Summary: The Laboratory Quality Analyst for Nijhuis Saur Industries in Stoke is responsible for ensuring the laboratory and Riventa business unit operate to the highest quality standards by managing accreditation compliance, internal and external audits, QA/QC processes, instrument calibration, data analysis, and documentation control. The role provides technical guidance to staff, supports method development, oversees customer satisfaction and performance metrics, leads accreditation audit representation, and manages non conformance investigations. It also involves collaborating with management and customers, producing performance reports, supporting routine and specialised testing, and maintaining ISO 9001 and ISO 17025 quality systems for both laboratory and manufactured parts environments. Duties and Responsibilities: Ensure compliance with laboratory accreditation, regulatory standards and provide guidance to staff to ensure that quality policies, processes and procedures are established, current and adhered to by all laboratory staff. Oversee laboratory internal audit processes, external proficiency testing programs, document control systems, competency assessment, training, and other quality processes. Support the development of instrument techniques, ensuring adequate calibrations and QC are in place. Monitor customer satisfaction and performance metrics of the laboratory. Liaise with management throughout the business as well as customers when reporting on quality and statistical data. Oversee the Riventa business unit quality system including manufactured parts QA/QC process, calibration of temperature probes to approved methods, warranty, repair and returns process for Riventa parts. Maintain a quality management system for Riventa. Work to the global NSI ISO 9001 accredited quality management system. Work to the NSI WTL ISO 17025 accredited quality management system. Manage, document and audit the Riventa incoming and assembled products/parts testing and acceptance QA/QC process at the Stoke facility, in collaboration with the Riventa team. Manage, document and audit the Riventa temperature and pressure probe calibration process to relevant standards. Conduct lab testing to high standards through busy periods or during periods of absence of Laboratory Analyst or Develop Analysts. Audit the analytical performance of the analysts, content of laboratory methodology and documentation to ensure compliance with the quality system. Represent the laboratory during annual accreditation audits. Oversee the laboratories non conformance log to ensure its appropriate use and investigations are completed in full, with appropriate actions. Analyse data, identify trends, monitor prevention and correction of quality deviations, and develop reports for management utilising regulatory knowledge, technical knowledge and laboratory experience. To provide quality support to the laboratory for routine testing when required as well as providing quality support to the Technical Development Scientist and the wider technical team with specialised testing and the growth of these methods. Report periodically to management, customers on the quality performance of the laboratory. Presenting data to stakeholders on laboratory performance statistics. Support the creation and reviewing of validation reports for new and current tests. Perform Uncertainty of Measurement calculations when required. This is not a fully comprehensive list of responsibilities, and other duties will be expected to be completed within the limits of the position. Required Skills/Qualifications (Essential): Knowledge and experience of quality management systems such as ISO 9001 and ISO 17025 and quality improvement tools and techniques Knowledge and experience of UKAS accreditation and audits is advantageous. Experienced in the auditing of quality systems and laboratory testing procedures. Experience working with a QC process for manufactured parts. Working knowledge of accreditation standards, practices, and guidelines sufficient to advise and guide the laboratory manager and laboratory team as they implement new methodology and maintain accreditation. Working knowledge of computer and analytical software programs sufficient for the evaluation of electronic data, data interpretation, and report development (A good understanding of the Microsoft Office Suite would be advantageous). Experience working with LIMS. Excellent organisational skills allowing the coordination of multi faceted QA activities. Experience in performing data analysis such as uncertainty of measurement. Working experience of overseeing the development of new analytical techniques. Good awareness of all HSE aspects in a laboratory environment (i.e., COSHH, RA). Required Skills/Qualifications (Desirable): Degree/HND in Biochemistry/Chemistry or related science (Highly Desirable) Consideration will be given to applicants with Certifications in Quality (Highly Desirable) Consideration will be given to those candidates with 2 years' experience in a similar position (Highly desirable) Knowledge and/or previous experience of GC FID, Ion chromatography, FT IR, wet chemistry, spectrophotometry experience of water, wastewater, cooling water and boiler water in the Oil & Gas, Petrochemical, food & beverage industries (Highly desirable). Working for us means: The salary is between £33,000 & £38,000 per year, depending on your professional experience. Hours of Work - 40 hours per week, Monday to Friday Holidays - 25 days + 8 statutory days (pro-rata) Probationary Period - 6 months. Pension - Can join immediately or auto enrolled after 3 months - Employee 5% and Employer 5% via salary sacrifice. Eligible to join Private Healthcare after successfully completing probation. Enrolled in Group Income Protection and Death in Service (4 x basic salary) upon commencement of employment. Notice - 1 Week during probation, increasing to 1 months thereafter. Nijhuis Saur Industries UK & Ireland are committed to maintaining Environmental & Social Impact goals: To reach Net Zero emissions across our value chain by 2040. To continuously meet high standards of social and environmental performance, transparency, accountability, maintaining B Corp Certification. To be a socially responsible company creating a positive impact to all stakeholders including workers, communities, customers, and our planet. Nijhuis Saur Industries UK & Ireland are an equal opportunity employer; we are committed to providing equal opportunities in all aspects of employment in line with the Equality Act 2010.
May 05, 2026
Full time
Summary: The Laboratory Quality Analyst for Nijhuis Saur Industries in Stoke is responsible for ensuring the laboratory and Riventa business unit operate to the highest quality standards by managing accreditation compliance, internal and external audits, QA/QC processes, instrument calibration, data analysis, and documentation control. The role provides technical guidance to staff, supports method development, oversees customer satisfaction and performance metrics, leads accreditation audit representation, and manages non conformance investigations. It also involves collaborating with management and customers, producing performance reports, supporting routine and specialised testing, and maintaining ISO 9001 and ISO 17025 quality systems for both laboratory and manufactured parts environments. Duties and Responsibilities: Ensure compliance with laboratory accreditation, regulatory standards and provide guidance to staff to ensure that quality policies, processes and procedures are established, current and adhered to by all laboratory staff. Oversee laboratory internal audit processes, external proficiency testing programs, document control systems, competency assessment, training, and other quality processes. Support the development of instrument techniques, ensuring adequate calibrations and QC are in place. Monitor customer satisfaction and performance metrics of the laboratory. Liaise with management throughout the business as well as customers when reporting on quality and statistical data. Oversee the Riventa business unit quality system including manufactured parts QA/QC process, calibration of temperature probes to approved methods, warranty, repair and returns process for Riventa parts. Maintain a quality management system for Riventa. Work to the global NSI ISO 9001 accredited quality management system. Work to the NSI WTL ISO 17025 accredited quality management system. Manage, document and audit the Riventa incoming and assembled products/parts testing and acceptance QA/QC process at the Stoke facility, in collaboration with the Riventa team. Manage, document and audit the Riventa temperature and pressure probe calibration process to relevant standards. Conduct lab testing to high standards through busy periods or during periods of absence of Laboratory Analyst or Develop Analysts. Audit the analytical performance of the analysts, content of laboratory methodology and documentation to ensure compliance with the quality system. Represent the laboratory during annual accreditation audits. Oversee the laboratories non conformance log to ensure its appropriate use and investigations are completed in full, with appropriate actions. Analyse data, identify trends, monitor prevention and correction of quality deviations, and develop reports for management utilising regulatory knowledge, technical knowledge and laboratory experience. To provide quality support to the laboratory for routine testing when required as well as providing quality support to the Technical Development Scientist and the wider technical team with specialised testing and the growth of these methods. Report periodically to management, customers on the quality performance of the laboratory. Presenting data to stakeholders on laboratory performance statistics. Support the creation and reviewing of validation reports for new and current tests. Perform Uncertainty of Measurement calculations when required. This is not a fully comprehensive list of responsibilities, and other duties will be expected to be completed within the limits of the position. Required Skills/Qualifications (Essential): Knowledge and experience of quality management systems such as ISO 9001 and ISO 17025 and quality improvement tools and techniques Knowledge and experience of UKAS accreditation and audits is advantageous. Experienced in the auditing of quality systems and laboratory testing procedures. Experience working with a QC process for manufactured parts. Working knowledge of accreditation standards, practices, and guidelines sufficient to advise and guide the laboratory manager and laboratory team as they implement new methodology and maintain accreditation. Working knowledge of computer and analytical software programs sufficient for the evaluation of electronic data, data interpretation, and report development (A good understanding of the Microsoft Office Suite would be advantageous). Experience working with LIMS. Excellent organisational skills allowing the coordination of multi faceted QA activities. Experience in performing data analysis such as uncertainty of measurement. Working experience of overseeing the development of new analytical techniques. Good awareness of all HSE aspects in a laboratory environment (i.e., COSHH, RA). Required Skills/Qualifications (Desirable): Degree/HND in Biochemistry/Chemistry or related science (Highly Desirable) Consideration will be given to applicants with Certifications in Quality (Highly Desirable) Consideration will be given to those candidates with 2 years' experience in a similar position (Highly desirable) Knowledge and/or previous experience of GC FID, Ion chromatography, FT IR, wet chemistry, spectrophotometry experience of water, wastewater, cooling water and boiler water in the Oil & Gas, Petrochemical, food & beverage industries (Highly desirable). Working for us means: The salary is between £33,000 & £38,000 per year, depending on your professional experience. Hours of Work - 40 hours per week, Monday to Friday Holidays - 25 days + 8 statutory days (pro-rata) Probationary Period - 6 months. Pension - Can join immediately or auto enrolled after 3 months - Employee 5% and Employer 5% via salary sacrifice. Eligible to join Private Healthcare after successfully completing probation. Enrolled in Group Income Protection and Death in Service (4 x basic salary) upon commencement of employment. Notice - 1 Week during probation, increasing to 1 months thereafter. Nijhuis Saur Industries UK & Ireland are committed to maintaining Environmental & Social Impact goals: To reach Net Zero emissions across our value chain by 2040. To continuously meet high standards of social and environmental performance, transparency, accountability, maintaining B Corp Certification. To be a socially responsible company creating a positive impact to all stakeholders including workers, communities, customers, and our planet. Nijhuis Saur Industries UK & Ireland are an equal opportunity employer; we are committed to providing equal opportunities in all aspects of employment in line with the Equality Act 2010.
QC Lab Analyst When registering to this job board you will be redirected to the online application form. Please ensure that this is completed in full in order that your application can be reviewed. We are seeking a QC Laboratory Analyst to support the delivery of a high-quality control service for our internal and external customers click apply for full job details
May 05, 2026
Full time
QC Lab Analyst When registering to this job board you will be redirected to the online application form. Please ensure that this is completed in full in order that your application can be reviewed. We are seeking a QC Laboratory Analyst to support the delivery of a high-quality control service for our internal and external customers click apply for full job details
Consent Cookie Name : Google Analytics What it does: Data Collection, Configuration, Data Processing and Reporting Why is it used: Tracks and Reports Traffic (Anonymised) for Web Analytics How long it lasts: At least 25 Months . Enquiries When contacted with an enquiry, we will hold the entity name and contact details only for the purposes of handling the enquiry. recognise you whenever you visit this website (this speeds up your access to the website as you do not have to log in each time); obtain information about your preferences, online movements and use of the internet; carry out research and statistical analysis to help improve our content, products and services and to help us better understand our customer requirements and interests; target our marketing and advertising campaigns more effectively by providing interest-based advertisements that are personalised to your interests; make your online experience more efficient and enjoyable.Senior GC Analyst (Team Lead) page is loaded Senior GC Analyst (Team Lead)locations: Southampton, UKtime type: Full timeposted on: Posted 2 Days Agojob requisition id: REQ106681 This role is located in Marchwood, within the Cawood Scientific Environment Division. Marchwood, part of Cawood, was established in 1998 and performs a range of specialist analytical testing services to customers operating in the Environmental, Industrial and Agricultural Sectors from its three laboratories based in the South and North of England. As a leading UK Dioxin and Furans analysis laboratory and the UK's leading specialist laboratory for independent occupational hygiene analysis, Marchwood offers a range of services for the environmental, occupational and food/feed sectors Job Description: Job Title: Senior GC Analyst (Team Lead) Location: Marchwood Southampton Company: Cawood Job Description: We are seeking a highly skilled and motivated Senior GC Analyst to join our dynamic team within our Dioxins Laboratory. The successful candidate will be responsible for performing routine analysis on customer samples, working to deadlines in accordance with the company Quality Management System and UKAS guidelines. Experience with High Resolution Mass Spectrometry advantages but not essential. Key Responsibilities: Perform routine analysis on customer samples, adhering to deadlines and quality standards (ISO 17025 and MCERTS). Accurately record and analyze data, identifying possible deviations and ensuring compliance with system suitability checks, calibrations, and AQC charts. Undertake and assist with the investigation of queries and non-conformance. Perform routine and non-routine instrument maintenance, troubleshooting, identifying root causes, and implementing corrective actions to minimize unplanned instrument downtime. Plan and perform validation work to improve existing methods and develop new methods to support client requests and company growth strategy. Assist with the validation of new instruments as required. Effectively communicate with co-workers and local management. Prepare standards and solutions and aid in the preparation/extraction of samples if required. Maintain a high standard of personal knowledge and skills relevant to the role through company-led and self-directed learning. Work with minimal supervision, prioritizing and managing workload for self and a small team of analysts. Act as a coach and mentor for less knowledgeable colleagues in areas of subject matter expertise. Comply with company health and safety requirements, adopting a proactive safety attitude to ensure the safety of self and others. Participate in wider laboratory support teams such as spill team, fire warden, first aid team, HS rep, quality team, or internal audit team. Qualifications: Bachelor's degree in Chemistry/Scientific discipline or equivalent experience within similar role. Proficiency in GC analysis and relevant software such as Xcalibur, Masslynx, Chromeleon or Masshunter. Strong analytical and problem-solving skills. Excellent communication and teamwork abilities. Knowledge of ISO 17025 and MCERTS standards.
May 05, 2026
Full time
Consent Cookie Name : Google Analytics What it does: Data Collection, Configuration, Data Processing and Reporting Why is it used: Tracks and Reports Traffic (Anonymised) for Web Analytics How long it lasts: At least 25 Months . Enquiries When contacted with an enquiry, we will hold the entity name and contact details only for the purposes of handling the enquiry. recognise you whenever you visit this website (this speeds up your access to the website as you do not have to log in each time); obtain information about your preferences, online movements and use of the internet; carry out research and statistical analysis to help improve our content, products and services and to help us better understand our customer requirements and interests; target our marketing and advertising campaigns more effectively by providing interest-based advertisements that are personalised to your interests; make your online experience more efficient and enjoyable.Senior GC Analyst (Team Lead) page is loaded Senior GC Analyst (Team Lead)locations: Southampton, UKtime type: Full timeposted on: Posted 2 Days Agojob requisition id: REQ106681 This role is located in Marchwood, within the Cawood Scientific Environment Division. Marchwood, part of Cawood, was established in 1998 and performs a range of specialist analytical testing services to customers operating in the Environmental, Industrial and Agricultural Sectors from its three laboratories based in the South and North of England. As a leading UK Dioxin and Furans analysis laboratory and the UK's leading specialist laboratory for independent occupational hygiene analysis, Marchwood offers a range of services for the environmental, occupational and food/feed sectors Job Description: Job Title: Senior GC Analyst (Team Lead) Location: Marchwood Southampton Company: Cawood Job Description: We are seeking a highly skilled and motivated Senior GC Analyst to join our dynamic team within our Dioxins Laboratory. The successful candidate will be responsible for performing routine analysis on customer samples, working to deadlines in accordance with the company Quality Management System and UKAS guidelines. Experience with High Resolution Mass Spectrometry advantages but not essential. Key Responsibilities: Perform routine analysis on customer samples, adhering to deadlines and quality standards (ISO 17025 and MCERTS). Accurately record and analyze data, identifying possible deviations and ensuring compliance with system suitability checks, calibrations, and AQC charts. Undertake and assist with the investigation of queries and non-conformance. Perform routine and non-routine instrument maintenance, troubleshooting, identifying root causes, and implementing corrective actions to minimize unplanned instrument downtime. Plan and perform validation work to improve existing methods and develop new methods to support client requests and company growth strategy. Assist with the validation of new instruments as required. Effectively communicate with co-workers and local management. Prepare standards and solutions and aid in the preparation/extraction of samples if required. Maintain a high standard of personal knowledge and skills relevant to the role through company-led and self-directed learning. Work with minimal supervision, prioritizing and managing workload for self and a small team of analysts. Act as a coach and mentor for less knowledgeable colleagues in areas of subject matter expertise. Comply with company health and safety requirements, adopting a proactive safety attitude to ensure the safety of self and others. Participate in wider laboratory support teams such as spill team, fire warden, first aid team, HS rep, quality team, or internal audit team. Qualifications: Bachelor's degree in Chemistry/Scientific discipline or equivalent experience within similar role. Proficiency in GC analysis and relevant software such as Xcalibur, Masslynx, Chromeleon or Masshunter. Strong analytical and problem-solving skills. Excellent communication and teamwork abilities. Knowledge of ISO 17025 and MCERTS standards.
Location: Swindon FTC - 18 month contract. Catalent are currently recruiting for a QC apprentice to join the Swindon site. The Apprentice QC Analyst will learn and assist in many aspects of the QC Chemistry role and then put these learnings into practice within the laboratories. The Apprentice will perform analysis for analytical samples in accordance with defined analytical methods and Standard Operating Procedures and within timelines as agreed with line management. Catalent seeks people with the desire to make a difference in the health of patients and consumers globally. Your talents, ideas and passion are essential to your success and our mission: to deliver more products, better treatments, reliably supplied. This is the opportunity you've been looking for to learn, develop, and be part of a growing business. The Role: Complete any college-based courses and be prepared to undertake any future training, internally or externally, as required by Catalent. Responsibilities To comply with all Catalent EH&S requirements. To ensure that all tasks are conducted in accordance with defined risk assessments and that tasks are carried out with regards to the safety of others. To understand the cGMP requirements as related to the role, to follow the training provided and ensure that all activities are performed according to the appropriate procedures. To participate in laboratory housekeeping and maintenance duties. To prepare laboratory chemicals and reagents as required for analysis and documenting/labelling them according to laboratory procedures. Gain a proficient understanding for the use of some of the simpler items of analytical equipment used within the laboratory, including analytical balances, pH meters, dissolution baths, disintegration bath. Help to troubleshoot these instruments when they do not work as expected. Provide timely feedback to more senior staff and to the laboratory analysts. Qualifications Basic knowledge of the main site Quality Systems for example LIMS and QUMAS. A minimum of 3 GCSEs (or equivalent) including English and Math's at grade C/5 or above. Good analytical thinking, dynamic, pro active approach to the workload. Have a positive attitude, taking personal accountability for your work. To demonstrate ability for attention to detail. Catalent offers rewarding opportunities to further your career. Legal Statements Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Proud member of the Disability Confident employer scheme.
May 04, 2026
Full time
Location: Swindon FTC - 18 month contract. Catalent are currently recruiting for a QC apprentice to join the Swindon site. The Apprentice QC Analyst will learn and assist in many aspects of the QC Chemistry role and then put these learnings into practice within the laboratories. The Apprentice will perform analysis for analytical samples in accordance with defined analytical methods and Standard Operating Procedures and within timelines as agreed with line management. Catalent seeks people with the desire to make a difference in the health of patients and consumers globally. Your talents, ideas and passion are essential to your success and our mission: to deliver more products, better treatments, reliably supplied. This is the opportunity you've been looking for to learn, develop, and be part of a growing business. The Role: Complete any college-based courses and be prepared to undertake any future training, internally or externally, as required by Catalent. Responsibilities To comply with all Catalent EH&S requirements. To ensure that all tasks are conducted in accordance with defined risk assessments and that tasks are carried out with regards to the safety of others. To understand the cGMP requirements as related to the role, to follow the training provided and ensure that all activities are performed according to the appropriate procedures. To participate in laboratory housekeeping and maintenance duties. To prepare laboratory chemicals and reagents as required for analysis and documenting/labelling them according to laboratory procedures. Gain a proficient understanding for the use of some of the simpler items of analytical equipment used within the laboratory, including analytical balances, pH meters, dissolution baths, disintegration bath. Help to troubleshoot these instruments when they do not work as expected. Provide timely feedback to more senior staff and to the laboratory analysts. Qualifications Basic knowledge of the main site Quality Systems for example LIMS and QUMAS. A minimum of 3 GCSEs (or equivalent) including English and Math's at grade C/5 or above. Good analytical thinking, dynamic, pro active approach to the workload. Have a positive attitude, taking personal accountability for your work. To demonstrate ability for attention to detail. Catalent offers rewarding opportunities to further your career. Legal Statements Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Proud member of the Disability Confident employer scheme.
We are seeking a Graduate QC Analyst to join our client's quality team in Lanarkshire, Scotland. The successful candidate will be responsible for conducting high-quality analytical testing of raw materials, intermediates, and finished products within a GMP-regulated environment. You will assist with validation, maintain laboratory equipment, and ensure compliance with industry standards. The role involves organising sample testing activities, updating documentation, and supporting batch release processes, with the aim of maintaining exemplary quality standards and efficient laboratory operations. BSc in Chemistry or equivalent Experience in a laboratory environment, GMP experience is advantageous Knowledge of EU GMP and analytical chemistry principles Attention to detail, problem-solving, and organisation skills Computer literacy and practical laboratory skills In return, you will enjoy excellent benefits. This permanent role offers ongoing development opportunities within a highly-regulated pharmaceutical environment, fostering growth in your analytical expertise and quality assurance skills.
Oct 05, 2025
Full time
We are seeking a Graduate QC Analyst to join our client's quality team in Lanarkshire, Scotland. The successful candidate will be responsible for conducting high-quality analytical testing of raw materials, intermediates, and finished products within a GMP-regulated environment. You will assist with validation, maintain laboratory equipment, and ensure compliance with industry standards. The role involves organising sample testing activities, updating documentation, and supporting batch release processes, with the aim of maintaining exemplary quality standards and efficient laboratory operations. BSc in Chemistry or equivalent Experience in a laboratory environment, GMP experience is advantageous Knowledge of EU GMP and analytical chemistry principles Attention to detail, problem-solving, and organisation skills Computer literacy and practical laboratory skills In return, you will enjoy excellent benefits. This permanent role offers ongoing development opportunities within a highly-regulated pharmaceutical environment, fostering growth in your analytical expertise and quality assurance skills.
Optimisation Functional SME Start: ASAP Duration: 6-12 months Location: Wokingham (3-days on site) Pay: Inside IR35, up to £425/day We are seeking a technically skilled Optimisation & Algorithm Test Engineer to join a high-impact programme within the Electricity System Operator's Balancing Transformation initiative. This pivotal role supports the development and quality assurance of a modern dispatch optimisation algorithm, working closely with Business Analysts, QA professionals, and Developers to ensure accurate and efficient algorithm functionality. Key Responsibilities - Collaborate with cross-functional teams to support the Dispatch Algorithm development and testing. - Contribute to the Quality Assurance of optimisation components within the broader Balancing Transformation Programme. - Review and validate algorithmic test scenarios with business and technical teams. - Perform exploratory testing and identify defects or irregularities in algorithm performance. - Assist in developing tools and automating testing processes for optimisation algorithms. - Work closely with developers and data scientists to refine algorithm outputs and ensure reliability. Essential Skills & Experience - Proven experience in solving optimisation problems using a variety of mathematical and computational techniques. - Familiarity with mathematical programming solvers such as Gurobi for LP, QP, and MIP (MILP, MIQP, MIQCP) problems. - Strong programming skills in Python and relevant libraries for optimisation and data analysis. - Solid understanding of data collection, pre-processing, and exploratory data analysis techniques. - Experience building and deploying custom data models and algorithms to solve real-world problems. - Experience working with large datasets and drawing actionable insights. - Strong communication skills to collaborate effectively with business stakeholders and technical teams. - Experience in QA or software testing environments, ideally within algorithmic or mathematical software contexts.
Sep 26, 2025
Contractor
Optimisation Functional SME Start: ASAP Duration: 6-12 months Location: Wokingham (3-days on site) Pay: Inside IR35, up to £425/day We are seeking a technically skilled Optimisation & Algorithm Test Engineer to join a high-impact programme within the Electricity System Operator's Balancing Transformation initiative. This pivotal role supports the development and quality assurance of a modern dispatch optimisation algorithm, working closely with Business Analysts, QA professionals, and Developers to ensure accurate and efficient algorithm functionality. Key Responsibilities - Collaborate with cross-functional teams to support the Dispatch Algorithm development and testing. - Contribute to the Quality Assurance of optimisation components within the broader Balancing Transformation Programme. - Review and validate algorithmic test scenarios with business and technical teams. - Perform exploratory testing and identify defects or irregularities in algorithm performance. - Assist in developing tools and automating testing processes for optimisation algorithms. - Work closely with developers and data scientists to refine algorithm outputs and ensure reliability. Essential Skills & Experience - Proven experience in solving optimisation problems using a variety of mathematical and computational techniques. - Familiarity with mathematical programming solvers such as Gurobi for LP, QP, and MIP (MILP, MIQP, MIQCP) problems. - Strong programming skills in Python and relevant libraries for optimisation and data analysis. - Solid understanding of data collection, pre-processing, and exploratory data analysis techniques. - Experience building and deploying custom data models and algorithms to solve real-world problems. - Experience working with large datasets and drawing actionable insights. - Strong communication skills to collaborate effectively with business stakeholders and technical teams. - Experience in QA or software testing environments, ideally within algorithmic or mathematical software contexts.
QC Analyst Location: Worthing, West Sussex Salary: £15.64 p/h Employment Type: 6 Month Contract CY Partners have an exciting contract opportunity for a QC Analyst with a background in pharmaceutical analysis. Do you have hands-on expertise with HPLC and other analytical techniques? If so, this could be a fantastic opportunity to further your career within a dynamic and fast-paced QC environment. This is a key role within the Quality function, supporting the release and stability testing of sterile and non-sterile products. Key Responsibilities: Perform physical and chemical testing of production and stability samples, meeting turnaround times and compliance standards. Analyse solid dose and antibiotic formulations using HPLC, Karl Fischer, dissolution, and other wet chemistry techniques. Calibrate, verify, and maintain analytical instruments and systems. Review and verify analytical results, ensuring data integrity and compliance with GMP/GLP. Support investigations into Out-of-Specification (OOS) results, working cross-functionally where needed. Contribute to the validation of analytical methods and equipment. About You: You ll ideally bring a strong background in pharmaceutical quality testing, with sound knowledge of GMP regulations and analytical chemistry. Requirements: HNC, HND, BSc or equivalent in Chemistry or a related scientific discipline. Proven experience in a GMP-regulated lab, with hands-on experience using HPLC. Strong documentation and data reporting skills. Detail-oriented, methodical, and safety-conscious. Able to communicate clearly and work effectively as part of a multidisciplinary team. A proactive, flexible approach to working in a fast-moving manufacturing environment. Whether you re looking to build on your experience or take the next step in your QC career, this is a great opportunity to make a meaningful impact within the pharmaceutical industry.
Sep 23, 2025
Contractor
QC Analyst Location: Worthing, West Sussex Salary: £15.64 p/h Employment Type: 6 Month Contract CY Partners have an exciting contract opportunity for a QC Analyst with a background in pharmaceutical analysis. Do you have hands-on expertise with HPLC and other analytical techniques? If so, this could be a fantastic opportunity to further your career within a dynamic and fast-paced QC environment. This is a key role within the Quality function, supporting the release and stability testing of sterile and non-sterile products. Key Responsibilities: Perform physical and chemical testing of production and stability samples, meeting turnaround times and compliance standards. Analyse solid dose and antibiotic formulations using HPLC, Karl Fischer, dissolution, and other wet chemistry techniques. Calibrate, verify, and maintain analytical instruments and systems. Review and verify analytical results, ensuring data integrity and compliance with GMP/GLP. Support investigations into Out-of-Specification (OOS) results, working cross-functionally where needed. Contribute to the validation of analytical methods and equipment. About You: You ll ideally bring a strong background in pharmaceutical quality testing, with sound knowledge of GMP regulations and analytical chemistry. Requirements: HNC, HND, BSc or equivalent in Chemistry or a related scientific discipline. Proven experience in a GMP-regulated lab, with hands-on experience using HPLC. Strong documentation and data reporting skills. Detail-oriented, methodical, and safety-conscious. Able to communicate clearly and work effectively as part of a multidisciplinary team. A proactive, flexible approach to working in a fast-moving manufacturing environment. Whether you re looking to build on your experience or take the next step in your QC career, this is a great opportunity to make a meaningful impact within the pharmaceutical industry.
Are you an experienced SAP B1 Support Analyst with strong ERP knowledge and a passion for supporting manufacturing operations? This is an exciting opportunity to join a growing global organisation and play a pivotal role in supporting and enhancing their SAP Business One and BEAS Manufacturing environment. The Role: You will provide 2nd (progressing to 3rd) line support for SAP Business One and BEAS across production, warehouse, QC and engineering departments. This is a hands-on role working closely with users, IT, and business teams to resolve issues, improve processes, and support ongoing rollout projects across multiple sites. Responsibilities: Troubleshooting and resolving SAP B1/BEAS issues within agreed SLAs Managing data, DTW templates, and integrations Supporting Item Master Data, BOMs, Routings, MRP and Capacity Planning Creating and maintaining Crystal Reports, SQL queries and layouts Developing Boyum B1UP functionalities and supporting BPA workflows Assisting with upgrades, testing and documentation to ISO standards Requirements: 2+ years' experience supporting SAP B1 BEAS highly desirable Strong understanding of production, warehouse or engineering environments Proficiency in SQL and data management concepts Excellent problem-solving and communication skills Experience with Crystal Reports, DTW and integrations is an advantage What's on Offer: Competitive salary Hybrid working - 3 days in the office and 2 days working from home Opportunity to progress into 3rd line support and project work Be part of a collaborative global IT team Exposure to SAP Business One, BEAS, Boyum and BPA automation tools If you're looking to build your career in SAP Business One support and want to work in a role where you'll directly impact production operations, this is the role for you. How to Apply: Please apply asap with your CV to be considered for this position. Henley Morgan is the leader in SAP Business One recruitment with SAP B1 jobs all over the globe.
Sep 21, 2025
Full time
Are you an experienced SAP B1 Support Analyst with strong ERP knowledge and a passion for supporting manufacturing operations? This is an exciting opportunity to join a growing global organisation and play a pivotal role in supporting and enhancing their SAP Business One and BEAS Manufacturing environment. The Role: You will provide 2nd (progressing to 3rd) line support for SAP Business One and BEAS across production, warehouse, QC and engineering departments. This is a hands-on role working closely with users, IT, and business teams to resolve issues, improve processes, and support ongoing rollout projects across multiple sites. Responsibilities: Troubleshooting and resolving SAP B1/BEAS issues within agreed SLAs Managing data, DTW templates, and integrations Supporting Item Master Data, BOMs, Routings, MRP and Capacity Planning Creating and maintaining Crystal Reports, SQL queries and layouts Developing Boyum B1UP functionalities and supporting BPA workflows Assisting with upgrades, testing and documentation to ISO standards Requirements: 2+ years' experience supporting SAP B1 BEAS highly desirable Strong understanding of production, warehouse or engineering environments Proficiency in SQL and data management concepts Excellent problem-solving and communication skills Experience with Crystal Reports, DTW and integrations is an advantage What's on Offer: Competitive salary Hybrid working - 3 days in the office and 2 days working from home Opportunity to progress into 3rd line support and project work Be part of a collaborative global IT team Exposure to SAP Business One, BEAS, Boyum and BPA automation tools If you're looking to build your career in SAP Business One support and want to work in a role where you'll directly impact production operations, this is the role for you. How to Apply: Please apply asap with your CV to be considered for this position. Henley Morgan is the leader in SAP Business One recruitment with SAP B1 jobs all over the globe.
