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Job Location Weybridge Job Description Procter & Gamble (P&G) is a leading global consumer goods company, with Personal Health Care brands including Vicks, Pepto Bismol, and Seven Seas. We are seeking a Qualified Person (QP) / Senior Quality Assurance Manager to lead quality and compliance activities across GMP, GDP and HACCP for food supplements and help safeguard consumer trust across our UK Personal Health Care portfolio. If you thrive at the intersection of regulatory excellence, safety, and quality leadership, this role could be your next career step. You will play a key part in ensuring products are manufactured, released, and distributed in full alignment with UK regulatory requirements and global quality standards. In this highly visible role, you will safeguard product quality, protect consumers, and act as a trusted partner to internal teams, suppliers, and regulatory authorities, making a real impact from manufacturing through distribution. This position will be primarily based in Weybridge (Surrey), with alternative options available in Reading or Skelmersdale. Candidates must be flexible to travel periodically to the Skelmersdale site as required. Role overview As the Qualified Person (QP) for Procter & Gamble UK, you will be accountable for ensuring that products are manufactured, tested, released, and distributed in full compliance with UK legislation and global quality standards. With us, you will: Act as Qualified Person for Procter & Gamble UK in accordance with UK legislation for Medicinal Products for Human Use, ensuring batch certification, release, and maintenance of the certification register. Ensure robust GMP, GDP, and HACCP compliance through effective documentation systems, quality and technical agreements, vendor qualification and auditing, and alignment with Marketing Authorisations and Global Healthcare procedures. Lead quality governance activities, including deviation management, CAPA definition and tracking, quality performance monitoring, and continuous improvement initiatives. Manage critical quality events such as incidents, complaints, recalls, and withdrawals, acting as the key interface with internal stakeholders, authorities, and drug and food safety bodies. Prepare for and manage regulatory inspections and approve and oversee annual training plans to ensure personnel are appropriately trained and qualified. What we offer you: Meaningful Work from Day 1: From Day 1, you'll step into a role with real accountability where you will directly influence product release, quality outcomes and regulatory confidence for P&G's UK portfolio, using your expertise to protect consumers and uphold trusted brands. You will be owning your part of the business and helping it grow, with continuous and supportive coaching from your manager and the wider team. Competitive Benefits: P&G take a Total Rewards approach meaning on top of your competitive salary, which is reviewed annually, you can expect a whole range of benefits including: a double matched pension scheme, private health insurance, participation in a stock ownership scheme, 25 days holiday and your very own 'Flex4Me' Fund which enables you to allocate a portion of your benefits package to the areas that matter most to you. Flexibility: We operate a flex at work approach, with flexibility built into the role. Our teams spend 3 days of their week collaborating together in our offices or at our external partners. This is balanced with 2 of their days spent on focused work which most tend to do from home. Of course, we do a bit of both every day, but we encourage our teams to choose where they work based on the jobs to be done. Job Qualifications What you'll bring Master's degree in pharmacy or another formal qualification in medicine, veterinary medicine, chemistry, pharmaceutical chemistry and technology or biology. Registration and approval as a Qualified Person with British Authorities in accordance with local regulations. Sufficient experience as a Qualified Person under UK regulations and solid experience in Quality Assurance. Advanced knowledge of GMP and GDP requirements. Fluency in English, both written and spoken Strong communication and collaboration skills with internal teams, suppliers, and regulators. A results driven, quality focused mindset with a strong sense of ownership. Proactivity, organization and ability to operate with urgency in a regulated environment. Right to Work For this role, P&G are willing to provide sponsorship to those who require a visa to live and work in the UK, subject to meeting all the necessary Home Office requirements. Full details on visa restrictions can be found on the Home Office website and immigration rules are subject to change. P&G is legally required to ensure all candidates have the right to work in the UK from Day 1 of their employment. All applicants will therefore be asked to provide evidence of their right to work at the conclusion of the recruitment process as a condition of employment. At P&G We are an equal opportunity employer and value diversity at our company. At P&G we strive to build a culture where everyone feels welcome, included, and able to bring their full selves to work. We ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process. Please click here if you require an accommodation during the application process. Please make sure to wait to hear back from us regarding your accommodation before proceeding with the online assessment, we thank you in advance for your patience. Job Schedule Full time Job Number R Job Segmentation Experienced Professionals Starting Pay / Salary Range

OVERVIEW Merrick & Company, an employee owned company, is seeking an experienced Senior Scientist in Biosafety and Laboratory Operations to join our growing team. The person would become a crucial part of a key Merrick growth initiative in Life Sciences, Biosafety & Biosecurity, and Laboratory Operations markets. This position is open for work in London, with ability to travel to client sites across the UK and Europe. The Scientist must be capable of coordinating and supporting a multi faced series of projects related to laboratory operations, operational planning, biosafety & biosecurity, regulatory compliance, and the integration of consensus standards (e.g., ANSI, ASHRAE), manufacturers use instructions, and industry best practices. This person would support the Science & Technology team with duties and coordination as part of a team of scientists, engineers, and subject matter experts. The position will work interactively with other teams responsible for laboratory design, commissioning, and operational planning, development of laboratory IT and IS systems, and development of laboratory programs (e.g., clinical, diagnostic, and research safety, bio risk management, small to large animal laboratory issues, etc.). This position requires the ability to not only be proficient in biosafety, but also clinical and research laboratory operations with an understanding of how laboratory activities, controls, and equipment function to support the containment and isolation of laboratory hazards. This person will support development of high level technical products and deliverables, problem solving and planning for high visibility projects, and as such must possess excellent communication skills. This position requires a high level of demonstrated effectiveness in working with HM government entities, regulators, and academic, clinical, and academic administrators, internal team members and outside consulting team members. The successful candidate will be required to interface with a broad spectrum of clients for Life Sciences projects located anywhere within the UK. Moderate travel (up to 50%) may be required. WHAT YOU'LL DO Provide strategy, development, execution, and technical knowledge for project deliverables related to laboratory operations, biological risk identification, assessment, characterization, management, exposure assessment and control, general safety, occupational hygiene, health and environmental management, animal care and use and regulatory compliance. Possess strong oral and written communications and interpersonal skills to effectively interface with clients and team members to: Ensure adherence to project quality of deliverables, products, and schedule Address issues related to the interface of laboratory operations, compliance, and operational planning Prepare complex studies, reports, plans, specifications, and other products for project deliverables. Support document preparation to aid clients in obtaining and maintaining regulatory registrations and permits. Support proposal development and marketing initiatives. Support leadership to ensure that project schedules and budgets are met and communicate with leadership any issues and concerns. Exercise initiative, judgment, and knowledge commensurate with the responsibilities of the position. Adopt and apply all Merrick policies and procedures and apply them on assignments. Educate clients on pertinent regulations, consensus standards, manufacturers use instructions, and best practices concerning their laboratories, operations, safety programs, hazard control systems, biocontainment, equipment, hazardous materials storage, waste treatment and disposal processes, and all associated documents and records. REQUIRED QUALIFICATIONS Applicant must be a U.K. Citizen This position may require vaccination as mandated by client polices Applicants must be willing to travel up to 50% domestically and internationally as needed to support client projects Technical Master's degree or higher in a science related field from an accredited program. Minimum of five (5) years of experience in laboratory operations, biosafety, & biosecurity. Previous experience in high and maximum containment laboratories (CL/BSL 3 or higher) is required. Must have technical knowledge of regulatory requirements regarding biosafety, HSE, ACDP, SAPO, GMO, and IATA. Technical knowledge of consensus standards (e.g., ANSI, ASHRAE, British Standards, CIBSE, HTM, ISO) is preferred. Experience performing laboratory assessments for biological, chemical, and physical hazards for all laboratory containment levels for human, animal, and plant materials. General awareness of clinical laboratory operations and hazards associated with diagnostic, clinical microbiology, chemistry, blood bank, histopathology, and gross sectioning is preferred. General awareness of laboratory operations and hazards associated with academic laboratories (e.g., chemistry, biology, microbiology) is preferred Ability to coordinate the collection of data from laboratory assessments to determine gaps and needs to meet design requirements. Computer Skills: Microsoft Office (Word, Excel, PowerPoint, Project, etc.). Ability to work on multiple projects which includes resourcing, tracking, follow up and follow through to project completion. Well organized, detail oriented, and self motivated professional with strong verbal and written communication skills. Strong desire to work in a team environment. Flexibility/adaptability to work in a fast paced environment. DESIRED QUALIFICATIONS Credentialed biosafety professional Advanced degree in the life and/or biological sciences (M.S. or Ph.D.) Past support of a ACDP or SAPO regulated entity Environment of Care committee member or participant Clinical laboratory operations General environment of care surveillance Clinical risk assessment and management PERKS Employee Owned - all eligible U.S. employees have an Employee Stock Ownership Account. Robust Employee Referral Program. Annual performance and compensation reviews. Professional Training and Development. Employee Recognition Awards. Peer Mentor Program And Much More! ADDITIONAL INFORMATION Apply online only. No e mail, hard copy or third party resumes accepted. At Merrick, every resume is carefully reviewed by our team of experienced human recruiters-never by AI. We are committed to a fully human centered hiring process, ensuring each candidate receives thoughtful, personalized attention at every stage. Merrick & Company offers a competitive compensation and benefits package which includes health insurance, dental and vision coverage, 401(k), and paid time off (PTO). Merrick is an Equal Opportunity Employer, including disability/vets. Employment with Merrick is contingent upon completion of a pre employment background check, MVR check, and drug screen.

Synthomer is a leading supplier of high-performance, highly specialised polymers and ingredients that play vital roles in key sectors such as coatings, construction, adhesives, and health and protection - growing markets that serve billions of end users worldwide. Headquartered in London, UK and publicly listed there since 1971, we employ c.3,900 employees across our 5 innovation centres of excellence and more than 29 manufacturing sites across Europe, North America and Asia. Around 20% of our sales volumes are from new and patent protected products. At our innovation centres of excellence in the UK, Germany, China, Malaysia and Ohio, USA we collaborate closely with our customers to develop new products and enhance existing ones tailored to their needs, with an increasing range of sustainability benefits. Since 2021, we have been proud holders of the London Stock Exchange Green Economy Mark, which recognises green technology businesses making a significant contribution to a more sustainable, low-carbon economy. The Role As an Advanced Method Development Chemist , you will play a key role in designing, developing, validating, and continuously improving analytical methods that underpin innovation, quality, and regulatory compliance at Synthomer. Working closely with Innovation, Technical, and Application teams, you'll help deliver harmonised, high quality analytical approaches across the organisation. We're looking for a methodical thinker and natural problem solver -someone who enjoys investigating challenges, troubleshooting complex analytical issues, and turning data into clear, actionable insight. Key Responsibilities Develop, optimise, and validate analytical methods to support innovation projects, long term analysis, and cross functional alignment Provide global analytical methodologies and support, reporting into the Analytical Manager Ensure a high level of analytical rigour, adhering to ISO standards and stringent validation protocols Train laboratory colleagues on newly developed methods and best practice Bridge analytical approaches across functions, presenting findings and updates to key stakeholders Maintain and ensure high standards of calibration and performance for GC, GC MS, HPLC, LC MS and FTIR equipment Drive continuous improvement of existing methodologies using Lean Enterprise techniques Take shared responsibility for laboratory safety and ensure full compliance with Synthomer's SHE directives What You'll Bring Essential Qualifications & Experience BSc or MSc in Analytical Chemistry, Polymer Chemistry, Materials Science, or a related discipline Minimum 2+ years' experience in analytical method development (ideally within polymer characterisation) Proven experience developing methods using GC MS, LC MS, GC and HPLC Strong data analysis skills with a logical, investigative approach to problem solving Hands on experience with analytical instrumentation and method validation Additional Technical Knowledge (Preferred) Rheometry FT IR GPC (with viscometry, RI and light scattering detectors) Sample preparation techniques including micro chamber, SPME and thermal desorption Desirable Experience Working within an ISO 17025 environment Understanding of polymer structure-property relationships Experience applying DoE or Lean Enterprise techniques to method development Location and Travel requirements: This role is part of the scientific team based at Synthomer's Harlow (UK) site . Due to the hands on, laboratory focused nature of the work, the successful candidate will be expected to work on site five days per week and be based within a reasonable commuting distance of the laboratories.At Synthomer, you'll be part of a collaborative, forward thinking scientific community where your expertise genuinely influences innovation and business outcomes. We offer a supportive environment, opportunities to grow your technical depth, and the chance to contribute to meaningful, real world applications on a global scale .At Synthomer we value the difference everyone brings to work, and we are committed to create a diverse and inclusive workplace, where people are supported to make their best contribution in creating a vibrant and successful business. Global Benefits Overview Competitive, market-aligned compensation Discretionary global bonus scheme Discretionary Long-Term Incentive Plan (LTIP) - for senior positions Company car or car allowance - varies by region and role Healthcare - tailored to regional locations Parental leave and family support - maternity, paternity, adoption (aligned with regional policies) Working options - flexibility where it matters, based on role and business needs Learning & development opportunities - training, online platforms, buddy/mentorship programs, Internal Synthomer University with L&D offers Wellbeing support - employee assistance program (EAP), mental health resources, wellbeing initiatives Retirement / pension contributions - plans vary by country Culture of Inclusion - where everyone can thrive Performance culture, global reward & recognition programmes

A leading supplier of polymers is seeking an Advanced Method Development Chemist to develop and validate analytical methods at their Harlow site. You will collaborate with various teams, ensuring compliance with ISO standards and training staff on best practices. The ideal candidate should have a BSc or MSc in a relevant field and at least 2 years of experience in analytical method development, particularly with GC-MS, HPLC, and LC-MS. This role requires on-site work five days a week in a dynamic laboratory environment.

A leading 3D printing company based in the United Kingdom is seeking a skilled Lead R&D Formulation Chemist. You will lead R&D projects and be involved in formulating and testing innovative 3D printable resins. The ideal candidate will have extensive experience in formulation chemistry, chemical synthesis, and the ability to work collaboratively with teams and clients. A strong focus on research and technical reporting is required. This is an exciting opportunity to contribute to cutting-edge manufacturing technology.

At the Ellison Institute of Technology (EIT), we're on a mission to translate scientific discovery into real world impact. We bring together visionary scientists, technologists, engineers, researchers, educators and innovators to tackle humanity's greatest challenges in four transformative areas: Health, Medical Science & Generative Biology Food Security & Sustainable Agriculture Climate Change & Managing CO Artificial Intelligence & Robotics This is ambitious work - work that demands curiosity, courage, and a relentless drive to make a difference. At EIT, you'll join a community built on excellence, innovation, tenacity, trust, and collaboration, where bold ideas become real-world breakthroughs. Together, we push boundaries, embrace complexity, and create solutions to scale ideas from lab to society. Explore more at . Welcome to the Pathogen Project Within this ecosystem, the Pathogen Mission exemplifies EIT's commitment to transformative science. It aims to revolutionise the diagnosis and treatment of infectious diseases by leveraging whole genome sequencing (WGS)-based metagenomic and pathogen specific analytical tools. This remit includes the development of a decentralised, sample to answer sequencing diagnostic platform for infectious diseases, enabling rapid and accurate analysis of patient samples without prior assumptions. Supported by Oracle Inc.'s cloud computing scale and security infrastructure, the Pathogen Mission is progressing towards certified diagnostic products for deployment in laboratories, hospitals, and public health organisations worldwide. Your Role We are seeking a Scientist or Senior Scientist with a strong interest in method development to join our growing Applications team, focused on advancing sequencing based diagnostics. In this role, you will contribute to the design and optimisation of novel targeted and semi targeted approaches for the rapid sequencing of clinically relevant pathogens. This laboratory based position encompasses end to end experimental workflows, including sample preparation, target enrichment and amplification, library preparation, and sequencing. You will support the development of strategies for comprehensive, high sensitivity sequencing across a large number of targets, using approaches such as targeted amplification, hybridisation, and related techniques. The role encourages creative problem solving, with opportunities to propose, explore, and evaluate new ideas. You will work collaboratively within a multidisciplinary team of microbiologists, molecular biologists, engineers, and data scientists to develop assays for integration into an automated, device based platform. Drawing on your experience, you will help define experimental strategies, design and execute studies, and contribute to advancing the application of sequencing technologies in pathogen detection and related areas. Key Responsibilities Design, develop, and optimise end to end sequencing assays (targeted and semi targeted) Execute experiments, analyse and interpret data, and contribute ideas for improvement Troubleshoot complex technical challenges across a range of sample types Maintain clear documentation to support reproducibility of experimental work Collaborate closely with colleagues across disciplines to progress shared goals Contribute to scientific discussions and decision making as projects evolve Essential Knowledge, Skills, and Experience PhD in molecular biology, microbiology, genomics, biochemistry or a related field Experience using molecular biology techniques (e.g. PCR, RT PCR, nucleic acid extraction, library preparation) Experience developing and optimising PCRs and/or related experimental workflows Ability to troubleshoot experimental challenges and adapt methods as needed Experience with DNA/RNA sequencing data Strong experimental design and data interpretation skills Good organisation, record keeping and communication skills Desirable We recognise that strong candidates may not meet every criterion below. Experience in any of the following would be beneficial: Multiplex PCR assay development, particularly for sequencing applications Enrichment or capture methods for pathogens or pathogen derived nucleic acids Work with bacteria, fungi, viruses, or other pathogens Handling clinical samples RNA based workflows (e.g. transcriptomics, viral genomics) Background in virology Exposure to metagenomics workflows Biochemistry knowledge relevant to assay development (e.g. enzyme optimisation, reaction conditions, assay development) Key Attributes Scientific and Technical Enjoys exploring new ideas and approaches to experimental challenges Curious and motivated to solve complex problems Able to balance scientific rigour with speed and pragmatism Working Style and Collaboration Takes ownership of work while valuing collaboration and shared success Proactive and supportive team member, with a willingness to contribute beyond immediate responsibilities Comfortable working in a dynamic research environment, with support from colleagues Our Benefits Salary: Competitive + travel allowance + bonus Enhanced holiday pay Pension Life Assurance Income Protection Private Medical Insurance Hospital Cash Plan Therapy Services Perk Box Electric Car Scheme Working Together - What It Involves You must have the right to work permanently in the UK with a willingness to travel as necessary. In certain cases, we can consider sponsorship, and this will be assessed on a case by case basis. For this role we would expect someone to be fully on site in Oxford You will live in, or within easy commuting distance of, Oxford (or be willing to relocate).

Energetics Chemist (Graduates considered) Kidderminster Aerospace & Defence Salary dependent on experience A truly unique opportunity to join a world leading Rocket Propulsion Technology organisation! Working within the Energetics and Materials Team you would be responsible for the research, development, clearance and manufacture of materials and products to meet demanding requirements click apply for full job details

Overview About Certara Certara accelerates the potential of bringing medicines to market and to patients using biosimulation software, technology, and services to transform traditional drug discovery and development. Our clients include more than 2,400 biopharmaceutical companies, academic institutions, and regulatory agencies across 70 countries. Our goal is to enable the life sciences industry's use of data, modeling, and analytics to make better decisions across the various phases of discovery and drug development. Our software and scientists incorporate modern advances in scientific understanding, drug development experience, data analysis, and AI resulting in significant opportunities to decrease the cost and increase the probability of success for new drug approval and commercialization. The Vice President of PBPK provides strategic, scientific, and organizational leadership for all physiologically based pharmacokinetic (PBPK) modeling and simulation activities across the company. This role is responsible for setting the vision for PBPK integration across discovery, preclinical, and clinical development, ensuring scientific excellence, regulatory impact, and business value. The SVP PBPK serves as a key scientific authority, internal advisor, and external thought leader in model-informed drug development (MIDD). Responsibilities Strategic Leadership Define and execute the company's PBPK strategy aligned with R&D, regulatory, and corporate objectives Drive integration of PBPK modeling into decision-making across discovery, translational science, clinical development, and lifecycle management Serve as a core member of senior leadership, influencing portfolio strategy and development prioritization Scientific & Technical Oversight Provide expert oversight of PBPK model development, qualification, validation, and application Ensure best-in-class scientific rigor, innovation, and adoption of emerging methodologies and platforms Guide PBPK applications including first-in-human dose selection, DDIs, special populations, pediatrics, formulation changes, and label claims Regulatory & External Engagement Lead PBPK strategy for global regulatory interactions (FDA, EMA, PMDA, etc.) Act as a primary scientific representative in regulatory meetings, advisory boards, and industry consortia Contribute to regulatory submissions, briefing documents, and responses related to PBPK and MIDD Organizational Leadership Build, mentor, and lead a high-performing PBPK and modeling organization Foster a culture of collaboration, scientific excellence, and continuous development Partner cross-functionally with clinical pharmacology, biostatistics, toxicology, chemistry, clinical, regulatory, and commercial teams Thought Leadership & Innovation Maintain external visibility through publications, presentations, and professional societies Evaluate and implement new modeling technologies, platforms, and data sources Shape industry standards and best practices in PBPK and model-informed drug development Qualifications Education PhD in Pharmacokinetics, Pharmaceutical Sciences, Biomedical Engineering, Chemical Engineering, Applied Mathematics, or a related field Experience 12+ years of progressive experience in PBPK modeling within pharma, biotech, CRO, or regulatory agencies Demonstrated leadership of PBPK or MIDD groups at a senior or executive level Proven track record of successful regulatory impact using PBPK approaches Experience influencing portfolio and development strategy at the enterprise level Skills & Competencies Deep technical expertise in PBPK theory, software platforms, and applications Strong regulatory knowledge and experience with global health authorities Exceptional leadership, communication, and stakeholder-management skills Strategic thinker with the ability to translate complex science into business value Preferred Attributes Recognized external expert or opinion leader in PBPK or MIDD Certara bases all employment-related decision on merit, taking into consideration qualifications, skills, achievement, and performance. We treat all applicants and employees without regard to personal characteristics such as race, color, ethnicity, religion, sex, sexual orientation, age, nationality, marital status, pregnancy, physical or mental condition, genetic information, military service or other characteristic protected by law.