SRG

Job Description - Maintenance Engineer Key Responsibilities: Perform preventative maintenance, repairs, calibrations, and electrical safety checks on laboratory, manufacturing, and biomedical equipment in line with established schedules and work orders Inspect and support the installation of new laboratory equipment, ensuring safe operation and overseeing Installation, Operation, and Performance Qualification (IQ/OQ/PQ) activities at assigned site(s) Troubleshoot and resolve equipment issues to minimise downtime and maintain high equipment availability Provide guidance to laboratory personnel on best practices for equipment use and operation Maintain accurate and up-to-date documentation for all equipment, including maintenance activities, repairs, and safety checks Continuously develop technical knowledge through training on relevant equipment and testing devices Manage and maintain the Computerised Maintenance Management System (CMMS), ensuring accuracy of asset records, maintenance schedules, and compliance documentation Process and track work orders through the CMMS and ensure timely completion of both planned and reactive maintenance tasks Coordinate third-party vendor activities, including scheduling, quote management, purchase order processing, and verification of completed work Work collaboratively with Quality teams to ensure ongoing regulatory compliance within maintenance systems and processes Experience & Qualifications: High school diploma (or equivalent) required; an Associate's degree in Manufacturing, Engineering, Electronics, or a related field is preferred Minimum of 2 years' experience in equipment maintenance ideally within a manufacturing or laboratory environment or similar technical environment Experience using CMMS platforms and managing external vendors is highly desirable Strong organisational and time management skills, with the ability to balance technical and administrative responsibilities Effective communication skills, both written and verbal Proficiency in Microsoft Excel and database management systems Ability to work independently with minimal supervision Additional Requirements: Ability to sit or stand for extended periods Ability to lift heavy weights Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Junior C++ Developer Manchester Digital Betting Technology Platform 2 days per week in office, flexible working hours A digital betting technology business in Manchester is hiring a Junior C++ Developer to work on customer-facing terminal software used in live retail environments.They are not looking for a finished expert. The main thing is attitude, curiosity and evidence of C++ project work, whether that is from university, internships, freelance work, personal projects or GitHub.This is a good step for someone early in their career who wants proper commercial C++ experience. You'll be learning around software that runs in the real world, where debugging, reliability, performance and hardware interaction actually matter.What you'll be doing Working on C++ software used across customer-facing terminal systems Learning from experienced engineers in a commercial team Supporting debugging, testing and improvements to existing software Getting exposure to Windows development, Visual Studio and production codebases Working around networking, hardware/peripherals and system reliability What they love to see: Some experience with C++ Evidence of C++ projects or genuine hands-on interest Comfortable with, or keen to improve around, OOP, debugging, pointers, memory management and STL Any exposure to Visual Studio, Windows, Unreal/C++, hardware or networking would be useful A positive attitude and willingness to get stuck in The long story short: This is a strong bridge from C++ project work into a proper commercial engineering role.You do not need to be the finished article. If you enjoy C++, like solving technical problems and want to build real software used in live environments. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Director, QA Manufacturing (Head of Front Line QA / QP) Liverpool Senior Leadership Role Salary Confidential About the Role We are seeking an experienced Director, QA Manufacturing (Head of Front Line QA) to take ownership of a well-established Quality function within a sterile manufacturing environment. Reporting to the Site Head of Quality Assurance, this is a senior leadership role responsible for providing independent QA oversight across all site operations, while shaping quality strategy, governance, and culture. You will lead a high-performing QA team delivering 24/7 operational support, ensuring that all products and processes meet the highest standards of cGMP, regulatory compliance, and data integrity. For candidates eligible to act as a Qualified Person (QP), the role also carries responsibility for certification and release of products, including oversight of manufacturing and intermediate product release. What You'll Be Responsible For: Front Line QA Operations Provide QA oversight across manufacturing, QC, engineering, and GMP operations Lead a team delivering continuous QA support to production operations Ensure robust systems for batch review, QA processes, and QA IT systems QP Responsibilities Certify or reject product for release in line with regulatory and legal requirements Provide oversight of product release across the manufacturing lifecycle Maintain QP eligibility through ongoing professional development Quality Leadership & Strategy Lead and develop a large QA team, setting clear direction, expectations, and performance standards Promote a strong quality culture and cGMP mindset across the organisation Act as a deputy to the Site Head of QA and contribute to overall site strategy Define and track quality KPIs and performance metrics Quality Systems & Governance Oversee the Pharmaceutical Quality System (PQS), including: Deviations, CAPA, and Change Management Document management and training systems Data integrity and compliance frameworks Ensure the site remains inspection-ready at all times Support management review processes and continuous improvement of quality systems Operational & Cross-Functional Oversight Provide QA leadership across key governance forums, including: Deviation Review Boards Change Review Panels Quality Management Reviews Collaborate with Supply Chain, External QA, and Contract Manufacturing teams Ensure compliant handling of all product across manufacturing, distribution, and third parties Regulatory & External Engagement Act as a key contact during regulatory inspections and audits Engage with regulatory authorities and ensure compliance with global GMP standards Support regulatory submissions, variations, and ongoing compliance requirements About You: You are a senior quality leader with deep experience in GMP-regulated manufacturing, ideally within sterile or aseptic environments. You'll bring: Significant experience in QA leadership roles within pharmaceutical manufacturing Strong knowledge of cGMP, regulatory frameworks, and quality systems Proven ability to lead teams, manage complexity, and drive quality performance Eligibility to act as a Qualified Person (QP) Highly desirable: Experience within sterile or aseptic manufacturing environments Experience leading QA functions in 24/7 operational settings Track record of supporting regulatory inspections and audits Location & Working Pattern Based on-site in Liverpool Senior leadership role with high on-site presence required Engagement across operational, strategic, and regulatory activities The Opportunity This is a rare opportunity for an experienced quality leader to step into a highly visible, business-critical role , taking ownership of an established QA function while driving forward quality excellence, regulatory compliance, and operational performance in a complex manufacturing environment. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Title: Regulatory Admin Assistant Location: Kingston upon Hull Salary: TBC Term: 22 week Temporary Contract - (potential for extension) Working Hours: 30h a week, 4 days a week flexibility on days and hours done per day to meet the 30h requirements, hybrid/remote once trained Benefits: enhanced training and development opportunities, industry exposure. SRG is working with a leading hygiene, personal care and home care manufacturer based in East Yorkshire. They are now looking for a Regulatory Admin Assistant to join the team. In this role, you will provide administrative support to the Regulatory team while assisting with a range of system, coordination, and communication tasks. This position would ideally suit a candidate with strong organisational skills who is looking to build experience in a fast-paced industry environment, with opportunities for and exposure to global regulatory processes in personal care and homecare sector. Role / Description Manage user access and workflow approvals within the Regulatory Intelligence PowerApp. Keep activity on track by sending clear communications, reminders, and guidance to users. Coordinate with global stakeholders across functions, cultures, and time zones to maintain smooth progress. Spot issues, raise system gaps, and work closely with the RI team to support improvements. Support testing, updates, and workshop scheduling to help deliver an effective and reliable system. Requirements Strong experience using Microsoft Excel, Outlook, and Teams Experience with PowerApps or similar systems is an advantage, but not essential if you are quick to learn new tools. Prior experience in an admin-based role is advantageous but not essential SRG 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 For more information regarding this position or any others, please call Rhi on (phone number removed). If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit (url removed) to view our other vacancies. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Marketing Communications Business Partner 12-month Fixed-Term Contract (Maternity Cover) North East England (Sedgefield, Darlington, Wilton) 43,108 - 55,108 About the Role: CPI is seeking a Marketing Communications Business Partner to join our Marketing team on a 12-month maternity cover, supporting the delivery of campaign-driven marketing activity across our Materials business. This is a highly varied, delivery-focused role where you will take ownership of multi-channel marketing campaigns, working closely with the Head of Marketing and wider business stakeholders. You will play a central role in executing established marketing plans, managing campaigns, and ensuring strong engagement across both digital and in-person channels. With autumn being a peak period for events and conferences, this role requires someone who can step in quickly, take ownership, and deliver with minimal supervision in a fast-paced environment. Hybrid working is supported, with travel required across CPI sites and events. What You'll Be Responsible For: Campaign Delivery & Execution Lead the delivery of integrated marketing campaigns aligned to business objectives Execute campaign activity across digital, inbound and outbound channels, including: Website content Social media Email and automation Work closely with content and communications teams to develop campaign assets Monitor performance and optimise campaigns through KPI tracking and reporting Events & External Engagement Lead the planning and delivery of events, conferences, and exhibitions Develop event plans, agendas, and supporting materials in collaboration with internal teams Maximise commercial opportunities from events, including lead generation and follow-up strategies Support delivery of webinars and hosted events across CPI facilities Stakeholder & Business Partnering Act as the Marketing Business Partner for the Materials side of the business Work closely with senior stakeholders to align campaigns with commercial objectives Provide best practice advice and guidance on marketing activity across teams Project Management & Coordination Manage multiple campaigns and activities simultaneously across the marketing calendar Coordinate timelines, stakeholders, and outputs across a busy programme of work Ensure consistent delivery against agreed plans and deadlines Strategy Contribution Support the development of future campaign strategy toward the latter part of the contract Provide insights and recommendations based on campaign performance and market trends About You: You are an experienced marketing professional who enjoys working autonomously, delivering campaigns end-to-end, and engaging with stakeholders across a complex organisation. You'll bring: Strong experience in B2B marketing, ideally in a campaign-driven role Proven ability to manage and deliver multi-channel marketing campaigns Experience planning and delivering events, conferences, or exhibitions Strong project management and organisational skills Confidence working with stakeholders and operating independently Desirable (but not essential): Experience working in technical, scientific, or sustainability-focused environments Familiarity with digital marketing tools, analytics, and automation platforms Experience working within matrix organisations or multi-site environments This role requires someone who is: Able to manage competing priorities and deliver at pace Strong in both execution and relationship-building Why Join CPI? Work within a highly regarded and supportive marketing team Deliver impactful campaigns across sustainability-driven materials programmes High level of responsibility and ownership Exposure to both digital campaigns and high-profile industry events Competitive salary 43,108 - 55,108 Location & Working Pattern Hybrid working (typically 2 days per week on-site) Travel required for events and conferences (UK-based) Full UK driving licence and access to a car required The Opportunity This is an excellent opportunity to step into a highly visible marketing role within a busy, well-established team - delivering real commercial impact while gaining exposure to multi-channel campaigns, events, and stakeholder-led marketing. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Senior Solicitor Northeast sites (Darlington, Sedgefield, Wilton) Hybrid working (minimum 2 days on-site) 52,000 - 64,800 About the Role CPI is seeking a Senior Solicitor to provide high-quality, commercially focused legal support across the organisation, working as part of an established in-house legal team. This is a hands-on, senior role in which you will take ownership of a broad range of legal matters, supporting the business across commercial, corporate, property, and regulatory activities . You will work closely with the General Counsel and existing solicitors to ensure timely, pragmatic legal advice across a diverse and fast-moving organisation. We are looking for someone who can hit the ground running - bringing prior in-house experience, strong commercial awareness, and the ability to manage competing priorities with minimal supervision. What You'll Be Responsible For: Commercial Legal Support Provide practical, commercially focused legal advice across: Commercial contracts and T&Cs Procurement and supplier agreements Corporate and transactional matters Draft, review, and negotiate a wide range of contracts and legal documentation Broad Legal Advisory Support the business across a variety of legal areas, including: Property and construction matters Regulatory and compliance advice Pre-contentious commercial disputes Intellectual property considerations Business Partnering Work closely with stakeholders across the organisation, providing clear and pragmatic guidance Support functions including procurement, HR, and operations on legal matters Build strong internal relationships and act as a trusted legal advisor Team & Operational Support Support the wider legal team in managing workload across multiple concurrent matters Maintain and develop legal templates and documentation frameworks Contribute to legal training and awareness across the business About You: You are an experienced, commercially minded solicitor with a strong background in in-house legal work , comfortable taking ownership of a broad and varied workload. You'll bring: Qualification as a Solicitor in England & Wales with a current practising certificate Proven experience working in-house (essential) Strong experience across commercial contracts and general corporate/legal matters Ability to manage multiple priorities and deliver high-quality advice in a fast-paced environment Confidence engaging with stakeholders at all levels across a business Desirable (but not essential): Experience across property, regulatory, or procurement-related legal work Exposure to working in complex or multi-disciplinary organisations Experience supervising or supporting junior team members This role is best suited to someone with a solid qualification period and meaningful in-house experience , rather than a purely private practice background. Why Join CPI? Join a well-established in-house legal team with broad exposure across the business Work on a diverse range of legal matters across multiple sectors High level of autonomy and responsibility Supportive and collaborative team environment Competitive salary ( 52k- 64.8k) Location & Working Pattern Based across CPI sites in the North East (Darlington, Sedgefield, Wilton) Hybrid working with typically 2+ days on-site per week Flexibility depending on meetings and workload The Opportunity This is an excellent opportunity for a confident, experienced in-house solicitor to step into a visible and impactful role, supporting a wide range of legal matters and helping the team deliver effectively during a key period. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Lead Bioprocess Engineer - Scale-Up & Pilot Operations Location: Somerset, UK (site-based) Type: Full-time We are seeking an experienced Lead Bioprocess Engineer to lead the scale-up and industrialisation of an innovative bioprocess platform . This role combines technical leadership with hands-on delivery , focusing on translating early-stage science into pilot-scale and commercially viable processes . The Role You will take ownership of bioprocess development and scale-up activities , working closely with R&D, engineering, and operations teams to move processes from lab through to pilot and beyond. A strong on-site presence is essential , and you will be actively involved in running experiments, troubleshooting processes, and optimising performance . Key responsibilities include: Leading end-to-end scale-up activities , from bench through pilot-scale demonstration Translating cell culture and tissue engineering processes into scalable manufacturing solutions Taking a hands-on role in process optimisation, troubleshooting, and system improvements across both unit operations and the wider platform Designing and overseeing scale-down models and experimental plans to support robust scaling strategies Driving improvements in process efficiency, cost of goods, and environmental performance Ensuring appropriate process documentation, validation, and technical standards are maintained Collaborating with internal teams and external partners to support technology development and delivery Managing and developing a team of engineers and scientists (3-5 direct reports) About You You will bring a strong combination of technical depth, practical experience, and leadership capability , with a clear track record in bioprocess scale-up and industrial biotechnology . Key requirements: Advanced qualification in bioprocess, biochemical, or chemical engineering Extensive industry experience in bioprocess development and scaling Proven track record working with bioreactors and associated unit operations from bench to pilot scale Strong understanding of upstream and/or downstream processing , including troubleshooting and optimisation Experience with CIP/SIP, contamination control, and operational challenges in bioprocess environments Demonstrated experience in leading teams and delivering complex technical programmes A practical, hands-on mindset , comfortable working directly with equipment and processes on-site A proactive, can-do attitude , with the ability to solve complex problems and adapt in a fast-paced environment Why Apply? This is an opportunity to play a central role in scaling a novel bioprocess technology , combining technical leadership with hands-on engineering and science . You will work in a collaborative, innovation-driven environment where your experience will directly influence the transition from R&D to real-world production. If you are a technically strong bioprocess expert who enjoys being close to the process, leading teams, and delivering scale-up in practice , this role offers a highly impactful next step. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

QC Officer - Analytical Chemistry SRG are delighted to be supporting a successful and growing organisation in the Central Belt of Scotland with the recruitment of a QC Analyst to join their analytical laboratory team. This is an excellent opportunity for someone with strong analytical chemistry experience gained in an industry-based GMP environment who is looking to take the next step in a hands-on quality control role. About the Opportunity Working as part of a busy QC laboratory, you will play a key role in supporting analytical testing activities across a range of materials and products. The position is well suited to a candidate who is confident using analytical instrumentation, particularly HPLC with Empower software, and who understands the importance of quality, compliance and high laboratory standards in a regulated environment. Key Responsibilities Perform a wide range of analytical chemistry testing within a GMP-regulated QC laboratory environment Operate analytical instrumentation with a particular focus on HPLC using Empower software Carry out testing using techniques such as HPLC, UV spectrophotometry and FTIR Complete compendial testing including osmolality, pH, appearance, conductivity, density and sub-visible particulate testing Support excipient testing, including compendial identification testing, as part of routine laboratory activities Undertake additional laboratory testing such as loss on drying and CCIT where required Review, record and trend analytical data in accordance with GMP requirements and internal procedures Assist with method transfer, validation, stability studies and laboratory investigations as needed Maintain excellent laboratory housekeeping standards, including stock management, reagent preparation, cleaning and waste disposal Ensure all documentation and laboratory activities are completed accurately and compliantly To succeed in this role, you will bring proven analytical chemistry experience from an industry setting and a practical, hands-on approach to laboratory work. Candidate Requirements Previous experience in an analytical chemistry or QC laboratory role within industry is essential Hands-on experience of HPLC with Empower software is strongly preferred Experience with some or all of the following techniques would be highly advantageous: HPLC, UV spectrophotometry, FTIR, compendial testing, excipient testing, loss on drying and CCIT A good understanding of GMP, laboratory compliance and quality documentation Practical awareness of day-to-day laboratory operations, including housekeeping, stock control, reagent preparation, waste disposal and cleaning A proactive and organised approach, with the ability to work effectively as part of a laboratory team This is a great opportunity to join a well-established and expanding organisation where you can further develop your analytical laboratory career in a supportive and quality-focused environment. If you have the relevant analytical chemistry experience and are looking for your next opportunity in a GMP laboratory environment, we would be pleased to hear from you. Please apply online or contact Emma for further information. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Shift QC Chemist West Yorkshire area - Commutable by car from Huddersfield, Halifax and surrounding areas Salary - 25,000 - 30,000 + shift allowance (depending on experience), may be more flexible for an ideal fit Permanent Hours - 2pm - 10pm (Monday - Friday) SRG is working with a manufacturer of industrial chemicals with products ranging from sealants to adhesives. Based in the West Yorkshire area, they have recently started hiring for a new member of their quality team. This opportunity would suit someone with an analytical chemistry background with some industrial experience or a graduate with an analytical specialism. You will join a close-knit team in a fast-paced manufacturing environment with opportunities to work on a wide range of processes within the organisation. Applications encouraged from graduates and people more experienced chemists Role Description Analytical testing of finished products, raw materials and finished products Quality checking under ISO 9001 (Quality), ISO 14001 (Environment), ISO 45001 (Health and Safety) policies Performing corrective action on manufactured products Preparing laboratory samples for analysis Interpreting data and providing detailed reports of findings Role Requirements Degree in chemistry, preferably with a focus on analytical or materials chemistry Numerate and problem solving skills Industrial experience in a QC role would be extremely beneficial Recent experience in a laboratory environment Ability to work within a team Computer literate Full right to work in the UK 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 Will on (phone number removed). If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit (url removed) to view our other vacancies. SRG 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. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Title: Site Chemist / Transfer Station Chemist Location: Hertfordshire Salary: 30,000 - 35,000 Term: Permanent SRG are working with a leading waste management and recycling company who have a long and very successful history of supporting the UK chemical industry. They are now looking for a site chemist to join the team. This is a hands-on role within the waste industry, you will be checking and testing incoming loads, processing hazardous and non-hazardous waste, ensuring segregation and storage of hazardous waste meets requirements, labelling waste and completing documents on all incoming and outgoing chemical materials. This role would suit candidates with 2+ years' experience as a chemist on a hazardous waste transfer station. Working Hours: 37.5 working hours per week, Monday to Friday, 24 days holiday + statutory bank holidays. Access to Rewards Gateway offering excellent discounts and cash back with many large retailers. Role/Description Receiving chemical waste on to site and ensure that per acceptance and acceptance of waste meets environmental requirements Ensuring paperwork for incoming waste is compliant and correctly completed Control waste streams through the plant/ transfer station to avoid delays and backlogs. Immediate testing of incoming waste to ensure conformity with paperwork using test strips Supervise, plan and prioritise the day to day activities of the Transfer Station Operatives Further laboratory testing as needed for further analysis using techniques including flash point testing, pH testing, visual checks, odour, viscosity. Working alongside site operatives to ensure that waste is processed, stored and transferred in a safe, compliant and timely manner Bulking/re-packing of waste to achieve maximum profitability Supporting other site chemists and operatives, ensuring all staff are working efficiently and collaboratively Requirements Minimum HND in Chemistry, or similar qualification with significant chemistry content 2+ years of recent experience in hazardous waste Any of the following qualifications or experience are considered advantageous: COTC, WAMITAB, NEBOSH, IOSH Willing to work outside in all weathers Full right to work in the UK - There is no sponsorship available for this role SRG 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. If you would like to apply for this position, please use the link provided. Alternatively, please email a copy of your CV For more information regarding this position or any others, please call Rhi on (phone number removed). If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit (url removed) to view our other vacancies. 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. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

SRG are working with an established CRO to help them find a new QA Officer. This is a great opportunity for someone looking for a new challenge in the QA field and is looking for a work/life balance as the company offer great benefits such as enhanced holidays and pension. The Role: QA monitoring of studies, on site facilities and where relevant suppliers and subcontractors to ensure compliance with Regulatory Standards Scheduling and conduct of audits - suppliers, subcontractors, facility, processes, critical phase, protocol, data and reports Review and provide QA approval of Standard Operating Procedures, Study Plans, protocols equipment calibration validation records and supporting documentation Maintain the Master Schedule Support in training on QA for other members of staff and departments Provide advice and guidance for any department on QA and regulatory queries Any other QA activities as required Requirements: A degree or equivalent experience in a life science discipline Previous experience in a QA/Quality focused role A sound knowledge/experience of Good Laboratory Practice (GLP) Experience of GLP (Apply online only) / OECD No 1 is essential Experience authoring and reviewing/auditing SOPs/study plans and reports Experience of equipment calibration would be beneficial Experience in quality auditing Working knowledge of databases, spreadsheets and other online quality and project management systems Strong communication skills and ability to work as part of a busy team If you meet the above requirements and are looking for a new role, then please apply online to find out more! Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Regulatory toxicologist needed for hybrid role in Manchester or Derbyshire Regulatory Toxicologist Hybrid working from Manchester or Derbyshire Salary - 40,000 - 60,000 depending on experience Permanent SRG is working with a leading global manufacturer of speciality chemicals. Recently a new vacancy has opened for a regulatory toxicologist with a background in human heath, environmental and ecotoxicology. This would be a great opportunity for someone with previous experience in the chemicals or pharmaceuticals sector to step into a global role and coordinate with regulatory agencies worldwide. Applications welcome from toxicologists and ecotoxicologists with a background in chemicals, pharmaceuticals, consultancy and similar industries. Role Description Interpreting test results and preparing submissions to regulatory agencies Presenting data and regulatory information both withing the company and externally Liaising with toxicologists and agencies globally to ensure product safety and compliance Conducting toxicological risk assessments Working closely with other areas of the business; such as R&D, procurement, supply chain, operations, legal and finance Requirements A strong academic background in toxicology, ecotoxicology or pharmacology; preferably at PhD level Recent industry experience working on toxicological risk assessments and regulatory dossiers An understanding of hazard communication and REACH regulations would be beneficial Experience working with IUCLID and CHESAR software Ability to work onsite in a hybrid set up in the Manchester or Derby area Full right to work in the UK. 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 Will on (phone number removed). If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit (url removed) to view our other vacancies. SRG 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. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Experienced Food/Flavours Technical Sales Manager looking to further develop their career required for a well-established chemical distributor in the West Midlands. Title: Technical Sales Manager - Food & Flavour Ingredients Location: Remote, occasional requirement on site in West Midlands office Salary: 45,000 - 65,000 (dependent upon experience) + benefits Term: Permanent SRG is exclusively partnering with a leading food ingredient distributor in the West Midlands, who offer a wide range of innovative raw materials to manufacturers and brands in the UK food, beverage and nutritional markets. With a big focus on in-house recipe development and manufacturing, collaboration and customer centricity, they have a well-known reputation for success in the market. Our client believes that delivering value starts with their people. By placing Employee Development at the heart of everything they do, they empower teams to grow, innovate and excel in their roles. This commitment not only enhances individual potential but also drives the exceptional service and solutions their customers deserve, ensuring they consistently exceed expectations and set new standards of excellence. Adopting a value-based sales approach, you will travel extensively across the UK, regularly meeting customers to continually build, develop and grow customer relationships across food and beverage manufacturers and brands. The role is suited to a business development hunter, with a target customer base of around 50 - 100. Benefits: Company car, 20% bonus (purely based on individual performance), company credit card and private healthcare amongst other benefits. Role / Description Identifying, contacting and developing new business using a variety of methods Promoting the company's range of innovative food ingredients Growing market presence across the UK food and beverage industries Growing existing customer relationships to ensure customer satisfaction and ultimately look to increase account spend Travelling approximately 1/3 of your time across the UK to visit customer sites Generating leads to identify new potential UK personal care customers Maintaining and updating the database to build a national customer pool Keeping abreast of product development & trends in the food and beverage industries. Requirements Direct experience in consultative and technical sales of food and beverage ingredients (experience with flavours specifically would be a benefit) Degree-level qualified (or equivalent) in Chemistry, Food Science or a closely related subject Experience with delivering technical presentations on food speciality ingredients Excellent communication and interpersonal skills Willing, and excited, to travel 1/3 of your time across the whole of the UK Full, clean UK driving licence A proactive approach and drive to deliver exceptional customer service. 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 Amy on (phone number removed). If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit (url removed) to view our other vacancies. SRG 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. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Job Title: Upstream Bioprocessing Technical Lead - 6 Month Contractor Vacancy type: 6 Month contract position - Potential to extend Salary: Great salary Location: Crumlin - Wales Are you a passionate bioprocess expert in Microbial Fermentation scale up seeking a new challenging contract? SRG are exclusively working with a global life science company who are looking for an Upstream Microbial Fermentation SME to support their scale up projects. If you have a proven track record in upstream process optimisation and scale-up, this could be the perfect role for you. The Upstream Bioprocess Technical Lead Role As the Upstream Bioprocess Technical Lead, you will be responsible for providing technical expertise throughout the early stages of design review, bioprocess optimisation, scale-up, and transfer strategy for Microbial Fermentation projects. You will support the technical inputs that drive successful design reviews and scale-ups, using your in-depth knowledge of bioreactor operations and maintenance, as well as mentoring junior staff. The Upstream Bioprocess Technical Lead will collaborate with cross-functional teams to ensure the successful delivery of the company's portfolio. This is an exciting opportunity to make a real impact and contribute to the company's growth and innovation. Key Responsibilities of the Upstream Bioprocess Technical Lead Provide subject matter expertise support for projects involving troubleshooting, scale-up, and downstream recovery of recombinant bacteria and yeasts Demonstrate a thorough understanding of biological processes, geometric factors, and mathematical models involved in scale-up Operate and maintain glass and stainless steel bioreactors at small (1L) and large scales (up to 250L) Drive optimization of existing processes to improve efficiency and reduce costs Proficiently use bioprocessing software and simulation tools to support operations Assist with the identification of technologies and equipment to improve and facilitate transfer and production programmes Maintain precise records of batch performance, reports, and analytics Qualifications and Experience To be successful in this role, you should have: A degree (ideally PhD) in microbiology, molecular biology, biotechnology, or chemical engineering Essential: Extensive recent experience in fermentation technologies for proteins, including antigens and enzymes using E.Coli and Yeast. Essential: Proven recent expertise in bioprocess optimization, scale-up, and transfer to regular production up to 100L (200L highly desirable) Essential: Bioreactor and Media Design for process scale up. Excellent understanding of microbiology, biotechnology, and biochemistry Proficiency in operating and maintaining glass and stainless steel bioreactors SRG are the UK number 1 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 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 Selby De Klerk at selby If you have a scientific background and this position is not relevant / suitable for you please feel free to get in touch or visit (url removed) to view our other vacancies. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Head of Operational Quality & Formulation North-East SRG is working with a leading sterile pharmaceutical company who has become a leader in specials with an ever-expanding footprint, supplying hard-to-source product to patients who need them. They are now looking for a Head of Operational Quality & Formulation to be based at their site in the North-East Near Newcastle and oversee the formulation and Safe & timely release of life saving products. The Role: As the Head of Operational Quality & Formulation you will be overseeing the Quality, Formulation & Production teams ensuring GMP & regulatory compliance of manufactured specials products, making sure they are released for the patients who need them. Key responsibilities: Act as the Quality Controller for the Manufacturers Specials Licence. Establish, review & monitor Key quality metrics and drive continuous improvement. Oversee new product introduction, assessing feasibility and guiding new formulations to production readiness. Design & oversee stability programs, pharmacovigilance systems and ensure compliance with GMP, GDP & MHRA. Lead investigations of deviations, complaints & root causes, implementing CAPAs. Required: A degree or higher qualification/ equivalent experience in relevant scientific field. GPhC registration is essential. Proven experience in a pharmaceutical formulation, QA or manufacturing with a strong knowledge of GMP, GDP & MHRA Specials guidance. Strong management & project coordination skills. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

QA Officer Derby 6-Month Contract SRG have a 6-month opportunity for a QA officer to join a leading provider of analytical services to the pharmaceutical industry. In this position you will be supporting the business through an exciting period of growth, assisting the Quality team with improvement projects and manging the QMS through a busy period. The Role: As a QA officer, you will: Maintain the QMS, ensuring GMP, GLP and data integrity compliance. Support QA activities, including QA review & release of data, Change controls, Document review & distribution and implementing CAPAs. Investigate OOS, deviations and complaints. Assist internal audits, maintaining audit readiness. Required: A degree or similar qualification in a relevant scientific field. Proven QA experience in a GMP / GLP Environment. Experience in supporting, preparing for or leading internal / External audits. Experience of investigation OOS, Deviations & Complaints Validation Experience would be highly advantageous. Attention to detail and the ability to manage multiple priorities. SRG are the UK number 1 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 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 have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit (url removed) to view our other vacancies Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Job Title: Regulatory Affairs Manager Location: Maidenhead Contract: 12 Months / Hybrid 3 days per week onsite Hours: 37.5 hours per week Rates: 80-90p/h Job Description SRG are seeking a regulatory affairs manager for a leading pharmaceutical company based in Maidenhead. For this role you will be working in collaboration with line manager and/or Area Product Lead, is responsible for implementation of registration strategy to ensure the regulatory approval of commercially successful pharma products in the Europe region. Is responsible for ensuring effective product maintenance and lifecycle management, in line with legal/regulatory requirements and regional business needs. May also support European regulatory strategy for assets in development. Duties and Responsibilities In consultation with line manager and/or Area Product Lead; Provides clear and constructive Europe Region (Area) regulatory input and intelligence to Area and Global Regulatory & Development Project Teams via the Area and/or Global Regulatory Lead (GRL) in accordance with Area & Commercial objectives. Ensure planned drug development activities comply with Area guidelines and if they do not provide a critical analysis of the risks and issues with a remediation proposal. Support global product development strategy(s); outlining options for Scientific Advice/PIP/IMPD, coordinating preparation of briefing packages and co-ordinating and leading agency meeting preparation. Prepare strategy recommendations to global regulatory and development teams in order to shape the global product strategy in line with Area regulatory and commercial objectives Define & implement Area filing strategy (including CP, MRP, DCP); identifying risks and proposing mitigation. Lead, plan, conduct and implement regulatory activities in support of lifecycle maintenance in Area. Identify compliance risks and remediation activities proactively. GRPT & ARPT representative ensuring regulatory requirements/interests of Area & Affiliate are represented at GRPT Supports co-ordination of the review of CMC, QRD, PSUR and labelling submissions and approval of product-related packaging as required to ensure regulatory compliance. Interface with EMA or Area Health Authority(s) for products within the Therapeutic Area on behalf of the Product Lead when required. Responsible for ensuring effective planning and tracking of activities, especially submissions and key correspondence. Ensures effective planning and tracking of activities via internal tools Supports co-ordination of the review of CMC, QRD, PSUR and labelling submissions and approval of product-related packaging as required to ensure regulatory compliance. People Establishes strong and effective relationships with affiliates, area and global regulatory teams as well as cross-functional teams thereby ensuring RA activities are in line with regional business priorities. Potential to mentor less experienced Area regulatory colleagues as required Processes Follows Global Regulatory policies and procedures. Ensures that new processes are developed and implemented in order to leverage the global infrastructure and maximise efficiency, ensures that new processes are aligned with global policies, but also meet regional regulations and needs. Responsible for the Notification of Regulatory activities and RIM system entry/data accuracy for allocated projects. Responsible for ensuring forecasts are developed and actuals managed in line with regional requirements and communicating these to Area TA Head, GRL and R&D finance for assigned projects. Experience and Qualifications Graduate in Life Sciences in a relevant area. Sound knowledge of both pharmaceutical regulations and guidelines and national regulations within Area. Pharmaceutical industry experience in European Regulatory strategy development and regulatory procedures, EU centralised procedure essential. Experience of EU strategy for development assets e.g. scientific advice, paediatric investigation plans preferred. Experience working effectively across cultures and in complex matrixed environment. Excellent organizational skills and solution driven leadership style Essential Skills and Abilities Ability to prioritise and manage workload including managing multiple projects. Ability to work effectively and collaboratively across the organisation. Experienced in working effectively across cultures and in complex matrix environment. Good interpersonal and negotiation skills and the ability to influence others. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Title: Business Development Executive - Graduate Location: Cambridgeshire Salary: 27,000 - 30,000 per annum + benefits Term: Permanent SRG is working with a well-respected, global company who supply a huge range of speciality chemicals and pharmaceutical intermediates to a wide range of industries including pharmaceutical, biotechnology and academic institutions. With a genuine drive for innovation, they are now looking for a Chemistry graduate to join them as a Business Development Executive and drive sales of their products to facilitate cutting-edge research. Adopting a value-based sales approach, you will travel extensively across the UK and Europe, meeting customers to continually develop and grow customer relationships. This would be an amazing opportunity for a Chemistry graduate looking to utilise their degree outside the lab and pivot into a customer-facing, commercial role. Benefits: Multinational chemicals supplier with a strong focus on innovation and a small, dynamic commercial team where you can really make a difference. Lots of opportunities for international travel, generous annual bonus scheme (up to 10%), relocation package, Christmas shutdown, flexible working, annual salary reviews and free on-site parking. Role / Description Building existing customer relationships to ensure customer satisfaction and ultimately look to increase account spend Travelling approximately 50% of your time across the UK and Europe to visit customer sites Generating leads to identify new potential customers in your region Using a variety of methods to target the new potential UK & European customers Spending approx. 80% of your time managing existing accounts and 20% new business development Maintaining and updating the database to build a global customer pool Keeping abreast of product development & trends in specific industry and project areas Requirements Degree-level qualified (or equivalent) in Chemistry, Biochemistry, Natural Sciences, Forensic Science or a closely related subject Full, clean UK driving licence. Willing, able and excited to travel across the UK and Europe A proactive approach and drive to deliver exceptional customer service Excellent communication and interpersonal skills Fluent in English, both written and verbal - fluency in other European languages would be highly desirable but not essential 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 Amy on (phone number removed). If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit (url removed) to view our other vacancies. SRG 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. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Title: Procurement Manager Location: Brighton, East Sussex Salary: 35,000 - 45,000 (dependent on experience) Term: Permanent SRG are working with a well-respected, global company who specialise in the creation of speciality chemicals for several different markets. Currently undergoing an exciting growth journey, they are now looking for a Procurement Manager to lead a small purchasing team and improve procurement strategies. This is an exciting opportunity to own and lead various procurement optimisation projects within the business! Benefits: An opportunity to join a speciality chemicals company at an exciting time for the company. Discretionary bonus scheme, Xmas shutdown period, company pension amongst others. 37.5 hours per week, with an early finish on a Friday. Role / Description Leading a small purchasing team internally Carrying out training, development and performance reviews of the team Understanding the current purchasing and stock management processes Identifying areas for improvement to increase efficiencies Using the internal ERP, and utilising the system to its full potential Managing the full procurement process for a range of speciality chemicals Negotiating contracts with suppliers Creating and maintaining relationships with key stakeholders within the suppliers Liaising with multiple departments in the business including Logistics and Sales. Requirements Recent CIPS qualification Proven recent experience as a Procurement Manager, ideally in a technical manufacturing environment but this is not essential Able to be on site near Brighton 5 days a week A proactive approach and drive to deliver exceptional service Willing and excited to implement positive change and process improvements Excellent communication and interpersonal skills. 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 Amy on (phone number removed). If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit (url removed) to view our other vacancies. SRG 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. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Job Title: Scientist 2 - Stability Contract: 9 months Location: Deeside Pay: 134 p/d SRG are partnered with a global medical products and technologies company. Our client is focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. We are seeking a Scientist to join their Deeside team. Duties and Responsibilities : To be responsible for maintaining compliance within the Stability Suites, Stability Laboratory and associated areas to support the determination of product shelf-life and product labelling. The focus of this role will be on Non-Conformance (NC), Corrective Action/Preventative Action (CAPA), and Out of Specification (OOS) investigations. Maintain compliance to ISO13485 & ISO9001 standards in accordance with GLP/GMP compliant procedures. Support maintenance, calibration, documentation and updating quality records for Stability equipment. Support any on-site maintenance, service and calibration activities performed by external vendors. Act as Subject Manner Expert (SME) and write Quality documentation such as Change Control Requests (CCRs), Non-Conformances (NCs), Corrective Action/Preventative Action (CAPAs) and Laboratory Out of Specifications (OOS'), ensuring accurate and thorough investigations are complete within required timeframes, incorporating problem-solving and troubleshooting for future improvements. Monitor compliance KPIs within the Stability department and proactively update the management team with trends and improvement initiatives. Ensure the Stability department is audit ready at all times. Supports and provides information for internal and external audits where required in a timely manner. Conduct training sessions on compliance for the Stability department. Support global testing laboratories with compliance requirements as needed. Actively execute improvement ideas (Lean/6S) for the Stability laboratories and suites. Actively supporting with the implementation of the LIMs system. Support bringing in new equipment when required, through planning and execution of Installation, Operational and Performance Qualification activities, liaising with vendors as per company procedures. Ensure the Stability lab, Stability Suites and storerooms are maintained as a safe and compliant working environment, raising near misses where needed. Supporting any other tasks required by the Laboratory Manager/Team Leaders. Skills & Experience: Pref erably 2-3 years' experience working in Medical Device/Pharmaceutical Industry within an R &D/product development or quality department role. Experience in quality and compliance Ability to react and respond positively to changes in priority and workload. Competent in following and adhering to pre-determined stability study protocols, SOPs, OCIs and TDs. Basic experience in the utilisation of computerised systems to manage data and information. Good working knowledge of Microsoft Office - specifically Word and Excel. Understanding of compliance with FDA and European Regulations (ICH), Quality Systems and GMP Guidelines. Proactive and positive mindset with an attitude that is open to change to embrace new ways of working and improvements. Proven experience leading thorough Quality investigations and implementing effective preventative and corrective measures. Strong communication skills to effectively collaborate cross-functionally. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.