Analytical chemistry jobs in United Kingdom

Are you a passionate Chemistry Teacher looking for your next opportunity in Hornchurch? Have you taught KS3-4 Chemistry in a secondary setting in Hornchurch or a similar school? Are you available to start after Easter term? Hornchurch, EssexASAP / April 2026Secondary School KS3-4Monday - Friday, 8:30am-3:30pmPay: MP3-6Applications close: 20/03/26Interviews: Interviews being held W/C 16th March, Trial Day - onboarded if successful. This Chemistry Teacher role in Hornchurch provides the opportunity to teach Chemistry across Key Stages 3 and 4 within a supportive department that values high-quality teaching, strong subject knowledge, and a passion for scientific enquiry. The trust prides itself on collaboration between its schools, ensuring that every Chemistry Teacher benefits from shared resources and best practice across the Hornchurch network. Job Overview: * This secondary school caters for students aged 11-16. * Full-time, Monday - Friday, Chemistry Teacher role. * You will deliver engaging and practical Chemistry lessons across KS3 and KS4 in Hornchurch. * Plan, prepare and assess in line with UK curriculum expectations as a Chemistry Teacher. * Inspire students to develop analytical thinking and a love for Chemistry. * Contribute to the wider trust network, collaborating with fellow Science colleagues. * Opportunity for TLR responsibilities for an experienced Chemistry Teacher. What we're looking for: Qualified Chemistry Teacher with QTS (or 5+ years' experience teaching Chemistry). * Strong subject knowledge and passion for Chemistry. * A proactive and committed Chemistry Teacher who can motivate learners in Hornchurch. * Excellent classroom management skills. * Commitment to contributing to trust-wide initiatives and upholding high standards across the Hornchurch school community. * Enhanced DBS on the Update Service. What's next? Click "Apply Now" and should your application be successful, you will be contacted for a phone call OR contact Ellie directly from Academics TODAY!

BioTalent are supporting a global leader in the development, manufacture, and distribution of innovative radiopharmaceutical products used in advanced diagnostic imaging and targeted therapies. With decades of industry expertise and international operations, they support millions of patients each year through high-quality, life-enhancing medicines. Our organization operates within highly regulated healthcare environments and is committed to innovation, operational excellence, and the highest standards of quality and patient safety. The Role We are seeking a Senior QA Specialist to design and implement analytical testing processes for radiopharmaceutical products while ensuring the QC Laboratory remains fully compliant with GMP and GLP standards. This is a hands-on, site-based role combining Quality Assurance oversight with active involvement in Quality Control activities. Key Responsibilities • Ensure production and analytical methods comply with GMP guidelines, pharmacopoeial standards (EP/BP), and product specifications., • Maintain and support the Quality Management System (QMS), including Deviations, OOS, CAPA, Change Control, Complaints, Recalls, Risk Assessments, Supplier Approval, and Validation documentation., • Review and approve QC analytical and microbiological results; manage investigations and ensure data integrity compliance., • Perform and oversee QC testing of radiopharmaceutical products in line with regulatory and internal standards., • Lead or support root cause investigations and implement effective corrective and preventive actions (CAPA)., • Maintain laboratory documentation, logbooks, validation master plan (VMP), equipment calibration schedules, and stock control., • Support batch release activities, audit readiness, and regulatory inspections., • Train technicians in SPECT and PET QC analytical testing across UK sites., • Support the QA Manager with day-to-day quality oversight and continuous improvement initiatives. Education & Experience • Degree in a related scientific discipline., • 2–3 years’ experience in radiopharmacy Quality Control., • Working knowledge of pharmaceutical chemistry and Good Manufacturing Practice (GMP)., • Strong attention to detail and practical laboratory skills., • Excellent communication and teamwork abilities., • Ability to work under pressure and manage priorities effectively., • Good customer-facing skills and professional conduct., • Basic computer literacy and strong time management. Reach out for more information to:

As a Biopolymer Scientist / Materials Engineer at Sealeo, you will take a central role in the development of a cutting-edge biomaterial system at the heart of the company’s technology. This is a hands-on, applied materials role with real ownership and responsibility. You will work directly with the founders on polysaccharide-based and soft-matter systems, generating new experimental data, structuring and interpreting existing results, and guiding technical decisions that shape Sealeo’s development trajectory. Your work will directly influence how a novel biomaterial progresses from early-stage development toward industrial readiness. This role suits someone who thrives in fast-moving, ambiguous environments and enjoys tackling complex materials challenges that do not yet have established playbooks. You will balance rapid experimentation with deeper materials understanding, making informed judgement calls that matter. You will collaborate with leading academic and industrial partners, engaging with advanced testing, validation, and scale-up capabilities beyond a single lab. This offers rare exposure to the full journey of novel biomaterials, from bench-scale science to real-world application. The role is part-time (2-3 days per week) with high flexibility in working hours and an outcome-driven approach. As Sealeo grows, there is clear potential to transition into a full-time position within 12 months, with scope for expanded responsibility and long-term technical leadership for the right person. Responsibilities Material Development & Evaluation: • Take a central scientific role in the development of novel biopolymer-based material systems, working with polysaccharides and soft-matter materials., • Contribute to Sealeo’s work within a large funded consortium, supporting and coordinating material validation, characterisation, and scale-up activities across partners., • Identify, evaluate, and select suitable biopolymer inputs and functional material components based on performance, manufacturability, and scale-up considerations., • Design and execute bench-scale experiments to develop, optimise, and characterise biomaterials., • Correlate material chemistry and structure with macroscopic properties relevant to real-world performance., • Structure, consolidate, and critically analyse existing experimental data to support clear technical decisions., • Design and generate new experimental data to resolve open technical questions and reduce development risk., • Develop and validate analytical test methods to ensure consistency and reproducibility in formulation performance., • Communicate material insights and formulation changes internally and externally, enabling effective collaboration with research organisations, scale-up partners, and manufacturing stakeholders., • Ensure experimental work remains aligned with manufacturing constraints, cost considerations, and downstream deployment requirements., • Contribute to the development of intellectual property, including patents and trade secrets. Qualifications Must-have: • PhD (ongoing or completed) in Materials Science, Polymer Chemistry, Chemical Engineering, or equivalent hands-on industry experience., • Demonstrated hands-on laboratory experience working with polysaccharides (e.g. alginate, cellulose, chitosan, starch) in material or formulation contexts., • Proven experience developing and testing physical material systems, such as foams, hydrogels, porous materials, or biopolymer-based composites., • Strong experimental skills, including designing experiments, generating reproducible data, and analysing results., • Experience working in exploratory R&D environments, with comfort navigating ambiguity and incomplete data., • Ability to translate experimental findings into clear technical conclusions and recommendations that support decision-making., • Strong written and verbal communication skills for technical documentation and partner-facing discussions. Nice-to-have: • Familiarity with thermal properties, heat transfer, and insulation-related material performance., • Exposure to thermal cycling, stability testing, or durability studies under repeated operating conditions., • Experience interfacing with scale-up, pilot manufacturing, or process engineering teams.

QC Analyst – Pharmaceuticals Location: South London (Fully Site-Based) Employment Type: Full-Time About the Role: We are seeking a highly skilled and motivated Quality Control Analyst to join a pharmaceutical team in South London. This is a fully site-based role, ideal for someone with a strong background in analytical chemistry and a passion for maintaining high standards in a GMP-regulated environment. Key Responsibilities: • Perform routine and non-routine analysis of raw materials and finished pharmaceutical products using HPLC (essential), GC, UV, and FTIR techniques (preferred)., • Demonstrate advanced troubleshooting skills with HPLC systems and lead Out of Specification (OOS) investigations., • Ensure all testing is conducted in compliance with GMP standards and internal SOPs., • Accurately document results and maintain laboratory records in accordance with regulatory requirements., • Support method development and validation activities as needed., • Collaborate with cross-functional teams to resolve quality issues and improve laboratory practices. Requirements: • Proven experience in a GMP-compliant pharmaceutical QC laboratory., • Strong proficiency in HPLC is essential, including troubleshooting and OOS investigations., • Experience with GC, UV, and FTIR techniques is highly desirable., • Excellent attention to detail and ability to work independently in a fast-paced environment., • Strong communication and documentation skills. What’s on Offer: • Competitive salary and benefits package., • Opportunity to work in a dynamic and supportive team., • Career development and training opportunities. Key Words: QC, quality control, analyst, analytical scientist, chemistry, chemist, chromatography, HPLC, GC, TLC, FTIR, UV Vis, techniques, GMP, Good Manufacturing Practice, laboratory technician, pharmaceutical, healthcare, supplement, medical.

We are seeking a Senior Biosensing Scientist to play a foundational role in building the biorecognition layer of our sensing platform. This is not a pure in-house discovery role; instead, you will focus on defining, guiding, and validating externally developed affinity reagents (such as aptamers and synthetic probes) to ensure they integrate with our proprietary continuous sensing hardware. About us (Stealth mode): We’re a stealth, VC-backed deep-tech startup building a next-generation molecular sensing platform, leveraging proprietary light-based sensing in a wearable form factor. Our mission is to turn the body’s molecular signals into a continuous source of truth - unlocking real-time biochemical clarity for areas like fertility, inflammation, metabolic health, and recovery. Today’s wearables track proxies (heart rate, sleep, movement), but the biology that drives health still lives in episodic, invasive lab tests. We’re closing that gap. The role: You will own the scientific interface between CHUNE’s hardware platform and our external affinity reagent partners. This means translating our unique continuous-sensing product requirements into precise technical specifications and guiding CROs through the development process. Once candidate reagents are delivered, you will lead internal validation, testing them in relevant biological matrices and on our solid-state sensor architectures to determine whether they meet platform performance requirements. You’ll work closely with our hardware, fluidics, and systems engineering teams to ensure reagent performance is evaluated within the real constraints of the device, not just in a vendor’s benchtop assay You will own: • Target Specifications: Defining target product requirements for affinity reagents, including physiological concentration ranges, matrix contexts, selectivity profiles, and binding kinetics (Kd, kon, koff)., • Vendor Management: Acting as the primary scientific lead with external aptamer/optimer vendors. You will guide them through reagent design, screening requirements, off-target panels, and success criteria., • Data Review & Downselection: Critically evaluating vendor outputs (sequence packages, binding data, selectivity reports) and deciding which candidates progress to in-house testing., • Internal Assay Validation: Developing and executing assays to test whether externally developed binders are fit for our specific use cases (e.g., performance in Interstitial Fluid, reproducibility, and reversibility for continuous monitoring)., • Hardware Integration: Collaborating with engineering teams to evaluate reagent compatibility with specific surface immobilisation techniques and our proprietary continuous readout systems., • Strategic Frameworks: Building an internal framework for reagent benchmarking, quality control, and acceptance criteria across our biomarker pipeline. You’ll collaborate closely with leaders across photonics, microfluidics, clinical, and product and play a key role in bringing a genuinely cutting-edge wearable technology from first prototypes to pilot-ready systems. The person: Ideal requirements: • PhD (or MSc + 2+ years’ experience) in biochemistry, bioengineering, or a related field, • Hands-on experience working with aptamers, optimers, or other synthetic affinity probes., • Deep understanding of binding performance metrics (affinity, specificity, sensitivity) and experience defining Kd, kon, and koff requirements for real-world assays., • Experience working with external partners, CROs, or vendors, with the ability to translate product needs into clear scientific briefs., • Proven track record of designing assays to validate binder performance in complex biological matrices (serum, plasma, ISF, etc.)., • Strong understanding of biomarker biology, including physiological concentration ranges, relevant interferents, and matrix effects, • Strong analytical skills to critically challenge vendor data and troubleshoot underperforming reagents. Nice to have (strong signals, not required) • Development of custom aptamers or nucleic-acid–based probes (e.g., optimisation, truncations/modifications, or SELEX exposure)., • Experience with SPR, BLI, QCM, or related kinetics / interaction analysis tools, • Familiarity with continuous or real-time biosensing platforms., • Experience working with microfluidic, wearable, or lab-on-chip systems., • Experience validating biomarkers in interstitial fluid (ISF)., • Experience handling skin tissue samples. Why work for us? • Foundational ownership: You’ll be a core contributor to the biorecognition layer of the platform, directly shaping sensor performance, biomarker selection, and long-term reliability. Your work will define what we can measure and how well we can measure it., • Deep-tech, real-world impact: Work on genuinely novel continuous biosensing technology with the potential to transform how health is monitored - moving biochemical insight from occasional lab tests to continuous, real-time understanding., • Work with exceptional people: collaborate with top-tier talent from Cambridge and Imperial College and leaders across sensing, chemistry, and product in a highly ambitious environment., • High-pace, high-support culture: a flat structure, fast iteration, and genuine room to experiment - with regular check-ins and feedback to support your growth and development., • Competitive compensation & meaningful equity: we offer competitive salary and early-stage share options, so you’ll own a real stake in what you’re building Apply / get in touch If you’re excited by wearable molecular monitoring and want to build something genuinely new, please apply here or email privately to

As a Biopolymer Scientist / Materials Engineer at Sealeo, you will take a central role in the development of a cutting-edge biomaterial system at the heart of the company’s technology. This is a hands-on, applied materials role with real ownership and responsibility. You will work directly with the founders on polysaccharide-based and soft-matter systems, generating new experimental data, structuring and interpreting existing results, and guiding technical decisions that shape Sealeo’s development trajectory. Your work will directly influence how a novel biomaterial progresses from early-stage development toward industrial readiness. This role suits someone who thrives in fast-moving, ambiguous environments and enjoys tackling complex materials challenges that do not yet have established playbooks. You will balance rapid experimentation with deeper materials understanding, making informed judgement calls that matter. You will collaborate with leading academic and industrial partners, engaging with advanced testing, validation, and scale-up capabilities beyond a single lab. This offers rare exposure to the full journey of novel biomaterials, from bench-scale science to real-world application. The role is part-time (2-3 days per week) with high flexibility in working hours and an outcome-driven approach. As Sealeo grows, there is clear potential to transition into a full-time position within 12 months, with scope for expanded responsibility and long-term technical leadership for the right person. Responsibilities Material Development & Evaluation: • Take a central scientific role in the development of novel biopolymer-based material systems, working with polysaccharides and soft-matter materials., • Contribute to Sealeo’s work within a large funded consortium, supporting and coordinating material validation, characterisation, and scale-up activities across partners., • Identify, evaluate, and select suitable biopolymer inputs and functional material components based on performance, manufacturability, and scale-up considerations., • Design and execute bench-scale experiments to develop, optimise, and characterise biomaterials., • Correlate material chemistry and structure with macroscopic properties relevant to real-world performance., • Structure, consolidate, and critically analyse existing experimental data to support clear technical decisions., • Design and generate new experimental data to resolve open technical questions and reduce development risk., • Develop and validate analytical test methods to ensure consistency and reproducibility in formulation performance., • Communicate material insights and formulation changes internally and externally, enabling effective collaboration with research organisations, scale-up partners, and manufacturing stakeholders., • Ensure experimental work remains aligned with manufacturing constraints, cost considerations, and downstream deployment requirements., • Contribute to the development of intellectual property, including patents and trade secrets. Qualifications Must-have: • PhD (ongoing or completed) in Materials Science, Polymer Chemistry, Chemical Engineering, or equivalent hands-on industry experience., • Demonstrated hands-on laboratory experience working with polysaccharides (e.g. alginate, cellulose, chitosan, starch) in material or formulation contexts., • Proven experience developing and testing physical material systems, such as foams, hydrogels, porous materials, or biopolymer-based composites., • Strong experimental skills, including designing experiments, generating reproducible data, and analysing results., • Experience working in exploratory R&D environments, with comfort navigating ambiguity and incomplete data., • Ability to translate experimental findings into clear technical conclusions and recommendations that support decision-making., • Strong written and verbal communication skills for technical documentation and partner-facing discussions. Nice-to-have: • Familiarity with thermal properties, heat transfer, and insulation-related material performance., • Exposure to thermal cycling, stability testing, or durability studies under repeated operating conditions., • Experience interfacing with scale-up, pilot manufacturing, or process engineering teams.

Science ECT | Bexley | September 2026 Are you an Early Career Teacher looking to launch your career in Science, whether thats career progression, relocation, or gaining leadership experience? A high-performing secondary school in Bexley is seeking a motivated and enthusiastic Science ECT to join their team. If you are passionate about inspiring young learners and developing your teaching skills in a supportive environment, this Science ECT role could be the ideal first step in your career. The Role | Science ECT: • Plan and deliver engaging lessons across Key Stages 3 and 4, with exposure to KS5 where possible., • Inspire students to develop curiosity, analytical thinking, and a love of Biology, Chemistry, and Physics., • Work closely with mentors and colleagues to refine teaching practice and meet ECF standards., • Contribute to whole-school initiatives and extracurricular science activities.Why Join This School?, • Excellent laboratories and well-resourced Science classrooms., • Inclusive and supportive school community., • Comprehensive ECT induction and ongoing professional development., • Clear pathways for career progression beyond the ECT year.What Were Looking For:, • Qualified teacher with QTS or completing ECT induction with a UK Bachelors degree., • Passion for Scie...

Science ECT | Bexley | September 2026 Are you an Early Career Teacher looking to launch your career in Science, whether thats career progression, relocation, or gaining leadership experience? A high-performing secondary school in Bexley is seeking a motivated and enthusiastic Science ECT to join their team. If you are passionate about inspiring young learners and developing your teaching skills in a supportive environment, this Science ECT role could be the ideal first step in your career. The Role | Science ECT: • Plan and deliver engaging lessons across Key Stages 3 and 4, with exposure to KS5 where possible., • Inspire students to develop curiosity, analytical thinking, and a love of Biology, Chemistry, and Physics., • Work closely with mentors and colleagues to refine teaching practice and meet ECF standards., • Contribute to whole-school initiatives and extracurricular science activities.Why Join This School?, • Excellent laboratories and well-resourced Science classrooms., • Inclusive and supportive school community., • Comprehensive ECT induction and ongoing professional development., • Clear pathways for career progression beyond the ECT year.What Were Looking For:, • Qualified teacher with QTS or completing ECT induction with a UK Bachelors degree., • Passion for Science education and commitment to pupils academic and personal development., • Collaborative approach and willingness to embrace guidance and mentoring. JBRP1_UKTJ

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, • 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., • 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 WR is acting as an Employment Agency in relation to this vacancy. JBRP1_UKTJ

Strong understanding of laboratory operations, quality requirements, and laboratory applications. Experience with global accounts and channel partner management in laboratory markets. Experience with water purification, analytical chemistry, or laboratory infrastructure.

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 Senior Director, Biological Analytical Development is responsible for providing both leadership and hands-on technical expertise for analytical aspects of biologic CMC programs. This role combines strategic oversight with direct scientific contributions ensuring delivery of high-quality methods, specifications, and regulatory documentation to enable clinical development and regulatory submissions. The role can manage a team as well as external partners/CMOs, balancing mentorship and oversight with active participation in experimental design, data interpretation, and issue resolution. Essential Functions Own and drive phase appropriate analytical development strategy for biologics programs from early clinical development through commercialisation, ensuring alignment with overall CMC and Pharmaceutical Development strategy. Serve as the analytical CMC lead for assigned programs, providing clear scientific judgment and decision making in cross functional forums with Drug Substance, Drug Product, Regulatory CMC, Quality, Manufacturing, and external partners. Define and implement analytical control strategies across the product lifecycle, including method scope, qualification and validation approach, specifications, stability programs, reference standards, extended characterization and comparability. Lead analytical input into process changes, tech transfers, PPQ, and lifecycle management activities, ensuring approaches are risk based, clinically relevant, and regulator ready. Personally author, review, and defend key analytical sections of regulatory submissions and responses, including IND, IMPD, BLA or MAA, comparability justifications, and health authority questions. Govern and oversee analytical activities at external CDMOs and contract laboratories, setting expectations, reviewing data critically, addressing underperformance, and ensuring inspection readiness Provide leadership to a small, senior analytical team through prioritisation, coaching, and development, while remaining sufficiently hands on to guide complex technical decisions Act as a senior analytical thought partner in a lean development environment, balancing scientific rigor with pragmatism, speed, and resource constraints Contribute to and in some cases lead non technical strategic initiatives across PharmDev or CMC, such as operating model improvements, governance processes, portfolio prioritisation, or capability strategy Where required, act as a CMC Development Team Lead or deputy, integrating analytical, DS, DP, regulatory, and quality considerations into a coherent program execution strategy Participate in Analytical Development and broader CMC leadership forums, contributing to strategy setting across modalities and programs Communicate clearly and credibly with internal stakeholders and external partners, adapting message depth and style to technical, regulatory, and executive audiences Travel as needed to support CDMO oversight, program reviews, and regulatory readiness activities Required/Preferred Knowledge, Skills, and Abilities At least 10 years experience in biologics analytical development across early and late stage development, including method qualification and validation from Phase 1 through approval Demonstrated experience in biologics characterization and analytical comparability assessments supporting regulatory filings Experience managing and governing external development and testing partners Direct experience authoring analytical sections of regulatory submissions and addressing health authority questions Preferred experience acting as a CMC Development Team Lead or senior CMC representative Demonstrated ability to operate at both strategic and execution levels, with sound scientific judgment and independence of thought Strong collaboration and influencing skills in matrix environments Excellent written and verbal communication skills Required/Preferred Education and Licenses B.Sc. in Analytical Chemistry, Biotechnology, Biochemistry, Chemical Engineering, or a related scientific discipline required M.Sc. or Ph.D. in a relevant discipline preferred 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

Field Service Chemist - Laboratory Instrumentation UK -50-75% Travel with Occasional International Travel (North West base would be desired) Up to £38,000 per annum Russell Taylor Group have an exciting opportunity for a hands-on Chemist who enjoys getting out of the lab and into the field. We are recruiting for a Field Service Chemist to join a leading scientific instrumentation organisation. This is a dynamic, customer-facing role combining chemistry, engineering, troubleshooting and travel across the UK. The Role: • Service, maintain and repair advanced analytical instrumentation • Install new systems and deliver customer training on how to upkeep maintenance tasks. • Be on hand for customers face to face, phone or email. • Diagnose mechanical, electrical and analytical faults • Provide remote and on-site technical support • Prepare paperwork and documentation following the installation of instrumentation. • Manage your own travel schedule and service planning The Person • Educated to degree level in Chemistry (or closely related discipline) • Strong practical lab skills • Understanding of electrical/electronic principles • Confident reading schematics and technical manuals • Excellent communication skills • Full UK driving licence • Happy to travel 50-75% UK wide and occasional international travel. 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 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

Exciting opportunity to join an innovative, industry leading laboratory equipment manufacturer and distributor. Our client is a leading provider of analytical instruments in the UK with products ranging from sample preparation systems to elemental analysis instrumentation. This opportunity calls for an ambitious scientist looking to drive sales whilst providing excellent service to customers. Within this role, you will support customers by identifying their key pain points and advising which products in your portfolio would best serve their requirements. Your position will focus on managing existing accounts and identifying new customers in academic, CRO, biotech and pharma laboratories. You will be based remotely and are expected to travel ~60% of your time to customer sites across the Southeast for instrument demonstrations, presentations and negotiation. To be considered for this position you will have: • BSc minimum in Chemistry or related subject, • Eligibility to work in the UK without sponsorship, • UK driver’s license and willingness to travel, • Proven experience within scientific sales and understanding of the sales process is highly desirable For your work you will be provided with a competitive basic salary, commission scheme, car and additional employee benefits. Please apply below to receive more details! Keywords: chemistry equipment, laboratory equipment, consumables sales, capital sales, business development, account management, sales, sales executive, technical sales, technical sales specialist, London, Cambridge, Oxford, Kent, Leicester, Northampton, Ipswich, St. Albans, Luton, Watford, VRS9389PC Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website

Regulatory CMC Technical Writer Fully Remote (UK/Europe) | Freelance Contract – Outside IR35 | Occasional International Travel About the Role We are seeking an experienced Regulatory CMC Technical Writer to support our client’s global regulatory and pharmaceutical development programmes. This is a fully remote, freelance position operating outside IR35, offering flexibility, autonomy, and the opportunity to collaborate with international teams across the life sciences sector. The ideal candidate will bring proven expertise in CMC documentation, regulatory submissions, and technical writing within pharmaceuticals, biologics, or advanced therapies. Key Responsibilities • Prepare, write, and review high‑quality CMC documentation for global regulatory submissions (e.g., Module 3, IMPD, IND, BLA, CTA)., • Translate complex scientific, manufacturing, and quality information into clear, compliant regulatory content., • Ensure all documentation aligns with FDA, EMA, MHRA and ICH guidelines., • Work closely with SMEs across Quality, Manufacturing, Analytical Development, Regulatory Affairs, and external partners., • Maintain document consistency, accuracy, and alignment across multiple projects and versions., • Contribute to gap analyses, data organisation, and dossier readiness activities., • Participate in virtual meetings and occasional international on‑site visits as needed. Experience & Skills Required • Demonstrable experience as a CMC Technical Writer or Regulatory Medical Writer within pharmaceuticals or biotech., • Strong understanding of CMC regulatory frameworks, quality systems, and manufacturing processes., • Prior experience supporting IND/IMPD/BLA/MAA submissions highly desirable., • Excellent written communication skills with the ability to simplify scientific content., • Ability to work independently, manage multiple deadlines, and collaborate with global project teams., • Degree in Life Sciences, Pharmacy, Chemistry, Biotechnology or related field. Contract Details • Freelance / Outside IR35, • Contract until September 2026 and extendable, • Fully remote, with flexibility on working hours, • Occasional international travel (project‑dependent), • Competitive day rate based on experience How to Apply If you are a detail‑driven Regulatory CMC specialist who thrives in a flexible freelance environment, we would love to hear from you. Please submit your CV today

An Excellent Career Opportunity for an Experienced Quality Control Analyst, Supporting the QC Supervisor and QC Lead Analyst ROLE * Perform Routine Analytical Testing on Incoming Materials and Finished Products * Ensuring All Analytical Standards, Methods, Sampling Processes, and Training Requirements are Executed in Full Compliance with SOP’s * Coordinate with QC Lead Analyst and Other Team Members to Ensure All Analytical Work Assigned is Achievable and Delivered in a Timely Manner * Peer-Review or Bench-Check QC Test Documentation and Results for the QC Analytical Team * Report Any Issue with Availability and Validity of Protocols, Reports, Specifications, or Retest Date for Calibration, Qualification and Validation of Equipment * Report on Any Issue with the Purchase, Replacement and Availability, or Delivery, of the Required Reference Standards, Chemicals, Reagents, etc * Consistently Follow the Data Integrity and Governance Requirements in SOP’s * Demonstrate Capabilities on HPLC, KF Titration, Dissolution Testing and Physical Testing of Dosage Forms and Packaging * Prepare and Check Analytical QC Data before Presenting Results for Review * Completing allocated training and making sure that the training is effective by implementing QC analytical work assigned correctly. * Perform Routine or Special Assigned Duties to Check/Verify/Draft SOP’s and Specifications Required to Meet Regulatory and Customer Requirements REQUIRED * Certificate, Diploma or BSc in Chemistry, Medical Laboratory Science, Analytical Sciences, or Equivalent Science Degree with Strong Practical and Analytical Component * Substantial Analytical Experience in a UK Pharmaceutical QC Laboratory * Experience of a Wide Range of Laboratory Instrumentation and Analytical Techniques * Experience with HPLC Analysis and Analytical Method Troubleshooting, Ideally with Agilent Systems and OpenLab Software * IT literate (Minimum Microsoft Office Suite) REMUNERATION * £32K p/a + Benefits RESPOND Call Terry Blaney on +44 (0)(phone number removed) to Learn More about this Career Opportunity

Are you a passionate Chemistry Teacher looking for your next opportunity in Hornchurch? Have you taught KS3-4 Chemistry in a secondary setting in Hornchurch or a similar school? Are you available to start after Easter term? Hornchurch, Essex ASAP / April 2026 Secondary School KS3-4 Monday - Friday, 8:30am-3:30pm Pay: MP3-6 Applications close: 20/03/26 Interviews: Interviews being held W/C 16th March, Trial Day - onboarded if successful. This Chemistry Teacher role in Hornchurch provides the opportunity to teach Chemistry across Key Stages 3 and 4 within a supportive department that values high-quality teaching, strong subject knowledge, and a passion for scientific enquiry. The trust prides itself on collaboration between its schools, ensuring that every Chemistry Teacher benefits from shared resources and best practice across the Hornchurch network. Job Overview: * This secondary school caters for students aged 11-16. * Full-time, Monday - Friday, Chemistry Teacher role. * You will deliver engaging and practical Chemistry lessons across KS3 and KS4 in Hornchurch. * Plan, prepare and assess in line with UK curriculum expectations as a Chemistry Teacher. * Inspire students to develop analytical thinking and a love for Chemistry. * Contribute to the wider trust network, collaborating with fellow Science colleagues. * Opportunity for TLR responsibilities for an experienced Chemistry Teacher. What we're looking for: Qualified Chemistry Teacher with QTS (or 5+ years' experience teaching Chemistry). * Strong subject knowledge and passion for Chemistry. * A proactive and committed Chemistry Teacher who can motivate learners in Hornchurch. * Excellent classroom management skills. * Commitment to contributing to trust-wide initiatives and upholding high standards across the Hornchurch school community. * Enhanced DBS on the Update Service. What's next? Click "Apply Now" and should your application be successful, you will be contacted for a phone call OR contact Ellie directly from Academics TODAY

Position: Early Career Teacher (Science) Contract Type: Full Time, Permanent Start Date: 03/09/2026 Salary: £37,868 – £39,851 per year Salary will be determined in line with the Outer London Main Pay Scale and aligned to the Early Career Teacher (ECT) pay range (M1–M2). The role is suitable for ECTs, with salary awarded at M1. Kick-Start Your Teaching Career in Science Are you a passionate science graduate ready to begin your journey as an Early Career Teacher? Teach Now is recruiting for a high-performing, Ofsted-rated Outstanding all-through school in Redbridge, where a full inspection in November 2023 confirmed it remains at the highest grade. The school is known for its strong academic standards, excellent behaviour for learning and commitment to pupil development. This is an ideal opportunity for an ECT to join a well-established, supportive Science department with modern facilities and a strong culture of collaboration. What You’ll Do • Deliver engaging Science lessons across Key Stages 3 and 4, covering Biology, Chemistry and Physics concepts., • Prepare students for GCSE Science, encouraging enquiry, experimentation and analytical thinking., • Support learners of all abilities, including those progressing to separate sciences., • Work collaboratively with experienced colleagues on curriculum planning and assessment strategies. What We’re Looking For • Qualified Teacher Status (QTS) • A degree in Biology, Chemistry, Physics or a related discipline • Strong subject knowledge and a genuine passion for inspiring scientific curiosity • A reflective and proactive approach to professional development What’s on Offer • Structured ECT induction programme with dedicated mentoring, • High-quality CPD and clear professional development pathways, • Collaborative department with modern teaching resources, • A school recognised for its academic excellence and supportive leadership Why work via Teach Now? Teach-Now are a widely recognised, education recruitment company. We pride ourselves on our high levels of customer service and professional development that we offer our teachers and support staff. We: • Ensure that you will have your own dedicated consultant who will provide ongoing support and guidance. • Offer an excellent ‘refer a friend’ scheme that pays you £150 for each candidate you refer to us after they have worked and been paid for their first 10 days. • Pay in line with the Agency Worker Regulations (AWR) meaning you will be paid equally to a permanent employee. • Give you access to a wide range of CPD training through our in-house team of experienced senior leaders Application Process: Do you feel you meet the criteria for this exciting opportunity? If so, please either apply below or contact Teach-Now directly. All applicants will require the appropriate qualification and training for this role. For teacher roles, we require a formally recognised teaching qualification. If you are not contacted within 2 working days, unfortunately, you have been unsuccessful for this role. However, we will keep your CV and continue to help you in your search for a job within education. Good luck with your application, we look forward to hearing from you. Teach Now operates stringent safer recruitment procedures. We are committed to promoting equality and challenging discrimination. Teach Now is committed to safeguarding and promoting the welfare of children, young people, and vulnerable adults and expects all staff and volunteers to share this commitment. This post will be subject to an Enhanced DBS Clearance

An Excellent Career Opportunity within the QC Department, with a Close Collaboration with Other Departments ROLE * Ensure Incoming Goods are Cleaned and Labelled in Accordance with SOP’s * Responsible for the Cleaning of Warehouse Staging Areas, Goods-In and Goods-Out Airlocks, and Sampling Booth, in Accordance with SOP’s and Written Procedures and Maintenance of Accurate Cleaning Records * Sampling and Inspection of All Incoming Packaging Components, in Accordance with Established Sampling Procedures and Specifications * Raising of Non-Conformance Reports if Any Material is Out of Specification * Maintaining Records for Stock Packing Material, Including Retaining Materials and Archiving. Records to be Prepared in Conformance with SOP’s and cGMP Requirements * Sampling and Identification of All Incoming Raw Materials in Accordance with SOP’s * Maintain Records for Receipt of Raw Materials, Including Retaining and Archiving. Records to be in Conformance with SOP’s and cGMP Requirements * Compliance with Company Personal Hygiene and Safety Procedures and Due Regard for Safety of Colleagues * Liaison with Warehouse Operatives, Packaging Manager, and Manufacturing Manager to Ensure All Materials are Sampled in a Timely Manner * Manage Laboratory Waste Disposal and Collection in Accordance with SOP’s * Undertake All Reasonable Instructions, as Directed by the Quality Control Supervisor REQUIRED * A Level in Chemistry or Another Relevant Subject, Higher Qualifications an Advantage * Previous Experience Working in a Laboratory Environment, Preferably Pharmaceutical * Appreciation of cGMP and cGLP and Working to SOP’s * Knowledge of a Range of Analytical Apparatus/Equipment and Methods/Techniques * Experienced User of Microsoft Office, Specifically Word and Excel * Excellent Attention to Detail REMUNERATION * £28K p/a + Benefits RESPOND Call Terry Blaney on +44 (0)(phone number removed) to Learn More about this Career Opportunity