28 jobs found

The Just Recruitment Group Ltd is currently recruiting for a Laboratory Technician for their client based in Felixstowe, Suffolk. Role will involve analytical testing on raw materials and finished products. Ensure the quality of the product range is controlled, maintained and appropriate documentation is updated, guarantee internal and external audit requirements. Key accountabilities: Perform analyses and operations to agreed work plans and schedules. Produce and report on time only valid accurate analytical results. Report immediately out-of-specification results, non-conformances or any aspects of laboratory operation which are prejudicial to the laboratory operation / service to the line manager. Achieve / maintain desired level of competency in all defined operations. Undertake operation to comply with world class operation practices. Carry out work activities to agreed work plans and schedules following the written standard operating procedures. Key attributes: Proven hands-on laboratory experience in Microbiological testing, sample preparation and serial dilution techniques, plating and plate reading. Practical experience in chemistry-based analysis Familiarity with aseptic techniques and contamination/cross contamination control Ability to prepare and handle media, reagents etc. Ability to operate basic laboratory equipment such as autoclaves, balances, microscopes and exposure to use of higher level equipment such as HPLC and any other equipment along those lines. Good understanding of GLP Accurate record keeping, completion of relevant spreadsheets, and associated databases Attention to detail for reporting and result verification Ability to interpret data For more information on this position, please contact Just Recruitment Group Ltd on telephone (phone number removed) quoting job reference TB34. Please note that if you have not been contacted within 7 days, your application for this position has been unsuccessful.

Job Title: Medical Lab Assistant (MLA) Agency Role via Trident Healthcare Solutions Location: Wexham Park Hospital, East Surrey Hospital , Frimley Park Hospital (1 site) Employment Type: Agency / Locum Experience Required: Minimum 1 year UK experience (applications without UK experience will not be considered) About the Role Trident Healthcare Solutions is seeking experienced Medical Lab Assistants (MLAs) to join our agency workforce supporting NHS laboratories. This is an excellent opportunity for professionals who are passionate about laboratory operations and want flexibility in their work schedule. As a Medical Lab Assistant , you will play a vital role in supporting the smooth running of laboratory services. We are happy to consider candidates with experience in Microbiology, Haematology, Biochemistry, or Histopathology, as well as those who have worked in specimen reception. Key Responsibilities Perform routine laboratory tasks under supervision, ensuring compliance with NHS standards. Handle and process patient samples accurately and efficiently. Support senior laboratory staff in maintaining workflow and quality control. Maintain accurate records and adhere to data protection and confidentiality guidelines. Assist in specimen reception and preparation for analysis. Requirements Minimum of 1 year UK experience as a Medical Lab Assistant (MLA) essential. Background in one or more of the following: Microbiology, Haematology, Biochemistry, Histopathology , or specimen reception. Strong attention to detail and ability to follow strict protocols. Excellent communication and teamwork skills. Eligibility to work in the UK with valid documentation. Why Join Trident Healthcare Solutions? Competitive agency rates. Flexible shifts across NHS hospitals. Dedicated support from our recruitment team. Opportunity to expand your experience across multiple disciplines.

Industrial Chemist Location: Knowsley Industrial Estate Salary: £27,674 per annum Shift Pattern: Weekly rotating shifts 6:00am 3:00pm 11:00am 8:00pm Bonus: Performance-related bonus schemes included About the Role: We are seeking an Industrial Chemist to join our operations team based at Knowsley Industrial Estate . This role is primarily carried out in an outdoor industrial environment and plays a key part in ensuring the safe handling, testing, and movement of materials across the site. The successful candidate will be responsible for testing, checking, and verifying materials at both intake and dispatch stages, ensuring compliance with operational, quality, and regulatory standards. Key Responsibilities: Sample, test, and assess incoming materials to ensure they meet required specifications Inspect and approve outgoing materials prior to dispatch Monitor, record, and report material testing data accurately Coordinate materials sent for outward processing Ensure all testing, handling, and documentation procedures are completed in line with company and regulatory requirements Liaise with internal departments and external processing partners Maintain high standards of health, safety, and environmental compliance Carry out duties within an outdoor, industrial working environment Qualifications and Experience: HMC qualification or a degree in Chemistry, Industrial Chemistry, Chemical Engineering, or a related scientific discipline Degree qualification strongly preferred Experience within an industrial, manufacturing, or chemical environment desirable Strong analytical skills and attention to detail Ability to follow technical and regulatory procedures Full UK driving licence (preferred) What We Offer: Salary of £27,674 per annum Weekly rotating shift system Performance-related bonus schemes Stable, long-term employment Ongoing training and development opportunities indliv

Laboratory Chemist (Hazardous Waste) Grays, Essex 34-38K dependent on experience Our client, a leading provider of hazardous waste management services, is looking to recruit a Laboratory Chemist for its operations in Grays, Essex. In this role you will carry out a variety of duties to enable the smooth running of the Hazardous Waste Laboratory. This will include logging and coordinating all samples and performing laboratory tests. Key duties and responsibilities: Take samples of routine wastes arriving at the Transfer Station Log all samples, record results, monitor and read samples sent to 3rd party labs Use of laboratory equipment which will include XRF, FTIR, Photometry, Closed Cup Flash point and Bomb calorimeter Look after and maintain the Laboratory equipment to a good standard Keep the laboratory tidy Ensure samples tested are kept and stored so they can be retrieved easily Organise disposal of old samples no longer needed Test unknown wastes for purposes of pricing and classification Test known wastes to confirm waste acceptance and flag any non-conformances Support the sales team with chemical knowledge and test results Read labs results and classify waste Ensure all activities are carried out in accordance with current Health & Safety and Environmental legislation and that Lab PPE requirements are adhered to Other duties may include: Classification of wastes Pricing of wastes leaving site Providing disposal costs for quotes for new enquiries at the Transfer Station Classify waste with appropriate EWC codes and assign ADR labels as required Supervision of vehicles loading with hazardous materials as required Perform other reasonable duties (Ad hoc) as requested to support the business needs which may include off site visits for sampling or technical advice. Candidate requirements: Applications are invited from candidates qualified to degree level in Chemistry or related subject with previous experience working in a laboratory environment using the equipment listed above. Candidates with experience working within the hazardous waste industry would be of particular interest. Ref: J9614

CK Group are recruiting for a Waste Operations Chemist to join an Environmental and Waste Management company at their site based near Darrington on a full time, permanent basis. the salary for this role ranges from 27,000 to 34,000 per annum, dependent on experience. The Company: A leading UK waste and resource management company, our client is part of a global group with a strong heritage in providing services for communities and businesses. Their aim is to be the environmental company of choice, delivering change for a sustainable future. The company's core business focuses on collection, resource recovery and renewable energy providing services for local authorities and commercial customers. They have a number of core services including municipal services, business waste solutions, recycling and green energy. Location: The Operations Chemist will be based at the company's site near Darrington, easily commutable from Wakefield, Knottingley, Castleford, Leeds, Bradford, Doncaster and Scunthorpe. Operations Chemist Role: Your main duties will be: Chemical and Physical analysis of Waste. Inspection and testing of waste for acceptance. Interpretation of laboratory results. Maintenance, QC and Calibration of laboratory equipment. Ensuring safety procedures are always upheld. Your Background: The ideal candidate for this role will have the following skills and experience: Chemistry degree/HND. Waste/Environmental testing experience. Hazardous Waste classification experience. Entitlement to work in the UK is essential. For more information or to apply for this Operations Chemist position, please contact Emily Mills on (phone number removed) or email (url removed). Please quote reference (phone number removed). If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page url removed)/) and follow us to see our latest jobs and company news.

Laboratory Technician (Contract) Location: Cumbria (onsite 5 days a week) Contract Length: 12 months Rate: 19.46 - 20.64 per hour (Umbrella) IR35 Status: Inside IR35 Clearance Required: BPSS Notice Period: 1 month The Role We are currently seeking a Laboratory Technician to join an analytical team, supporting the delivery of an efficient and high-quality analytical service. This is an agency-based position, working in line with strict safety, quality, and environmental standards. The successful candidate will play a key role in supporting laboratory operations, ensuring analytical results are delivered to time and quality expectations while maintaining compliance with all relevant procedures. Key Responsibilities Assist in the delivery of assigned programmes of work to support timely and accurate analytical results Work in compliance with laboratory quality management systems to support accreditation Follow processes and procedures to ensure safe working practices at all times Support the analytical team to deliver a consistent and efficient service Assist with the waste management of samples and consumables Carry out routine laboratory cleaning and maintenance activities Take responsibility for personal development and ongoing learning Ensure compliance with legislation, policies, and procedures Promote efficient operational practices to minimise financial and material waste Essential Experience & Skills Science GCSEs at grades A-C (or equivalent) Good organisational skills with strong attention to detail Awareness of conventional and radiological safety IT literate Ability to work effectively as part of a team Desirable Previous experience in an analytical chemistry or laboratory environment Additional Information This role is well suited to candidates looking to develop or build on laboratory experience within a regulated and safety-critical environment.

Operations Support Assistant Location : Site-based (either site) Earby, BB18 6JZ Salary : £26,000 £28,000 per annum + Excellent Benefits Hours : 40 hours per week, Monday Friday (8-hour days, 30-minute lunch break) Contract Type : Full time, Permanent Benefits : Annual Bonus: £1,200 based on company and personal performance, Holidays: 25 days plus statutory holidays (option to purchase additional week), Broughton Day: Option for a fixed day off every 2 3 weeks via salary sacrifice, Pension: Auto-enrolment, LifeInsurance: 2x death in service and Healthcare: Cash plan Broughton s mission is to improve public health and well-being. As a global contract research organisation, we partner with future-focused organisations and category innovators to bring products to market across the Pharmaceutical, Healthcare, and Lifestyle sectors. Our integrated solutions are delivered by world-leading scientists and regulatory consultants through our contract laboratories. We are seeking an Operations Support Assistant to join our team! This role is essential in supporting laboratory operations and ensuring timely completion of analyses. While this is not a scientific role, it offers the chance to work closely with our laboratory teams and gain insight into the workings of an analytical environment. We are not looking for anyone with a scientific degree for this role. You ll play a vital role in supporting the smooth running of our laboratories. This is an opportunity to join a collaborative team where attention to detail and pride in your work make a real difference to the success of our operations. You ll be involved in a variety of tasks that keep our labs functioning efficiently, from managing stock and glassware to registering client samples and supporting physical testing. If you enjoy working in a structured environment and take satisfaction in ensuring everything runs seamlessly, this role is for you! As our Operations Support Assistant, you will: Support laboratory teams in day-to-day tasks. Perform laboratory housekeeping and ensure compliance with regulations. Register client samples and manage sample receipt and reconciliation. Maintain availability of clean glassware and perform routine stocktakes. Follow the KANBAN process to ensure timely ordering of stock and reagents. Book chemicals and consumables in and out, ensuring accurate records. Prepare high-demand diluents and other solutions as required. Perform some physical chemistry testing and operate vaping simulation hardware. Travel between sites occasionally to support stability and archive activities. Maintain and understand the QMS and produce quality documents in line with data integrity requirements. Support the laboratory team as required and perform other duties as needed. In order to be successful in this role you must have / be: Good attention to detail and ability to follow instructions carefully. Good IT skills, including working knowledge of Microsoft applications. Strong verbal, numerical, and literacy skills. It would be great if you had: Good written English and organisational skills. GCSE or equivalent in a science-related subject with a desire to learn the workings of an analytical laboratory. Join us and be part of a team that s shaping the future of health and well-being through science. If you are interested in this role, please do submit a copy of your CV by clicking on APPLY today! No agencies please. Right to work in the UK is essential for this role.

We ae looking for a Business Chemist who is an expert in the development, application and interpretation of analytical chemistry to support our sodium bicarbonate and sodium chloride operations in Northwich, Cheshire. This role is ideal for a motivated professional with a strong scientific background and proven experience leading laboratory teams within a pharmaceutical or food manufacturing env click apply for full job details

Technical Assessor - Waste Management Location: Southampton, UK Salary: up to 28,000 - 34,000 (DOE) Working Hours: Monday to Friday - 8:00am-5:00pm Are you experienced in the waste management or environmental services industry? Are you looking to start or develop your career with an accredited and renowned waste management company? My client is offering a fantastic package for a Hazardous Waste and Recycling Technical Assessor to join their team based in Southampton. The right candidate will possess a degree or HNC in Chemistry, Environmental Science or similar and ideally have worked previously for a UK based Waste and Recycling Management Company. Candidates looking to start their career in Waste Management, are also encouraged to apply. Package Benefits: 21 days Holiday + Banks - increasing to 25 days with service Company Pension Private Health Care + Dental Scheme Annual Salaries Reviews Annual Discretionary Bonus On-site parking Excellent and on-going training programme Opportunity for growth and development within the company Key Responsibilities: Review and classify hazardous and non-hazardous waste streams using chemical data, site information, and relevant legislation (e.g., EWC/LoW codes). Assess analytical results, risk assessments, method statements, waste profiles, and safety data to determine appropriate disposal or treatment pathways. Keep up to date with UK and EU environmental regulations (e.g., Environmental Permitting Regulations, ADR, CLP) and ensure assessments reflect legal obligations. Produce clear technical reports, audit records, waste acceptance criteria, and recommendations for clients or internal teams. Work with operations, health & safety, logistics, and laboratory teams to resolve technical issues and approve waste movements. Contribute to process improvements, technical standards, and quality assurance systems. Requirements: Bachelor's degree in Chemistry or related field Previous experience as a Technical Assessor, Site/Mobile Chemist, Lab Analyst, or similar is desirable Good lab practice and Site H&S knowledge Experience in the Waste Management industry is desirable, but not essential Forklift Licence desirable, but not essential WR Logistics are the recruitment partner for all vacancies in the logistics industry. We recruit in the UK & USA for permanent jobs. WR is acting as an Employment Agency in relation to this vacancy.

Our client is a global leader in the food manufacturing sector, supplying high-quality products to major retailers. Due to continued growth and innovation, they are now seeking an experienced Senior Process Technologist to join their Product Development team. This is a hands-on role suited to someone who enjoys being close to the factory floor while also working cross-functionally with technical, commercial, operations, and external partners to deliver new and improved products to market. The successful candidate will play a key role in driving process development, supporting product launches, and ensuring consistency, safety, and quality across production. The role will involve supporting the Process Development Manager with the preparation and coordination of new and modified product launches. You will arrange and oversee production trials, ensuring processes are robust, repeatable, and compliant with food safety requirements. You will coordinate trial follow-ups, product sampling, and lessons learned, and work closely with Technical and Production teams to develop product specifications and support accurate set-up within the business ERP system. You will collaborate with Production, Engineering, and Technical colleagues to resolve production issues, work with ingredient and packaging suppliers to establish or improve supply solutions, and take responsibility for artwork approval across your product portfolio. The role includes regular contact with retailer technologists, occasional store visits for product evaluation, and ad-hoc travel to customers and suppliers. The successful candidate must hold a third-level qualification (diploma or degree) in Food Science, Chemistry, Microbiology, or a related discipline. A recognised Food Safety qualification such as REHIS would be advantageous. A thorough understanding of food processing and the systems that underpin food safety is essential. This role requires flexibility, as working hours may include weekends, night shifts, and other non-standard hours in line with business needs. Business travel is required on an ad-hoc basis. You will bring a genuine enthusiasm for food and food manufacturing, strong problem-solving skills, and a proactive, collaborative approach to your work. You will be well organised, highly detail-focused, and able to perform under pressure while adapting quickly to changing situations. Excellent written and verbal communication skills are essential, along with a willingness to continuously learn and stay up to date with customer and market requirements. Applicants must have proven experience in a similar role within food manufacturing, ideally working with major retail customers, and a demonstrable track record of delivering high-quality work to deadlines. The role offers a competitive salary, pension, and a comprehensive employee benefits package, including gym membership, retail discount vouchers, and health and wellbeing support. Ongoing training, development, and progression opportunities are also available. A full job description and company brief will be provided to shortlisted candidates. If you are interested in this opportunity, please forward your most up-to-date CV to Simon Norris.

A leading FMCG manufacturing are actively seeking a Assistant Quality Manager, you'll be joining a company committed to excellence and innovation, working in a dynamic environment where your expertise will drive quality and technical standards to new heights. This is your opportunity to be part of a forward-thinking organisation that values collaboration and continuous improvement. What You Will Do: - Conduct audits of designated suppliers to ensure compliance with industry and company standards. - Manage supplier relationships from a quality and technical perspective, ensuring timely issue resolution using CAPA and PDCA tools. - Lead incident committees and support strategic quality objectives, driving continuous improvement initiatives. - Maintain and enhance a contemporary Quality Management System for all activities within scope. - Represent the quality function in technical transfer activities and new programme introductions. - Collaborate with cross-functional teams, including R&D, procurement, and regulatory, to achieve shared goals. What You Will Bring: - A degree in biological sciences, chemistry, food sciences, microbiology, or a related scientific discipline. - Hands-on experience within a manufacturing or technical environment, particularly in food and beverage production. - Certificated HACCP and auditing skills. - Strong analytical and problem-solving skills, paired with excellent organisational abilities. - The ability to communicate confidently at all levels, with diplomacy and ambassadorial skills. This role is integral to ensuring the highest standards of quality and safety across the company's external supply chain operations. The Assistant Quality Manager will play a pivotal role in driving efficiency, innovation, and compliance, contributing to the company's commitment to delivering exceptional products to its customers. Location: This position is based in Coleford, offering a unique opportunity to work in a vibrant and accessible location. Interested?: If you're ready to take the next step in your career and make a real difference in the food and beverage industry, apply now to become the Assistant Quality Manager. Don't miss this chance to join a company that recognises and rewards talent! Your CV will be forwarded to Jonathan Lee Recruitment, a leading engineering and manufacturing recruitment consultancy established in 1978. The services advertised by Jonathan Lee Recruitment are those of an Employment Agency. In order for your CV to be processed effectively, please ensure your name, email address, phone number and location (post code OR town OR county, as a minimum) are included.

Process Development Chemist - Renewables / Biofuels - Scotland - Permanent Our client is a leading force in renewable energy across the UK. At present, they are seeking a Process Development Chemist on a permanent basis at their site in Ayrshire, Scotland. This is an excellent opportunity for an experienced Process Development Chemist to support the scale up and delivery of major projects. Responsibilities: To use expert knowledge to chemistry and related fields to devise, plan and execute research programmes with the overall aim of making operations more efficient and/or reduce operational impacts. The Process Development Chemist will conduct and report on laboratory, Midi Plant and Full-Scale Plant trials. Key Duties Laboratory Experiments - Develop and document experimental plans for improving performance in anaerobic digestion and associated activities. - Operate lab scale anaerobic digestion test facilities (AMPTS and Continuous Reactors) for the measurement of biogas potential, digestate quality for various feedstocks under different operating conditions. Midi and Plant Trials - Assist in Midi and Plant Trials as required. - Implementation of process improvement trials across the operational sites. - Prepare Management of Change, Risk and COSHH assessments for Midi and Plant Trials as required - Contribute to safe working environment by complying with written procedures e.g. risk and COSHH assessments. - Development methods and procedures for trials at Midi and across operational sites, which will include trials of new technologies. - Optimisation of existing site processes following successful trials. Documentation: - Write reports of laboratory, Midi and Plant Trials, including descriptions of test method and results, including cross-refencing to plant data or previous tests and analysing and interpreting data. Safety - Complete training on analytical techniques, company procedures, and HSE as tasked. - Work in accordance with SOP s, COSHH and risk assessments and keep working areas clean Other: - Fully participate in innovation process by presenting improvements/innovations at scheduled meetings. - Carry out experimental work at other company locations from time-to-time where on site investigations are required. - Where required; collect, prepare and perform chemical analysis of effluent, process liquors, feedstock, sea water, carbon dioxide and biogas samples according to standard operating procedures, COSHH and Risk Assessment - Analyse samples using advanced instrumental techniques including GC - MS, ICP, and Elemental Analyser. - Perform analysis using basic techniques including colourimetric techniques, gravimetric, titrations etc. - Complete training as tasked on analytical techniques, company procedures, HSE etc. Experience & Qualifications: Strong Laboratory work background. Ability to collate data and produce meaningful & concise reports from data Strong IT skills particularly Excel & use of ERP system or databases. Ability to manage own time and prioritise workload accordingly Ability to present complex scientific information to a non-scientific work group Some experience of training non-scientific colleagues to understand data and reason for treatment of same. Able to challenge established norms with a professional and fact driven approach Ability to work independently. First Degree in Biology, Chemistry; Biochemistry; Microbiology or similar. Desirable: Masters in similar subject area.

Job Title: Upstream Bioprocessing Technical Lead - 6 Month Contractor Vacancy type: 6 Month contract position - Potential to extend Salary: Great salary Location: Crumlin - Wales Are you a passionate bioprocess expert in Microbial Fermentation scale up seeking a new challenging contract? SRG are exclusively working with a global life science company who are looking for an Upstream Microbial Fermentation SME to support their scale up projects. If you have a proven track record in upstream process optimisation and scale-up, this could be the perfect role for you. The Upstream Bioprocess Technical Lead Role As the Upstream Bioprocess Technical Lead, you will be responsible for providing technical expertise throughout the early stages of design review, bioprocess optimisation, scale-up, and transfer strategy for Microbial Fermentation projects. You will support the technical inputs that drive successful design reviews and scale-ups, using your in-depth knowledge of bioreactor operations and maintenance, as well as mentoring junior staff. The Upstream Bioprocess Technical Lead will collaborate with cross-functional teams to ensure the successful delivery of the company's portfolio. This is an exciting opportunity to make a real impact and contribute to the company's growth and innovation. Key Responsibilities of the Upstream Bioprocess Technical Lead Provide subject matter expertise support for projects involving troubleshooting, scale-up, and downstream recovery of recombinant bacteria and yeasts Demonstrate a thorough understanding of biological processes, geometric factors, and mathematical models involved in scale-up Operate and maintain glass and stainless steel bioreactors at small (1L) and large scales (up to 250L) Drive optimization of existing processes to improve efficiency and reduce costs Proficiently use bioprocessing software and simulation tools to support operations Assist with the identification of technologies and equipment to improve and facilitate transfer and production programmes Maintain precise records of batch performance, reports, and analytics Qualifications and Experience To be successful in this role, you should have: A degree (ideally PhD) in microbiology, molecular biology, biotechnology, or chemical engineering Essential: Extensive recent experience in fermentation technologies for proteins, including antigens and enzymes using E.Coli and Yeast. Essential: Proven recent expertise in bioprocess optimization, scale-up, and transfer to regular production up to 100L (200L highly desirable) Essential: Bioreactor and Media Design for process scale up. Excellent understanding of microbiology, biotechnology, and biochemistry Proficiency in operating and maintaining glass and stainless steel bioreactors SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors. As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients. If you would like to apply for this position, please use the link provided. Alternatively, please email a copy of your CV to Selby De Klerk at selby If you have a scientific background and this position is not relevant / suitable for you please feel free to get in touch or visit (url removed) to view our other vacancies. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Your new company An exciting opportunity has arisen for a Quality Manager to join a leading manufacturing organisation at their Cheshire-based facility. Reporting directly to the Plant Manager, you will be responsible for leading all quality and hygiene activities across the site, ensuring compliance with ISO standards, HACCP and GMP, while driving continuous improvement initiatives. Your new role You will manage the site's Quality Management System, oversee QC operations, lead internal audits and complaints investigations, and act as the CI pillar lead. This role also includes responsibility for the site laboratory and quality approval of incoming and finished goods. What you'll need to succeed With a degree in Chemistry, Food Science or a related field, you will bring proven experience in manufacturing quality processes within the chemicals, food or FMCG sectors. Strong knowledge of ISO9001, HACCP, GMP and IMS is essential, along with excellent communication skills and the ability to lead and motivate cross-functional teams. What you'll get in return The salary on offer is up to 55,000 plus benefits. This is a key leadership role within the plant management team, offering the chance to shape quality culture and standards across a high-performing site. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career. Hays Specialist Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C's, Privacy Policy and Disclaimers which can be found at (url removed)

Senior Lab Technician - Chemicals / Detergents Location: Stafford Salary: 45,000 - 50,000 DOE KO2's client, a specialist in advanced cleaning technology, is looking to recruit an experienced Senior Lab Technician to join their growing team in Stafford. This is an exciting opportunity for someone with a strong background in chemicals or detergents who is keen to play a key role in product development, process optimisation, and lab management. As a Lab Technician, you will take responsibility for the smooth running of the laboratory, including maintaining equipment, designing and carrying out experiments, and ensuring compliance with test standards. You will work closely with colleagues in software, mechanical design, and operations to optimise wash performance through a deep understanding of chemicals, water, energy, and time. The successful candidate will be confident in experimental design, data analysis, and presenting results up to board level. This role suits someone with an inquisitive mindset who can bring scientific rigour and practical solutions to the challenges of cleaning systems using detergents and chemicals. Key responsibilities: Manage day-to-day laboratory operations, including calibration and test standards. Design and carry out experiments to optimise cleaning cycles. Analyse and interpret results, focusing on the role of chemicals and detergents. Present findings and recommendations to senior stakeholders. Contribute to the development of new testing methodologies and measurable parameters. The ideal Senior Lab Technician will have: A degree in Chemistry, Chemical Engineering, or a related discipline. Proven experience in a laboratory environment working with detergents or chemicals. Strong knowledge of experimental design and process optimisation. Excellent communication and presentation skills. The ability to work independently while contributing to a collaborative team. Benefits: Competitive salary ( 45,000 - 50,000 depending on experience). Flexible working hours (Monday-Friday, early finish on Fridays). Opportunity to play a pivotal role in shaping future cleaning technologies. This is a fantastic opportunity for a Lab Technician who wants to step up into a senior role with real influence in a dynamic, forward-thinking business. If you have the expertise in detergents and chemicals to drive innovation, KO2's client would love to hear from you.

We are seeking a Graduate QC Analyst to join our client's quality team in Lanarkshire, Scotland. The successful candidate will be responsible for conducting high-quality analytical testing of raw materials, intermediates, and finished products within a GMP-regulated environment. You will assist with validation, maintain laboratory equipment, and ensure compliance with industry standards. The role involves organising sample testing activities, updating documentation, and supporting batch release processes, with the aim of maintaining exemplary quality standards and efficient laboratory operations. BSc in Chemistry or equivalent Experience in a laboratory environment, GMP experience is advantageous Knowledge of EU GMP and analytical chemistry principles Attention to detail, problem-solving, and organisation skills Computer literacy and practical laboratory skills In return, you will enjoy excellent benefits. This permanent role offers ongoing development opportunities within a highly-regulated pharmaceutical environment, fostering growth in your analytical expertise and quality assurance skills.

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. The Principal will be responsible for supporting complex or leading singular projects related to data engineering requirements and initiatives across Jazz Research and Development. The Principal will support data projects from across the business including Clinical, Pre-Clinical, Non-Clinical, Chemistry, RWD and Omics. Essential Functions Support the design, development and maintenance of data pipelines for processing Research and Development data from diverse sources (Clinical Trials, Medical Devices, Pre-Clinical, Omics, Real World Data) utilizing the AWS technology platform. Create and optimize ETL/ELT processes for structured and unstructured data using Python, R, SQL, AWS services and other tools. Build and maintain data repositories using AWS S3 and FSx technologies. Establish data warehousing solutions using Amazon Redshift. Build and maintain standard data models. Develop data quality frameworks, validation processes and KPIs to ensure accuracy and consistency of data pipelines. Implement data versioning and lineage tracking to support data traceability, regulatory compliance and audit requirements. Create and maintain documentation for data processes, architectures, and workflows. Implement modern software development best practices (e.g. Code Versioning, DevOps, CD/CI). Support collaboration with RnD Researchers, Data scientists and Stakeholders to understand data requirements and deliver appropriate solutions in a global working model. Maintain compliance with data privacy regulations such as HIPAA, GDPR May be required to develop, deliver or support data literacy training across R&D. Required Knowledge, Skills and Abilities Strong knowledge of data engineering tools such as Python, R and SQL for data processing. Strong proficiency with AWS services particularly S3, Redshift, FSx, Glue, Lambda. Strong proficiency with relational databases. Strong background in data modeling and database design. Familiarity with unstructured database technologies (e.g. NoSQL) and other database types (e.g. Graph). Familiarity with Containerization such as Docker and EKS/Kubernetes. Familiarity with one or more RnD research process and associated regulatory requirements. Exposure to healthcare data standards (CDISC, HL7, FHIR, SNOMED CT, OMOP, DICOM). Exposure to big data technologies and handling. Knowledge of machine learning operations (MLOps) and model deployment. Strong problem-solving and analytical abilities. Excellent communication skills for collaborating with stakeholders. Experience working in an Agile development environment. Required/Preferred Education Bachelor's Degree in Computer Science, Statistics, Mathematics, Life Sciences, or other relevant scientific fields; Master's Degree preferred 3-5 years of experience in data engineering, with at least 1.5 years focusing on healthcare, research or clinical related data Description of Physical Demands Occasional mobility within office environment Routinely sitting for extended periods of time Constantly operating a computer, printer, telephone and other similar office machinery 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: .

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. The Principal will be responsible for supporting complex or leading singular projects related to data engineering requirements and initiatives across Jazz Research and Development. The Principal will support data projects from across the business including Clinical, Pre-Clinical, Non-Clinical, Chemistry, RWD and Omics. Essential Functions Support the design, development and maintenance of data pipelines for processing Research and Development data from diverse sources (Clinical Trials, Medical Devices, Pre-Clinical, Omics, Real World Data) utilizing the AWS technology platform. Create and optimize ETL/ELT processes for structured and unstructured data using Python, R, SQL, AWS services and other tools. Build and maintain data repositories using AWS S3 and FSx technologies. Establish data warehousing solutions using Amazon Redshift. Build and maintain standard data models. Develop data quality frameworks, validation processes and KPIs to ensure accuracy and consistency of data pipelines. Implement data versioning and lineage tracking to support data traceability, regulatory compliance and audit requirements. Create and maintain documentation for data processes, architectures, and workflows. Implement modern software development best practices (e.g. Code Versioning, DevOps, CD/CI). Support collaboration with RnD Researchers, Data scientists and Stakeholders to understand data requirements and deliver appropriate solutions in a global working model. Maintain compliance with data privacy regulations such as HIPAA, GDPR May be required to develop, deliver or support data literacy training across R&D. Required Knowledge, Skills and Abilities Strong knowledge of data engineering tools such as Python, R and SQL for data processing. Strong proficiency with AWS services particularly S3, Redshift, FSx, Glue, Lambda. Strong proficiency with relational databases. Strong background in data modeling and database design. Familiarity with unstructured database technologies (e.g. NoSQL) and other database types (e.g. Graph). Familiarity with Containerization such as Docker and EKS/Kubernetes. Familiarity with one or more RnD research process and associated regulatory requirements. Exposure to healthcare data standards (CDISC, HL7, FHIR, SNOMED CT, OMOP, DICOM). Exposure to big data technologies and handling. Knowledge of machine learning operations (MLOps) and model deployment. Strong problem-solving and analytical abilities. Excellent communication skills for collaborating with stakeholders. Experience working in an Agile development environment. Required/Preferred Education Bachelor's Degree in Computer Science, Statistics, Mathematics, Life Sciences, or other relevant scientific fields; Master's Degree preferred 3-5 years of experience in data engineering, with at least 1.5 years focusing on healthcare, research or clinical related data Description of Physical Demands Occasional mobility within office environment Routinely sitting for extended periods of time Constantly operating a computer, printer, telephone and other similar office machinery 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: .

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. The Principal will be responsible for supporting complex or leading singular projects related to data engineering requirements and initiatives across Jazz Research and Development. The Principal will support data projects from across the business including Clinical, Pre-Clinical, Non-Clinical, Chemistry, RWD and Omics. Essential Functions Support the design, development and maintenance of data pipelines for processing Research and Development data from diverse sources (Clinical Trials, Medical Devices, Pre-Clinical, Omics, Real World Data) utilizing the AWS technology platform. Create and optimize ETL/ELT processes for structured and unstructured data using Python, R, SQL, AWS services and other tools. Build and maintain data repositories using AWS S3 and FSx technologies. Establish data warehousing solutions using Amazon Redshift. Build and maintain standard data models. Develop data quality frameworks, validation processes and KPIs to ensure accuracy and consistency of data pipelines. Implement data versioning and lineage tracking to support data traceability, regulatory compliance and audit requirements. Create and maintain documentation for data processes, architectures, and workflows. Implement modern software development best practices (e.g. Code Versioning, DevOps, CD/CI). Support collaboration with RnD Researchers, Data scientists and Stakeholders to understand data requirements and deliver appropriate solutions in a global working model. Maintain compliance with data privacy regulations such as HIPAA, GDPR May be required to develop, deliver or support data literacy training across R&D. Required Knowledge, Skills and Abilities Strong knowledge of data engineering tools such as Python, R and SQL for data processing. Strong proficiency with AWS services particularly S3, Redshift, FSx, Glue, Lambda. Strong proficiency with relational databases. Strong background in data modeling and database design. Familiarity with unstructured database technologies (e.g. NoSQL) and other database types (e.g. Graph). Familiarity with Containerization such as Docker and EKS/Kubernetes. Familiarity with one or more RnD research process and associated regulatory requirements. Exposure to healthcare data standards (CDISC, HL7, FHIR, SNOMED CT, OMOP, DICOM). Exposure to big data technologies and handling. Knowledge of machine learning operations (MLOps) and model deployment. Strong problem-solving and analytical abilities. Excellent communication skills for collaborating with stakeholders. Experience working in an Agile development environment. Required/Preferred Education Bachelor's Degree in Computer Science, Statistics, Mathematics, Life Sciences, or other relevant scientific fields; Master's Degree preferred 3-5 years of experience in data engineering, with at least 1.5 years focusing on healthcare, research or clinical related data Description of Physical Demands Occasional mobility within office environment Routinely sitting for extended periods of time Constantly operating a computer, printer, telephone and other similar office machinery 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: .