286 jobs found

Head of Technology and Projects - Chemical and Recycling Abingdon, commutable from Swindon, Oxford, Didcot, Wantage, Thame and Wallingford 80,000 - 90,000 + Life Assurance + Share Options + Training + Progression + Cutting edge technology + Flexible Working + Excellent Company Benefits Are you an engineering leader looking to guide major projects, shape next generation recycling technology and play a key role in a company driving the circular economy forward? On offer is the change to join an ambitious organisation developing advanced recycling technology that converts hard to recycle plastics into valuable chemical feedstocks. The business is scaling through development, demonstration and commercial projects with strong investment into new capability, giving you the chance to influence technical direction and progress into senior management. You will lead engineering activity across process, mechanical, electrical, EC&I and CAD, oversee major projects in the UK and mainland Europe, guide technical strategy, coordinate internal and external engineering work and support delivery across all project stages. Occasional UK and European travel will be required. This role suits an engineering leader with strong project delivery experience who wants real influence at company level and clear progression. The Role Lead the technology and projects function Manage engineering teams across process, mechanical, electrical, EC and I and CAD Oversee major projects across development, design, construction and operations Guide technical strategy and support continuous improvement The Person Engineering professional with experience leading multidisciplinary teams Background in major industrial, petrochemical or related projects Experience delivering large scale projects from concept to operations Strong knowledge of engineering work processes, industry standards and coordination Reference Number: BBBH(phone number removed) To apply for this role or to be considered for further roles, please click "Apply Now" or contact Matilda Hocknell at Rise Technical Recruitment. Rise Technical Recruitment Ltd acts an employment agency for permanent roles and an employment business for temporary roles. The salary paid will be dependent on your level of experience, qualifications and skill set. We are an equal opportunities employer and welcome applications from all suitable candidates.

If you are a Laboratory Technician in the South of England with experience in Plant Monitoring and Process Engineering, and are looking for a new role in 2026, please get in touch! UK RTW REQUIRED Job Title: Laboratory Technician I Location: Fawley Contract Length: 12 Months Job Description: Support/assist the lab supervisors/chemists by performing routine and non-routine laboratory analysis/wet chemistry on product and in-process samples, to support plant operations for the purpose of quality assurance/control. Perform calibration and maintenance of test equipment. Prepare samples and ensure accurate data generation and records, in accordance with the standard operating procedures. Utilize analytical instruments to address quality assurance/control issues. Prepare chemical stock solutions and reagents, as well as set preparation standards. Position will receive direction and support. SKILLS AND QUALIFICATIONS Polytechnic graduate with the background in Chemical/Process/Technical Engineering. Computer-literate. Preferable experience in quality control systems. Scope of Work The Environmental Technician carries out daily routine Environmental analysis of plant effluent streams and performs environmental analysis in response to Company incidents. Plant monitoring analysis includes metals by AA method, MBG testing and other titration analysis. This is a full-time temporary role to run for 12 months, requiring 37.5 hours per week, Monday to Friday, with the possibility of contract extension. Perform routine and non-routine laboratory analysis/wet chemistry on product and process samples for the purpose of quality assurance and control. Prepare samples and ensure accurate data generation and records, in accordance with the standard operating procedures. Knowledge and experience in environmental water analysis is highly desirable. Specialized knowledge in GC-MS, AA testing, calibration and maintenance is highly desirable. With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.

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. Brief Description: The Process Technician Senior Coordinator is required to assist in development and manufacture of research pharmaceutical formulations for use in clinical trials, as well as assisting in all commercial manufacturing and packaging processes within Botanical Drug Product (BDP), including Clinical Trial packing using a series of well-defined and documented manufacturing procedures whilst being in compliance with Health and Safety (H&S) and current Good Manufacturing Practices (cGMP) requirements. Essential Functions/Responsibilities Quality is a primary focus to ensure all aspects of cGMP are met and product quality is not compromised. The workload is varied with the core areas of responsibility listed below: The job holder is responsible for maintaining cGxP and EH&S knowledge applicable to the job. Execute manufacture of clinical formulations. Maintenance of the manufacturing facility, including cleaning and 6S. Ensure delivery against schedule, for all production activities. Assist in the departmental controlled drug reconciliation. Ensure all Production batch documentation has been processed in accordance with cGMP and current procedures. To perform a leading and proactive role within the production areas to ensure procedures are followed correctly and tasks completed in a timely manner. Perform routine micro testing in the GMP facilities Liaising with other departments regarding production scheduling, including supply chain, warehouse, engineering, Pharm Dev, QC and QA. Training of other technicians on new processes/changes to manufacturing techniques. Identifying areas for improvement and implementing these improvements where applicable across all Production processes/working practices. Completing additional tasks assigned by production management that are outside the core duties described above. Required Knowledge, Skills, and Abilities Carries out their work in a way that will not adversely affect their own, or others, health, safety and security or the environment and reports any shortcomings in company arrangements. Responsible all aspects of the manufacturing processes to ensure all product are made accordance with cGMP standards, both as an initiator and checker. Recording of manufacturing/process conditions in batch documentation and equipment/area logbooks. Complete area/equipment cleaning procedures to high standards as illustrated in cGMP practices. The job holder may be called upon to provide cover for other internal departments, when the PDMF production schedule allows. Ensures that all activities undertaken comply with cGMP and EH&S standards as detailed in relevant SOP's and working practices. Authors and updates batch documentation, standard operating procedures and associated forms. Responsible for the completion of quality related documentation, such as deviations, CAPA's, protocols and change controls. The nature of the work requires the job holder to be flexible, with regards to working hours to ensure that they are available to complete a production process should it overrun. Trains and coaches new starters (re-train individuals) in Production manufacturing and packaging processes. Looks for areas of improvement across all Production manufacturing and packaging processes, in order to improve efficiency and reduce costs. Informs department management of any atypical events/deviations immediately. Executes additional tasks in order to meet department objectives. Potential to act as the Production department EH&S representative and undertake all of the tasks associated with that role. Potential to take responsibility for consumable and critical to quality ordering within the department. Required/Preferred Education and Licenses Minimum of 3 years experience gained in a regulated production environment, ideally within the pharmaceutical/chemical or food industry. Ideally hold qualifications gained in the Pharmaceutical industry i.e. NVQ's or similar Displays the attributes encompassed in the company values and encourages their development in others. Good level of numeracy. Good communication skills including written. A good working knowledge of standard Microsoft packages, i.e. Excel and Word. Excellent attention to detail. Develops and maintains positive working relationships with key stakeholder groups, both internal and external. Prepared to challenge the norm and look for areas of improvement, share own ideas and information. Good team worker assists colleagues as and when required. Demonstrates a 'can do' attitude. 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. Brief Description: The Process Technician Senior Coordinator is required to assist in development and manufacture of research pharmaceutical formulations for use in clinical trials, as well as assisting in all commercial manufacturing and packaging processes within Botanical Drug Product (BDP), including Clinical Trial packing using a series of well-defined and documented manufacturing procedures whilst being in compliance with Health and Safety (H&S) and current Good Manufacturing Practices (cGMP) requirements. Essential Functions/Responsibilities Quality is a primary focus to ensure all aspects of cGMP are met and product quality is not compromised. The workload is varied with the core areas of responsibility listed below: The job holder is responsible for maintaining cGxP and EH&S knowledge applicable to the job. Execute manufacture of clinical formulations. Maintenance of the manufacturing facility, including cleaning and 6S. Ensure delivery against schedule, for all production activities. Assist in the departmental controlled drug reconciliation. Ensure all Production batch documentation has been processed in accordance with cGMP and current procedures. To perform a leading and proactive role within the production areas to ensure procedures are followed correctly and tasks completed in a timely manner. Perform routine micro testing in the GMP facilities Liaising with other departments regarding production scheduling, including supply chain, warehouse, engineering, Pharm Dev, QC and QA. Training of other technicians on new processes/changes to manufacturing techniques. Identifying areas for improvement and implementing these improvements where applicable across all Production processes/working practices. Completing additional tasks assigned by production management that are outside the core duties described above. Required Knowledge, Skills, and Abilities Carries out their work in a way that will not adversely affect their own, or others, health, safety and security or the environment and reports any shortcomings in company arrangements. Responsible all aspects of the manufacturing processes to ensure all product are made accordance with cGMP standards, both as an initiator and checker. Recording of manufacturing/process conditions in batch documentation and equipment/area logbooks. Complete area/equipment cleaning procedures to high standards as illustrated in cGMP practices. The job holder may be called upon to provide cover for other internal departments, when the PDMF production schedule allows. Ensures that all activities undertaken comply with cGMP and EH&S standards as detailed in relevant SOP's and working practices. Authors and updates batch documentation, standard operating procedures and associated forms. Responsible for the completion of quality related documentation, such as deviations, CAPA's, protocols and change controls. The nature of the work requires the job holder to be flexible, with regards to working hours to ensure that they are available to complete a production process should it overrun. Trains and coaches new starters (re-train individuals) in Production manufacturing and packaging processes. Looks for areas of improvement across all Production manufacturing and packaging processes, in order to improve efficiency and reduce costs. Informs department management of any atypical events/deviations immediately. Executes additional tasks in order to meet department objectives. Potential to act as the Production department EH&S representative and undertake all of the tasks associated with that role. Potential to take responsibility for consumable and critical to quality ordering within the department. Required/Preferred Education and Licenses Minimum of 3 years experience gained in a regulated production environment, ideally within the pharmaceutical/chemical or food industry. Ideally hold qualifications gained in the Pharmaceutical industry i.e. NVQ's or similar Displays the attributes encompassed in the company values and encourages their development in others. Good level of numeracy. Good communication skills including written. A good working knowledge of standard Microsoft packages, i.e. Excel and Word. Excellent attention to detail. Develops and maintains positive working relationships with key stakeholder groups, both internal and external. Prepared to challenge the norm and look for areas of improvement, share own ideas and information. Good team worker assists colleagues as and when required. Demonstrates a 'can do' attitude. 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: .

Senior Process Safety Consultant to join a leading engineering consultancy, delivering complex safety projects across high-hazard industries including Pharmaceuticals, Medical Technologies, Food & Beverage, Energy, and Chemicals. This Senior Process Safety Consultant position is a hybrid role, requiring 2-3 days per week to be based in the site office in Edinburgh, offering up to £75,000 per annum, click apply for full job details

Product Formulation Manager (Full-time, Permanent) Hybrid; 2 days in the office Aylesford, Kent Unlock your potential with Our Client Our client is a leading global supplier of ingredients and premix manufacturing solutions, and trusted by the world s best-known food, beverage, and nutrition brands. Their expertise lies in Ingredient Distribution, Manufacturing Solutions, and Customised Services. Their global network of colleagues, located in offices and manufacturing facilities around the world, delivers sustainable value-added solutions to their customers. They are recognised for their deep expertise, commitment to excellence, and bold innovation, which have earned them a strong reputation as a trusted industry leader. Wherever your career is headed, you ll find direction, opportunity, and belonging with them. What does a Product Formulation Manager mean at Our Client? Lead and grow the department responsible for the design, scale-up, and manufacture of nutritional pre-mixes (vitamins, minerals, functional ingredients) and sports nutrition products (powders, RTM, ready-to-drink support). Own the end-to-end value chain, from concept through to commercialisation, ensuring products meet regulatory, quality, safety, and commercial targets. You ll manage the Product Formulation team and commercial interfaces, while building robust systems and driving continuous improvement. What s in it for you? Personal growth, including training and development opportunities Health Cash Plan Subsidised gym membership Discretionary bonus Access to flexible pay with Aslan What to expect? Strategy and Leadership: Develop and execute the department strategy aligned to business goals (NPD pipeline, margin mix, category growth, customer satisfaction). Lead, coach, and build high performing teams across formulation and product development. Coach and mentor Junior-level Managers within the department to strengthen leadership capability and succession planning. Own annual budget, resource planning and capability. Assure that you and the Product Formulation team maintain a broad and sound knowledge of all products sold (premix blends and straight ingredients), to provide input to all requests for technical, nutritional and labelling information. Product Development and Formulation: Oversee design of vitamin/mineral premixes, functional blends (pre and probiotics, botanicals, amino acids), and sports nutrition products (whey/plant proteins, creatine, BCAAs, electrolytes, pre workout/energy blends). Ensure science-based formulations Efficacy, stability, bioavailability, sensory, and cost-in-use; Validate through pilot trials and shelf life studies. Approve specifications. Build expertise on functional ingredients, nutrients and additives assuring that the Product Formulation team are up to date with market trends and changes in regulatory/legislative landscape to support usage of nutritional ingredients and additives. Support raw material substitution in formulations. Support dual sourcing of raw materials to reduce risk and optimise cost in use. Support customer compliance projects (infant qualification, GB compliance and other regulatory requirements which orientate around raw materials and premixes). Provide technical inputs for supplier raw material approval. Commercial and Customer Interface: Partner with commercial teams to scope customer briefs, translate requirements to technical specs, and present technical proposals. Deliver on-time launch execution, support key customers with technical service and post-launch improvements. Assure that robust scoping of customer requirements is completed together with indicative costings prior to formulation development commencing. Work to right first time on the development of premix formulations for customer requirements on the basis that robust scoping has been completed. Support customer compliance projects (infant qualification, GB compliance and other regulatory requirements which orientate around raw materials and premixes). Provide technical support to commercial, customer care, quality and production. Assure that you are a subject matter expert in Product Vision capability understanding the interface with Access Supply Chain and FBSS. Lead improvements in Product Vision capability for our client to improve efficiency and reduce complexity. Data, Systems and Continuous Improvement: Establish robust documentation and SOPs. Implement and drive KPI dashboards for the department which demonstrate ROIC. Does this sound like you? Degree (BSc/MSc) in Food Science, Nutrition, Chemistry, Biochemistry, Pharmacology, or Chemical/Process Engineering. 5+ years in food/nutrition manufacturing, with 3+ years in people leadership and cross functional stakeholder management. Direct experience with premix formulation (vitamins, minerals, amino acids, botanicals, probiotics), sports nutrition categories (whey/plant proteins, creatine/BCAA/EAA, electrolytes, pre workouts), and powder technologies (blending, flowability/segregation, hygroscopic management, encapsulation/granulation, sieving, milling). Demonstrated ability to design science-based formulations. Sensory understanding (flavour/sweetener systems, masking, texture) in RTM/RTD formats. Interested? Our client would love to hear from you! Click apply and submit your CV.

You will like Design & Applications engineering for Cirencester area specialist in Engineering & Sealing Solutions firm supplying a range of markets including Formula 1, Motorsport, Oil & Gas, Pumps, Chemical Processing and other Fluid Handling applications. Dealing with high performance sealing components, rubber, plastic and composite technology manufactured from the highest quality materials to exacting specifications, ensuring long-term reliability in the most demanding applications. You will like The Design Engineer/Applications Engineer job itself, which is a hands-on, customer-facing engineering role owning the application design journey from initial enquiry through to release. You will interface with customers and suppliers, generate and approve design proposals, and ensure solutions are manufacturable, compliant and delivered on time. More specifically: Design of products for customers using SolidWorks (CAD), ensuring these are to customer expectations Provide technical guidance to highly technical external customers, visiting customer sites Liaising with the Sales team, customers and suppliers Generate and approve design proposals utilizing our client's extensive design and material expertise to ensure the best application solution for customers Knowledge and experience of Quality Systems, familiarity with the Quality Procedures of ISO9001:2015, PPAP, First Article Inspection, Non-Conformances, Quality Audits etc Support with Goods Inwards Inspection of manufactured parts to ensure conformity Work closely with suppliers to ensure quality of product Hours: Full Time: Monday to Thursday: 8:30 to 17:00 Friday: 8:30 to 16:00 Incl. 30 minutes lunch You will have To be successful as the Design Engineer/Applications Engineer, you will have a healthy mix of the following: Worked in a Design Engineer role Understanding of applications in Hydraulics, Pumps, Valves, Compressors is a benefit Worked within / comfortable with having direct contact with customers Knowledge of manufacturing and processes in relevant industries IT usage of ERP & CAD systems, Microsoft Office (Outlook, Excel, Word and PowerPoint) You will get As Design Engineer/Applications Engineer, you will enjoy a competitive salary of £45K-£50K + Package. Monday Thursday: 08 00, Fridays: 08 00 25 days holiday + Bank Holidays, increasing with length of service Company Bonus Medical (BUPA) and Dental Childcare Vouchers and Cycle to Work Scheme Potentially more for a stand-out candidate so please apply irrespective of salary! You can apply For the Design Engineer/Applications Engineer by pushing the button on this job posting (recommended), or by sending CV in confidence to (url removed) UK_MS

About LJMU At Liverpool John Moores University, our students thrive because of the people who teach, guide, and inspire them, we truly make a difference. Every year, our commitment to exceptional education attracts talented students from across the UK and the world. This growth is fuelled by inspirational academics, professionals who bring vision, passion, and expertise to their disciplines. Driven by our continued growth in student numbers and our commitment to delivering outstanding learning, teaching, and research opportunities for our students, we are expanding our academic community. As part of this growth, we are creating a number of key academic positions that will play an integral role in shaping our university's next chapter. About the School of Pharmacy and Biomolecular Sciences The School of Pharmacy and Biomolecular Sciences is at the forefront of higher education in Pharmacy, Biomedical Science, Forensic Science, Pharmaceutical and Cosmetic Science, and related areas. As a result of this expertise, the school has excellent working relationships with law enforcement agencies, pharmaceutical providers, the NHS, and industry. From investigating human diseases, including diagnostic and treatment strategies; new methods of drug delivery; to working with police forces to provide new forensic analytical methods and techniques; the school has a wide range of expertise and areas of interest. What we're looking for We are seeking a highly professional, enthusiastic and committed individual to join our academic team in the area of cosmetic science. You will hold a PhD in a chemistry discipline relevant to cosmetic science, with particular expertise in the formulation and analysis of cosmetic products. We welcome applicants with research and/or teaching experience in this field. In this role, you will contribute to the teaching and administration of our foundation, undergraduate and postgraduate programmes. We are looking for someone whose expertise complements our existing research and teaching strengths, and you will be encouraged to develop your own research interests as you build your academic career with us. What we offer This is a key moment to join a welcoming, ambitious, and research-informed university community that places students at the heart of everything we do. We value and invest in our staff, offering meaningful opportunities for professional development, scholarship support, and clear internal promotion routes. As well as outstanding development support, we also offer: A low contractual 35-hour week Generous annual leave entitlement and Christmas period closure with the option to purchase additional annual leave Excellent pension scheme Access to an Employee Assistance Programme Family friendly policies Car and travel loan schemes We are also investing in our staff and students by creating a busy and thriving campus, the hubs of which are our friendly and inclusive Student Life, Redmonds, Tithebarn and Byrom Street buildings. Our staff are visible and present for our students and this all adds to the fantastic student experience of living and studying in such a vibrant city. We see our staff as very much part of this community and value their contribution to the success of LJMU, Liverpool and the wider northwest region. If you're inspired by the idea of joining a growing university and bringing your expertise to a community where you can truly make a difference, we look forward to hearing from you. Informal enquiries may be made to Professor Satya Sarker, Director of School, Tel: or e-mail: or Dr Steve Enoch, Head of Subject, Chemical and Pharmaceutical Sciences, Tel: or email: s For other enquiries, you may contact . Interviews for the post are expected to be held mid-January 2026. The School of Pharmacy and Biomolecular Sciences is committed to promoting equality and diversity, including the Athena Swan Gender Equality Charter for promoting the career of Women in STEM (science, technology, engineering, mathematics) in higher education. We encourage applications from all individuals who meet the advert criteria but would particularly welcome applications from women for this post. All appointments will be made on merit. Please let us know if you require reasonable adjustments during the recruitment process.Please note all of our vacancies will be closed to applications at midnight on the advertised closing date, unless otherwise stated.

We are currently recruiting for a full time Laboratory Technician. This is full time position working on-site in Fawley. This is a temporary on-going contract. A DBS check and a drug and alcohol test will be required. MAIN FUNCTIONS Support/assist the lab supervisors/chemists by performing routine and non-routine laboratory analysis/wet chemistry on product and in-process samples, to support plant operations for the purpose of quality assurance/control. Perform calibration and maintenance of test equipment. Prepare samples and ensure accurate data generation and records, in accordance with the standard operating procedures. Utilise analytical instruments to address quality assurance/control issues. Prepare chemical stock solutions and reagents, as well as set preparation standards. Position will receive direction and support. SKILLS AND QUALIFICATIONS Polytechnic graduate with the background in Chemical/Process/Technical Engineering. Computer-literate. Preferable experience in quality control systems. Scope of Work The Environmental Technician carries out daily routine Environmental analysis of plant effluent streams and performs environmental analysis in response to Company incidents. Plant monitoring analysis includes metals by AA method, MBG testing and other titration analysis. This is a full-time temporary role to run for 12 months, requiring 37.5 hours per week, Monday to Friday, with the possibility of contract extension. Perform routine and non-routine laboratory analysis/wet chemistry on product and process samples for the purpose of quality assurance and control. Prepare samples and ensure accurate data generation and records, in accordance with the standard operating procedures. Knowledge and experience in environmental water analysis is highly desirable. Specialised knowledge in GC-MS, AA testing, calibration and maintenance is highly desirable.

Our client is seeking a detail oriented Environmental Technician to support routine and incident based environmental testing within their oil refining and petrochemical complex. The successful candidate will conduct daily environmental analyses / laboratory analyses on plant effluent streams, perform laboratory testing in response to company incidents, and contribute to overall environmental monitoring efforts. This position is ideal for a candidate with a strong chemistry background and a passion for environmental quality assurance. Key Responsibilities: Perform routine and ad-hoc laboratory analyses (wet chemistry) on plant product and process samples to support quality assurance and compliance. Conduct tests including, but not limited to, metals analysis using Atomic Absorption (AA), Microbial Growth (MBG), Gas Chromatography (GC), Fourier Transform Infrared Spectroscopy (FTIR) and various titrations. Prepare chemical stock solutions, reagents, and calibration standards according to standard procedures. Ensure accurate and timely data recording and reporting using the Laboratory Information Management System (LIMS). Maintain lab cleanliness and safety in accordance with established protocols. Support the resolution of quality control issues using appropriate analytical methods and equipment. Qualifications and Skills: Bachelor's degree (or equivalent) in Chemistry, Environmental Science, Engineering, or a related STEM discipline. Alternatively, relevant and demonstrable laboratory work experience will be considered. Proficiency with computers; experience using quality control or LIMS systems is preferred. Strong attention to detail with the ability to work independently and manage priorities effectively. Experience in environmental water analysis is highly desirable. Knowledge of and hands-on experience with analytical instruments such as GC, FTIR, and AA, including calibration and maintenance, is a strong asset. This role is Inside IR35. The rates advertised are PAYE.

Laboratory Technician Benefits: Competitive pay: 18.10 - 22.35 per hour (PAYE) or 23.86 - 28.79 per hour (Umbrella). Inside IR35 contract for 12 months, with potential extension. Full-time hours: 37.5 per week, Monday to Friday. Belcan Workforce Solutions is seeking a Laboratory Technician to join our team at a leading refinery site in Southampton. This is an exciting opportunity to work in a dynamic environment where your expertise will directly support plant operations and quality assurance processes. As a Laboratory Technician, you will assist lab supervisors and chemists by performing routine and non-routine laboratory analysis on product and in-process samples. Your role will include calibration and maintenance of test equipment, preparation of chemical stock solutions and reagents, and ensuring accurate data generation in line with standard operating procedures. You will also contribute to environmental monitoring and analysis, supporting compliance and safety standards. Essential Requirements: Polytechnic graduate with a background in Chemical, Process, or Technical Engineering. Computer literacy and familiarity with quality control systems. Knowledge of environmental water analysis and techniques such as GC-MS and AA testing. Ability to perform calibration and maintenance of analytical instruments. Ready to take the next step in your career? Apply now to join our team and make an impact as a Laboratory Technician. This vacancy is being advertised by Belcan

Are you an experienced Quality Assurance Leader looking for a challenge with a really exciting CDMO focused on Pharmaceutical Manufacturing? Job Title: Quality Assurance Manager Type: Permanent Salary: Highly attractive Location: Northwest, England SRG is currently working exclusively with a highly successful, award winning, contract development and manufacturing organisation focused on providing expert intelligence and support to their partners, driven by their capabilities. As a result of expansion, we are looking for a Quality Assurance Manager to join their quality team. Typical responsibilities/accountabilities: Ensure full compliance with UK/EU GMP Regulatory Standards and company procedures. Lead and manage the Quality Assurance Team at an IMP manufacturing site, focused on Phase I and Phase II clinical trial materials. Maintain QA systems and processes, reviewing and supporting ongoing improvement activities. Ensure effective management of documents through lifecycle, ensuring compliance with regulations and industry best practices. This includes - creating, reviewing, and approving key documentation such as specifications, SOPs, protocols, and methods associated with all products and procedures. Support batch documentation review and provide quality oversight for the certification and release of IMPs by the QP. Investigating and approval of deviations, complaints and OOS to prevent future reoccurrences of nonconformance, providing support on SMART CAPA plans. Supplier Management: Managing supplier approval and ongoing performance. Evaluating site compliance and implementing improvements through the internal audit process, as an Internal Auditor and Report approver. Supporting Client projects as a Quality Assurance representative and Customer liaison Support generation and cascade of quality training packages, including but not limited to GMP induction and annual refresher. Assist with management of Regulatory inspections: inspection readiness, inspection and response. Essential Requirements: Minimum of 5 years' of recent experience in Quality Assurance within a Pharmaceutical (GMP) facility, preferably Investigational Medicinal Products (IMPs) Proven Leadership/ Management experience Degree or equivalent in a relevant scientific discipline desired Experience in working with analytical laboratories and/ or GMP production areas. 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 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. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Applications Engineer E astbourne, East Sussex Salary: Neg (depending on experience) MUST HAVE THE RIGHT TO WORK IN THE UK IN PLACE AS OUR CLIENT DOES NOT OFFER SPONSORSHIP - PLEASE ONLY APPLY IF YOU HAVE PERMANENT RIGHT TO WORK IN THE UK STATUS. To provide technical and commercial support for the global sales activity, within markets such as Oil and Gas, Chemical, Pharmaceutical, etc. Responsible for enquiry handling, technical evaluation, proposal creation and customer support, through to generation of post-order contractual documentation and supporting the handover process to relevant departments. Duties/Responsibilities Act as the pre-order point of contact for the external sales team, global representatives and customers, responding to enquiries and technical clarifications for new unit sales. Evaluate clients needs and create proposals, reviewing project specifications and generating comments/deviations. Attend pre-order technical and commercial clarification meetings with customers, as necessary. Raise contract documentation and support the order handover process to the Project Manager and Product Engineer. Communicate and build working relationships with external sales teams, global representatives and customers. Operate within bid deadlines and contractual guidelines set down by the client. Liaise with other departments, as necessary, to ensure that contractual requirements are understood. Support training activity for external sales teams and global representatives. The successful individual should possess the following: Bachelor s Degree in Mechanical Engineering, or equivalent. Strong interpersonal skills and good communication skills is essential at all levels. Ability to prioritise a heavy and variable workload. A methodical approach with attention to detail. Highly organised and able to work under minimal supervision, capable of dealing with high pressure situations. Competent with MS Office (Word, Excel, PowerPoint). Fluent in English language. Please note this role is based on-site, but travel may be required to support the external sales teams/ global representatives and attend bid clarification meetings with customers.

Manufacturing Process Technician (12 month FTC) Join a global leader in solid oxide technology, developing next-generation fuel cell and electrolyser solutions that power innovation in green hydrogen, advanced power systems, and distributed energy for mission-critical sectors like data centres. With more than 5 million test hours behind our proven designs, we're accelerating the clean energy revolution-and you can be part of it. Redhill, Surrey Salary is £26,481 + 20% shift allowance = £31,777 The roles will be shift work. 1 week on early shift (06.00 - 14.00) and the following week on late shift (13.45 - 10.00) All training will be provided As a Manufacturing Process Technician , you'll play a hands-on part in producing high-quality fuel cell products that meet strict quality, safety, and performance standards. You'll be responsible for: Following detailed work instructions to manufacture fuel cells Accurately weighing, measuring, and recording production data Operating process equipment under tightly controlled conditions Performing visual and in-process quality checks Identifying and reporting non-conformances and supporting corrective actions Maintaining stocks of raw materials Collaborating with R&D and Engineering teams on continuous improvement Ensuring full compliance with Health & Safety requirements Full training provided - bring your attention to detail, willingness to learn, and commitment to quality. What We're Looking For Basic engineering, scientific, chemical or manufacturing process skills (preferred) Previous manufacturing or production experience Experience working in controlled areas (GMP, cleanroom) is an advantage Familiarity with quality control measurement and reporting Strong numeracy and literacy skills A proactive mindset and high accuracy in your work Why Join Us? Be part of a team where innovation is Embedded in the culture and where your work contributes directly to cleaner, more sustainable energy solutions. Ready to make an impact? Apply now and help power the future.

Are you an experienced Field Service Engineer with a background in pneumatics, electrical or mechanical engineering? If so, we have an exciting opportunity providing support for customers throughout the UK. Salary: £30,000 - £35,000 (depending on experience) Overtime Company car Bonus Field-based nationwide About Us Alpeco has over 30 years' experience specialising in the design, supply and build of high-quality liquid handling solutions to the petroleum road tanker and chemical process industries around the world. We pride ourselves on our ability to deliver complete, innovative and tailored liquid handling solutions, customised to suit clients' specific needs. We are seeking an experienced, highly skilled Field Service Engineer to join our dynamic team supporting customers throughout the UK. The successful candidate will be responsible for providing technical support, maintenance, and installation services at customer sites. The ideal applicant will possess strong problem-solving abilities, excellent communication skills, and a proactive approach to service delivery. Responsibilities Full responsibility for the installation, service, repair, and calibration of a range of flowmeter, PD pumps and associated equipment in accordance with company standards. Maintenance of clients' mobile and static liquid handling equipment. Utilise strong fault-finding skills to identify any issues and offer resolutions from within the field. Provide a high level of customer service to our clients from start to finish whilst developing strong working relationships. Collaborate with the internal team to escalate complex issues and ensure customer satisfaction. Carry out duties to a high standard whilst complying with all relevant health and safety requirements. Skills and experience Proven experience as a Field Service Engineer or similar technical role. Strong communication skills. Excellent problem-solving skills with the ability to diagnose issues efficiently. Good organisational skills with the capacity to manage multiple service appointments effectively. Able to work individually or as part of a team. IT literate, proficient in MS Office. Valid driving licence is essential; willingness to travel extensively is required. This is a fantastic opportunity for an enthusiastic individual wanting to progress their career whilst working for a forward thinking, dynamic and growing company. Apply today to be considered for the Field Service Engineer role. Equals One is an advertising and recruitment agency working on behalf of our client to promote this vacancy. You may be contacted directly by the employer should they wish to progress your application. Due to the number of applications we receive, we are unable to provide specific feedback if your application is unsuccessful.

As the Control Systems Engineer, you will need to have / be: Proficient in the configuration and programming of Allen Bradley control systems through RSLogix 500, Studio 5000 and FactoryTalk View. Basic knowledge of BS / IEC 61003, 61131, 61508, 61511 and 62443 standards. Good understanding in the design of functional safety, SIL, LOPA and Safety Instrumented Systems. Familiar with project and engineering documents including Cause & Effect diagrams, Loop Drawings, Control Philosophy, Electric Schematics, URS, FDS, Datasheets, etc. Experience of working on various communication protocols including Industrial Ethernet, DH+, Modbus, ProfiNet, Serial, etc. Knowledge of OT Cyber Security, IIOT and AI would be a plus. Prior understanding of chemicals manufacturing, large scale processes, Hazardous Areas (ATEX) and Intrinsic Safety would be preferred. Prior experience of instrumentation engineering would be highly advantageous. Familiarity with AutoCAD or similar engineering drawing tool. Qualifications: A minimum of a HNC in Controls/Electronic/Instrument Engineering. A further 5 years practical experience, post HNC, in an industrial manufacturing environment. The job requires a flexible attitude to deal with multiple complex jobs simultaneously, to meet the required changes in operational priorities. Role of the Control Systems Engineer: Maintenance - Diagnose and rectify control system failures. Project work - Design, specification, and installation of control and safety systems (PLCs, BPCS, SIS, DCS, SCADA, HMI, etc.). Management of Change - Review/approval of MOC proposals and subsequent programming and modification of control systems. Liaison at all levels inside the Company. Outside contacts typically would include control system suppliers, system integrators and contractors. Safety, Health & Environmental - To maintain and promote a safe operating culture within the E&I Department ensuring that in all its aspects of installation and maintenance it operates to the highest levels of safety and meets all legal and statutory requirements, company rules and procedures. To assist with the development and training of department resource in control systems.

Teknikal Specialist Recruitment are recruiting for a Maintenance Technician with an Electronics Bias. £45,000 DOE + Bonus + Private Healthcare + Profit Share Bedford (Ampthill area) Double Day Shift Further Education Support Award-Winning Employer What s In It for You?: Salary up to £45,000 DOE Profit share bonus scheme (up to 8%) Private healthcare package Financial support for further education 24 days holiday + bank holidays Gym and cinema discounts Ongoing technical and professional training Clear route for career development Double Days shift: Mon Fri (6am 2pm / 2pm 10pm) No weekend work The Role: Our client, a respected leader in precision components and advanced technology, is seeking a Maintenance Technician with an electronics bias to join their Bedfordshire facility. This role is ideal for someone experienced in electronic fault-finding who is keen to work in a cleanroom environment on a variety of high-spec equipment. You will be responsible for conducting preventative maintenance, diagnosing, and repairing electronic faults, and supporting production efficiency across electrical, electronic and some mechanical systems. You ll also play a part in stock management, process improvement, and ensuring high safety standards. What You ll Need: Apprenticeship or Level 3 qualification in Electronics or Electrical Engineering Experience working in a cleanroom or wafer fabrication setting (preferred) Strong skills in PCB fault-finding, soldering, and working with motors/control panels Ability to read electrical/electronic schematics Confident working with PPE and chemicals A proactive, team-oriented approach and willingness to learn This is a rare opportunity to join a growing business that invests in its people. APPLY NOW to take the next step in your maintenance engineering career. REFER A FRIEND AND GET UP-TO £250! Call me to find out how it works

Location: Skipton, North Yorkshire Type: Permanent Salary: £55,000 per annum Hours Monday-Thursday 16:00-1:45 Are you interested in joining a company that truly values its employees? Our client is looking to recruit an experienced electrically biased Maintenance Engineer. The Role: Respond quickly to Maintenance support on manufacturing equipment, to achieve production output standards. Support to environmental and utilities systems at our manufacturing facility. Delivery of excellent customer service resulting in asset uptime, first time fix and quality workmanship. Actively involved in the development of departmental processes, procedures. Lead maintenance activities in areas of responsibility, both breakdown support and improvement work. Proactive support of a continuous improvement culture that develops factory assets, procedures, processes and systems. Comply with planned maintenance / calibration regimes, ensure work is completed and recorded in a timely manner within the CMMS. Ensure effective communications with stakeholders regarding equipment status, during breakdown support and any engineering requirements within Operational areas. Comply with site Health Safety and Environmental procedures and standards; ensure safe working conditions are maintained. The Person: Will hold a HNC or equivalent in Mechanical or Electrical Engineering Experience working as a Maintenance Engineer in a Pharmaceutical, Chemical, FMCG, Food setting is essential. The ideal candidate will hold additional electrical qualifications. Strong fault finding and problem solving skills (electrical with some mechanical). Proficient in IT / Microsoft applications (Word, Excel, Outlook, PowerPoint etc). Good interpersonal skills, effective communication skills needed. Good team player and able to work independently when needed. Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or GDPR please get in touch with us here. JBRP1_UKTJ