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Scientist II (12-Month Contract) \n Job Title: Scientist II \n Location: Deeside \n Contract Duration: 12 Months \n PAYE Rate: £142.32 per day \n \n Position Overview \n The Scientist II is responsible for performing analytical testing on existing and new medical devices, skincare products, and raw materials in accordance with approved protocols, Standard Operating Procedures (SOPs), Operating Control Instructions (OCIs), and Technical Documents (TDs). The role supports product claims generation, analytical method development, validation activities, and laboratory operations while maintaining compliance with applicable quality standards and regulatory requirements. \n The successful candidate will contribute to research and development projects, ensure high standards of laboratory compliance, and provide technical expertise across a range of analytical techniques and equipment. \n \n Key Responsibilities \n Analytical Testing & Data Management \n\n • Conduct analytical testing of medical devices, skincare products, and raw materials in line with approved protocols and procedures.\n, • Analyse, interpret, document, and report laboratory data in accordance with GMP and GLP requirements.\n, • Compile laboratory results and generate technical reports to support product development and business objectives.\n, • Perform technical data reviews for analytical testing activities.\n, • Carry out technical approval checks for reports generated by the Analytical function.\n\n Method Development & Validation \n\n • Design, develop, optimise, and validate analytical methods for new products, raw materials, and analytical techniques.\n, • Support planned and ad-hoc analytical testing and method development projects.\n, • Execute method validation activities to ensure suitability for intended use.\n, • Troubleshoot analytical methods and laboratory issues to drive continuous improvement.\n\n Laboratory Compliance & Quality \n\n • Maintain compliance with ISO 13485 and ISO 9001 quality standards through adherence to GLP/GMP-compliant procedures.\n, • Prepare and manage quality documentation, including:\n, • Change Control Records\n, • Non-Conformance Reports\n, • Out-of-Specification (OOS) Investigations\n, • Participate in laboratory investigations and root cause analysis activities with appropriate supervision.\n, • Support internal and external audits by providing accurate and timely information.\n\n Equipment & Laboratory Operations \n\n • Maintain, calibrate, document, and update quality records for laboratory equipment.\n, • Act as a technical expert for designated analytical instrumentation, particularly HPLC systems.\n, • Operate and maintain a broad range of analytical equipment, including:\n, • HPLC\n, • FTIR\n, • ICP-MS\n, • Balances\n, • Pipettes\n, • Other analytical instrumentation\n, • Coordinate with external vendors regarding equipment servicing, maintenance, calibration, and service contracts.\n, • Monitor laboratory stock levels and initiate reordering of consumables, chemicals, and reagents as required.\n\n Documentation & Systems \n\n • Author and maintain SOPs, OCIs, and Technical Documents.\n, • Submit controlled documentation through the Electronic Data Management System (EDMS) for review and approval.\n, • Utilise software packages for data management, analysis, and reporting, including:\n, • Microsoft Word\n, • Microsoft Excel\n, • SAP\n, • Waters Empower\n, • ChemStation\n, • MassHunter\n, • Minitab\n\n Training & Collaboration \n\n • Train and mentor new or less experienced laboratory personnel on equipment operation and testing procedures.\n, • Support other R&D teams through laboratory testing and technical expertise when required.\n, • Collaborate effectively with Scientists, Senior Scientists, Team Leaders, and laboratory management to achieve project goals.\n, • Participate actively in team activities and continuous improvement initiatives.\n\n Continuous Improvement & Safety \n\n • Maintain a safe laboratory working environment and report near misses, hazards, and safety concerns.\n, • Implement and support Lean and 6S initiatives within the Analytical Laboratory.\n, • Drive improvements to analytical processes, testing methods, and laboratory procedures.\n, • Ensure the correct handling and disposal of chemicals, reagents, and solvents in accordance with site and environmental procedures.\n\n \n Skills & Experience \n Essential \n\n • Bachelor's degree (BSc) or equivalent in a scientific discipline.\n, • Strong understanding of laboratory health and safety practices.\n, • Experience with analytical chemistry techniques and laboratory operations.\n, • Ability to follow and comply with SOPs, OCIs, and Technical Documents.\n, • Experience in analytical method validation.\n, • Proficiency in Microsoft Office applications, particularly Word and Excel.\n, • Strong data interpretation, reporting, and problem-solving skills.\n, • Ability to work effectively within a regulated environment and manage multiple priorities.\n\n Preferred \n\n • Degree in Analytical Chemistry or a related scientific discipline.\n, • 3-4 years' experience within the Medical Device, Pharmaceutical, or related regulated industry in an R&D or Product Development environment.\n, • Experience operating advanced analytical instruments such as HPLC, FTIR, and ICP-MS.\n, • Working knowledge of FDA regulations, ICH guidelines, Quality Systems, and GMP requirements.\n, • Experience with laboratory data systems and analytical software platforms including Empower, ChemStation, MassHunter, and Minitab.\n\n \n Qualifications \n Required \n\n • BSc degree or equivalent in a scientific discipline.\n

Scientist II (12-Month Contract) Job Title: Scientist II Location: Deeside Contract Duration: 12 Months PAYE Rate: £142.32 per day Position Overview The Scientist II is responsible for performing analytical testing on existing and new medical devices, skincare products, and raw materials in accordance with approved protocols, Standard Operating Procedures (SOPs), Operating Control Instructions (OCIs), and Technical Documents (TDs). The role supports product claims generation, analytical method development, validation activities, and laboratory operations while maintaining compliance with applicable quality standards and regulatory requirements. The successful candidate will contribute to research and development projects, ensure high standards of laboratory compliance, and provide technical expertise across a range of analytical techniques and equipment. Key Responsibilities Analytical Testing & Data Management Conduct analytical testing of medical devices, skincare products, and raw materials in line with approved protocols and procedures. Analyse, interpret, document, and report laboratory data in accordance with GMP and GLP requirements. Compile laboratory results and generate technical reports to support product development and business objectives. Perform technical data reviews for analytical testing activities. Carry out technical approval checks for reports generated by the Analytical function.Method Development & Validation Design, develop, optimise, and validate analytical methods for new products, raw materials, and analytical techniques. Support planned and ad-hoc analytical testing and method development projects. Execute method validation activities to ensure suitability for intended use. Troubleshoot analytical methods and laboratory issues to drive continuous improvement.Laboratory Compliance & Quality Maintain compliance with ISO 13485 and ISO 9001 quality standards through adherence to GLP/GMP-compliant procedures. Prepare and manage quality documentation, including: Change Control Records Non-Conformance Reports Out-of-Specification (OOS) Investigations Participate in laboratory investigations and root cause analysis activities with appropriate supervision. Support internal and external audits by providing accurate and timely information.Equipment & Laboratory Operations Maintain, calibrate, document, and update quality records for laboratory equipment. Act as a technical expert for designated analytical instrumentation, particularly HPLC systems. Operate and maintain a broad range of analytical equipment, including: HPLC FTIR ICP-MS Balances Pipettes Other analytical instrumentation Coordinate with external vendors regarding equipment servicing, maintenance, calibration, and service contracts. Monitor laboratory stock levels and initiate reordering of consumables, chemicals, and reagents as required.Documentation & Systems Author and maintain SOPs, OCIs, and Technical Documents. Submit controlled documentation through the Electronic Data Management System (EDMS) for review and approval. Utilise software packages for data management, analysis, and reporting, including: Microsoft Word Microsoft Excel SAP Waters Empower ChemStation MassHunter MinitabTraining & Collaboration Train and mentor new or less experienced laboratory personnel on equipment operation and testing procedures. Support other R&D teams through laboratory testing and technical expertise when required. Collaborate effectively with Scientists, Senior Scientists, Team Leaders, and laboratory management to achieve project goals. Participate actively in team activities and continuous improvement initiatives.Continuous Improvement & Safety Maintain a safe laboratory working environment and report near misses, hazards, and safety concerns. Implement and support Lean and 6S initiatives within the Analytical Laboratory. Drive improvements to analytical processes, testing methods, and laboratory procedures. Ensure the correct handling and disposal of chemicals, reagents, and solvents in accordance with site and environmental procedures.Skills & Experience Essential Bachelor's degree (BSc) or equivalent in a scientific discipline. Strong understanding of laboratory health and safety practices. Experience with analytical chemistry techniques and laboratory operations. Ability to follow and comply with SOPs, OCIs, and Technical Documents. Experience in analytical method validation. Proficiency in Microsoft Office applications, particularly Word and Excel. Strong data interpretation, reporting, and problem-solving skills. Ability to work effectively within a regulated environment and manage multiple priorities.Preferred Degree in Analytical Chemistry or a related scientific discipline. 3-4 years' experience within the Medical Device, Pharmaceutical, or related regulated industry in an R&D or Product Development environment. Experience operating advanced analytical instruments such as HPLC, FTIR, and ICP-MS. Working knowledge of FDA regulations, ICH guidelines, Quality Systems, and GMP requirements. Experience with laboratory data systems and analytical software platforms including Empower, ChemStation, MassHunter, and Minitab.Qualifications Required BSc degree or equivalent in a scientific discipline.Working Relationships Key Internal Contacts Scientists and Senior Scientists Team Leaders Analytical Laboratory Manager R&D TeamsKey External Contacts Equipment and service vendors Calibration and maintenance providers External training organisations Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy

Technical Manager | Permanent | Cheshire | Speciality Chemicals Industry | £60,000-£70,000 | Immediate Start Available Location: Cheshire Salary: £60,000 - £70,000 per annum DOE Contract Type: Permanent Hours: Monday to Thursday 8:00am-4:00pm, Friday 8:00am-3:00pm Start Date: ASAP The Opportunity Are you an experienced technical leader looking to play a pivotal role within a growing speciality chemicals manufacturer? An exciting opportunity has arisen for a Technical Manager to join a well-established chemical manufacturing business with an international customer base and a strong reputation for innovation. As a key member of the senior leadership team, you will shape technical strategy, drive new product development, oversee product quality and compliance, and act as the technical authority across the organisation. This role would suit a highly motivated chemist with significant industrial experience who enjoys combining hands-on technical problem solving with strategic leadership, customer engagement, and team development. What you'll be doing Lead the technical function and provide strategic direction across product development, quality, compliance and customer support. Manage and develop a small technical team including Quality Control, Product Development and Quality/Food Safety personnel. Drive innovation through the development and optimisation of new and existing chemical formulations. Support commercial teams by translating customer requirements into technical solutions. Act as the primary escalation point for technical enquiries and customer complaints. Work closely with manufacturing teams to ensure efficient product scale-up and process optimisation. Maintain high standards of product quality, regulatory compliance and technical governance. Develop strong relationships with key suppliers and collaborate on raw material innovation and product improvements. Oversee product validation, testing programmes and continuous improvement initiatives. Contribute to business growth through technical expertise, leadership and customer-focused problem solving. Ensure appropriate food safety, quality and risk management processes are maintained where applicable. Support international customers and stakeholders, including occasional global travel. What we're looking for Degree qualified in Chemistry, Polymer Science, Emulsion Science or a related scientific discipline. MSc or PhD qualification highly desirable. Extensive experience within speciality chemical manufacturing, formulation or industrial chemicals. Strong background in product development and formulation chemistry. Previous experience leading technical, quality or R&D teams. Proven ability to work directly with customers and suppliers in a technical capacity. Willingness to travel internationally when required.Benefits Competitive salary of £60,000-£70,000 DOE Discretionary annual bonus scheme Employer pension contribution of 10% with no employee contribution required 25 days annual leave plus bank holidays Excellent work-life balance with an early finish every Friday How to Apply If you'd like to apply, please use the link provided or email your CV to For more information, please call Tom on (phone number removed). If this role isn't right for you, feel free to get in touch or visit (url removed) to view other opportunities. About SRG SRG is the UK's leading specialist recruiter across the scientific, engineering, clinical, pharmaceutical, FMCG, energy, biotech, chemical and medical device sectors. As scientists ourselves, our deep technical understanding means we're passionate about finding the right roles for our candidates and the right talent for our clients. Keywords Technical Manager, Chemistry, PhD Chemist, Formulation Chemistry, Chemical Manufacturing, Specialty Chemicals, Product Development, R&D Manager, Quality Control, Regulatory Compliance, HACCP, Process Improvement, Technical Leadership, Polymer Science, Emulsion Technology, Industrial Chemicals, New Product Development, Quality Management, Supplier Management, Chemical Industry Jobs, Cheshire Jobs, Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy

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