug discovery process. You will collaborate with scientists from other disciplines within Jazz Pharmaceuticals and with external collaborators to build an innovative portfolio of therapeutics across our exciting and growing oncology and neuroscience pipelines. Working at the forefront of drug discovery you will advance projects from target selection to preclinical drug candidates and FiH trials, and contribute to the growth of the medicinal chemistry team. Key Responsibilities: Utilize modern molecular modelling methods to support different stages of R&D programs. Collaborate effectively with other departments and functions to advance research discovery projects expeditiously from hit identification to high quality preclinical candidates. Design, lead and drive computational studies on projects throughout the several discovery phases and ensure execution on agreed deliverables. Opportunities to lead or co-lead projects in addition to drive discipline-specific endeavours. Set the vision and strategy for computational chemistry. Foster innovative thinking in all areas of departmental activities, with a particular focus on computational and medicinal chemistry. Manage CRO compchem activities, providing expertise and guidance. Present plans and results internally, including at board level, and externally at conferences. Contribute to the writing of patent applications, scientific publications, and internal reports. Develop and mentor less experienced staff. Keep up to date with the latest scientific advances and trends in drug discovery to deliver the next-generation therapies. Undertake ongoing professional development by attending relevant training and conferences. Requirements & Qualifications: MSc/PhD in a relevant scientific discipline (Pharmaceutical Sciences, Chemistry, Computational Chemistry) with a solid foundation in molecular modelling built in a pharma/biotech/CRO setting. Expert knowledge in CADD software packages and modern molecular modelling techniques. Sound knowledge in cutting-edge cheminformatic tools, AI/ML-enabled technologies, and in silico drug design, including both structure- and ligand-based methodologies. Passion for drug discovery with a deep entrepreneurial and problem-solving attitude. Mastery of all the theoretical and practical principles of medicinal chemistry and drug design. Broad knowledge of biophysical, biochemical, and cell-based assays used in the early stages of the drug discovery process. In depth understanding of multi-parameter optimization and ability to integrate disease biology, ADME/DMPK and toxicology data to solve complex drug discovery problems. Excellent leadership, management, organizational and team-working skills, and a talent to deliver project milestones within the expected time frame. Demonstrated track record of scientific publications. Exceptional oral, written, and interpersonal communication skills, and ability to develop and grow strong cross-functional collaborations. Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: .
Nov 17, 2025
Full time
If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases - often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. Job Role: We are looking for dynamic, creative, and talented computational chemist to join our expanding Discovery & Medicinal Chemistry Department. Reporting to the Director of Medicinal Chemistry, you will apply your expertise, leadership and guidance to discover and develop novel small-molecule therapeutic agents. You will be working within a patient-focused, science-driven, and multi-disciplinary biopharmaceutical environment, covering all stages of the drug discovery process. You will collaborate with scientists from other disciplines within Jazz Pharmaceuticals and with external collaborators to build an innovative portfolio of therapeutics across our exciting and growing oncology and neuroscience pipelines. Working at the forefront of drug discovery you will advance projects from target selection to preclinical drug candidates and FiH trials, and contribute to the growth of the medicinal chemistry team. Key Responsibilities: Utilize modern molecular modelling methods to support different stages of R&D programs. Collaborate effectively with other departments and functions to advance research discovery projects expeditiously from hit identification to high quality preclinical candidates. Design, lead and drive computational studies on projects throughout the several discovery phases and ensure execution on agreed deliverables. Opportunities to lead or co-lead projects in addition to drive discipline-specific endeavours. Set the vision and strategy for computational chemistry. Foster innovative thinking in all areas of departmental activities, with a particular focus on computational and medicinal chemistry. Manage CRO compchem activities, providing expertise and guidance. Present plans and results internally, including at board level, and externally at conferences. Contribute to the writing of patent applications, scientific publications, and internal reports. Develop and mentor less experienced staff. Keep up to date with the latest scientific advances and trends in drug discovery to deliver the next-generation therapies. Undertake ongoing professional development by attending relevant training and conferences. Requirements & Qualifications: MSc/PhD in a relevant scientific discipline (Pharmaceutical Sciences, Chemistry, Computational Chemistry) with a solid foundation in molecular modelling built in a pharma/biotech/CRO setting. Expert knowledge in CADD software packages and modern molecular modelling techniques. Sound knowledge in cutting-edge cheminformatic tools, AI/ML-enabled technologies, and in silico drug design, including both structure- and ligand-based methodologies. Passion for drug discovery with a deep entrepreneurial and problem-solving attitude. Mastery of all the theoretical and practical principles of medicinal chemistry and drug design. Broad knowledge of biophysical, biochemical, and cell-based assays used in the early stages of the drug discovery process. In depth understanding of multi-parameter optimization and ability to integrate disease biology, ADME/DMPK and toxicology data to solve complex drug discovery problems. Excellent leadership, management, organizational and team-working skills, and a talent to deliver project milestones within the expected time frame. Demonstrated track record of scientific publications. Exceptional oral, written, and interpersonal communication skills, and ability to develop and grow strong cross-functional collaborations. Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: .
Laboratory Technician We now have an excellent opportunity for an organised and professional team player to join the Research and Operational Support team as Laboratory Technician. Position: Laboratory Technician Location: Brookfield Farm, near Honiton, East Devon (an area of outstanding natural beauty) Hours: Part-time 30 hours per week, Monday-Thursday Salary: £29,076 pro rata Contract: Fixed term role starting as soon as possible until 1 January 2027 Closing Date: Sunday 16 November 2025 About the Role Under the direction of the Laboratory Manager, you will provide in-house clinical and pathological laboratory services, interpret results and communicate relevant findings to the clinical veterinary teams and other relevant teams or personnel. Key responsibilities include: Carrying out routine haematology, biochemistry and endocrinology on blood samples submitted by the veterinary teams and promptly highlighting abnormal results. Carrying out routine faecal parasitology on faecal samples submitted to the laboratory for intestinal parasites, liver fluke and lungworm. Monitoring the worm burden of charity donkeys by regular testing of a representative sample as determined by the Research Department. Processing blood and faecal samples from rehomed donkeys, private donkeys, holding bases and Ireland as part of an advisory service. Performing PCR tests on a variety of bodily fluid and tissue samples submitted for donkeys and mules with suspected infections and reporting the results to the case Veterinary Surgeon. Providing laboratory-based support to research and veterinary team projects. Supporting the Laboratory Manager in the training of new staff and the teaching of students and visitors. About You You will have: Previous biological laboratory experience. Knowledge and practical experience of laboratory principles. Educated to degree level (or equivalent) in a biological or animal science. Competent IT Skills. Knowledge of equine parasitology and experience in using PCR (desirable). Self-motivated with a flexible attitude. Committed to making a difference for donkeys and the people that rely on them. As part of the process, you will be asked to upload your CV and Cover Letter once you click to apply. Benefits include: Competitive pension. Life assurance Healthshield. 31 days holiday (including Bank holidays), rising to 34 will each full year of service. Wellbeing team. Recorded Pilates and Yoga classes. Long service awards. Healthshield plan Free parking. Subsidised restaurant and shop. About the Organisation The sanctuary is one of the UK s largest international animal welfare charities, currently supporting projects in over 35 countries worldwide, working for a world where donkeys and mules live free from suffering and their contribution to humanity is fully valued. The Charity is a Disability Confident Employer, committed to safeguarding and promoting the welfare of vulnerable people (children and adults) and expects all staff and volunteers to undertake this commitment. Applicants will be subject to safer recruitment processes, including an application for a Disclosure and Barring Service (DBS) check where required for the post. You may also have experience in areas such as Lab, Laboratory, Lab Technician, Laboratory Technician, Lab Assistant, Laboratory Assistant, Animal Lab, Animal Laboratory, Animal Lab Technician, Animal Laboratory Technician, Animal Lab Assistant, Animal Laboratory Assistant, Clinical Lab Technician, Clinical Laboratory Technician, Pathological Lab Technician, Pathological Laboratory Technician PLEASE NOTE: This role is being advertised by NFP People on behalf of the organisation
Nov 03, 2025
Contractor
Laboratory Technician We now have an excellent opportunity for an organised and professional team player to join the Research and Operational Support team as Laboratory Technician. Position: Laboratory Technician Location: Brookfield Farm, near Honiton, East Devon (an area of outstanding natural beauty) Hours: Part-time 30 hours per week, Monday-Thursday Salary: £29,076 pro rata Contract: Fixed term role starting as soon as possible until 1 January 2027 Closing Date: Sunday 16 November 2025 About the Role Under the direction of the Laboratory Manager, you will provide in-house clinical and pathological laboratory services, interpret results and communicate relevant findings to the clinical veterinary teams and other relevant teams or personnel. Key responsibilities include: Carrying out routine haematology, biochemistry and endocrinology on blood samples submitted by the veterinary teams and promptly highlighting abnormal results. Carrying out routine faecal parasitology on faecal samples submitted to the laboratory for intestinal parasites, liver fluke and lungworm. Monitoring the worm burden of charity donkeys by regular testing of a representative sample as determined by the Research Department. Processing blood and faecal samples from rehomed donkeys, private donkeys, holding bases and Ireland as part of an advisory service. Performing PCR tests on a variety of bodily fluid and tissue samples submitted for donkeys and mules with suspected infections and reporting the results to the case Veterinary Surgeon. Providing laboratory-based support to research and veterinary team projects. Supporting the Laboratory Manager in the training of new staff and the teaching of students and visitors. About You You will have: Previous biological laboratory experience. Knowledge and practical experience of laboratory principles. Educated to degree level (or equivalent) in a biological or animal science. Competent IT Skills. Knowledge of equine parasitology and experience in using PCR (desirable). Self-motivated with a flexible attitude. Committed to making a difference for donkeys and the people that rely on them. As part of the process, you will be asked to upload your CV and Cover Letter once you click to apply. Benefits include: Competitive pension. Life assurance Healthshield. 31 days holiday (including Bank holidays), rising to 34 will each full year of service. Wellbeing team. Recorded Pilates and Yoga classes. Long service awards. Healthshield plan Free parking. Subsidised restaurant and shop. About the Organisation The sanctuary is one of the UK s largest international animal welfare charities, currently supporting projects in over 35 countries worldwide, working for a world where donkeys and mules live free from suffering and their contribution to humanity is fully valued. The Charity is a Disability Confident Employer, committed to safeguarding and promoting the welfare of vulnerable people (children and adults) and expects all staff and volunteers to undertake this commitment. Applicants will be subject to safer recruitment processes, including an application for a Disclosure and Barring Service (DBS) check where required for the post. You may also have experience in areas such as Lab, Laboratory, Lab Technician, Laboratory Technician, Lab Assistant, Laboratory Assistant, Animal Lab, Animal Laboratory, Animal Lab Technician, Animal Laboratory Technician, Animal Lab Assistant, Animal Laboratory Assistant, Clinical Lab Technician, Clinical Laboratory Technician, Pathological Lab Technician, Pathological Laboratory Technician PLEASE NOTE: This role is being advertised by NFP People on behalf of the organisation
