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SRG
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  • CAD Technician  

    - Chester
    Job Title: CAD TechnicianPosition Overview: We are seeking a skilled C... Read More
    Job Title: CAD TechnicianPosition Overview:
    We are seeking a skilled CAD Technician to design, draft, modify, and maintain engineering plans using advanced CAD software. The ideal candidate will have a strong technical foundation in engineering design and proficiency in CAD tools. Experience with Teamcenter software is highly desirable.Key Responsibilities:Design & Drafting:Create accurate and detailed 2D and 3D models using CAD software.Develop engineering drawings, schematics, and layouts based on specifications.Ensure designs comply with engineering standards, codes, and regulations.Collaborate with engineers and project managers to refine designs and ensure feasibility.Technical Support:Provide CAD support during product development, including design modifications and updates.Review and revise existing CAD drawings to improve design efficiency.Assist in creating detailed documentation for manufacturing processes.Collaboration:Work closely with cross-functional teams, including designers, engineers, and manufacturers.Participate in design reviews and provide feedback on improvements and challenges.Coordinate with other departments to meet project deadlines.Quality Control & Compliance:Ensure CAD designs adhere to industry standards and regulatory requirements.Perform regular checks for accuracy and completeness of CAD models.Use version control to manage design revisions and updates.Required Skills & Qualifications:BTEC, HNC, or Degree in Mechanical, Electrical, Civil Engineering, Industrial Design, or related field.Proven experience with CAD software (e.g., AutoCAD, SolidWorks, Teamcenter).Strong understanding of engineering principles, materials, and manufacturing processes.Proficiency in 2D and 3D design and modelling.Knowledge of GD&T (Geometric Dimensioning and Tolerancing) standards.Excellent problem-solving skills and attention to detail.Strong communication skills for effective collaboration.Guidant, Read Less
  • Regulatory Coordinator  

    - West Yorkshire
    Regulatory Coordinator needed in West Yorkshire on permanent basis. Re... Read More
    Regulatory Coordinator needed in West Yorkshire on permanent basis. Requiring a degree in Chemistry (or a similar field) and recent, proven experience of SDS authoring, REACH and CLP regulations.Title: Regulatory Coordinator Location: West YorkshireSalary: £28,000 - £35,000 (dependent on experience)Term: PermanentSRG are working with a global, market leading specialist developer and manufacturer of a range of industrial chemicals including fluids, lubricants, oils and other speciality products. They are now seeking a Regulatory Coordinator to join their Regulatory team to be based at their site in West Yorkshire. This role will support in continuing the development of regulatory compliance across a growing product portfolio and formulation changes, whilst keeping up to date with regulatory updates within the industry. This role would suit candidates who have experience of Regulatory Affairs and are looking to advance their careers in this field. Alternatively, this role would suit candidates that have laboratory experience but would like to switch to an office-based role. Suitable experience would include working knowledge of UK and EU REACH, chemical labelling and SDS & MSDS writing.Benefits: You will join a highly successful company, with an opportunity to make a great impact. 35 hours - Monday to Friday, with flexibility on start and finish times. 25 days holiday and plus bank holidays.Role/DescriptionUsing knowledge and experience in the industry to generate and execute regulatory documentationSupporting with authoring Safety Data Sheets (SDS) and Material Safety Data Sheets (MSDS) relating to products across the businessDevelop product dossiers, flag issues when they arise, ensuring transparency, candour and a solution mindsetResearching and checking various sources for updated regulations, new consultative documents and regulatory information relevant to the business and their productsProviding regulatory assistance and advice/support when needed across the businessSupporting with Chemical registrations including REACHAssisting with the administration of relevant regulatory documentation including SDS, MSDS, SOPs, controlled documents and product datasheetsRequirementsDegree in Chemistry (or similar)Demonstrable experience and understanding of regulatory affairs within the chemicals industryKnowledge of UK and EU REACH RegistrationsKnowledge and experience of chemical labelling, SDS and MSDSSRG is the UK's number one recruitment company specialising in the scientific, engineering, clinical, pharmaceutical, food/FMCG, energy & renewables, biotech, chemical and medical device sectors.
    As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.If you would like to apply for this position, please use the link provided. Alternatively please email a copy of your CV to For more information regarding this position or any others, please call Chris on 0161 667 795.If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit to view our other vacancies. Keywords: SDS, Safety Data Sheet, MSDS, Material Safety Data Sheet, TDS, Technical Data Sheet, regulatory, compliance, excel, chemical data, REACH, chemical safety, product safety, registration, regulatory affairs, regulations, labelling, UK, EUGuidant, Read Less
  • Health Economics Modeller  

    - Maidenhead
    Health Economics ModellerLocation: Maidenhead / RemoteDuration: 12 mon... Read More
    Health Economics ModellerLocation: Maidenhead / RemoteDuration: 12 months initial

    SRG are partnering exclusively with a leading pharmaceutical companywho currently require an experienced Health Economics Modeller to come and join them on a temporary basis. This assignment is expected to span an initial 12 months and allows a lot of flexibility to work remotely.
    Within this role, the successful candidate will provide the global Value Analytics team with Excel-based economic modelling support and you will have the opportunity to work on projects in different therapy areas and in different phases of development (from early pricing models to submission models).
    Main Responsibilities may include: Build new, modify existing, or review Health Economic (HE) deliverables (cost-utility, budget impact, and other HE tools) for use in HTA submissions globallyAct as a primary point of contact for guidance, advice, and support on HE deliverablesConduct quantitative health economics analyses (cost-utility, budget impact) to inform HTA and pricing strategies from early on in asset development working with partners across the Global Market Access & Pricing team.Build tools and help establish standards to improve efficiencies within the global HTA team
    Skills/experience required:

    MSc or MPhil (required) or PhD (preferred) in Health Economics, Econometrics or any other related fieldExpert knowledge and experience in economic modelling and budget impact analysisHands-on knowledge of EXCEL for the development of economic models and/or BIMs including VBAITC experience (Indirect Treatment Comparisons) - also show ability to develop these from scratchAbility to be proactive and motivated under a high-pressure environmentExperience/ability to work in a global matrix environment and operate cross-functionally as neededAbility to work independently and take full accountability over projectsStrong communication skillsTo ApplyPlease click below and/or to discuss further, contact Theo Charles for more information
    Guidant, Read Less
  • Europe Regulatory Strategist  

    - Tadworth
    Job Title: Europe Regulatory StrategistLocation: Hybrid / Walton OaksC... Read More
    Job Title: Europe Regulatory StrategistLocation: Hybrid / Walton OaksContract: Jan Oct 2026Hours: 37 hours per weekPay: PAYE rate up to £33.78 p/h Umbrella rate up to £37.86 p/h DOEWe are seeking an enthusiastic Europe Regulatory Strategist to join a leading global pharmaceutical organisation.ROLE SUMMARYRepresent a particular region for regulatory sciences (US, EU or EM)Provide regional strategic expertise as a member of the Global Regulatory Strategic Team (GRST).Lead and implement regional regulatory strategies in agreement with key stakeholders for assignedprojects/products and in line with the commercial goals.Accountable for timely submissions and approvals with commercially attractive labelling in the designated regionAccountable for ensuring optimal regulatory interactions with Health Authorities, in relation to the assignedproject(s) within the designated region.Role can be combined with other Regulatory Role(s) (i.e., Global Regulatory Lead).
    ROLE RESPONSIBILITIES:Accountable for ensuring regional (US, EU or EM) contribution to Global Regulatory Strategies and implementation plans (including core labels, risk registers) for assigned projects.Ensures regulatory contributions achieve the objectives in the strategy, achieve agreed standards, maximizing overall project delivery time and probability of success and facilitating post-filing activities.Partners with project teams and other customer groups to ensure required regulatory contributions (line plans, label, CTA, MAA/IRD, variations, license renewals etc.) meet business needs and are provided to the project teams, to agreed time and quality standards.Ensures regulatory plans are monitored, progress/variance communicated to Global Regulatory Lead and Senior Management, and any risks (from emerging technical data, changing internal objectives or external threats) mitigated.Ensures an aligned regional regulatory position is reached and communicated for all key issues for assigned project/s, and that these regulatory positions supporting the regional business are championed and communicated.Engages in appropriate activities in order to influence the regional regulatory environment through OGRS-In Country colleagues, Agency contacts, and/or Trade Associations as appropriate.Ensures business compliance and implementation of and adherence to Regulatory standards.Develops and maintains, directly or indirectly, constructive working relationship with Health Authority contacts in the assigned regionQUALIFICATIONS/SKLLS:Scientific Degree. A higher degree may be an advantage but is not essential.Proven experience in managing national and/or regional regulatory process and registration aspects of the drug development process particularly clinical trials experience at least in one country.Previous experience as a national and/or regional regulatory liaison for at least one product in different therapeutic areas and in different stages of the product life cycle is highly desirable. Equivalent experience, either at a regulatory agency or working on substantive industry -government collaborations, can be considered.Experience in communicating with FDA or major EU regulatory agency(ies) for US and EU regulatory strategists respectively, as well as participating in/leading such interactions, is preferred.Knowledge of drug development practice rules, regulations and guidelines - Familiarity with f actors likely to influence the regulatory environment, including new and emerging guidelines.Proven ability in developing and implementing regulatory strategy - Understanding of regulatory agency philosophy and guidelines. Experience preparing and submitting INDs and/or CTAs, NDAs / MAA/IRDs. Working with and influencing regulators and opinion leaders, facilitating approval of submissions with labelling meeting corporate expectations.Communication skills - Ability to communicate complex information and analyses to a variety of scientific audiences in both verbal and written format, including to senior management.Presentation skills - Is effective in a variety of formal presentation settings; one- on-one, small and large groups, with peers, direct reports and senior manager.Negotiation skills - Can negotiate skilfully in tough situations with both internal and external groups. Can be direct and forceful as well as diplomatic. Gains trust quickly of other parties to the negotiations.Guidant, Read Less
  • HSE Lead  

    - Bracknell
    HSE LeadContract: 6 months contract - rollingLocation: Bracknell, UKPa... Read More
    HSE Lead
    Contract: 6 months contract - rolling
    Location: Bracknell, UK
    Pay rate:£33.65 per hour (£63k perm equivalent) - PAYE£47 per hour - Umbrella
    We are seeking an experienced and proactive HSE Lead to oversee and implement health, safety, and environmental policies and procedures on a construction project in the UK. This role ensures compliance with UK legislation, CDM Regulations 2015, and environmental regulations, while fostering a proactive safety culture to protect all personnel, subcontractors, and stakeholders on-site.Key Responsibilities:Act as the primary point of contact for HSE-related queries on-site and liaise with the principal contractor and external stakeholders.Provide proactive project HSE management guidance and communication to ensure HSE Management requirements are integrated into the project lifecycle.Champion the project safety culture, behaviours, and engagement activities.Drive HSE commitment across the project to meet HSE goals and targets.Manage compliance with contractual obligations and UK legal requirements.Review and approve contractor procedures to ensure alignment with HSE requirements.Establish safe systems of work including RAMS, permit to work systems, and LOTO procedures.Identify, evaluate, and resolve HSE issues during all project phases.Coordinate with project teams and cross-functional disciplines for HSE activities.Schedule and conduct internal HSE evaluations and audits; issue reports and monitor action closure.Investigate accidents, incidents, and near-misses; produce reports and implement corrective actions.Provide regular feedback to HSE and Project teams including lessons learned.Liaise with regulatory bodies such as the Health and Safety Executive and local authorities.Lead regular safety inspections and audits.Ensure all personnel are inducted and trained on site-specific safety protocols.Develop and maintain the project-specific Health and Safety Plan.Monitor contractor and subcontractor HSE performance and provide monthly reports.Ensure escalation of incidents and delivery of emergency response drills.Review and report on all construction project activities from preconstruction to commissioning.Prepare regular HSE performance reports for leadership teams.Identify opportunities for improving safety and environmental practices.Deliver toolbox talks, safety briefings, and training sessions.Skills and Qualifications:NEBOSH National Diploma in Occupational Health and Safety (or equivalent).Proficiency in Microsoft Office applications - Outlook, Word, Excel, PowerPoint, Visio, SharePoint.Understanding of UK HSE regulatory requirements for construction site operations including CDM 2015, LOLER, WAH, EPA 1990.Lead Auditor training (ISO 14001 or ISO 45001).5 - 7 years' experience in health, safety, and environmental management.Experience in construction site HSE management.Environmental management qualification (e.g., IEMA or equivalent).Experience with ISO 45001 and ISO 14001 standards.Experience conducting risk assessments, audits, emergency response, and incident investigations.Fire Safety/First Aid at Work certification (desirable).Guidant, Read Less
  • Analytical Laboratory Analyst  

    - Cambridge
    Analytical Laboratory AnalystStart: ASAP Contract: 12 Months initially... Read More
    Analytical Laboratory Analyst
    Start: ASAP
    Contract: 12 Months initially with potential to extend to 18 months
    Hours: 37.5 hrs/week (9:00 AM - 5:00 PM, 30 mins unpaid lunch)
    Location: Onsite
    Salary: £26,000 - £28,000 Requirements* Experience with general laboratory glassware and equipment including pipettes, filters and filtration equipment
    * Experience using HPLC is a bonus
    * Knowledge of ALCOA++ and proven good documentation practice
    * Good organisation skills
    * Good time management
    * Experience working with Microsoft Office package - Word, Excel, PowerPoint and OutlookEducation and Qualifications* BSc in Life Science subject desirable
    * Minimum A level chemistry or equivalentPurposeProvides analytical laboratory support for Medical Device and Combination Product (MDCP) development as required.Responsibilities* Comply with applicable GxP regulations, SOPs, HSE, DQP & other Guidelines in the laboratory.
    * Maintain up-to-date documentation of laboratory work carried out including documentation sample storage and laboratory notebook archiving.
    * Ensure consistent flow of laboratory and project consumables by contacting approved suppliers and executing purchase orders.
    * Support establishment and maintenance of lab instructions, SOPs, templates.
    * Support cleaning, maintenance, qualification, and calibration of laboratory equipment with accompanying documentation.
    * Prepare laboratory solutions for analytical test and chromatographic analysis.
    * Ensure proper laboratory cleaning, housekeeping, and waste disposal.
    * Execute and document analytical tests for products assigned in the context of process transfer, process improvement and process validation.
    * Perform experiments to support root cause investigation based on written protocols.
    * Execute and document experiments according to written protocols.
    * Recognize, communicate, and contribute to solving problems (including OOT and OOS results).
    * Supports inhalation product development by conducting analytical test packages, including finished product characterization.
    * Daily set up of the analytical laboratory for testingGuidant, Read Less
  • R&D Chemist  

    - Herefordshire
    Join Our Client as a Research & Development Chemist!Hiring a Research... Read More
    Join Our Client as a Research & Development Chemist!Hiring a Research & Development Chemist to develop polymers. Starting asap, competitive salary, based in Herefordshire, permanent position.Location: Herefordshire
    Contract: Full-time, Permanent
    Salary: competitive
    Start date: ASAP

    Are you detail-oriented and passionate about innovation? Our client is seeking a Research & Development Chemist to join their dynamic Divisional R&D team. This is your chance to work at the cutting edge of polymer technology, developing advanced polyurethane and phenolic resin systems and conducting performance testing on polymer foams.What You'll DoPrepare and cut polyurethane and phenolic foam samples.Mix and run foam formulations using laboratory chemicals.Perform small-scale fire tests and operate advanced lab equipment (FTIR, GC-MS, thermal conductivity instruments, etc.).Plan and execute experimental production trials.Analyse data, write reports, and present findings to senior staff.Provide technical support and stay up-to-date with scientific developments.What We're Looking ForRecent chemistry/ related graduate or experience within the polymer industryStrong analytical skills and attention to detail.IT literacy (Microsoft Outlook, Word, Excel).Full UK driving licence.What's on OfferCompetitive salary + profit-related bonus.25 days annual leave + bank holidays.Contributory pension scheme.Life assurance (4x salary).Enhanced family leave, buy & sell annual leave.Professional development support.Employee Assistance Programme, cycle-to-work scheme, discounted healthcare.Keywords: graduate, chemistry, development, formulation, product development, npd, new product development, materials, developing, formulate, formulating, construction, adhesive, cement, sealant, grout, coating, elastomer, silicone, mould, paint, plastic.Guidant, Read Less
  • Senior Scientist - Modeller  

    - Manchester
    Job Title: Senior Scientist, Modeller (up to Principal Scientist) Vaca... Read More
    Job Title: Senior Scientist, Modeller (up to Principal Scientist)
    Vacancy Type: Permanent
    Area: South Manchester
    Salary: DOEExciting Opportunity: Senior Scientist, Modeller
    Are you a data-driven problem solver with a passion for applying mathematical modelling to real-world pharmaceutical challenges? This innovative company is seeking a talented Senior Scientist, Modeller to join their Clinical Pharmacology & Modelling Group in South Manchester. The ideal candidate will have already worked in a pharmaceutical environment, within PKPD and ADME.The Role of the Senior Scientist, ModellerAs a Senior Scientist within the ClinPharm & Modelling Group, you will play a pivotal role in supporting pharmaceutical development projects through advanced data analysis and mathematical modelling. Your key responsibilities will include:Leading modelling projects and delivering scientific insight to clients through data visualisation, analysis, and pharmacometric modellingDesigning pragmatic experiments and applying robust scientific thinking to enhance understanding of drug behaviourIntroducing and qualifying new modelling techniques and analysis methodsSupporting the development of new service offerings to drive company growthPerforming scientific computing tasks, including software maintenance and safety assessmentsCoaching and mentoring junior modelling staffPresenting at internal meetings, networking events, and conferencesThe Ideal Candidate for the Senior Scientist, Modeller RoleTo thrive in this role, you will need:A PhD in a numerate discipline (e.g. Mathematics, Physics, Engineering) with applied modelling experience, ideally in biological systems
    (Alternatively, a relevant degree with 5+ years of experience applying mathematical models to real-world problems, preferably pharmaceutical projects) - Happy to hear from junior candidates for more junior roles.Recent proficiency in programming languages, especially RIdeally worked in PKPD and ADME recently.A strong track record of working to high scientific standards in data analysis and modellingThe ability to operate independently and provide scientific leadershipExcellent problem-solving skills and a solution-oriented mindsetEffective communication and presentation skillsA passion for self-development and mentoring othersIf you're a modelling enthusiast with a drive to make a meaningful impact in pharmaceutical development, this is a fantastic opportunity to elevate your career. Apply now and be part of a team that's shaping the future of drug development through data and innovation!For more information, please contact Selby De Klerk at SRG.SRG are the UK's number one recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.
    As scientists ourselves, our specialist sector knowledge and passion are second to none. We're committed to providing outstanding career opportunities and expert recruitment services across all levels.If this position isn't quite right for you, feel free to get in touch or visit to explore other vacancies.Guidant, Read Less
  • QC Team Leader  

    - Stirling
    Are you a passionate Quality Control (QC) professional seeking a dynam... Read More
    Are you a passionate Quality Control (QC) professional seeking a dynamic and rewarding role? Our client is looking for a driven QC Team Leader to join their team and contribute to their ongoing success.About the QC Team Leader RoleAs the QC Team Leader, you will play a crucial role in maintaining the company's comprehensive quality control systems. Responsible for ensuring adherence to quality control protocols, you will be instrumental in upholding the high standards required for Investigational Medicinal Product and Licensed Medicinal Product manufacturing.Key responsibilities of the QC Team Leader include:Developing, monitoring, and improving quality control procedures to ensure compliance with Good Manufacturing Practice (EU/FDA and other relevant standards)Overseeing the QC team's day-to-day operations, including performance management and trainingCollaborating with technical and supply chain departments to ensure materials meet quality requirementsProviding QC guidance and support to cross-functional teamsRepresenting the company during third-party audits, regulatory inspections, and client auditsWhat We're Looking ForThe ideal candidate for the QC Team Leader role will possess:Extensive experience in a quality control or quality assurance role within the pharmaceutical industryExperience working as a Microbiologist or QC Micro is essential for this positionProven track record of leading and developing a team of QC professionalsExcellent understanding of GMP requirements and quality control best practicesStrong problem-solving and analytical skillsEffective communication and interpersonal abilitiesCommitment to continuous improvement and quality excellenceWhy Join This Company?This company offers a competitive salary, comprehensive benefits package, and opportunities for professional development. As the QC Team Leader, you will be part of a dynamic and supportive team, contributing to the company's mission of delivering high-quality pharmaceutical products.If you're ready to take your career to the next level as a QC Team Leader, we encourage you to apply to be a part of this thriving organisation. Read Less
  • Director of Research  

    - Altrincham
    Director of ResearchPermanentCheshire SRG is delighted to be working w... Read More
    Director of ResearchPermanentCheshire SRG is delighted to be working with a seed-stage biotech to help them find a Director of Research. The organisation is developing a non-viral gene-delivery platform targeting glioblastoma cells and has shown incredibly positive results in pre-clinical models.Reporting directly to the founders as the Director of Research you will be the operational engine that drives the platform from final GLP tox through first-patient-in. You will co-ordinate academics, CROs, manufacturing, vendors and regulators to drive this exciting project into clinic.Key responsibilitiesProject leadership to build and maintain the integrated project plan (timeline, budget, risk log) for GLP tox, CMC, regulatory and clinical work-streams.Regulatory operations - compile and submit CTA/IND, ethics track RFIs, manage agency correspondence (MHRA, FDA, EMA).Vendor & CRO management - source, contract, kick-off and oversee CROs and specialist labs; track KPIs and invoices.Study start-up - support protocol development, investigator brochure, site selection and green-light packages.Stakeholder communication - prepare dashboards and board packs; chair weekly cross-functional calls.Ideal profilePhD (or equivalent) in a related discipline with working knowledge of oncology or gene-therapy terminology.Significant experience coordinating or managing Phase I/II trials in a CRO, biotech or pharma.Proven experience with CTA or IND submission and tracking.Experience with liposomes or lipid nanoparticles would be advantageous.Familiar with GxP, ICH, and MHRA processes.Strong communication and vendor management skillsAre you ready to shape the future of gene therapy and make a real impact in oncology?Join a passionate team at the forefront of biotech innovation, where your expertise will drive breakthrough science into the clinic. If you thrive in dynamic environments and want to be part of something truly transformative, we want to hear from you!Apply now by attaching your CV in Word, or contact Paige Keenan () or Nathan Fairhurst () for further information about this new role.Guidant, Read Less

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