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SRG
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  • QA Document Reviewer  

    Join a Growing Life Science Leader! About the Opportunit y Are you exp... Read More
    Join a Growing Life Science Leader! About the Opportunit y Are you experienced in reviewing quality or batch documentation in a regulated GMP environment? This expanding life science organisation is seeking a committed QA Document Reviewer to support their Quality Assurance function and ensure documentation excellence across the business. This role is also suitable for driven science graduates looking to start their career in QA. Reporting to the Quality Assurance Manager, you will play a critical role in maintaining compliant, accurate, and well controlled documents, data, and records. Key Responsibilities Review quality and batch documentation with accuracy and attention to detail Provide document control functions, support, and guidance across the business Maintain trackers and generate accurate status reports to support batch compilation activities Support document archiving, ensuring controlled and compliant material movement Coordinate SOP review cycles and ensure revisions meet required timelines Ensure all documents are updated, mastered, and maintained according to established procedures Contribute to GMP compliance activities and continuous QA improvement Requirements HNC/HND minimum; degree preferred Experience in document review within a regulated GMP environment is preferred but they will consider graduates with demonstrable skills Strong written and verbal communication skills at all levels Knowledge of Quality Systems (desirable) Excellent organisational skills, with the ability to work independently and as part of a team Analytical approach to problem solving and decision making Proficiency in Microsoft Office and confident data entry skills Read Less
  • Global Product Manager  

    Global Product Manager required, based in Cheshire West on a permanent... Read More
    Global Product Manager required, based in Cheshire West on a permanent basis. Candidates will hold significant experience within the chemical industry, including product management and commercialisation of speciality chemicals across international markets. A degree (or higher) in Chemistry (or similar) is required. Title: Global Product Manager Location: Cheshire West Salary: Up to £80,000 (dependent on experience), plus car allowance and bonus potential Term: Permanent SRG are working with a well-respected, global speciality chemicals manufacturer with a strong reputation for innovation and market-led product development. They are now looking for a Global Product Manager to lead the strategic direction, commercialisation and lifecycle management of a portfolio of performance chemical products across international markets. This is a highly visible, strategic role, responsible for driving global product strategies, leading cross-functional collaboration and supporting commercial growth through effective portfolio management. The successful candidate will operate within a matrix organisation, working closely with R Read Less
  • Quality Assurance Regulatory Affairs Manager  

    - Berkshire
    p strong Manager - Regulatory Affairs Submission Management /strong /p... Read More
    p strong Manager - Regulatory Affairs Submission Management /strong /p p br /p p strong Contract: /strong Temporary - 12 months (extension possible) /p p strong Location: /strong Maidenhead – hybrid working (or remote if needed) /p p strong Rate: em (INSIDE IR35) /em /strong /p p - circa. £22-25 per hour (PAYE) /p p br /p p SRG are seeking a Regulatory Affairs professional with Submission Management skills experience to assist a leading pharmaceutical company on a temporary basis. Join a dynamic regulatory affairs team and play a pivotal role in delivering complex regulatory submissions that support the development, approval, and lifecycle management of innovative healthcare products. /p p br /p p strong Key Responsibilities /strong /p ul li Lead and manage complex regulatory submission projects, ensuring high-quality dossiers are delivered on time and in line with regulatory requirements. /li li Act as the primary regulatory submission management contact for cross-functional project teams, providing guidance on processes, timelines, and deliverables. /li li Coordinate and facilitate submission planning meetings, driving progress across multiple concurrent projects and stakeholders. /li li Oversee publishing activities and collaborate with external publishing partners to ensure successful submission delivery. /li li Perform quality reviews of published submissions, ensuring compliance with technical standards and regulatory authority requirements. /li li Contribute to continuous improvement initiatives, enhancing regulatory processes, standards, and systems. /li /ul p br /p p strong Skills Experience Required /strong /p ul li Bachelors degree or equivalent combination of education and relevant industry experience. /li li Experience within the pharmaceutical, biotechnology, healthcare, or related regulated industry. /li li Strong project management skills, with experience managing complex, cross-functional activities and competing priorities. /li li Knowledge of regulatory operations, submission management, and/or submission publishing processes. /li li Excellent written and verbal communication skills, with the ability to influence stakeholders in a matrix environment. /li li Demonstrated leadership capability, including mentoring colleagues and driving process improvements. PMP and/or RAC certification is advantageous. /li /ul p br /p p strong To Apply /strong /p p Please click and submit your profile and/or to discuss further, contact Theo Charles on 07836 251472 /p p Umbrella also possible – please enquire for more information /p p br /p Read Less
  • NPD Chemist  

    - Cheshire East
    p em New Product Development (NPD) Chemist required in Cheshire East,... Read More
    p em New Product Development (NPD) Chemist required in Cheshire East, on a permanent basis. Requiring a degree in Chemistry, Materials Science (or similar) and recent, proven industrial experience of product development within a manufacturing environment. Candidates with coatings, adhesives, paper, film or related materials experience are encouraged to apply. /em /p p br /p p strong Title: New Product Development (NPD) Chemist /strong /p p strong Location: Cheshire East /strong /p p strong Salary: £40,000 - £46,000 /strong em (dependent on experience) /em /p p strong Term: Permanent /strong /p p br /p p SRG are working with a highly successful company that develop and manufacture a range of specialist coated products. They are now seeking a New Product Development Chemist to join their technical team in Cheshire East on a permanent basis. This role is designed for someone with proven experience of managing development projects from concept through to commercial launch and will involve taking ownership of a portfolio of new product and process development activities to support business growth. This role will suit candidates with recent and proven industrial experience in product development, project management and formulation, as well as being comfortable working with customers, suppliers and internal stakeholders. Experience within coatings, adhesives, paper or film manufacturing is desirable but not essential. /p p br /p p strong Benefits: Joining a highly successful, employee-owned business that values employees. Flexible working hours, annual bonus, healthcare cash plan and strong pension. /strong /p p br /p p strong Role/Description /strong /p ul li Manage, plan and execute product and process development projects from ideation through to commercial launch. /li li Deliver sales growth through the development of new and improved products. /li li Assess new product ideas and opportunities, including costs, benefits, resourcing requirements and timescales. /li li Plan and prioritise development activities to ensure projects are delivered on time. /li li Report project progress and provide clear technical recommendations and go/no-go proposals. /li li Coordinate and support laboratory work, production trials and scale-up activities. /li li Manage NPD projects through to full production implementation. /li li Identify and engage with suppliers, consultants, test houses and academic partners to support development activities. /li li Share technical learning and project outcomes across the wider business. /li li Provide technical support relating to specifications, material changes, customer complaints and operational troubleshooting. /li /ul p br /p p strong Requirements /strong /p ul li Degree in Chemistry, Materials Science or a related scientific discipline. /li li Proven industrial experience within product development, R D or process development. /li li Experience managing projects from concept through to commercial launch. /li li Strong analytical and problem-solving skills with the ability to assess opportunities technically and commercially. /li li Excellent communication skills and ability to work effectively with customers, suppliers and internal stakeholders. /li li Experience within coatings, adhesives, paper, film or a related materials manufacturing environment is desirable. /li li Formulation experience is highly desirable. /li /ul p br /p p em For more information please call Chris Beckenham on 0161 667 1795. /em /p p br /p p strong Keywords: /strong em new product development, NPD, research and development, R D, chemist, development chemist, coatings, adhesives, paper, film, product development, process development, formulation, formulating, project management, innovation, scale-up, commercialisation, technical support, specifications, materials science, chemistry, chemicals, laboratory, manufacturing, trials, product launch. /em /p Read Less
  • Global Product Manager  

    p em Global Product Manager required, based in Cheshire West on a perm... Read More
    p em Global Product Manager required, based in Cheshire West on a permanent basis. Candidates will hold significant experience within the chemical industry, including product management and commercialisation of speciality chemicals across international markets. A degree (or higher) in Chemistry (or similar) is required. /em /p p br /p p strong Title: Global Product Manager /strong /p p strong Location: Cheshire West /strong /p p strong Salary: Up to £80,000 (dependent on experience), plus car allowance and bonus potential /strong /p p strong Term: Permanent /strong /p p br /p p SRG are working with a well-respected, global speciality chemicals manufacturer with a strong reputation for innovation and market-led product development. They are now looking for a Global Product Manager to lead the strategic direction, commercialisation and lifecycle management of a portfolio of performance chemical products across international markets. /p p br /p p This is a highly visible, strategic role, responsible for driving global product strategies, leading cross-functional collaboration and supporting commercial growth through effective portfolio management. The successful candidate will operate within a matrix organisation, working closely with R D, sales, regulatory and operations teams to deliver value across the product lifecycle. /p p br /p p strong Benefits: Multinational chemicals business with a strong focus on innovation and collaboration. Attractive salary, car allowance and bonus scheme. Excellent pension scheme and private healthcare. /strong /p p br /p p strong Role / Description /strong /p ul li Leading the strategic direction and lifecycle management of a global portfolio of speciality chemical products /li li Developing and implementing product strategies, including market positioning, pricing and portfolio optimisation /li li Conducting market analysis, including customer needs, competitive landscape and regulatory considerations /li li Driving global product launches, coordinating cross-functional teams to ensure successful commercialisation /li li Collaborating closely with R D, regulatory, operations and sales teams to align product development and execution /li li Supporting sales teams with technical product knowledge, training and go-to-market strategies /li li Monitoring product performance and implementing continuous improvement initiatives /li li Establishing standardised product management processes and best practices across regions /li li Building and aligning global teams, fostering a collaborative and high-performance culture /li /ul p br /p p strong Requirements /strong /p ul li Degree (BSc/MSc or higher) in Chemistry or a related scientific discipline /li li Extensive experience within the chemical industry, ideally within speciality chemicals. Other sectors of industrial or performance chemicals will be considered /li li Proven success managing products in international markets within a matrix organisation /li li Strong understanding of commercialisation, product lifecycle management and market dynamics /li li Knowledge of regulatory environments (e.g. REACH, TSCA) is advantageous /li li Excellent communication, leadership and stakeholder management skills /li li Willingness to travel internationally /li /ul p br /p p For more information, please call Chris Beckenham on 0161 667 1795. /p p br /p p strong Keywords: /strong em Product Manager, Global Product Manager, speciality chemicals, performance chemicals, chemical industry, product lifecycle management, commercialisation, portfolio management, go-to-market, strategy, coatings, paints, additives, surfactants, innovation, product strategy, regulatory, REACH, TSCA, international markets, management, manager. /em /p Read Less
  • Chief Technologist  

    - Glasgow City
    p strong Chief Technologist – Synthetic Therapeutics (Peptides Oligonu... Read More
    p strong Chief Technologist – Synthetic Therapeutics (Peptides Oligonucleotides) /strong /p p br /p p strong FTC until March 2028 | Glasgow | /strong /p p br /p p strong £64,394 – £84,394 + £491 Monthly Car Allowance /strong /p p br /p p strong About the Role: /strong /p p We are seeking a Chief Technologist – Synthetic Therapeutics to provide strategic technical leadership across peptide and oligonucleotide technologies, helping shape future capability, support commercial growth, and drive innovation in one of the fastest-growing areas of advanced therapeutics. /p p br /p p This is a highly influential role for a recognised subject matter expert who combines deep scientific expertise with strong market awareness and commercial insight. You will help identify future opportunities, advise on technology strategy, engage with customers and partners, and support the development of capabilities that address emerging industry needs. /p p br /p p The successful candidate will act as a senior technical leader across both internal and external activities, supporting business development, customer engagement, technology strategy, and scientific delivery while helping build capability in peptides and oligonucleotides. /p p br /p p strong What Youll Be Responsible For: /strong /p p br /p p strong Technical Leadership Domain Expertise /strong /p ul li Act as the recognised technical authority in peptide and/or oligonucleotide chemistry /li li Provide expert guidance across customer programmes, strategic initiatives, and capability development activities /li li Support scientists and technical teams with specialist knowledge and technical problem-solving /li li Ensure emerging scientific developments are translated into practical and commercially relevant applications /li /ul p br /p p strong Technology Strategy Capability Development /strong /p ul li Shape future capability in synthetic therapeutics, identifying technology gaps, market opportunities, and investment priorities /li li Inform long-term technology strategy and help develop deliverable plans aligned to business objectives /li li Anticipate new developments within peptide and oligonucleotide technologies and assess their commercial relevance /li li Support the translation of advanced chemistry into scalable and commercially viable capabilities /li /ul p br /p p strong Market Engagement Business Development /strong /p ul li Work closely with commercial and business development teams to identify and develop new opportunities /li li Engage directly with customers, industry partners, investors, and stakeholders to understand market needs /li li Support proposal development, bid activities, and customer-facing technical discussions /li li Contribute to technical and commercial assessments of new opportunities and partnerships /li /ul p br /p p strong Capability Building Mentorship /strong /p ul li Mentor scientists and technical teams, helping build expertise across the organisation /li li Promote knowledge sharing and capability development across internal and external networks /li li Support the development of future scientific leaders and specialists /li li Foster a culture of innovation and continuous learning /li /ul p br /p p strong About You /strong /p p You are a senior technical expert with deep knowledge of peptides, oligonucleotides, or synthetic therapeutic modalities, coupled with strong commercial awareness and an ability to influence strategic direction. /p p Youll bring: /p ul li Significant industrial experience within peptides and/or oligonucleotides /li li Strong expertise in areas such as: /li li Peptide synthesis, modification, and conjugation /li li Complex or constrained peptides /li li Peptide-drug conjugates /li li Oligonucleotide chemistry /li li Oligo conjugates /li li Modified backbones and delivery-enabled constructs /li li A proven track record of translating scientific knowledge into commercially relevant capabilities and opportunities /li li Strong understanding of market dynamics, customer needs, and future industry trends /li li Excellent stakeholder management, networking, and influencing skills /li li Experience operating at a strategic level within pharmaceutical, biotech, CDMO, or advanced therapeutics environments /li /ul p strong Desirable (but not essential): /strong /p ul li PhD or equivalent research background in peptide, oligonucleotide, or synthetic chemistry disciplines /li li Experience contributing to technology strategy and capability development /li li Existing industry network within peptides, oligonucleotides, or related therapeutic modalities /li li Knowledge of broader synthetic therapeutic approaches and emerging modalities /li li Membership of relevant professional bodies and active engagement with the wider scientific community /li /ul p strong Importantly, this role is not focused on routine GMP manufacturing operations. /strong The emphasis is on strategic technical leadership, market engagement, capability development, and helping define where future investment and technological growth should occur. /p p br /p p strong Why Join Us? /strong /p ul li Influence the future direction of peptide and oligonucleotide technology development /li li Shape capability in a rapidly growing area of advanced therapeutics /li li Work with leading scientific, commercial, and industry stakeholders /li li Play a key role in identifying and developing future market opportunities /li li High-profile position with significant external engagement /li li Competitive package including salary up to £84,394 plus monthly car allowance /li /ul p br /p p strong Location Working Pattern /strong /p ul li strong FTC until March 2028 (potential to extend) /strong /li li Hybrid working available /li li Regular engagement with customers, partners, and external stakeholders /li li Travel to industry events, customer meetings, and scientific forums as required /li /ul p br /p Read Less
  • Graduate Chemist  

    - Glasgow City
    p SRG are delighted to be working once again with one of Scotlands lea... Read More
    p SRG are delighted to be working once again with one of Scotlands leading start-up companies as they continue to expand into new sites and new regions. /p p br /p p As part of their growth they are looking to bring in a number of graduate chemists to join their large scale production team on a full-time permanent basis. /p p br /p p strong The Role /strong /p p br /p p As a chemist within the production department you will work as part of a large, multi-skilled team to ensure the efficient manufacture of the companies small-organic molecule products. When joining the production team you will enter in one of the below positions; /p p br /p ul li Production Chemist /li li Purification Technician /li li Analytical Technician /li /ul p br /p p strong The Right Candidate /strong /p p br /p ul li Recent or upcoming graduate in chemistry, applied sciences or similar (HNC up to Masters) /li li Demonstrable experience in a laboratory environment /li li Fundamental knowledge of the principles of lab Health and safety /li li strong MUST /strong be open to working in a variety of shifts - including weekends /li /ul p br /p p This role is unable to provide sponsorship and as such candidates will require full, indefinite right to work in the UK. /p Read Less
  • Senior Associate Device Engineer  

    - Cambridgeshire
    p strong Senior Associate Device Engineer /strong /p p strong Location... Read More
    p strong Senior Associate Device Engineer /strong /p p strong Location: /strong Cambridge /p p strong Contract Length: /strong 12 Months /p p strong Hours: /strong 37 Hours per Week /p p br /p p strong Pay Rates: /strong /p ul li PAYE: £21.31 per hour /li li Umbrella: £23.88 per hour /li /ul p br /p p strong The Opportunity /strong /p p An exciting opportunity has arisen for a strong Senior Associate Device Engineer /strong to join a leading global pharmaceutical organisation supporting the development of innovative drug delivery devices and combination products. /p p br /p p Working within a multidisciplinary engineering and scientific team, you will provide technical support across device development programmes, contributing to the testing, analysis, verification and evaluation of drug delivery devices, components and primary packaging systems. This role offers the opportunity to work on cutting-edge healthcare technologies while supporting the delivery of safe, effective and compliant products to patients. /p p br /p p strong Key Responsibilities /strong /p ul li Support the development and verification of drug delivery devices through testing, data analysis and engineering assessments. /li li Design and develop test methods, experimental rigs and laboratory-based test setups. /li li Contribute to risk management activities, including design and usability FMEA assessments. /li li Support the preparation, review and maintenance of design control documentation. /li li Analyse experimental data using statistical and scientific techniques to support decision-making. /li li Assist with design verification, stability studies, transportation assessments and specification development. /li li Collaborate with internal teams and external partners on device design, testing and manufacturing activities. /li li Prepare technical reports and ensure accurate documentation in line with quality requirements. /li li Maintain laboratory equipment and support compliance activities within a regulated environment. /li /ul p br /p p strong About You /strong /p p To be successful in this role, you will bring: /p ul li A degree, HND or equivalent qualification in an Engineering or Scientific discipline. /li li Experience working with device testing, device development or engineering investigations. /li li Knowledge of design verification, specification setting and analytical test methods. /li li Experience applying structured problem-solving techniques and statistical analysis. /li li Strong technical writing and documentation skills. /li li Excellent attention to detail and the ability to work within regulated procedures and quality systems. /li li Effective communication skills and the ability to work within multidisciplinary teams. /li /ul p br /p p strong Desirable Experience /strong /p ul li Medical device, pharmaceutical or combination product development experience. /li li Knowledge of ISO 13485, GMP and/or GLP environments. /li li Experience with risk management tools such as dFMEA and uFMEA. /li li CAD experience (ideally Creo). /li li Understanding of engineering calculations, FEA or mechanical testing techniques. /li li Experience developing and validating test methods. /li /ul p br /p Read Less
  • Clinical Scientist  

    - Cambridgeshire
    p strong Clinical Scientist /strong /p p br /p p strong Cambridge /str... Read More
    p strong Clinical Scientist /strong /p p br /p p strong Cambridge /strong /p p br /p p strong Permanent /strong /p p br /p p SRG is delighted to be partnering with an innovative and growing diagnostics organisation to support the appointment of an experienced Clinical Scientist. This is a hands-on role combining clinical leadership, diagnostic assay delivery, and laboratory operations within a company developing cutting-edge diagnostic solutions across multiple disease areas. /p p br /p p The successful candidate will play a key role in ensuring diagnostic services are delivered safely, accurately, and in line with the highest clinical and quality standards. Working closely with laboratory leadership, you will provide scientific expertise, support clinical governance activities, and contribute to the introduction and validation of new diagnostic services. /p p br /p p Key Responsibilities: /p ul li Lead clinical activities relating to the implementation, validation, and ongoing optimisation of diagnostic testing platforms /li li Perform and oversee the processing, analysis, interpretation, and reporting of clinical diagnostic assays /li li Provide clinical oversight and support for molecular and immunochemistry-based diagnostic services /li li Review and sign off validation and verification studies for new and existing assays /li li Support ISO 15189 compliance and contribute to quality management and clinical governance activities /li li Assess clinical risks associated with diagnostic workflows and support corrective and preventative actions /li li Provide training, mentorship, and supervision to laboratory staff involved in clinical testing activities /li li Work closely with laboratory, quality, and technical teams to ensure services meet patient and user needs /li /ul p br /p p Requirements: /p ul li HCPC registration as a Clinical Scientist or a Medical Degree /li li Experience working within a clinical diagnostic laboratory environment /li li Hands-on experience with molecular and/or immunochemistry assays, including PCR-based testing /li li Strong understanding of clinical governance, risk assessment, and quality systems /li li Experience working within ISO 15189 accredited or regulated laboratory environments /li li Working knowledge of ISO 13485 would be incredible beneficial /li li Excellent communication skills with the ability to provide clinical guidance and support across multidisciplinary teams /li li A proactive and collaborative approach with the confidence to challenge where patient safety or clinical appropriateness may be affected /li li Proven ability to balance clinical responsibilities with hands-on laboratory activities /li /ul p br /p p Desirable Experience: /p ul li Experience with genotyping assays and probe-based PCR workflows /li li Exposure to assay validation, verification, and implementation of new diagnostic tests /li li Experience supervising or mentoring laboratory personnel /li li Knowledge of TaqMan arrays, KingFisher extraction systems, or similar molecular diagnostic technologies /li li Experience supporting service development and laboratory operational improvement initiatives /li /ul p br /p p Apply now by attaching your CV in Word, or contact Paige Keenan for further information about this opportunity: strong paige.keenan@srgtalent.com /strong . /p Read Less
  • Principal Food Scientist  

    - Gloucestershire
    p strong Principal Food Scientist /strong /p p br /p p 📍 Southwest Eng... Read More
    p strong Principal Food Scientist /strong /p p br /p p 📍 Southwest England /p p 💷 Competitive Salary + Bonus + Excellent Package /p p ⏰ Full Time | Site-Based (5 Days Per Week) /p p br /p p SRG are supporting an exciting, innovative company in recruiting a Principal Food Scientist to lead an advanced research programme focused on how food processing methods impact food and beverage products. /p p br /p p This is a senior, hands-on role for an experienced food scientist with strong expertise in food processing, food chemistry and analytical techniques. You will design and deliver investigative research to understand how processing conditions influence product functionality, stability and performance. This is a fantastic opportunity to shape and lead high-impact food science research with long-term technical and leadership progression /p p br /p p strong The Role /strong /p p br /p ul li Develop and lead an investigative food science research programme focused on processing and treatment methods /li li Design and deliver experimental testing to assess both physical and chemical product changes /li li Generate insight across processing techniques including frying, roasting, baking, blending and mixing /li li Apply food chemistry principles such as oxidation, hydration and ingredient interactions /li li Use a range of analytical techniques to evaluate product behaviour and performance /li li Translate complex findings into clear, actionable insights /li li Work cross-functionally to support innovation and technical decision making /li li Manage your own research priorities, planning and delivery /li /ul p br /p p strong About You /strong /p p br /p ul li Degree in Food Science, Nutrition or a related discipline /li li Strong industry experience in food science, food processing or product development /li li Deep understanding of how processing conditions affect food properties /li li Strong knowledge of both physical and chemical analytical approaches /li li Able to design and lead scientifically robust research programmes /li li Confident communicator, able to engage technical and non-technical stakeholders /li li Comfortable working in a highly hands-on, site-based environment /li /ul p br /p p em If you would like to apply for this position, please use the link provided. Alternatively, please email a copy of your CV to /em strong em amy.hallworth@srgtalent.com /em /strong em For more information regarding this position or any others, please call /em strong em Amy /em /strong em on /em strong em 0161 667 1792. /em /strong em If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit a www.srgtalent.co.uk /a to view our other vacancies. /em /p p br /p p SRG is a UK leader in specialist recruitment across science and engineering, including chemicals, pharmaceuticals, FMCG, medical devices and biotech. With deep sector expertise and a strong scientific background, we connect talent with high-quality roles and deliver tailored recruitment solutions to clients across the UK. /p p br /p p strong Keywords em : /em /strong em Food Science, FMCG Innovation, Food Processing, Food Chemistry, Product Development, Food Research, Food Scientist /em /p Read Less

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