14 jobs found

Quality Control Specialist - Chemicals North London Full time and permanent role Excellent salary and benefits Are you a detail-driven scientist with strong experience in laboratory testing, documentation, and regulatory compliance? Our client is seeking a proactive Laboratory Specialist to support day-to-day QC operations, ensure accurate certification documentation, and contribute to new product development activities. This role offers the chance to work closely with internal teams, customers, and the Head of Laboratory while developing your technical and regulatory expertise. Key Responsibilities Perform routine and non-routine quality control testing across raw materials, intermediates, and finished products. Maintain accurate laboratory records and ensure equipment calibration and maintenance. Prepare and manage technical documentation, including Certificates of Analysis (CoA), Certificates of Conformity (CoC), and Safety Data Sheets (SDS). Support new product development activities through testing, method development, and stability studies. Provide technical and regulatory support to customers, managing incoming queries in a professional and timely manner. Skills & Experience Required Degree in Chemistry, Chemical Engineering, or a related scientific discipline. Experience working in a laboratory or quality control environment. Knowledge of CLP and REACH regulations, with experience preparing SDS documentation. Strong analytical, organisational, and problem-solving skills. Excellent communication skills, with the ability to liaise effectively with internal teams and external customers. If this looks like an opportunity of interest, and you possess the required skills and experience, then please follow the link to apply.

Job Title: Biomedical Scientist Team Manager- Haematology Location: Manchester Salary: £47,810- £54,710 + £5,000 joining bonus and £1,500 wellbeing allowance per annum Job Type: Full Time, Permanent The Pathology Partnership's Haematology Department, based on-site at the specialist Hospital, is seeking an experienced and motivated Biomedical Scientist Team Manager to join our Blood Sciences team. The hospital is a world-leading cancer treatment centre and a specialist site with no Accident & Emergency or Maternity services. The Pathology Partnership was formed in 2014 and is a joint venture between two companies including the largest provider of laboratory pathology and diagnostic services in Europe. We provide Pathology services for The hospital, which is the largest single cancer centre site in Europe and the first UK centre to be accredited as a comprehensive cancer centre. We treat more than 60,000 patients a year. Our Haematology laboratory processes approximately 270000 samples per year and is equipped with Siemens Advia analysers, Coagulation ACL Tops, and manual assays/techniques which deliver a comprehensive service for patients undergoing cancer treatment. This is an exciting opportunity to contribute to a busy, high-quality diagnostic service at one of the UK's most respected specialist hospitals. The role operates within core laboratory hours only (Monday to Friday), with no requirement for shift or out-of-hours work. At the organisation we believe in nurturing a culture of well-being and ensuring our employees are supported both professionally and personally. That's why we're thrilled to offer an exhilarating rewards package, including our incredible Wellbeing Allowance worth up to £1500 per annum and a £5,000 joining bonus. Please note that this company does not offer sponsorship and therefore candidates must have the legal right to live and work in the UK to be considered. Responsibilities: Perform and interpret complex analytical investigations within Haematology. Provide specialist advice on troubleshooting analyser and assay issues. Undertake validation and verification of new methods and equipment. Participate in EQA (External Quality Assessment) interpretation and reporting. Organise and manage a team of Biomedical Scientists, junior staff and support staff. Provide professional leadership and contribute to training and supervision of Specialist Biomedical Scientists, Trainee BMS and Pathology Support staff. Engage actively in quality management and research, including internal audits and document review. Operate and maintain competence with the Laboratory Information Management System (LIMS) and associated middleware applications. About you: Qualifications: HCPC registration as a Biomedical Scientist with evidence of Continued Professional Development MSc/FIBMS by examination and is currently in possession of Fellowship of the IBMS Blood Sciences or Haematology or demonstrates equivalent experience IBMS Specialist portfolio in Haematology or equivalent specialist qualifications with proven experience at this level High level working knowledge of biomedical techniques and practices at post honours degree level. Expert interpretive and diagnostic skills. Knowledge of National guidelines and protocols relating to specific discipline Strong leadership qualities Please click the APPLY button to send your CV and Cover Letter for this role. Candidates with the relevant experience or job titles of; Biomedical Scientist, Biomedical Scientist Team Leader, Biochemist, HCPC Registered Specialist, Haematology Team Manager, Haematology may also be considered for this role.

Talent STEM are partnering with a highly specialised chemical manufacturing organisation operating within regulated industrial markets. This is a key senior laboratory position within a small, technically driven site where quality, precision and continuous improvement are central to success. The successful candidate will play a pivotal role in leading day to day analytical and quality control activities while supporting production, technical development and wider operational objectives. The Opportunity This is not a routine testing role. You will be the technical authority within the laboratory, ensuring analytical robustness, data integrity and regulatory compliance in a fast paced manufacturing environment. You will work cross functionally with operations, technical and quality teams to ensure materials and finished products meet defined specifications and client expectations. The role offers significant autonomy and influence within a growing and evolving business. Key Responsibilities - Lead the daily operation of the analytical laboratory in a deadline driven production setting - Perform and oversee analysis of raw materials, intermediates and finished products using GC, HPLC, FTIR, Karl Fischer and classical wet chemistry techniques - Develop, optimise and validate analytical methods to ensure accuracy, repeatability and fitness for purpose - Review and trend analytical data, identifying shifts, deviations and opportunities for improvement - Maintain and improve quality systems aligned to ISO 9001 standards - Manage laboratory documentation including specifications, SOPs, investigations and CAPA activities - Support internal and external audits - Troubleshoot instrumentation including GC, HPLC and associated gas generation systems - Coordinate external service engineers for calibration, preventative maintenance and repair - Mentor and develop junior analysts, setting clear technical expectations - Drive continuous improvement initiatives across laboratory and production processes - Support technical and R&D activities including process development and specification setting About You You will be an experienced analytical chemist who thrives in a hands on manufacturing environment. - Degree in Analytical Chemistry or closely related discipline - Significant experience in a QC or analytical laboratory within chemical, fine chemical or pharmaceutical manufacturing - Strong working knowledge of GC and HPLC operation and troubleshooting - Experience with FTIR, Karl Fischer and titration techniques - Understanding of analytical method development and validation - Experience operating within ISO 9001 or comparable quality systems - Strong data review skills with the ability to interpret trends and anomalies - Excellent organisational skills with the ability to prioritise under pressure Working Environment This is a site based laboratory role within a production facility. The environment is fast moving and requires adaptability, resilience and strong collaboration skills. The role involves handling chemicals and operating analytical instrumentation daily. Candidates must have the right to work in the UK as sponsorship is not available. If you are a technically strong analytical chemist looking for a senior role where you can influence laboratory standards, mentor others and support operational growth, Talent STEM would be pleased to speak with you. To apply or request further information, please contact Talent STEM directly for a confidential discussion.

Blue Arrow is recruiting a Quality Control (QC) Analyst to join our clients team based in the Llantrisant area. Salary : 27,000p.a / 14.79 per hour Hours: 4 days on, 4 days off, 10-hour shifts from 07:00 to 18:00 Contract: 6 month fixed term contract Role Overview As a QC Analyst, you will be responsible for conducting a variety of laboratory tests and analyses to ensure our products meet regulatory standards and client specifications. You will play a key role in monitoring production processes, identifying deviations, and implementing corrective actions to maintain the integrity and safety of our products. Main Responsibilities Perform routine and non-routine analyses of raw materials, in-process samples, and finished products using established analytical techniques (e.g., FPLC, UV-Vis, FTIR, titration, wet chemistry). Interpret and report analytical results accurately, maintaining detailed and organised records in compliance with Good Laboratory Practices (GLP) and company SOPs. Calibrate, operate, and maintain laboratory equipment, ensuring all instruments are functioning optimally and maintaining calibration logs as required. Participate in method development, method validation, and continuous improvement initiatives to optimise laboratory performance. Conduct investigations into non-conforming results and work collaboratively to determine root causes and implement effective corrective actions. Assist in the preparation and review of technical documents such as SOPs, test methods, specifications, and validation protocols. Support internal and external audits by providing necessary documentation, data, and explanations regarding laboratory practices and results. Ensure all laboratory activities are conducted in accordance with health, safety, and environmental regulations. Collaborate with cross-functional teams, including production, quality assurance, and research and development, to resolve quality issues and drive continuous improvement. Stay current with advances in analytical techniques, regulatory requirements, and industry best practices. Requirements Bachelor's degree in chemistry, Biochemistry, Pharmaceutical Science, Microbiology, Food Science, or a related scientific discipline. Familiarity with analytical instrumentation (e.g., HPLC, GC, UV-Vis, FTIR) and associated software. Strong understanding of GLP, GMP, or ISO standards as applicable to the industry. Excellent attention to detail, time management, and organisational skills. Strong communication abilities, both written and verbal, and ability to convey technical information clearly. Problem-solving skills and an investigative mindset. Ability to work independently as well as collaboratively in a fast-paced, team-oriented environment. Proficient in using standard office and laboratory software (e.g., Microsoft Office, LIMS). Desirable Skills Experience with method development and validation. Knowledge of statistical analysis and data interpretation. Familiarity with regulatory submissions and documentation (e.g., MHRA, FDA, EMA). Previous experience in root cause analysis and CAPA (Corrective and Preventive Action) processes. Additional language skills are an advantage. If you feel you would be suitable for the above role, please submit your CV for immediate response. Blue Arrow is proud to be a Disability Confident Employer and is committed to helping find great work opportunities for great people.

Role Name: Laboratory Technician Site location: Stevenage, UK Hourly Rate: £16 per hour via PAYE Duration of contract: 6 months initially, possibility for extension. Weekly hours: 37.5 hours LABORATORY TECHNICIAN (CHEMISTRY R&D) STEVENAGE Help us improve access to life-changing therapies that can transform human health A global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups, and sauces - they need to work better, faster, and safer, leading to better patient outcomes. We are looking for an organized, self-motivated, enthusiastic, and disciplined Laboratory Technician (Chemistry R&D) to work with our dynamic chemistry team with employees across the world. Would you be excited to be part of a global science leader's company dedicated that advance and accelerate the development, manufacture, and delivery of therapeutics? Then we would love to hear from you. What you'll do Work closely with chemists, materials scientists, engineers and biologists to support activities including membrane fabrication and materials analysis. Perform chemical modification of Fibro membranes supporting R&D and production. Perform both routine and one-off laboratory testing such as Raman Spectroscopy, Differential Scanning Calorimetry, SEM, FT-IR, BET and dry weight testing. Support good housekeeping practices and adhering to Laboratory Health and Safety standards Lab management support, including order, restock and maintain inventory of chemicals and consumables and arrange deliveries between sites. Document and arrange safe disposal of all laboratory waste Take detailed lab notes, documenting and clearly communicating results with the team. Who you are Either Bachelor's degree in a scientific discipline with minimum of 3 months laboratory experience, or Science A-levels (or equivalent) with minimum 2 years laboratory experience. Knowledge of organic chemistry and/or membrane fabrication techniques. Experience in one or more of the analytical methods listed above would also be an advantage, but on the job training will be provided. Proficiency in MS Office Applications such as Word, Excel, and PowerPoint. Strong written and oral communication skills. Teamworking ability, attention to detail and interpersonal skills. Strong organisational and prioritisation skills, able to multi-task efficiently.

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.

CK Group are recruiting for a Laboratory Technician to join a global chemical manufacturing company at their facilities located near Durham on a 2 month contract basis. The Company: Our client is a leading manufacturer of PVC Compounds and they work at the forefront of technology with a comprehensive range of products. Location: This position is located near Durham and is site based. Pay rate: 14.00/hr PAYE Role: Conduct and report upon programmes of analytical testing so that the required results are produced within defined timescales and in an appropriate format. Participate in improvement opportunities through effective process monitoring. Support the day-to-day running and resource requirements of the laboratory including the ordering of consumables as required. Provide content for internal and external customer communications relating to both services received and delivered by the laboratory. To participate in COSHH assessments and the safety-assurance of equipment and processes To contribute to the development and updating of test procedures. . Participate in the effective management of the Laboratory waste. Participate in instrument training programmes to ensure lab and production teams are properly trained to deliver accurate analytical results. Support the maintenance and calibration of all laboratory equipment to maintain a high reliability of the service. Your Background: Educated to degree level or equivalent in Chemistry or a Scientific discipline. An understanding of appropriate test methods together with an understanding of the associated equipment with respect to maintenance and calibration. Hands on experience with ICP and of numerous chemicals/materials in wet chemistry, analytical processes. Excellent IT (specifically, word processing and spreadsheet) and communication skills (report writing). Understanding of risk assessment relating to the ChemiLab activities including COSHH. Ability to report results in written and oral form to internal and external customers. Apply: For more information, or to apply for this Laboratory Technician position please contact Mary Bolt on (phone number removed) or email (url removed). Please quote job reference (phone number removed) in all correspondence. It is essential that applicants hold entitlement to work in the UK INDLS

CMDO is Seeking to Appoint a Qualified Person. The Organisation is Engaged in Developing and Manufacturing New Medicines and Novel Formulations, Including a Wide Range of Oral Solid and Liquid Dosage Forms, Sterilised and Aseptically Filled Products, as well as Manufacturing and QP Certification of a Range of Phase I/II Clinical Trials for the UK and EU Markets, ROLE Perform the Legal Duties of a Qualified Person (QP) on the MIA(IMP) as Specified under EC Directive 2001/20/EC and Human Medicines Regulations 2012 Ensure Compliance with the Requirements of Eudralex Volume 4, Part 1, Annexes 13 and 16 Undertake QP Batch Certification and Release Functions within Departments Named on the Relevant Site Manufacturers Authorisation (IMP) Responsible for All QP Activities and Associated Resource Planning, Training, Development and Management Ensuring the Completeness and Effectiveness of the of Pharmaceutical Quality Management System and Pharmaceutical Quality Control Service as per the requirements for the Qualified Person, Described in Human Medicines Regulations 2012 and EudraLex Volume 4, Part 1, Annex 13 and Annex 16. REQUIRED Masters Degree in Pharmacy, Biochemistry, Chemistry, or Life Sciences Extensive Specialist Knowledge and Experience of Batch Certification/Release of Sterile Injectable Manufacture, Manufacture of Specials (Unlicensed) Medicinal Products, Investigational Medicinal Products for Clinical Trials and Radiopharmaceuticals Eligibility to Function as an EU QP for Investigational Medicinal Products under Statutory Instrument 2004:1031 Eligibility to Function as an EU QP Under the Permanent Provisions for Medicinal Products Under Statutory Instrument 2012:1916 Extensive Experience in GMP Validation of Pharmaceutical Facilities, Utilities, Equipment, Processes and Analytical Methods Managerial Experience in a Pharmaceutical Organisation and a Track Record of Compliance at Regulatory Inspections Experience of Research and Supply of IMP Medicines for Clinical Trials Expert Knowledge of GCP, GMDP, Quality Systems and Pharmaceutical Analysis Expert Knowledge of Pharmaceutical Microbiology and Quality Control Expert Practical Knowledge of GCP, GMDP, QA and All Current Relevant Regulations Expert Technical Knowledge of Pharmaceutical Sterile and Non -Sterile Manufacturing Demonstrable Ability to Risk Assess, Perform Root Cause Analysis and Resolve Deviations and Out of Specification Results and Develop Suitable CAPAs Demonstratable Ability to Ensure Quality through Set-Up, Manufacturing and Release of IMPs under a MAIMP to Comply Fully with the Requirements of GMP and GCP REMUNERATION 90K, Subject to Qualifications and Experience

Walker Cole International is searching for a Senior R&D Scientist - E&L and Nitrosamine Method Development - to join a global pharmaceutical company at their R&D and GMP-regulated site in the UK. As the Senior Scientist, you will play a key role in developing and validating analytical methods to support Extractables, Leachables, and Nitrosamine testing across pharmaceutical products and materials. Your responsibilities will include: Leading and supporting risk assessments and analytical method development for E&L and Nitrosamines. Developing, validating, and transferring LC-MS and GC-MS methods in compliance with GMP and regulatory guidelines. Performing data interpretation, troubleshooting, and technical investigations to resolve analytical issues. Preparing technical reports and regulatory documentation to support product filings and submissions. Collaborating with QC, QA, and Regulatory Affairs teams to ensure analytical compliance and product quality. Contributing to continuous improvement within analytical R&D and supporting method optimisation projects. To be successful, you will have: Proven experience in Extractables & Leachables and/or Nitrosamine analysis within a GMP-regulated laboratory. Hands-on experience with LC-MS or GC-MS and method validation techniques. Strong problem-solving, communication, and documentation skills. Analytical Chemistry Extractables & Leachables Nitrosamines LC-MS GC-MS Method Development Validation GMP Pharmaceuticals R&D

Title: Material Technologist (Compounds) Salary: Dependent on experience Working hours: Monday - Thursday 8:30am - 5:00pm and Friday 8:30am - 2:00pm (37.5 hours per week) Location: Leicester, Leicestershire VH Talent is delighted to partner with our renowned client, a leading global engineering company, to appoint a skilled Material Technologist (Compounds). The Material Technologist will support the development, testing, and evaluation of raw materials, chemical solutions, and compound formulations used in manufacturing. Whilst also assisting in analysing material properties to ensure performance, quality, and suitability for production applications. If you re ready for the challenge, we d love to hear from you! Please note this is a site based role not hybrid The Material Technologist Role: Assist in developing, testing, and evaluating new compounding materials and mixing processes to ensure they meet required specifications Identify, investigate and assist in addressing production and process-related failures Evaluate chemical risks in accordance with COSHH regulations and provide corresponding hazard warning cards Update, monitor and maintain process and solution specifications Assist with failure analysis and root cause analysis/investigation Regular communication with internal departments, other sites, customers, suppliers and other external personnel Support with carrying out testing methods Conduct laboratory experiments and physical testing of materials Generate and maintain Bill of Materials for all production compound recipes Accurate report writing, documenting and filing Maintain a commitment to continuous improvement Compliance with health, safety, and housekeeping standards Work to department targets and wider business objectives Support with other duties and activities within the department as required You ll Need: Analytical approach and excellent problem-solving skills Experience of interpreting test results and identify trends or anomalies Basic understanding of compound formulation principles and curing systems Experience of reporting writing and reading specifications Has attention to detail and methodical approach Some knowledge of rubber polymers and their compounding procedures Experience in assessment of risks and hazardous materials Experience in conducting physical and chemical testing of rubber compounds (e.g., tensile, hardness, rheometry) would be highly advantageous Proficient in Microsoft packages and various IT systems Engineering or Scientific (Chemistry or Polymer) qualification(s) would be advantageous What s in it for you: 25 Days annual leave + Bank Holidays Early finish Fridays Onsite subsidised canteen Health and wellbeing activities Employee Assistance Program Company pension VH Talent, your Permanent and FTC Recruitment Partner!

We are seeking an accomplished ICP-MS/OES expert to join our client as a Senior Scientist, where you will provide technical support and insight across the business. In this pivotal site-based role, you will lead the development, validation, and optimisation of ICP-MS and ICP-OES methods for a range of projects within the food and drinks testing sector. Key responsibilities: Method development and optimisation : You will hold a large responsibility for developing and improving ICP-MS/OES methods across trace metal analysis. Instrument maintenance and troubleshooting: Acting as main point of contact, you will take the lead in any maintenance and troubleshooting required, with the aim to reduce our clients service engineering contracts. Training: Provide guidance and training to colleagues across the ICP department where required. Customer support: You will utilise your technical expertise and excellent communication skills to support customer enquiries and ensure timely project delivery. Leadership support : Assisting the Manager with the day-to-day running and scheduling of projects for the team. To be considered you must have: A strong background working with ICP-MS/OES instrumentation Experience developing, optimising or validating methods Confidence undertaking instrument maintenance and troubleshooting Excellent interpersonal and team working skills In return you will receive a highly competitive salary and benefits package, working within a friendly and welcoming team, in a picturesque location in the Cotswolds! Due to the location of the laboratory you must have a driving licence and access to your own transport. If this sounds like the next step up for you then apply to be considered today! Key words: inorganic, ICP, ICP-MS, ICP-OES, laboratory, analytical, chemistry, food, drink, environmental, agrochemical, method development, ISO 17025, ISO17025, Gloucestershire, Cotswolds, Stratford Upon Avon, Midlands, South West, VRS9044AW

ROLE OVERVIEW We are currently looking for a GC / GC-MS Technical Specialist to join a leading analytical company based in the North West or South East GB area. As the GC / GC-MS Technical Specialist, you will be responsible for delivering exceptional technical expertise and support to both the sales team and customers. KEY DUTIES AND RESPONSIBILITIES: Your duties as the GC / GC-MS Technical Specialist will be varied however the key duties and responsibilities are as follows: 1. Provide technical expertise during pre-sales activities, including conducting technical discussions, assessing customer needs, and recommending tailored solutions. 2. Plan and execute product demonstrations, analyse customer samples, and generate proof data to support sales efforts. 3. Deliver comprehensive training, method development support, and troubleshooting advice to ensure customer success with GC and GC-MS products. 4. Develop new application notes, technical materials, and relevant content to support product portfolio growth and expand into new markets. ROLE REQUIREMENTS: To be successful in your application to this exciting role as the GC / GC-MS Technical Specialist we are looking to identify the following on your profile and past history: 1. Relevant degree in a scientific discipline such as chemistry, analytical chemistry, or environmental chemistry. 2. Proven industry experience with GC, GC-MS, and related technologies. 3. A working knowledge and practical experience with mass spectrometry software systems. Key Words: GC / GC-MS / chromatography / mass spectrometry / analytical chemistry / technical specialist / product demonstrations / customer training / application development / scientific instrumentation / technical support Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.

D365 Operations Process Lead Full-Time PermanentHybrid Runcorn (with occasional international travel) Are you a D365 operations expert with a passion for driving operational excellence? Do you have a proven ability to optimise ERP platforms and embed process improvements across supply chain and operations? We are looking for an experienced D365 Operations Process Lead to take ownership of optimising and driving operational processes across a leading chemical and life science group. What's on offer Generous holiday allowance with buy/sell scheme. Flexible hours and hybrid working. Professional development through internal and external training. Mental health and wellbeing initiatives, including free therapy/counselling. Active support for physical wellbeing and fitness challenges. The Role In this pivotal role, you'll be responsible for shaping, enhancing, and embedding best practice business processes within Microsoft Dynamics 365, ensuring alignment with strategic objectives. This is a highly collaborative role, engaging with group companies, operational sites, suppliers, customers, and cross-functional teams. Strong analytical, problem-solving, and stakeholder management skills are key to success. What you'll be doing Acting as the subject matter expert for Microsoft Dynamics 365 (WMS, production, and transport modules). Ensuring optimal utilisation of handheld devices and related technology to streamline workflows. Applying Lean methodologies to eliminate waste, reduce lead times, and improve throughput. Embedding customer-centric improvements using Net Promoter Score (NPS) insights. Upskilling operational staff on D365 best practice, building in-house capability. Driving cross-functional business transformation to deliver measurable value and sustainable change. Improving process reliability, reducing operational errors, and enhancing customer satisfaction. What we're looking for Essential skills & experience: Strong technical and functional expertise in Microsoft Dynamics 365 (WMS, production, transport). Proven track record of delivering ERP-enabled process improvements within operations and supply chain. Knowledge and application of Lean methodologies. Experience embedding NPS-driven initiatives into business processes. Ability to translate business requirements into system solutions and operational practices. Excellent communication and stakeholder engagement skills. Experience training and upskilling teams on ERP best practice. Graduate-level education or equivalent ERP/operations qualifications. Desirable: Background in chemicals, manufacturing, or distribution. Experience leading business transformation or ERP implementation projects. Knowledge of compliance within supply chain operations. Full UK driving licence. About the organisation This is an international group of Material & Life Science companies with customers in over 90 countries. Headquartered in the UK and established in 2004, they are market leaders in the chemical industry, delivering chemistry-based solutions for a better life today and a better world tomorrow. With a culture of innovation, collaboration, and creativity, the group empowers its people to make a real impact. Next steps If you feel this role matches your skills and ambitions, please apply with your CV. If you are shortlisted for this role, the client will contact you directly to discuss your experience and suitability further. Unsuccessful applicants will be informed once we have received feedback from the client. Key Appointments UK Ltd will assess your suitability for the role based on the information contained in your CV and application. This includes skills, experience, education, and location. By applying for this role, you give consent for your CV to be processed by Key Appointments for recruitment purposes. Our full Privacy Policy is available at key-appointments.

Cosmetic Chemist - Liverpool - Personal care We're working with an industry leader in lash, brow, haircare, and skincare treatments to recruit a Cosmetic Formulation Chemist to join their Liverpool-based lab. This is an exciting opportunity to work on innovative professional-grade cosmetic treatment products with a focus on sustainability, efficacy, and stability. Key Requirements: Expertise in formulating for lash, brow, skincare, and haircare products Strong practical lab skills in formulation and stability testing Proven ability to develop sustainable carriers and bases Degree-qualified in Chemistry or Analytical Chemistry (or similar) Solid understanding of raw materials and performance testing Experience in developing and validating methods for new formulations and packaging compatibility Strong communication and data management skills Proactive, detail-driven, and self-motivated You'll play a pivotal role in driving innovation and ensuring high-quality standards for market-leading cosmetic treatments. If you're passionate about lab work, product development, and clean science in beauty, we'd love to hear from you. To apply or find out more, get in touch today.