Get Staffed Online Recruitment Limited
Bedford, Bedfordshire
Systems Engineer - Embedded and Hardware £60,000 to £70,000 depending on skills and experience + Bonus + Benefits Bedford The Vacancy Our client is seeking an experienced and Senior Systems Engineer - Embedded and Hardware to take ownership of the electronics and software workstream for their IVD medical devices. This is a senior role where you will act as technical design authority, ensuring robust system architecture, supplier governance and regulatory compliance while working at system level rather than as a day to day coder. Based in Bedford and working closely with both in house teams and international third party suppliers, this role offers the opportunity to influence products from early architecture through regulatory approval and post market readiness. Reporting to the Head of Engineering, you will provide technical governance and leadership across hardware, embedded firmware and PC software, ensuring all development activities meet quality, safety and regulatory requirements. You will operate as the system-level technical owner, shaping architecture, design controls and verification strategies, while ensuring supplier outputs are delivered to the highest standards. Key Responsibilities: Third Party Oversight and Governance : Partner with external suppliers to develop electronics, embedded firmware, and software for an IVD medical device, leading supplier governance across design controls, KPIs, risk management, schedules, budgets, quality, and regulatory compliance. Supplier Management and Deliverables : Author and manage supplier agreements (quality agreements, SOWs, acceptance criteria, configuration management) and review / approve all supplier outputs, including designs, code, risk documentation, testing artifacts, traceability, and release records Design Controls and Technical Leadership: Own system and software requirements (including safety, EMI / ESD protection, and usability) and ensure full bidirectional traceability from user needs through design, verification, and validation. Architecture, V&V, and Design Transfer: Lead system architecture decisions across electronics, firmware, and software; define and execute verification and validation strategies (including qualified tools and fixtures); and lead design transfer activities. Regulatory Compliance and QMS: Ensure supplier activities operate under ISO 13485 - compliant processes and deliver complete DHF / Technical Documentation regulatory expectations; align development to applicable standards. Risk, Submission and Audit Support: Lead and document risk management (ISO 14971), ensure readiness for UDI, labelling, post market surveillance, and change control, and support regulatory submissions and notified body audits by presenting clear technical rationales and objective evidence. Cross Functional and Stakeholder Integration: Integrate the electronics / software workstream with assay / chemistry, mechanical design, manufacturing / operations, and service, collaborating closely with Quality, Regulatory, Clinical, and Customer Support to ensure end to end readiness. Risk, Performance and Delivery Management: Proactively identify and mitigate risks, manage non conformities and CAPAs with root cause analysis, and track / report KPIs including quality, schedule adherence, test coverage, and audit outcomes. International travel required approximately 4 - 5 times per year. They're Looking for Someone Who Has: Proven experience in medical devices or IVDs, with hands on exposure to embedded electronics, firmware and software development within a regulated environment. Bachelor's Degree in electrical engineering, software engineering or a related discipline; a Master's Degree would be advantageous. Demonstrable experience overseeing third party design partners, OEMs and ODMs. Strong background in real time embedded systems and instrument control. Solid understanding of design controls, verification and validation. Familiarity with statistical methods for V&V, measurement system analysis and design for reliability. Highly organised with exceptional attention to detail. Clear and confident communicator, both written and verbal. Comfortable working within Microsoft 365; Outlook, Teams, Word, Excel, PowerPoint. Strong sense of ownership and accountability. Able to quickly interpret complex information and identify key technical and programme risks. They Can Offer You: An excellent working environment. Hybrid working - three days a week in the office with two days a week working from home. 25 days paid annual leave plus bank holidays. Company pension scheme including competitive employer's contribution. Private Medical Insurance package with additional medical cash plan scheme. Enhanced maternity and paternity pay. Company supported employee Health and Wellbeing programme. Life assurance. Free plentiful car parking and electrical car charging points. Beautiful parkland setting with excellent transportation links to Cambridge, Milton Keynes and London. The Company Our client is a world leader in the research, design and marketing of advanced consumer diagnostic products. Their research centre is at the cutting edge of innovation and is fully engaged in the development of reliable diagnostic products to empower women on their reproductive journey. They are committed to answering the needs of their existing and future consumers, through a continuous flow of new and innovative products. Interested Click apply and you will be redirected to our client's careers page to complete your application.
May 17, 2026
Full time
Systems Engineer - Embedded and Hardware £60,000 to £70,000 depending on skills and experience + Bonus + Benefits Bedford The Vacancy Our client is seeking an experienced and Senior Systems Engineer - Embedded and Hardware to take ownership of the electronics and software workstream for their IVD medical devices. This is a senior role where you will act as technical design authority, ensuring robust system architecture, supplier governance and regulatory compliance while working at system level rather than as a day to day coder. Based in Bedford and working closely with both in house teams and international third party suppliers, this role offers the opportunity to influence products from early architecture through regulatory approval and post market readiness. Reporting to the Head of Engineering, you will provide technical governance and leadership across hardware, embedded firmware and PC software, ensuring all development activities meet quality, safety and regulatory requirements. You will operate as the system-level technical owner, shaping architecture, design controls and verification strategies, while ensuring supplier outputs are delivered to the highest standards. Key Responsibilities: Third Party Oversight and Governance : Partner with external suppliers to develop electronics, embedded firmware, and software for an IVD medical device, leading supplier governance across design controls, KPIs, risk management, schedules, budgets, quality, and regulatory compliance. Supplier Management and Deliverables : Author and manage supplier agreements (quality agreements, SOWs, acceptance criteria, configuration management) and review / approve all supplier outputs, including designs, code, risk documentation, testing artifacts, traceability, and release records Design Controls and Technical Leadership: Own system and software requirements (including safety, EMI / ESD protection, and usability) and ensure full bidirectional traceability from user needs through design, verification, and validation. Architecture, V&V, and Design Transfer: Lead system architecture decisions across electronics, firmware, and software; define and execute verification and validation strategies (including qualified tools and fixtures); and lead design transfer activities. Regulatory Compliance and QMS: Ensure supplier activities operate under ISO 13485 - compliant processes and deliver complete DHF / Technical Documentation regulatory expectations; align development to applicable standards. Risk, Submission and Audit Support: Lead and document risk management (ISO 14971), ensure readiness for UDI, labelling, post market surveillance, and change control, and support regulatory submissions and notified body audits by presenting clear technical rationales and objective evidence. Cross Functional and Stakeholder Integration: Integrate the electronics / software workstream with assay / chemistry, mechanical design, manufacturing / operations, and service, collaborating closely with Quality, Regulatory, Clinical, and Customer Support to ensure end to end readiness. Risk, Performance and Delivery Management: Proactively identify and mitigate risks, manage non conformities and CAPAs with root cause analysis, and track / report KPIs including quality, schedule adherence, test coverage, and audit outcomes. International travel required approximately 4 - 5 times per year. They're Looking for Someone Who Has: Proven experience in medical devices or IVDs, with hands on exposure to embedded electronics, firmware and software development within a regulated environment. Bachelor's Degree in electrical engineering, software engineering or a related discipline; a Master's Degree would be advantageous. Demonstrable experience overseeing third party design partners, OEMs and ODMs. Strong background in real time embedded systems and instrument control. Solid understanding of design controls, verification and validation. Familiarity with statistical methods for V&V, measurement system analysis and design for reliability. Highly organised with exceptional attention to detail. Clear and confident communicator, both written and verbal. Comfortable working within Microsoft 365; Outlook, Teams, Word, Excel, PowerPoint. Strong sense of ownership and accountability. Able to quickly interpret complex information and identify key technical and programme risks. They Can Offer You: An excellent working environment. Hybrid working - three days a week in the office with two days a week working from home. 25 days paid annual leave plus bank holidays. Company pension scheme including competitive employer's contribution. Private Medical Insurance package with additional medical cash plan scheme. Enhanced maternity and paternity pay. Company supported employee Health and Wellbeing programme. Life assurance. Free plentiful car parking and electrical car charging points. Beautiful parkland setting with excellent transportation links to Cambridge, Milton Keynes and London. The Company Our client is a world leader in the research, design and marketing of advanced consumer diagnostic products. Their research centre is at the cutting edge of innovation and is fully engaged in the development of reliable diagnostic products to empower women on their reproductive journey. They are committed to answering the needs of their existing and future consumers, through a continuous flow of new and innovative products. Interested Click apply and you will be redirected to our client's careers page to complete your application.
Senior Project Manager Location: Basingstoke (Remote) Pay Rate: 40 per hour Shifts: Office hours, flexible Increased innovation, along with substantial growth in the Specialty Diagnostics Group, has resulted in a need for a senior project manager with focus on business transformation and change control. The individual in this role will be a leader in ensuring that the project management teams achieve goals and objectives set by Group leadership. In addition, he/she will be responsible for identifying and mitigating risks, helping guide and mentor staff in project leadership, and communicating as needed on any issues and challenges that constitute obstacles to success. The Senior Project Manager will also make substantial contributions to setting strategic direction for business transformation and will be expected to partner with all functions in ensuring that the organisation achieves its goals. Performance of this individual's responsibilities will require good knowledge of regulatory requirements and quality systems required for in vitro diagnostic (IVD) products Responsibilities: The duties and responsibilities include, but are not limited to the following: The manager of project management, will be responsible for managing complex projects cross division and group level with duties and responsibilities as follows: o Developing project tasks, deliverable, dependencies and resource requirements Creating, maintaining and organising necessary documentation and records; responsible for the quality of project deliverables and documentation Facilitates the completion of various validation deliverables, such as product risk analyses, master validation master plan, related activities & documentation. Oversees and prepares project team budget including resources and costs collaborating with finance and other cross-functional departments. Identifying, documenting and communicating project risks and contingency plans. Tracking and communicating project status, plans, issues, timelines, action items, and budgets. Communicate, document, and archive project team activities and decisions; act as a primary contact for project team related information. Facilitate project team meetings, cross-functional communication and decision making, ensuring alignment with internal and external stakeholders. Exercising scope management with consideration for the customer, team, and company needs Promoting a proactive, professional culture and contributing to the group's success. Significant contribution to the development of strategy for the organisation and the implementation of strategy by project teams in Product Life Cycle. Leadership in the development of processes and tools for value streams including Change Management and business transformation project funnel capture and management and prioritisation. Conduct lessons learned sessions to identify areas for improvement and maintain tracker for implementation of short and longer-term corrective and improvement measures into standard project management practices. Contribute to the standardisation of the project management best practices and seeking opportunities to harmonise processes and systems across programs Minimum Requirements/Qualifications: Bachelor's degree from an accredited higher learning program in Molecular Biology, Cell Biology, Biochemistry, Immunology or related discipline. 9 years industry experience including 5 year's experience in progressively more responsible project management roles required. Previous experience in a regulated manufacturing environment. Previous experience in academic research or biotech industry, preferably including familiarity with reagent production and QA/Regulatory standards. Technical skills in laboratory techniques, manufacturing techniques, FDA & GMP compliance, especially DC. Advanced understanding and ability adhere to established quality standards and regulatory compliance requirements for medical device or diagnostics. Demonstrated skills using MS Project or related project management software, MS Office, Outlook, and the Internet. Strong understanding of product development challenges and methods for resolution. Ability to resolve most day-to-day issues and develop mitigation plans. Superior organisational skills with ability to multi-task and balance complex and routine work activities. Demonstrated ability to lead program teams from concept to market successfully, direct and manage cross-functional teams and projects, influence business partners, get results through others and work effectively in a matrixed environment. High-level business acumen. Advanced presentation skills and interpersonal and communication skills, both written and verbal, with the ability to work as a team player and team builder. Demonstrated experience using financial reports, budgeting and other related reporting tools. Strong problem solving and scientific skills and ability to work independently. Desired Qualifications: An advanced degree in the sciences or an M.B.A. would be an advantage. PMP (Project Management Professional) certification is a plus. IVD Industry experience with proven history of delivering commercially successful results and working under Design Controls is a plus. Top skills: Senior Project Management (Complex, Cross-Functional Projects) Regulatory & Quality Expertise (IVD / Medical Devices) Business Transformation & Change Control Excellent Gantt chart and critical path management skills; great attention to detail Project Planning, Risk Management If you receive suspicious outreach claiming to be from us, please contact us via the ManpowerGroup website.
May 14, 2026
Contractor
Senior Project Manager Location: Basingstoke (Remote) Pay Rate: 40 per hour Shifts: Office hours, flexible Increased innovation, along with substantial growth in the Specialty Diagnostics Group, has resulted in a need for a senior project manager with focus on business transformation and change control. The individual in this role will be a leader in ensuring that the project management teams achieve goals and objectives set by Group leadership. In addition, he/she will be responsible for identifying and mitigating risks, helping guide and mentor staff in project leadership, and communicating as needed on any issues and challenges that constitute obstacles to success. The Senior Project Manager will also make substantial contributions to setting strategic direction for business transformation and will be expected to partner with all functions in ensuring that the organisation achieves its goals. Performance of this individual's responsibilities will require good knowledge of regulatory requirements and quality systems required for in vitro diagnostic (IVD) products Responsibilities: The duties and responsibilities include, but are not limited to the following: The manager of project management, will be responsible for managing complex projects cross division and group level with duties and responsibilities as follows: o Developing project tasks, deliverable, dependencies and resource requirements Creating, maintaining and organising necessary documentation and records; responsible for the quality of project deliverables and documentation Facilitates the completion of various validation deliverables, such as product risk analyses, master validation master plan, related activities & documentation. Oversees and prepares project team budget including resources and costs collaborating with finance and other cross-functional departments. Identifying, documenting and communicating project risks and contingency plans. Tracking and communicating project status, plans, issues, timelines, action items, and budgets. Communicate, document, and archive project team activities and decisions; act as a primary contact for project team related information. Facilitate project team meetings, cross-functional communication and decision making, ensuring alignment with internal and external stakeholders. Exercising scope management with consideration for the customer, team, and company needs Promoting a proactive, professional culture and contributing to the group's success. Significant contribution to the development of strategy for the organisation and the implementation of strategy by project teams in Product Life Cycle. Leadership in the development of processes and tools for value streams including Change Management and business transformation project funnel capture and management and prioritisation. Conduct lessons learned sessions to identify areas for improvement and maintain tracker for implementation of short and longer-term corrective and improvement measures into standard project management practices. Contribute to the standardisation of the project management best practices and seeking opportunities to harmonise processes and systems across programs Minimum Requirements/Qualifications: Bachelor's degree from an accredited higher learning program in Molecular Biology, Cell Biology, Biochemistry, Immunology or related discipline. 9 years industry experience including 5 year's experience in progressively more responsible project management roles required. Previous experience in a regulated manufacturing environment. Previous experience in academic research or biotech industry, preferably including familiarity with reagent production and QA/Regulatory standards. Technical skills in laboratory techniques, manufacturing techniques, FDA & GMP compliance, especially DC. Advanced understanding and ability adhere to established quality standards and regulatory compliance requirements for medical device or diagnostics. Demonstrated skills using MS Project or related project management software, MS Office, Outlook, and the Internet. Strong understanding of product development challenges and methods for resolution. Ability to resolve most day-to-day issues and develop mitigation plans. Superior organisational skills with ability to multi-task and balance complex and routine work activities. Demonstrated ability to lead program teams from concept to market successfully, direct and manage cross-functional teams and projects, influence business partners, get results through others and work effectively in a matrixed environment. High-level business acumen. Advanced presentation skills and interpersonal and communication skills, both written and verbal, with the ability to work as a team player and team builder. Demonstrated experience using financial reports, budgeting and other related reporting tools. Strong problem solving and scientific skills and ability to work independently. Desired Qualifications: An advanced degree in the sciences or an M.B.A. would be an advantage. PMP (Project Management Professional) certification is a plus. IVD Industry experience with proven history of delivering commercially successful results and working under Design Controls is a plus. Top skills: Senior Project Management (Complex, Cross-Functional Projects) Regulatory & Quality Expertise (IVD / Medical Devices) Business Transformation & Change Control Excellent Gantt chart and critical path management skills; great attention to detail Project Planning, Risk Management If you receive suspicious outreach claiming to be from us, please contact us via the ManpowerGroup website.
Systems Engineer Embedded and Hardware £60,000 to £70,000 depending on skills and experience + Bonus + Benefits Bedford The Vacancy We are seeking an experienced and Senior Systems Engineer Embedded and Hardware to take ownership of the electronics and software workstream for our IVD medical devices. This is a senior role where you will act as technical design authority, ensuring robust system architecture, supplier governance and regulatory compliance while working at system level rather than as a day to day coder. Based in Bedford and working closely with both in house teams and international third party suppliers, this role offers the opportunity to influence products from early architecture through regulatory approval and post market readiness. Reporting to the Head of Engineering, you will provide technical governance and leadership across hardware, embedded firmware and PC software, ensuring all development activities meet quality, safety and regulatory requirements. You will operate as the system-level technical owner, shaping architecture, design controls and verification strategies, while ensuring supplier outputs are delivered to the highest standards. Key Responsibilities: Third Party Oversight and Governance: Partner with external suppliers to develop electronics, embedded firmware, and software for an IVD medical device, leading supplier governance across design controls, KPIs, risk management, schedules, budgets, quality, and regulatory compliance. Supplier Management and Deliverables: Author and manage supplier agreements (quality agreements, SOWs, acceptance criteria, configuration management) and review / approve all supplier outputs, including designs, code, risk documentation, testing artifacts, traceability, and release records Design Controls and Technical Leadership: Own system and software requirements (including safety, EMI / ESD protection, and usability) and ensure full bidirectional traceability from user needs through design, verification, and validation. Architecture, V&V, and Design Transfer: Lead system architecture decisions across electronics, firmware, and software; define and execute verification and validation strategies (including qualified tools and fixtures); and lead design transfer activities. Regulatory Compliance and QMS: Ensure supplier activities operate under ISO 13485 compliant processes and deliver complete DHF / Technical Documentation regulatory expectations; align development to applicable standards. Risk, Submission and Audit Support: Lead and document risk management (ISO 14971), ensure readiness for UDI, labelling, post market surveillance, and change control, and support regulatory submissions and notified body audits by presenting clear technical rationales and objective evidence. Cross Functional and Stakeholder Integration: Integrate the electronics / software workstream with assay / chemistry, mechanical design, manufacturing / operations, and service, collaborating closely with Quality, Regulatory, Clinical, and Customer Support to ensure end to end readiness. Risk, Performance and Delivery Management: Proactively identify and mitigate risks, manage non conformities and CAPAs with root cause analysis, and track / report KPIs including quality, schedule adherence, test coverage, and audit outcomes. International travel required approximately 4 5 times per year. We re Looking for Someone Who Has: Proven experience in medical devices or IVDs, with hands on exposure to embedded electronics, firmware and software development within a regulated environment. Bachelor s Degree in electrical engineering, software engineering or a related discipline; a Master s Degree would be advantageous. Demonstrable experience overseeing third party design partners, OEMs and ODMs. Strong background in real time embedded systems and instrument control. Solid understanding of design controls, verification and validation. Familiarity with statistical methods for V&V, measurement system analysis and design for reliability. Highly organised with exceptional attention to detail. Clear and confident communicator, both written and verbal. Comfortable working within Microsoft 365; Outlook, Teams, Word, Excel, PowerPoint. Strong sense of ownership and accountability. Able to quickly interpret complex information and identify key technical and programme risks. We Can Offer You: An excellent working environment. Hybrid working three days a week in the office with two days a week working from home. 25 days paid annual leave plus bank holidays. Company pension scheme including competitive employer s contribution. Private Medical Insurance package with additional medical cash plan scheme. Enhanced maternity and paternity pay. Company supported employee Health and Wellbeing programme. Life assurance. Free plentiful car parking and electrical car charging points. Beautiful parkland setting with excellent transportation links to Cambridge, Milton Keynes and London. The Company Swiss Precision Diagnostics GmbH (SPD) is a world leader in the research, design and marketing of advanced consumer diagnostic products. Our SPD research centre is at the cutting edge of innovation and is fully engaged in the development of reliable diagnostic products to empower women on their reproductive journey. We are committed to answering the needs of our existing and future consumers, through a continuous flow of new and innovative products. Interested Click apply and you will be redirected to our careers page to complete your application.
May 14, 2026
Full time
Systems Engineer Embedded and Hardware £60,000 to £70,000 depending on skills and experience + Bonus + Benefits Bedford The Vacancy We are seeking an experienced and Senior Systems Engineer Embedded and Hardware to take ownership of the electronics and software workstream for our IVD medical devices. This is a senior role where you will act as technical design authority, ensuring robust system architecture, supplier governance and regulatory compliance while working at system level rather than as a day to day coder. Based in Bedford and working closely with both in house teams and international third party suppliers, this role offers the opportunity to influence products from early architecture through regulatory approval and post market readiness. Reporting to the Head of Engineering, you will provide technical governance and leadership across hardware, embedded firmware and PC software, ensuring all development activities meet quality, safety and regulatory requirements. You will operate as the system-level technical owner, shaping architecture, design controls and verification strategies, while ensuring supplier outputs are delivered to the highest standards. Key Responsibilities: Third Party Oversight and Governance: Partner with external suppliers to develop electronics, embedded firmware, and software for an IVD medical device, leading supplier governance across design controls, KPIs, risk management, schedules, budgets, quality, and regulatory compliance. Supplier Management and Deliverables: Author and manage supplier agreements (quality agreements, SOWs, acceptance criteria, configuration management) and review / approve all supplier outputs, including designs, code, risk documentation, testing artifacts, traceability, and release records Design Controls and Technical Leadership: Own system and software requirements (including safety, EMI / ESD protection, and usability) and ensure full bidirectional traceability from user needs through design, verification, and validation. Architecture, V&V, and Design Transfer: Lead system architecture decisions across electronics, firmware, and software; define and execute verification and validation strategies (including qualified tools and fixtures); and lead design transfer activities. Regulatory Compliance and QMS: Ensure supplier activities operate under ISO 13485 compliant processes and deliver complete DHF / Technical Documentation regulatory expectations; align development to applicable standards. Risk, Submission and Audit Support: Lead and document risk management (ISO 14971), ensure readiness for UDI, labelling, post market surveillance, and change control, and support regulatory submissions and notified body audits by presenting clear technical rationales and objective evidence. Cross Functional and Stakeholder Integration: Integrate the electronics / software workstream with assay / chemistry, mechanical design, manufacturing / operations, and service, collaborating closely with Quality, Regulatory, Clinical, and Customer Support to ensure end to end readiness. Risk, Performance and Delivery Management: Proactively identify and mitigate risks, manage non conformities and CAPAs with root cause analysis, and track / report KPIs including quality, schedule adherence, test coverage, and audit outcomes. International travel required approximately 4 5 times per year. We re Looking for Someone Who Has: Proven experience in medical devices or IVDs, with hands on exposure to embedded electronics, firmware and software development within a regulated environment. Bachelor s Degree in electrical engineering, software engineering or a related discipline; a Master s Degree would be advantageous. Demonstrable experience overseeing third party design partners, OEMs and ODMs. Strong background in real time embedded systems and instrument control. Solid understanding of design controls, verification and validation. Familiarity with statistical methods for V&V, measurement system analysis and design for reliability. Highly organised with exceptional attention to detail. Clear and confident communicator, both written and verbal. Comfortable working within Microsoft 365; Outlook, Teams, Word, Excel, PowerPoint. Strong sense of ownership and accountability. Able to quickly interpret complex information and identify key technical and programme risks. We Can Offer You: An excellent working environment. Hybrid working three days a week in the office with two days a week working from home. 25 days paid annual leave plus bank holidays. Company pension scheme including competitive employer s contribution. Private Medical Insurance package with additional medical cash plan scheme. Enhanced maternity and paternity pay. Company supported employee Health and Wellbeing programme. Life assurance. Free plentiful car parking and electrical car charging points. Beautiful parkland setting with excellent transportation links to Cambridge, Milton Keynes and London. The Company Swiss Precision Diagnostics GmbH (SPD) is a world leader in the research, design and marketing of advanced consumer diagnostic products. Our SPD research centre is at the cutting edge of innovation and is fully engaged in the development of reliable diagnostic products to empower women on their reproductive journey. We are committed to answering the needs of our existing and future consumers, through a continuous flow of new and innovative products. Interested Click apply and you will be redirected to our careers page to complete your application.
Process Development Chemist - Renewables / Biofuels - Scotland - Permanent Our client is a leading force in renewable energy across the UK. At present, they are seeking a Process Development Chemist on a permanent basis at their site in Ayrshire, Scotland. This is an excellent opportunity for an experienced Process Development Chemist to support the scale up and delivery of major projects. Responsibilities: To use expert knowledge to chemistry and related fields to devise, plan and execute research programmes with the overall aim of making operations more efficient and/or reduce operational impacts. The Process Development Chemist will conduct and report on laboratory, Midi Plant and Full-Scale Plant trials. Key Duties Laboratory Experiments - Develop and document experimental plans for improving performance in anaerobic digestion and associated activities. - Operate lab scale anaerobic digestion test facilities (AMPTS and Continuous Reactors) for the measurement of biogas potential, digestate quality for various feedstocks under different operating conditions. Midi and Plant Trials - Assist in Midi and Plant Trials as required. - Implementation of process improvement trials across the operational sites. - Prepare Management of Change, Risk and COSHH assessments for Midi and Plant Trials as required - Contribute to safe working environment by complying with written procedures e.g. risk and COSHH assessments. - Development methods and procedures for trials at Midi and across operational sites, which will include trials of new technologies. - Optimisation of existing site processes following successful trials. Documentation: - Write reports of laboratory, Midi and Plant Trials, including descriptions of test method and results, including cross-refencing to plant data or previous tests and analysing and interpreting data. Safety - Complete training on analytical techniques, company procedures, and HSE as tasked. - Work in accordance with SOP s, COSHH and risk assessments and keep working areas clean Other: - Fully participate in innovation process by presenting improvements/innovations at scheduled meetings. - Carry out experimental work at other company locations from time-to-time where on site investigations are required. - Where required; collect, prepare and perform chemical analysis of effluent, process liquors, feedstock, sea water, carbon dioxide and biogas samples according to standard operating procedures, COSHH and Risk Assessment - Analyse samples using advanced instrumental techniques including GC - MS, ICP, and Elemental Analyser. - Perform analysis using basic techniques including colourimetric techniques, gravimetric, titrations etc. - Complete training as tasked on analytical techniques, company procedures, HSE etc. Experience & Qualifications: Strong Laboratory work background. Ability to collate data and produce meaningful & concise reports from data Strong IT skills particularly Excel & use of ERP system or databases. Ability to manage own time and prioritise workload accordingly Ability to present complex scientific information to a non-scientific work group Some experience of training non-scientific colleagues to understand data and reason for treatment of same. Able to challenge established norms with a professional and fact driven approach Ability to work independently. First Degree in Biology, Chemistry; Biochemistry; Microbiology or similar. Desirable: Masters in similar subject area.
Oct 07, 2025
Full time
Process Development Chemist - Renewables / Biofuels - Scotland - Permanent Our client is a leading force in renewable energy across the UK. At present, they are seeking a Process Development Chemist on a permanent basis at their site in Ayrshire, Scotland. This is an excellent opportunity for an experienced Process Development Chemist to support the scale up and delivery of major projects. Responsibilities: To use expert knowledge to chemistry and related fields to devise, plan and execute research programmes with the overall aim of making operations more efficient and/or reduce operational impacts. The Process Development Chemist will conduct and report on laboratory, Midi Plant and Full-Scale Plant trials. Key Duties Laboratory Experiments - Develop and document experimental plans for improving performance in anaerobic digestion and associated activities. - Operate lab scale anaerobic digestion test facilities (AMPTS and Continuous Reactors) for the measurement of biogas potential, digestate quality for various feedstocks under different operating conditions. Midi and Plant Trials - Assist in Midi and Plant Trials as required. - Implementation of process improvement trials across the operational sites. - Prepare Management of Change, Risk and COSHH assessments for Midi and Plant Trials as required - Contribute to safe working environment by complying with written procedures e.g. risk and COSHH assessments. - Development methods and procedures for trials at Midi and across operational sites, which will include trials of new technologies. - Optimisation of existing site processes following successful trials. Documentation: - Write reports of laboratory, Midi and Plant Trials, including descriptions of test method and results, including cross-refencing to plant data or previous tests and analysing and interpreting data. Safety - Complete training on analytical techniques, company procedures, and HSE as tasked. - Work in accordance with SOP s, COSHH and risk assessments and keep working areas clean Other: - Fully participate in innovation process by presenting improvements/innovations at scheduled meetings. - Carry out experimental work at other company locations from time-to-time where on site investigations are required. - Where required; collect, prepare and perform chemical analysis of effluent, process liquors, feedstock, sea water, carbon dioxide and biogas samples according to standard operating procedures, COSHH and Risk Assessment - Analyse samples using advanced instrumental techniques including GC - MS, ICP, and Elemental Analyser. - Perform analysis using basic techniques including colourimetric techniques, gravimetric, titrations etc. - Complete training as tasked on analytical techniques, company procedures, HSE etc. Experience & Qualifications: Strong Laboratory work background. Ability to collate data and produce meaningful & concise reports from data Strong IT skills particularly Excel & use of ERP system or databases. Ability to manage own time and prioritise workload accordingly Ability to present complex scientific information to a non-scientific work group Some experience of training non-scientific colleagues to understand data and reason for treatment of same. Able to challenge established norms with a professional and fact driven approach Ability to work independently. First Degree in Biology, Chemistry; Biochemistry; Microbiology or similar. Desirable: Masters in similar subject area.
Senior Lab Technician - Chemicals / Detergents Location: Stafford Salary: 45,000 - 50,000 DOE KO2's client, a specialist in advanced cleaning technology, is looking to recruit an experienced Senior Lab Technician to join their growing team in Stafford. This is an exciting opportunity for someone with a strong background in chemicals or detergents who is keen to play a key role in product development, process optimisation, and lab management. As a Lab Technician, you will take responsibility for the smooth running of the laboratory, including maintaining equipment, designing and carrying out experiments, and ensuring compliance with test standards. You will work closely with colleagues in software, mechanical design, and operations to optimise wash performance through a deep understanding of chemicals, water, energy, and time. The successful candidate will be confident in experimental design, data analysis, and presenting results up to board level. This role suits someone with an inquisitive mindset who can bring scientific rigour and practical solutions to the challenges of cleaning systems using detergents and chemicals. Key responsibilities: Manage day-to-day laboratory operations, including calibration and test standards. Design and carry out experiments to optimise cleaning cycles. Analyse and interpret results, focusing on the role of chemicals and detergents. Present findings and recommendations to senior stakeholders. Contribute to the development of new testing methodologies and measurable parameters. The ideal Senior Lab Technician will have: A degree in Chemistry, Chemical Engineering, or a related discipline. Proven experience in a laboratory environment working with detergents or chemicals. Strong knowledge of experimental design and process optimisation. Excellent communication and presentation skills. The ability to work independently while contributing to a collaborative team. Benefits: Competitive salary ( 45,000 - 50,000 depending on experience). Flexible working hours (Monday-Friday, early finish on Fridays). Opportunity to play a pivotal role in shaping future cleaning technologies. This is a fantastic opportunity for a Lab Technician who wants to step up into a senior role with real influence in a dynamic, forward-thinking business. If you have the expertise in detergents and chemicals to drive innovation, KO2's client would love to hear from you.
Oct 06, 2025
Full time
Senior Lab Technician - Chemicals / Detergents Location: Stafford Salary: 45,000 - 50,000 DOE KO2's client, a specialist in advanced cleaning technology, is looking to recruit an experienced Senior Lab Technician to join their growing team in Stafford. This is an exciting opportunity for someone with a strong background in chemicals or detergents who is keen to play a key role in product development, process optimisation, and lab management. As a Lab Technician, you will take responsibility for the smooth running of the laboratory, including maintaining equipment, designing and carrying out experiments, and ensuring compliance with test standards. You will work closely with colleagues in software, mechanical design, and operations to optimise wash performance through a deep understanding of chemicals, water, energy, and time. The successful candidate will be confident in experimental design, data analysis, and presenting results up to board level. This role suits someone with an inquisitive mindset who can bring scientific rigour and practical solutions to the challenges of cleaning systems using detergents and chemicals. Key responsibilities: Manage day-to-day laboratory operations, including calibration and test standards. Design and carry out experiments to optimise cleaning cycles. Analyse and interpret results, focusing on the role of chemicals and detergents. Present findings and recommendations to senior stakeholders. Contribute to the development of new testing methodologies and measurable parameters. The ideal Senior Lab Technician will have: A degree in Chemistry, Chemical Engineering, or a related discipline. Proven experience in a laboratory environment working with detergents or chemicals. Strong knowledge of experimental design and process optimisation. Excellent communication and presentation skills. The ability to work independently while contributing to a collaborative team. Benefits: Competitive salary ( 45,000 - 50,000 depending on experience). Flexible working hours (Monday-Friday, early finish on Fridays). Opportunity to play a pivotal role in shaping future cleaning technologies. This is a fantastic opportunity for a Lab Technician who wants to step up into a senior role with real influence in a dynamic, forward-thinking business. If you have the expertise in detergents and chemicals to drive innovation, KO2's client would love to hear from you.
Principal Air Quality Consultant - Bristol Location: Bristol Salary: Competitive + Benefits Penguin Recruitment is partnering with a leading environmental consultancy to appoint a Principal Air Quality Consultant to its high-performing team in Bristol . This is a senior opportunity to lead complex projects across infrastructure, transport, urban development and industry, shaping healthier, more sustainable environments while mentoring a growing team. The Role Based in Bristol , you'll own the technical and commercial delivery of major air quality commissions - scoping, directing and reviewing impact assessments and dispersion modelling (ADMS / AERMOD), setting methodologies, and ensuring outputs meet regulatory and client standards. You'll act as a trusted advisor to developers, planners and local authorities, and will help drive frameworks, bids and strategic client relationships. Key Responsibilities Lead and sign off air quality assessments, ES/EIA chapters and planning/permit submissions. Set modelling strategies, assure quality, and troubleshoot complex technical issues. Grow client accounts: bid writing, fee proposals, frameworks and thought leadership. Line-manage, mentor and develop consultants; coordinate resourcing and training. Oversee monitoring campaigns, data QA/QC and evidence for inquiries/examinations. Track and interpret UK air quality policy, LAQM TG(22), IAQM/EPUK guidance and emerging best practice. About You 7-10+ years' experience in air quality consultancy or regulatory practice. Advanced proficiency with ADMS/AERMOD/Breeze and robust understanding of uncertainty and verification. Strong report writing and review skills; confident presenting to clients and stakeholders. Degree in Environmental/Atmospheric Science, Chemistry, Engineering or related discipline. Chartered or working toward (CEnv/MIEnvSc/IAQM) strongly preferred. Commercial acumen: pricing, programmes, risk management and client development. The Offer Competitive salary and annual bonus, plus private healthcare and pension. Flexible/hybrid working with excellent support from national subject-matter experts. Funded CPD, professional memberships and clear progression to Associate/Technical Director. A modern, centrally located Bristol office. Ready to step up and lead as a Principal Air Quality Consultant in Bristol ? Contact Abi King at Penguin Recruitment to apply.
Sep 22, 2025
Full time
Principal Air Quality Consultant - Bristol Location: Bristol Salary: Competitive + Benefits Penguin Recruitment is partnering with a leading environmental consultancy to appoint a Principal Air Quality Consultant to its high-performing team in Bristol . This is a senior opportunity to lead complex projects across infrastructure, transport, urban development and industry, shaping healthier, more sustainable environments while mentoring a growing team. The Role Based in Bristol , you'll own the technical and commercial delivery of major air quality commissions - scoping, directing and reviewing impact assessments and dispersion modelling (ADMS / AERMOD), setting methodologies, and ensuring outputs meet regulatory and client standards. You'll act as a trusted advisor to developers, planners and local authorities, and will help drive frameworks, bids and strategic client relationships. Key Responsibilities Lead and sign off air quality assessments, ES/EIA chapters and planning/permit submissions. Set modelling strategies, assure quality, and troubleshoot complex technical issues. Grow client accounts: bid writing, fee proposals, frameworks and thought leadership. Line-manage, mentor and develop consultants; coordinate resourcing and training. Oversee monitoring campaigns, data QA/QC and evidence for inquiries/examinations. Track and interpret UK air quality policy, LAQM TG(22), IAQM/EPUK guidance and emerging best practice. About You 7-10+ years' experience in air quality consultancy or regulatory practice. Advanced proficiency with ADMS/AERMOD/Breeze and robust understanding of uncertainty and verification. Strong report writing and review skills; confident presenting to clients and stakeholders. Degree in Environmental/Atmospheric Science, Chemistry, Engineering or related discipline. Chartered or working toward (CEnv/MIEnvSc/IAQM) strongly preferred. Commercial acumen: pricing, programmes, risk management and client development. The Offer Competitive salary and annual bonus, plus private healthcare and pension. Flexible/hybrid working with excellent support from national subject-matter experts. Funded CPD, professional memberships and clear progression to Associate/Technical Director. A modern, centrally located Bristol office. Ready to step up and lead as a Principal Air Quality Consultant in Bristol ? Contact Abi King at Penguin Recruitment to apply.
