SRG

Customer Advisor Edinburgh, Part Time (17.5 hours/week - overtime available if you wish to do more). This is an exciting opportunity to join a large Customer Engagement Centre (CEC) as a Customer Advisor , based at our client's Edinburgh office on a part-time basis. You'll keep customers and stakeholders informed about works and service interruptions, working closely with your team to deliver the highest quality of service at all times. What you'll do You'll build strong relationships across the team to make sure our customers are always in the loop. Day to day, you'll: Manage inbound customer contacts across a wide range of subjects Provide customers with information and guidance, logged accurately on our internal systems Work reactively and precisely during operational incidents Work proactively, collaborating with stakeholders to gather up-to-date information What you'll bring Your communication skills, attention to detail and ability to prioritise will be key. You'll have strong verbal and written information-management skills, and the confidence to learn a range of systems and technology quickly. You'll use your organisational skills to manage your own workload while working as part of a team to ensure every task is carried out to the highest standard. Your adaptability will let you switch to reactive work when it's needed - meeting customer needs and supporting your colleagues. Previous experience in a fast-paced environment is advantageous. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Operations Manager Permanent Glasgow £44,497 - £60,497 About the Role We are seeking an experienced Operations Manager to lead operational delivery across a regulated manufacturing environment, ensuring facilities, people, systems, and processes are set up to support safe, efficient, and compliant operations. Reporting to the Head of Operations, this is a key leadership role with responsibility for operational activities across the site, including production support, warehousing, facilities, and operational readiness. The successful candidate will play a critical role in maintaining operational excellence while helping shape future site capability through strategic planning, continuous improvement, and capital investment initiatives. This is a highly visible role that requires someone who is proactive, solutions-focused, and able to deliver results while working effectively across multiple functions and stakeholders. What You'll Be Responsible For: Operational Leadership Lead day-to-day operational activities across the facility, ensuring safe, compliant, and efficient operations Manage and develop a team of operational staff, setting priorities, objectives, and performance expectations Ensure facilities, equipment, materials, and resources are available to support project and production delivery Drive a culture of accountability, continuous improvement, and operational excellence Health, Safety & Compliance Take a leading role in maintaining site compliance with Health & Safety, quality, and regulatory requirements Ensure safe systems of work are developed, implemented, and continuously improved Promote a strong compliance culture within a highly regulated environment Support site readiness for audits and inspections as required Facilities & Asset Management Oversee the effective operation and maintenance of site facilities and equipment Support operational planning to maximise facility utilisation and asset availability Contribute to future CAPEX planning and investment decisions Ensure equipment testing, maintenance, and accreditation activities remain compliant and up to date Continuous Improvement Drive initiatives to improve operational performance, efficiency, and cost effectiveness Improve systems, processes, documentation, housekeeping, and resource management Identify opportunities to streamline operations and enhance service delivery Ensure lessons learned are captured and applied to future activities Stakeholder Management Work closely with project teams, central functions, technical teams, and external suppliers Build strong relationships across the organisation to resolve challenges and deliver outcomes Influence stakeholders and navigate complex environments to achieve operational objectives Support the delivery of projects through effective planning and cross-functional collaboration About You: You are an experienced operations leader who enjoys taking ownership, solving problems, and driving delivery within regulated environments. You'll bring: Proven operational management experience within a regulated industry Experience managing teams and operational activities in manufacturing or production environments Strong understanding of Health & Safety, quality, and compliance requirements Experience managing operational budgets, resources, and facility requirements Excellent stakeholder management and influencing skills A proactive, "can-do" approach with the confidence to make decisions and drive outcomes Desirable (but not essential): Experience within pharmaceutical, food manufacturing, GMP, or similarly regulated environments NEBOSH or equivalent Health & Safety qualification Experience managing CAPEX projects or facility improvements Exposure to Lean, 5S, or continuous improvement methodologies This role would suit someone who has operated in highly regulated sectors such as pharmaceuticals, food production, nuclear, advanced manufacturing, or similar environments where quality, compliance, and operational discipline are critical. Why Join Us? Opportunity to lead operational delivery at a strategically important manufacturing facility Influence site operations, future improvements, and long-term capability plans Work in a collaborative environment with strong cross-functional support Flexible approach to working hours Competitive salary (£44,497 - £60,497) Location & Working Pattern Based primarily on-site in Glasgow High on-site presence expected, with occasional home working flexibility 37 hours per week Monday-Thursday: 08:30 - 17:00, Friday: 08:30 - 16:00 Flexible working arrangements available around core business needs The Opportunity This is an excellent opportunity for an experienced operations professional to step into a highly influential role where you will help shape the future of site operations while leading teams, improving processes, and ensuring operational excellence within a regulated manufacturing environment. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Chief Technologist - Synthetic Therapeutics (Peptides & Oligonucleotides) FTC until March 2028 Glasgow £64,394 - £84,394 + £491 Monthly Car Allowance About the Role: 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. 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. 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. What You'll Be Responsible For: Technical Leadership & Domain Expertise Act as the recognised technical authority in peptide and/or oligonucleotide chemistry Provide expert guidance across customer programmes, strategic initiatives, and capability development activities Support scientists and technical teams with specialist knowledge and technical problem-solving Ensure emerging scientific developments are translated into practical and commercially relevant applications Technology Strategy & Capability Development Shape future capability in synthetic therapeutics, identifying technology gaps, market opportunities, and investment priorities Inform long-term technology strategy and help develop deliverable plans aligned to business objectives Anticipate new developments within peptide and oligonucleotide technologies and assess their commercial relevance Support the translation of advanced chemistry into scalable and commercially viable capabilities Market Engagement & Business Development Work closely with commercial and business development teams to identify and develop new opportunities Engage directly with customers, industry partners, investors, and stakeholders to understand market needs Support proposal development, bid activities, and customer-facing technical discussions Contribute to technical and commercial assessments of new opportunities and partnerships Capability Building & Mentorship Mentor scientists and technical teams, helping build expertise across the organisation Promote knowledge sharing and capability development across internal and external networks Support the development of future scientific leaders and specialists Foster a culture of innovation and continuous learning About You 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. You'll bring: Significant industrial experience within peptides and/or oligonucleotides Strong expertise in areas such as: Peptide synthesis, modification, and conjugation Complex or constrained peptides Peptide-drug conjugates Oligonucleotide chemistry Oligo conjugates Modified backbones and delivery-enabled constructs A proven track record of translating scientific knowledge into commercially relevant capabilities and opportunities Strong understanding of market dynamics, customer needs, and future industry trends Excellent stakeholder management, networking, and influencing skills Experience operating at a strategic level within pharmaceutical, biotech, CDMO, or advanced therapeutics environments Desirable (but not essential): PhD or equivalent research background in peptide, oligonucleotide, or synthetic chemistry disciplines Experience contributing to technology strategy and capability development Existing industry network within peptides, oligonucleotides, or related therapeutic modalities Knowledge of broader synthetic therapeutic approaches and emerging modalities Membership of relevant professional bodies and active engagement with the wider scientific community Importantly, this role is not focused on routine GMP manufacturing operations. The emphasis is on strategic technical leadership, market engagement, capability development, and helping define where future investment and technological growth should occur. Why Join Us? Influence the future direction of peptide and oligonucleotide technology development Shape capability in a rapidly growing area of advanced therapeutics Work with leading scientific, commercial, and industry stakeholders Play a key role in identifying and developing future market opportunities High-profile position with significant external engagement Competitive package including salary up to £84,394 plus monthly car allowance Location & Working Pattern FTC until March 2028 (potential to extend) Hybrid working available Regular engagement with customers, partners, and external stakeholders Travel to industry events, customer meetings, and scientific forums as required Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

SRG are looking for an experienced Formulation Scientist to join a team within a successful organisation who are known across the world. This is an excellent opportunity to join a company at an exciting time for the business. This is a technical position, with your role primarily involved in pre-formulation, formulation and process development activities of sterile dosage forms in a laboratory setting. Main Responsibilities: Completing all aspects of the formulation design and development process related to sterile dosage forms Working with the formulation of small molecules and biologics Use of analytical and lyophilisation equipment Working to and maintaining set quality standards and GMP guidelines Updating procedures Working to set deadlines Liaising with customers Qualifications and Experience required: Must have a degree or equivalent in a relevant scientific discipline along with extensive industry experience Must have experience in pharmaceutical product formulation and process development Hands on experience in pre-formulation work including measuring physical properties (e.g. pKa, partition coefficients, pH-solubility profiles, etc.) Hands on experience in wet chemistry and characterisation methods. Experience in the formulation of both small molecules and biologics Knowledge and experience of working to GMP guidelines Experience of pre-formulation and lyophilisation cycle development would be beneficial Excellent communication skills Driven and passionate individual who can move projects forward and work within set timeframes Benefits: The client offer an comprehensive benefits package with an excellent pension, health insurance and additional lifestyle benefits among others. This is an excellent opportunity for the right individual to make the next step in their career within a highly successful company. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Exciting Opportunity: Medical Device Regulatory Administrator Are you a highly organised administrator with excellent attention to detail and a passion for working in a regulated environment? This growing healthcare organisation is seeking a Regulatory & Quality Administrator to join its Clinical and Regulatory Affairs team, providing vital support across product safety, quality, and regulatory processes. This is a fantastic opportunity for someone with strong administrative skills who wants to build experience within a regulated healthcare environment. You'll gain exposure to regulatory processes, quality systems, document control, and cross-functional project coordination while working within a supportive and collaborative team. Job Title: Medical Device Regulatory Administrator Vacancy Type: Permanent (Full right to work in the UK Required Location: Gosmore Salary: DOE Hours: Monday-Friday, 9am-5pm (Hybrid role after training) Extra: Candidates would need to be able to commute to site without the use of public transport due to office location (drive/Cycle) About the Organisation This organisation develops and supplies healthcare products to customers across the UK and international markets. Operating within a highly regulated environment, the business places a strong emphasis on product quality, patient safety, regulatory compliance, and continuous improvement. The Clinical and Regulatory Affairs function plays a key role in supporting product lifecycle management, maintaining essential documentation, monitoring product feedback, and ensuring compliance with relevant standards and regulations. The Role of the Regulatory & Quality Administrator This is an excellent opportunity for an organised and detail-oriented administrator to support a busy regulatory team. You will be responsible for coordinating documentation, maintaining databases, preparing reports, and ensuring important product information is accurately recorded and managed. Key responsibilities include: Managing and recording customer feedback relating to product quality and safety matters Coordinating communication between internal departments, customers, distributors, and external partners Maintaining document control systems, including SOPs, work instructions, and other controlled documents Supporting the preparation of reports and data summaries used for monitoring product performance and quality trends Reviewing regulatory standards, specifications, and guidelines, and assisting with gap analysis activities Supporting artwork review and approval processes Conducting document checks prior to manufacturing activities to ensure compliance requirements are met Maintaining databases and ensuring records remain accurate, complete, and up to date The Ideal Candidate for the Regulatory & Quality Administrator Role To succeed in this role, you will need: Previous experience in an administrative, document control, compliance, quality, or regulatory support role Strong organisational skills with the ability to manage multiple priorities simultaneously Excellent verbal and written communication skills High levels of accuracy and attention to detail Confidence using Microsoft Office applications, particularly Word and Excel Experience working with databases and electronic record systems The ability to work independently while collaborating effectively with multiple teams Experience in Pharmacovigilance, Medical Devices, Regulatory Affairs, or a scientific discipline is advantageous, but not essential. The organisation is primarily looking for a strong administrator who can manage documentation, coordinate information effectively, and work accurately within a regulated environment. SRG are the UK's number one recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors. As scientists ourselves, our specialist sector knowledge and 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 this position isn't quite right 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.

Shift Analytical Chemist required on a permanent basis, based in North Cheshire. Recent and proven industrial experience using GC, HPLC and wet chemistry is required. Manual Driving license is essential. Title: Shift Analytical Chemist Location: North Cheshire Salary: 32,084 + Shift Allowance ( 10,900) Term: Permanent SRG are working with a multinational chemicals manufacturer who produce a highly varied range of products. Based in North Cheshire, their central Analytical Team is now looking to hire a Shift Analytical Chemist on a permanent basis. This role will see the successful candidate support with testing of samples from across the site, from multiple departments and customers. This would be an excellent opportunity for Chemists with good analytical skills and experience to join a company with a fantastic reputation. Recent and proven industrial experience with wet chemistry, GC and/or HPLC is essential. Benefits: You would be joining a team in a respected and successful company, with an outstanding reputation. Generous salary and shift allowance, 26 days holiday as standard plus 8 statutory days. Shift Pattern: 4 on (2 days: 6.00am-6.00pm; 2 nights: 6.00pm-6.00am), 6 days off. 7 shift rotations, followed by a 20-day break. Role / Description Collecting liquid and gaseous samples from various locations across site Analysing collected samples and samples sent from internal teams or external customers, including organic, inorganic and environmental samples Using instrumentation including GC, HPLC, ICP, MS and Atomic Absorption Spectroscopy to conduct analysis, as well as density, colour and wet chemistry tests. Validating and reporting on analytical results, identifying anomalies and taking appropriate action. Responding to unscheduled analytical requirements and site emergencies, as necessary Basic instrument maintenance and calibration Using prescribed analytical procedures and maintaining records to ensure required standards are met Conducting environmental measurements for any emergency response situations on or off site Requirements HND or BSc degree in Chemistry, Analytical Science, Forensic Science or similar preferred Good practical analytical skills - recent hands-on industrial experience of GC (Gas Chromatography) and HPLC in particular, ICP or MS is preferrable. Valid driving licence essential Excellent time management skills, able to adapt according to priorities and think clearly under pressure A strong team player, able to collaborate and support colleagues as needed If you would like to apply for this position, please use the link provided. Alternatively, please email a copy of your CV to For more information regarding this position or any others, please call Chris on (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.

Development Chemist require based in West Yorkshire on a permanent basis. Requiring a degree in Chemistry (or similar), with recent and extensive experience in formulating products such as lubricants, oils, greases, coatings (other aligned industries considered). Title: Development Chemist Location: West Yorkshire Salary: 32,000 - 40,000 per annum (dependent on experience) Term: Permanent SRG are working with a global, market leading specialist developer and manufacturer of a range of industrial chemicals including fluids, lubricants, oils and other speciality products. They are now seeking a Development Chemist to join their R&D team in West Yorkshire to support in developing both new and existing products within the portfolio. This is a hands-on development position within an established R&D team. The role will also involve testing products, supporting in analysis and scale-up activities and supporting in process improvements. Benefits: You will join a highly successful company, with an opportunity to make a great impact. 35 hours - Monday to Friday, with flexibility on start and finish times. 25 days holiday and plus bank holidays. Potential for an annual bonus and company pension scheme. Role/Description Support in the formulation and development of both new and existing products Testing new formulations Prepare technical reports, documentation and procurement records for new products Support with analysis and developing new analytical methods Assist in scale-up activities of new and existing formulations Support other departments as necessary Requirements Degree-level qualification (BSc or higher) in Chemistry or a closely related discipline Extensive practical laboratory experience in formulation or development chemistry within a materials, chemicals or speciality products environment (lubricants, oils, greases, coatings etc.) Sound understanding of laboratory HSE, COSHH and risk assessment principles 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 to For more information regarding this position or any others, please call Chris 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.

Title: QC Technician Location: West Yorkshire Salary: £27000 DOE Term: Permanent SRG is working with an independent contract manufacturer of personal care and skincare products, based in West Yorkshire. They are now looking for a Production and Quality Technician to join the team.This is a hands-on opportunity to sit at the heart of operations, balancing quality, production planning, materials, and stock control to help keep everything running smoothly. You will be responsible for carrying out wet chemistry and bench chemistry testing, supporting product quality checks, and ensuring finished goods meet the required customer and company specifications.Working closely with the QC Manager and wider production team, you will help maintain high standards across the manufacturing process, support documentation and batch record accuracy, and play a key role in ensuring products are made, checked, and released to the right standard. Working Hours: Monday to Friday 7:30am to 4:15pm (Mon-Fri), 30 minute lunch break Role / Description Carry out quality checks across raw materials, production, and finished goods to ensure standards are met Support production scheduling, helping align output with customer demand and forecasts Monitor stock levels and coordinate ordering to keep materials flowing without disruption Track production progress, highlighting risks or delays before they impact delivery Investigate quality issues and support corrective actions to prevent reoccurrence Oversee goods in/out processes, ensuring accuracy, traceability, and efficient storage Contribute to process improvements across planning, quality, and stock control Requirements Experience in quality, production planning, manufacturing, or stock control Strong organisation skills with a high level of attention to detail Willing and able to work stood up in a Fast-paced manufacturing environment on the production / factory floor in a hands of role Strong communication skills and can relay information accurately 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.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 .If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit to view our other vacancies. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Technical Service Chemist required in Cheshire East, on a permanent basis. Requiring a degree or relevant qualification in Chemistry, Materials Science (or similar) and recent, proven industrial experience within laboratory testing, technical services, quality control or R&D. Candidates with coatings, adhesives, paper, film or related manufacturing experience are encouraged to apply. Title: Technical Service Chemist Location: Cheshire East Salary: 36,000 - 40,000 (dependent on experience) Term: Permanent SRG are working with a market-leading materials manufacturer specialising in the development and production of advanced coated products for a range of industrial applications. They are now seeking a Technical Service Chemist to join their technical team in Cheshire East on a permanent basis. This role is designed for someone with strong laboratory and technical support experience and will involve coordinating technical service activities, laboratory testing and customer-focused technical support projects. This role will suit candidates with recent and proven industrial experience within technical service, quality control, laboratory testing or R&D and who are comfortable managing multiple priorities in a fast-paced manufacturing environment. Experience within coatings, adhesives, paper or film manufacturing is desirable but not essential. Benefits: Joining a highly successful, employee-owned business that values employees. Flexible working hours, annual bonus, healthcare cash plan and strong pension. Role/Description Prioritise and coordinate technical service requests to ensure timely and high-quality delivery. Support customer requirements and short-term product development activities. Conduct laboratory testing safely, accurately and in line with agreed procedures and standards. Ensure testing data is recorded, analysed and communicated effectively. Coordinate and support production and customer trials when required. Work closely with technical teams and wider stakeholders to align priorities and resources. Support investigations into quality issues, customer enquiries and product performance concerns. Assist with technical reports and recommendations based on laboratory findings. Maintain a safe working environment and ensure all H&S, compliance and training standards are met. Contribute to continuous improvement initiatives across technical and laboratory activities. Requirements Degree, HNC, HND or equivalent qualification in Chemistry, Materials Science or a related discipline. Proven industrial experience in laboratory testing, technical service, quality control or R&D. Strong analytical and problem-solving skills with the ability to interpret data effectively. Ability to manage and prioritise multiple workstreams in a fast-paced environment. Strong communication skills and ability to work collaboratively across teams and with customers. Experience within coatings, adhesives, paper, film or a related manufacturing environment is desirable. Knowledge of statistics, data analysis or design of experiments would be advantageous. Project management experience is beneficial 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 to For more information regarding this position or any others, please call Chris 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.

Title: Head Of science Location: UK Wide, Hybrid / Remote Salary: Competitive Term: Permanent SRG is supporting an award-winning climate technology organisation that is driving innovation in carbon removal at a global scale. Following significant growth and industry recognition, they are now looking for an experienced scientific leader to shape strategy, guide a high-performing team, and help deliver credible, scalable solutions that contribute directly to tackling climate change. You'll join the senior leadership team and take ownership of the scientific direction of the business, ensuring robust science underpins both operational delivery and future growth. Key Responsibilities Lead and develop a team of senior scientists, fostering a collaborative and high-performing culture. Define and deliver the scientific roadmap in line with business objectives and product strategy. Drive the evolution of carbon removal quantification methods and scientific best practice. Translate complex scientific research into practical protocols that support large-scale project delivery. Partner with internal teams, external stakeholders and project developers to ensure successful implementation of scientific programmes. Represent the science function at a senior level, influencing business decisions and industry standards. Manage departmental budgets, scientific investment and technical input for funding, investor and due diligence activities. Requirements Advanced expertise in a relevant scientific discipline such as geochemistry, soil science, geology, hydrology, plant science, soil science, ERW or CDR or similar preferred. Proven people leadership experience, with a track record of delivering commercial objectives while maintaining scientific excellence. Excellent communication skills, able to influence stakeholders and translate complex science into clear business outcomes. 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. 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.

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. Title: New Product Development (NPD) Chemist Location: Cheshire East Salary: 40,000 - 46,000 (dependent on experience) Term: Permanent 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. Benefits: Joining a highly successful, employee-owned business that values employees. Flexible working hours, annual bonus, healthcare cash plan and strong pension. Role/Description Manage, plan and execute product and process development projects from ideation through to commercial launch. Deliver sales growth through the development of new and improved products. Assess new product ideas and opportunities, including costs, benefits, resourcing requirements and timescales. Plan and prioritise development activities to ensure projects are delivered on time. Report project progress and provide clear technical recommendations and go/no-go proposals. Coordinate and support laboratory work, production trials and scale-up activities. Manage NPD projects through to full production implementation. Identify and engage with suppliers, consultants, test houses and academic partners to support development activities. Share technical learning and project outcomes across the wider business. Provide technical support relating to specifications, material changes, customer complaints and operational troubleshooting. Requirements Degree in Chemistry, Materials Science or a related scientific discipline. Proven industrial experience within product development, R&D or process development. Experience managing projects from concept through to commercial launch. Strong analytical and problem-solving skills with the ability to assess opportunities technically and commercially. Excellent communication skills and ability to work effectively with customers, suppliers and internal stakeholders. Experience within coatings, adhesives, paper, film or a related materials manufacturing environment is desirable. Formulation experience is highly desirable. 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 to For more information regarding this position or any others, please call Chris 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.

Recruitment Administrator (Temporary Assignment - 6 Months) Sedgefield On-site £13.45 per hour About the Role We are seeking a Recruitment Administrator to join a busy recruitment team on a 6-month temporary assignment, providing essential support across a high-volume recruitment function. This is a fast-paced, process-driven role that would suit someone who enjoys working with people, thrives in a busy environment, and takes pride in delivering excellent customer service. You will play a key role in supporting candidates, hiring managers, and recruitment partners throughout the recruitment process, ensuring a professional and efficient experience for all stakeholders. What You'll Be Responsible For Recruitment Administration Manage recruitment-related enquiries and act as a first point of contact for candidates and hiring managers Coordinate interviews and support recruitment activities across multiple vacancies Maintain accurate recruitment records and candidate information Support onboarding and pre-employment screening processes Systems & Data Management Work extensively with Microsoft Office applications, including: Outlook Excel Microsoft Lists Coordinate and maintain job advertisements across the intranet, careers website, and external online platforms Raise purchase orders using Microsoft D365 Maintain trackers, records, and recruitment reports Ensure all data is accurate, up-to-date, and confidential Customer Service & Stakeholder Support Deliver a responsive and customer-focused service to candidates, managers, and external partners Build positive relationships across the business Keep stakeholders informed throughout the recruitment process Support the successful delivery of recruitment activities within a fast-paced HR environment. Administrative Support Process recruitment documentation accurately and efficiently Support invoice processing and purchase order administration Assist with reporting and recruitment metrics where required About You You are organised, resilient, and enjoy working in a fast-paced environment where priorities can change quickly. You'll bring: Experience working in a busy office or administrative environment Strong Microsoft Office skills, particularly Outlook, Teams and Excel Excellent attention to detail and data accuracy Strong communication and customer service skills Confidence using business systems and learning new processes quickly Desirable (but not essential): Experience of Microsoft D365 or similar systems Experience of Microsoft Lists Experience within recruitment, HR, or administration Experience processing purchase orders or invoices Most importantly, we're looking for someone who: Enjoys helping people Remains calm under pressure Is positive, proactive, and adaptable Takes pride in delivering a great service Why Join Us? Opportunity to build your recruitment experience in a fast-paced, collaborative team environment. Varied role with exposure to different stakeholders and processes Supportive and collaborative environment Immediate opportunity to make an impact Competitive hourly rate (£13.45 per hour) Location & Working Pattern Based in Sedgefield, based onsite 37 hours per week Monday-Thursday: 08:30 - 17:00, Friday: 08:30 - 16:30 The Opportunity This is an excellent opportunity for a highly organised administrator who enjoys working with people and delivering excellent customer service. If you're looking for a busy, varied role where you can make an immediate contribution, we'd love to hear from you. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Recruitment Administrator (Temporary Assignment - 6 Months) Sedgefield On-site 13.45 per hour About the Role We are seeking a Recruitment Administrator to join a busy recruitment team on a 6-month temporary assignment, providing essential support across a high-volume recruitment function. This is a fast-paced, process-driven role that would suit someone who enjoys working with people, thrives in a busy environment, and takes pride in delivering excellent customer service. You will play a key role in supporting candidates, hiring managers, and recruitment partners throughout the recruitment process, ensuring a professional and efficient experience for all stakeholders. What You'll Be Responsible For Recruitment Administration Manage recruitment-related enquiries and act as a first point of contact for candidates and hiring managers Coordinate interviews and support recruitment activities across multiple vacancies Maintain accurate recruitment records and candidate information Support onboarding and pre-employment screening processes Systems & Data Management Work extensively with Microsoft Office applications, including: Outlook Excel Microsoft Lists Coordinate and maintain job advertisements across the intranet, careers website, and external online platforms Raise purchase orders using Microsoft D365 Maintain trackers, records, and recruitment reports Ensure all data is accurate, up-to-date, and confidential Customer Service & Stakeholder Support Deliver a responsive and customer-focused service to candidates, managers, and external partners Build positive relationships across the business Keep stakeholders informed throughout the recruitment process Support the successful delivery of recruitment activities within a fast-paced HR environment. Administrative Support Process recruitment documentation accurately and efficiently Support invoice processing and purchase order administration Assist with reporting and recruitment metrics where required About You You are organised, resilient, and enjoy working in a fast-paced environment where priorities can change quickly. You'll bring: Experience working in a busy office or administrative environment Strong Microsoft Office skills, particularly Outlook, Teams and Excel Excellent attention to detail and data accuracy Strong communication and customer service skills Confidence using business systems and learning new processes quickly Desirable (but not essential): Experience of Microsoft D365 or similar systems Experience of Microsoft Lists Experience within recruitment, HR, or administration Experience processing purchase orders or invoices Most importantly, we're looking for someone who: Enjoys helping people Remains calm under pressure Is positive, proactive, and adaptable Takes pride in delivering a great service Why Join Us? Opportunity to build your recruitment experience in a fast-paced, collaborative team environment. Varied role with exposure to different stakeholders and processes Supportive and collaborative environment Immediate opportunity to make an impact Competitive hourly rate ( 13.45 per hour) Location & Working Pattern Based in Sedgefield, based onsite 37 hours per week Monday-Thursday: 08:30 - 17:00, Friday: 08:30 - 16:30 The Opportunity This is an excellent opportunity for a highly organised administrator who enjoys working with people and delivering excellent customer service. If you're looking for a busy, varied role where you can make an immediate contribution, we'd love to hear from you. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Job title: Plant Manager Location: Lancashire Job Type: Permanent Salary: Competitive + Benefits SRG are currently recruiting for an experienced Plant Manager on a permanent basis, based in Lancashire. This is a key leadership position, responsible for driving operational excellence and leading continuous improvement initiatives across the site. The successful candidate will be a proven manufacturing leader with experience managing plant operations within a chemical, process, or manufacturing environment. You will play a critical role in delivering business objectives through effective people management, operational efficiency, and change management programmes. Key Responsibilities (including but not limited to): Provide overall leadership and direction for site operations, ensuring safe, efficient and compliant plant performance Manage and develop multidisciplinary teams, creating a high-performance and accountable culture Lead and promote a proactive Health, Safety and Environmental (HSE) culture, ensuring compliance with all regulatory and company requirements Drive continuous improvement initiatives focused on productivity, quality, cost reduction and operational performance Develop and implement change management strategies to support business growth Monitor and improve key performance indicators (KPIs) relating to safety, production, quality and maintenance Ensure effective resource planning to meet customer demand and operational targets Lead investigations into incidents, identifying root causes and implementing corrective actions. Criteria: Previous experience in a similar role with leadership role within chemical/ COMAH manufacturing or a related process industry Demonstrable experience leading teams in a manufacturing environment Strong knowledge of HSE legislation, compliance and best practices Experience leading and embedding organisational and operational change Excellent leadership, communication and stakeholder management skills Strong commercial awareness and problem-solving abilities. If interested, please apply or contact Julia for more information: / (phone number removed) Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Content Officer (12-Month Fixed-Term Contract - Maternity Cover) Hybrid Working North East (primarily Sedgefield) 36,044 - 46,044 About the Role CPI is seeking a talented Content Officer to join our Communications, Content & Channels team on a 12-month maternity cover contract. This is an exciting opportunity for an experienced writer, editor, and communicator who can take complex scientific, technical, and innovation-focused topics and transform them into clear, engaging content for a range of audiences. The successful candidate will act as a key editorial voice within the team, helping to shape content quality, tone of voice, and storytelling across multiple channels. We're looking for someone who is comfortable operating independently, leading conversations with stakeholders, challenging contributors where necessary, and ensuring all content meets the highest editorial standards. Above all else, we're looking for somebody who can write exceptionally well. What You'll Be Responsible For: Content Creation & Editorial Leadership Write, edit, and publish compelling content across CPI's website, social media channels, campaigns, and communications materials. Act as a guardian of CPI's tone of voice, editorial standards, and content quality. Review, edit, and approve content produced by colleagues and contributors. Develop engaging stories that showcase CPI's expertise, innovation, and impact. Science & Technical Communication Interview scientists, engineers, technical specialists, and business leaders to gather information and develop engaging content. Translate complex scientific, technical, manufacturing, and innovation-related topics into clear and accessible language. Create content that resonates with both technical and non-technical audiences, including industry, government, partners, and wider stakeholder groups. Media Relations & Communications Write press releases, editorial articles, case studies, website copy, blogs, and campaign content. Support media relations activities and engage with journalists and external media contacts. Contribute to communications campaigns designed to raise awareness of CPI's capabilities and impact. Stakeholder Engagement Lead content-focused discussions with stakeholders across the organisation. Guide subject matter experts and contributors to develop stronger, more audience-focused content. Build effective relationships across teams to ensure content is accurate, timely, and impactful. Digital Content & Performance Support the management and maintenance of website and digital content. Monitor content effectiveness and channel performance. Contribute ideas for continuous improvement and audience engagement. About You You are an experienced content professional who is equally comfortable writing from scratch, editing the work of others, and confidently engaging stakeholders to improve communications outcomes. You'll bring: Exceptional writing, editing, and proofreading skills. Experience creating content across websites, publications, digital channels, and communications campaigns. Proven ability to simplify complex information and develop compelling stories. Confidence managing multiple projects and deadlines simultaneously. Strong interpersonal and stakeholder management skills. The ability to work independently and take ownership of content delivery. Desirable (but not essential): Experience in journalism, publishing, media, communications, marketing, or science communication. Experience working with technical experts or scientific organisations. Media relations experience and confidence engaging with journalists. Understanding of SEO and digital content best practice. Experience within science, technology, engineering, manufacturing, research, or innovation environments. We'd particularly like to hear from candidates who have experience in: Journalism or editorial roles Science communication Technical or B2B content marketing Publishing or media organisations Agency environments where content creation is central to the role Why Join CPI? Join a highly regarded and supportive Communications team. Work across a diverse portfolio of science, innovation, manufacturing, and technology projects. Opportunity to shape how complex innovation stories are communicated externally. High degree of autonomy and ownership. Competitive salary ( 36,044 - 46,044). Location & Working Pattern Hybrid working arrangement. Primarily based at NETPark, Sedgefield. Typically 2 days per week on-site, with flexibility depending on business needs. Occasional travel to other CPI locations may be required. The Opportunity This role would suit a confident content professional who enjoys finding stories, building relationships, and creating content that makes complex topics accessible and engaging. Whether your background is journalism, science communication, publishing, content marketing, or editorial work, this is an opportunity to play a key role in communicating some of the UK's most exciting innovation and technology programmes. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Technical Bid Writer - CDMO services Manchester Full Time 37.5 hours per week About the Role: We are working with a growing pharmaceutical services organisation seeking a Technical Bid & Proposal Writer to join their Business Development team. This is a high impact role responsible for leading the creation of compelling, high quality proposals and bid submissions that clearly articulate complex scientific and technical capabilities to prospective clients. You will act as the bridge between technical subject matter experts and commercial teams, ensuring proposals are accurate, persuasive and aligned with client needs while supporting the company's continued growth. What You'll Be Responsible For: Lead the end to end delivery of bids and proposals, including RFPs, RFIs, tenders and client documentation. Translate complex scientific and technical content into clear, client focused language. Collaborate with internal teams across pharmaceutical development, ADME sciences, clinical manufacturing and operations. Manage timelines, inputs and internal review processes to ensure high quality, on time submissions. Ensure all proposals meet quality, compliance and governance standards. Support continuous improvement by developing content libraries, templates and best practices. Work closely with commercial and finance teams to ensure pricing accuracy and consistency. Provide written support for business development materials and, where required, participate in client interactions. About You: A scientific or technical background within pharmaceuticals, biotech, CRO/CDMO or a related environment. Proven experience producing high quality technical documentation (e.g. proposals, protocols, reports). Exceptional written communication skills with the ability to simplify complex information. Strong organisational skills with the ability to manage multiple deadlines and priorities. Comfortable working cross-functionally with both technical and commercial stakeholders. Desirable (but not essential): Experience in bid/proposal writing within pharma, biotech, CRO or CDMO environments Exposure to clinical development, GMP manufacturing or analytical services Familiarity with regulated or audited documentation processes Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Operations Manager Permanent Glasgow 44,497 - 60,497 About the Role We are seeking an experienced Operations Manager to lead operational delivery across a regulated manufacturing environment, ensuring facilities, people, systems, and processes are set up to support safe, efficient, and compliant operations. Reporting to the Head of Operations, this is a key leadership role with responsibility for operational activities across the site, including production support, warehousing, facilities, and operational readiness. The successful candidate will play a critical role in maintaining operational excellence while helping shape future site capability through strategic planning, continuous improvement, and capital investment initiatives. This is a highly visible role that requires someone who is proactive, solutions-focused, and able to deliver results while working effectively across multiple functions and stakeholders. What You'll Be Responsible For: Operational Leadership Lead day-to-day operational activities across the facility, ensuring safe, compliant, and efficient operations Manage and develop a team of operational staff, setting priorities, objectives, and performance expectations Ensure facilities, equipment, materials, and resources are available to support project and production delivery Drive a culture of accountability, continuous improvement, and operational excellence Health, Safety & Compliance Take a leading role in maintaining site compliance with Health & Safety, quality, and regulatory requirements Ensure safe systems of work are developed, implemented, and continuously improved Promote a strong compliance culture within a highly regulated environment Support site readiness for audits and inspections as required Facilities & Asset Management Oversee the effective operation and maintenance of site facilities and equipment Support operational planning to maximise facility utilisation and asset availability Contribute to future CAPEX planning and investment decisions Ensure equipment testing, maintenance, and accreditation activities remain compliant and up to date Continuous Improvement Drive initiatives to improve operational performance, efficiency, and cost effectiveness Improve systems, processes, documentation, housekeeping, and resource management Identify opportunities to streamline operations and enhance service delivery Ensure lessons learned are captured and applied to future activities Stakeholder Management Work closely with project teams, central functions, technical teams, and external suppliers Build strong relationships across the organisation to resolve challenges and deliver outcomes Influence stakeholders and navigate complex environments to achieve operational objectives Support the delivery of projects through effective planning and cross-functional collaboration About You: You are an experienced operations leader who enjoys taking ownership, solving problems, and driving delivery within regulated environments. You'll bring: Proven operational management experience within a regulated industry Experience managing teams and operational activities in manufacturing or production environments Strong understanding of Health & Safety, quality, and compliance requirements Experience managing operational budgets, resources, and facility requirements Excellent stakeholder management and influencing skills A proactive, "can-do" approach with the confidence to make decisions and drive outcomes Desirable (but not essential): Experience within pharmaceutical, food manufacturing, GMP, or similarly regulated environments NEBOSH or equivalent Health & Safety qualification Experience managing CAPEX projects or facility improvements Exposure to Lean, 5S, or continuous improvement methodologies This role would suit someone who has operated in highly regulated sectors such as pharmaceuticals, food production, nuclear, advanced manufacturing, or similar environments where quality, compliance, and operational discipline are critical. Why Join Us? Opportunity to lead operational delivery at a strategically important manufacturing facility Influence site operations, future improvements, and long-term capability plans Work in a collaborative environment with strong cross-functional support Flexible approach to working hours Competitive salary ( 44,497 - 60,497) Location & Working Pattern Based primarily on-site in Glasgow High on-site presence expected, with occasional home working flexibility 37 hours per week Monday-Thursday: 08:30 - 17:00, Friday: 08:30 - 16:00 Flexible working arrangements available around core business needs The Opportunity This is an excellent opportunity for an experienced operations professional to step into a highly influential role where you will help shape the future of site operations while leading teams, improving processes, and ensuring operational excellence within a regulated manufacturing environment. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Job Title: Technical Writer Contract Type: Fixed Term Contract (FTC) Contract Length: 6 Months Location: Hampshire (Site based) SRG are currently searching for a Technical Writer to join a regulated manufacturing company on a 6-month fixed-term contract. You will be responsible for producing clear, accurate, and compliant documentation, including SOPs, work instructions, investigation reports, deviation records, and CAPA documentation. Working closely with Operational, Quality, and Technical teams, you'll ensure documentation remains audit-ready and aligned with quality standards. Key Requirements: Experience in technical writing within a manufacturing or regulated environment. Strong report writing and document control skills. Ability to translate complex technical information into clear, user-friendly documentation. Experience with SOPs, investigations, CAPAs, or quality documentation is highly desirable. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

MSAT Manager Permanent Darlington Up to 70,000 About the Role: We are seeking an MSAT Manager to lead technology transfer activities into GMP manufacturing within an advanced biopharmaceutical manufacturing environment. Reporting into the leadership team, this is a highly visible role responsible for bridging the gap between process development and GMP operations, ensuring manufacturing processes are successfully transferred, implemented, and executed within a regulated setting. This role combines technical leadership, people management, and customer engagement, making it ideal for someone who understands both clinical-stage bioprocessing and the practical realities of GMP manufacturing. You'll work closely with Development, Manufacturing, QA, QC, Bioengineering, Procurement, and external customers to ensure successful technology transfer and operational delivery. What You'll Be Responsible For: Technology Transfer & MSAT Leadership Lead the transfer of development processes into GMP manufacturing facilities Act as the primary technical point of contact for customers throughout technology transfer projects Ensure new processes are robust, scalable, and suitable for GMP manufacture Coordinate activities across Process Development, Manufacturing, QA, QC, Bioengineering, and external stakeholders to ensure successful implementation GMP Manufacturing Support Manage the day-to-day delivery of manufacturing support and preparation activities Ensure production activities are executed safely, compliantly, and to schedule Support the introduction of new products and processes into manufacturing operations Lead deviation investigations, impact assessments, CAPAs, and technical reviews associated with transferred processes People Leadership Lead a small operational team, including GMP operators and manufacturing support personnel Set objectives, manage performance, and support development of team members Ensure appropriate training, competency, and resource planning to support manufacturing activities Foster a culture of collaboration, accountability, and continuous improvement Cross-Functional Project Leadership Lead complex multidisciplinary projects involving technical, operational, and quality functions Coordinate delivery across multiple stakeholders and competing priorities Support strategic resource, capacity, and equipment planning Ensure projects are delivered on time, to budget, and to required quality standards Customer & Business Engagement Work directly with customers to support process transfer and manufacturing readiness Contribute technical expertise to business development activities and proposal development Support future work-winning activities through technical input and customer engagement Build strong relationships internally and externally to support successful project delivery About You You are an experienced bioprocessing or manufacturing professional who enjoys working across multiple functions and taking ownership of complex technical programmes. You'll bring: Significant experience within bioprocessing, biologics manufacturing, or MSAT environments Strong understanding of GMP manufacturing and quality systems Experience transferring development processes into clinical or GMP manufacturing environments Knowledge of upstream, downstream, and analytical bioprocessing activities Experience leading technical projects and coordinating cross-functional teams Strong problem-solving capability and the confidence to make decisions in complex environments Excellent stakeholder management and customer-facing skills Highly desirable: Clinical-stage manufacturing experience MSAT, process transfer, or process validation experience Experience managing GMP operators or production teams Knowledge of biologics manufacturing and CMC principles Experience within mRNA, RNA therapeutics, or advanced biologics environments Project management experience Why Join Us? Opportunity to play a pivotal role in the transfer of innovative products into GMP manufacture Lead technically complex, customer-facing projects Combine scientific, operational, and leadership responsibilities Be part of a growing manufacturing organisation supporting cutting-edge therapies Competitive salary package of up to 70,000 Location & Working Pattern Based in Darlington Full-time permanent position Primarily site-based due to manufacturing and operational activities Flexible working arrangements available around core business requirements The Opportunity This is an outstanding opportunity for an experienced GMP or bioprocessing professional to step into a role that sits at the heart of manufacturing delivery. You'll combine technical expertise, customer engagement, technology transfer, and people leadership to ensure innovative therapies successfully move from development into GMP production. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

QC Chemist required on a permanent basis, based in the Greater Manchester. Requiring proven industrial experience within quality control (QC) testing with wet chemistry techniques, ideally within paints & coatings. A range of other industrial chemical QC experience can be considered. Title: QC Chemist Location: Greater Manchester Salary: 28,000 - 34,000 (dependent on experience) Term: Permanent SRG are working with a respected and well-established manufacturer of premium coating products. Renowned for high-quality formulations, expertise and product performance, they are now seeking to hire a QC Chemist to join their technical team in Greater Manchester. This role will be laboratory-based and hands-on, focusing on quality control (QC) testing, batch approval support and technical problem-solving across raw materials, intermediates and finished products. This represents an excellent opportunity for candidates with proven QC or technical laboratory experience within paints, coatings, chemicals or other related manufacturing environments within industrial chemicals. Benefits: You will join a well-established and highly successful coatings manufacturer. 39 hours per week. 8:30am-5:00pm Mon-Thurs and 8:30am-4:00pm on Friday. 25 days holiday plus bank holidays. Role / Description Perform quality control (QC) assessments on incoming raw materials, products in manufacture and finished goods to ensure compliance with established quality standards. Undertake a variety of laboratory evaluations including colour, viscosity, density, pH, gloss, opacity, drying characteristics, adhesion, stability and application performance testing. Contribute to batch release activities by interpreting test data, identifying deviations and highlighting any quality concerns requiring further investigation. Support the investigation of manufacturing, product quality and customer-related issues, helping to identify root causes and implement effective solutions. Assist with colour verification, tint accuracy checks and shade correction activities to maintain consistency across product ranges. Produce test panels, drawdowns and application samples to assess both the visual appearance and functional performance of coating products. Ensure all laboratory results, quality records, specifications and supporting documentation are completed accurately and maintained in accordance with company procedures. Carry out routine calibration, verification and upkeep of laboratory instruments to guarantee reliable and reproducible test results. Liaise with colleagues across production, technical and commercial functions to support product quality objectives and continuous improvement projects. Provide support with raw material assessments, competitor product reviews and formulation-related activities where required. Requirements Proven industrial experience within a QC, or analytical testing laboratory within the chemicals sector. Experience gained within decorative paints, surface coatings, chemicals or a manufacturing environment would be advantageous. A degree, HNC, HND or similar qualification in Chemistry or a related scientific discipline would be beneficial. Practical understanding of paint and coatings testing methods including colour, viscosity, pH, density and applied coating performance. Excellent attention to detail with strong documentation and record-keeping skills. Ability to investigate technical and quality issues and provide practical solutions. Good communication skills with the ability to work collaboratively across technical and production teams. Knowledge of laboratory safety procedures and quality systems. Full UK driving licence would be advantageous. 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 Chris 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.