Complaints Investigator (Night Shift) Location: Witney, Oxfordshire (OX29 0YL) Shift Pattern: 4 on, 4 off - 7:00 PM to 7:00 AM Pay Rate: 17.19 per hour Contract: Temporary About the Role Are you passionate about quality and committed to improving healthcare outcomes? Do you thrive in a structured, process-driven environment and enjoy getting to the root of complex problems? We're hiring Complaints Investigators to join a leading global healthcare and medical device manufacturer in Witney. This is not a customer service position - instead, you will play a vital part in analysing returned medical products , identifying causes of issues, and contributing to ongoing product and process improvements. Key Responsibilities Product Investigations: Conduct detailed investigations into returned medical products, identifying root causes and ensuring compliance with regulatory and quality standards. Data Analysis: Utilise internal software systems to track complaint trends and emerging patterns. Your analytical skills will be key to recognising recurring issues. Continuous Improvement: Suggest and implement improvements in workflows and documentation processes to boost efficiency and reliability. Cross-Functional Collaboration: Liaise with internal stakeholders and international colleagues to share findings and support broader quality assurance objectives. New Product Readiness: Participate in pre-launch readiness activities, ensuring complaint handling systems are in place for new product introductions. What We're Looking For IT Proficiency: Comfortable using Excel, Word, and internal systems for documentation and analysis. Detail-Oriented: Strong focus on accuracy and process compliance. Analytical Thinking: Able to identify trends, draw insights, and support data-driven decision-making. Excellent Communication: Able to clearly document findings and collaborate with global colleagues. Minimum Education: GCSEs or equivalent in Maths and English. Desirable (Not Essential) Exposure to lab practices, root cause analysis, or regulated environments. Familiarity with complaint handling in healthcare, pharma, or diagnostics. What We Offer Full training provided - no prior experience required! Work that matters - support the delivery of safe and effective medical devices. Career progression opportunities in a growing and supportive team. Clean, modern facilities with on-site perks including free parking and subsidised canteen. Additional Requirements Eligibility to live and work in the UK. Ability to provide a 5-year referencing history (employment or alternative activity). Ready to Make a Difference? Apply now via this advert or email to or call (phone number removed) and ask for Akhil to learn more! Randstad Business Support is acting as an Employment Business in relation to this vacancy.
Nov 08, 2026
Seasonal
Complaints Investigator (Night Shift) Location: Witney, Oxfordshire (OX29 0YL) Shift Pattern: 4 on, 4 off - 7:00 PM to 7:00 AM Pay Rate: 17.19 per hour Contract: Temporary About the Role Are you passionate about quality and committed to improving healthcare outcomes? Do you thrive in a structured, process-driven environment and enjoy getting to the root of complex problems? We're hiring Complaints Investigators to join a leading global healthcare and medical device manufacturer in Witney. This is not a customer service position - instead, you will play a vital part in analysing returned medical products , identifying causes of issues, and contributing to ongoing product and process improvements. Key Responsibilities Product Investigations: Conduct detailed investigations into returned medical products, identifying root causes and ensuring compliance with regulatory and quality standards. Data Analysis: Utilise internal software systems to track complaint trends and emerging patterns. Your analytical skills will be key to recognising recurring issues. Continuous Improvement: Suggest and implement improvements in workflows and documentation processes to boost efficiency and reliability. Cross-Functional Collaboration: Liaise with internal stakeholders and international colleagues to share findings and support broader quality assurance objectives. New Product Readiness: Participate in pre-launch readiness activities, ensuring complaint handling systems are in place for new product introductions. What We're Looking For IT Proficiency: Comfortable using Excel, Word, and internal systems for documentation and analysis. Detail-Oriented: Strong focus on accuracy and process compliance. Analytical Thinking: Able to identify trends, draw insights, and support data-driven decision-making. Excellent Communication: Able to clearly document findings and collaborate with global colleagues. Minimum Education: GCSEs or equivalent in Maths and English. Desirable (Not Essential) Exposure to lab practices, root cause analysis, or regulated environments. Familiarity with complaint handling in healthcare, pharma, or diagnostics. What We Offer Full training provided - no prior experience required! Work that matters - support the delivery of safe and effective medical devices. Career progression opportunities in a growing and supportive team. Clean, modern facilities with on-site perks including free parking and subsidised canteen. Additional Requirements Eligibility to live and work in the UK. Ability to provide a 5-year referencing history (employment or alternative activity). Ready to Make a Difference? Apply now via this advert or email to or call (phone number removed) and ask for Akhil to learn more! Randstad Business Support is acting as an Employment Business in relation to this vacancy.
Are you an experienced Civil or Site Engineer? Would you like to be part of a transformational and historic project within the Steel industry? Are you based in or around South Wales? Tata Steel are looking for an established Engineer to support on Project invictus - a project that will modernise and transform the UK Steelmaking sector. The successful applicant will be someone with substantial experience within the Construction, heavy industry and/or Power industry. It is with the expectation that the post holder already holds full Right To Work in the UK, Site Management experience and a strong knowledge of UK Health and Safety legislation within a complex environment. Role: Site Engineer Location: Tata Steel, Port Talbot, SA13 2NG Rate: competitive (dependent upon experience) Shift Patterns: Mon-Fri, 08:00-16:15 Mon-Thu and 08:00-15:15 Fri Duration: Until 31/12/2027 initially Start: ASAP (within one month) but pending the result of a medical assessment. This does include a drug and alcohol test. Responsibilities: Supporting the civil engineering within Project Invictus Reviewing inspection reports raised by the asset inspection team on civil/structural engineering assets Developing a process for the delivery of the reduction of inspection reports Generating necessary documentation for the emerging works department Analysing and interpreting information from the electronic system Liaising with relevant department to obtain information relative for the pre engineering function Conducting investigations for the emerging works department Inspecting works areas to ensure safe working conditions Spearheading a strong, high performing and safe culture Essential requirements: Time served apprenticeship (Mechanical, Electrical Engineering or equivalent) Proven experience within a large construction, industrial or power site Driving Licence and access to own vehicle Previous experience conducting site management Excellent verbal and written communication skill Ability to conduct stakeholder management effectively Strong UK Health and Safety knowledge and experience within a high risk environment Proactive approach to tasks and ability to deliver on compliance and innovation Large capital project experience Desirable requirements: Degree educated/HNC/HND in Mechanical, Electrical Engineering or equivalent Black CSCS Card Completion of the SMTS course Benefits: Advice and editing on your current CV Dedicated team throughout your journey within the role Paid holiday (35 days per annum, including Bank Holidays) Exclusive online services including restaurant and retail discounts Chance to receive 300 for referring a friend Opportunity for progression into permanent roles Free Access to Employee Assistance programme for Mental, Physical and Financial support Does this role sound interesting? Apply today and a member of the team will be in contact if you meet our requirements. All applicants are subject to vetting checks including: Right to work check, medical check and reference check.
Nov 08, 2026
Contractor
Are you an experienced Civil or Site Engineer? Would you like to be part of a transformational and historic project within the Steel industry? Are you based in or around South Wales? Tata Steel are looking for an established Engineer to support on Project invictus - a project that will modernise and transform the UK Steelmaking sector. The successful applicant will be someone with substantial experience within the Construction, heavy industry and/or Power industry. It is with the expectation that the post holder already holds full Right To Work in the UK, Site Management experience and a strong knowledge of UK Health and Safety legislation within a complex environment. Role: Site Engineer Location: Tata Steel, Port Talbot, SA13 2NG Rate: competitive (dependent upon experience) Shift Patterns: Mon-Fri, 08:00-16:15 Mon-Thu and 08:00-15:15 Fri Duration: Until 31/12/2027 initially Start: ASAP (within one month) but pending the result of a medical assessment. This does include a drug and alcohol test. Responsibilities: Supporting the civil engineering within Project Invictus Reviewing inspection reports raised by the asset inspection team on civil/structural engineering assets Developing a process for the delivery of the reduction of inspection reports Generating necessary documentation for the emerging works department Analysing and interpreting information from the electronic system Liaising with relevant department to obtain information relative for the pre engineering function Conducting investigations for the emerging works department Inspecting works areas to ensure safe working conditions Spearheading a strong, high performing and safe culture Essential requirements: Time served apprenticeship (Mechanical, Electrical Engineering or equivalent) Proven experience within a large construction, industrial or power site Driving Licence and access to own vehicle Previous experience conducting site management Excellent verbal and written communication skill Ability to conduct stakeholder management effectively Strong UK Health and Safety knowledge and experience within a high risk environment Proactive approach to tasks and ability to deliver on compliance and innovation Large capital project experience Desirable requirements: Degree educated/HNC/HND in Mechanical, Electrical Engineering or equivalent Black CSCS Card Completion of the SMTS course Benefits: Advice and editing on your current CV Dedicated team throughout your journey within the role Paid holiday (35 days per annum, including Bank Holidays) Exclusive online services including restaurant and retail discounts Chance to receive 300 for referring a friend Opportunity for progression into permanent roles Free Access to Employee Assistance programme for Mental, Physical and Financial support Does this role sound interesting? Apply today and a member of the team will be in contact if you meet our requirements. All applicants are subject to vetting checks including: Right to work check, medical check and reference check.
Our client is a world-renowned, global healthcare and medical device manufacturer with a major state-of-the-art facility based in Witney. Known for their life-changing medical technologies, they offer an incredibly stable, supportive, and structured working environment We are looking for graduate or early career scientist. Some experience in industry is preferable but not essential. Role : Scientist Location : Witney Salary: 30,000 p.a- 35,000 p.a Work hours : 37.5 hours a week Job type: 12 Months Roles and Responsibilities Perform testing to protocol or procedure whilst adhering to good laboratory practice Develop protocols to accomplish goals Produce prototype product or communicate protoype requirements to support experiments. Utilise analytical instruments and train others in their operation Participate in experimental design discussions, identify variables that may impact experimental results Analyse data, evaluate results and form conclusions Prepares effective summaries of results and communicates these to wider team Compile and maintain records as required by good laboratory practice Writes clear and technically correct reports with feedback from colleagues Liase with other departments and present technical information to team meetings Have awareness of change control procedures applicable to role Know and apply knowledge of health and safety procedures Responsible for own laboratory notebook and for the accuracy, quality and timeliness of experimental results Ensures that all work complies with the quality system Uses scientific and industry literature to broaden technical and theoretical understanding Highlights improvement opportunities to manager Basic Qualifications Good written and oral communication skills Good working knowledge of software packages such as Word, Excel and Powerpoint to analyse data, present results and write reports Experience of working in a laboratory, scientific or technical environment Randstad Business Support is acting as an Employment Business in relation to this vacancy.
Nov 08, 2026
Contractor
Our client is a world-renowned, global healthcare and medical device manufacturer with a major state-of-the-art facility based in Witney. Known for their life-changing medical technologies, they offer an incredibly stable, supportive, and structured working environment We are looking for graduate or early career scientist. Some experience in industry is preferable but not essential. Role : Scientist Location : Witney Salary: 30,000 p.a- 35,000 p.a Work hours : 37.5 hours a week Job type: 12 Months Roles and Responsibilities Perform testing to protocol or procedure whilst adhering to good laboratory practice Develop protocols to accomplish goals Produce prototype product or communicate protoype requirements to support experiments. Utilise analytical instruments and train others in their operation Participate in experimental design discussions, identify variables that may impact experimental results Analyse data, evaluate results and form conclusions Prepares effective summaries of results and communicates these to wider team Compile and maintain records as required by good laboratory practice Writes clear and technically correct reports with feedback from colleagues Liase with other departments and present technical information to team meetings Have awareness of change control procedures applicable to role Know and apply knowledge of health and safety procedures Responsible for own laboratory notebook and for the accuracy, quality and timeliness of experimental results Ensures that all work complies with the quality system Uses scientific and industry literature to broaden technical and theoretical understanding Highlights improvement opportunities to manager Basic Qualifications Good written and oral communication skills Good working knowledge of software packages such as Word, Excel and Powerpoint to analyse data, present results and write reports Experience of working in a laboratory, scientific or technical environment Randstad Business Support is acting as an Employment Business in relation to this vacancy.
Role : Operations scientist Location : Witney Salary: 33,500 p.a Work hours : 37.5 hours a week Job type: 6 Months Client: Abbott Roles and Responsibilities Perform testing to protocol or procedure whilst adhering to good laboratory practice Develop protocols to accomplish goals Produce prototype product or communicate protoype requirements to support experiments. Utilise analytical instruments and train others in their operation Participate in experimental design discussions, identify variables that may impact experimental results Analyse data, evaluate results and form conclusions Prepares effective summaries of results and communicates these to wider team Compile and maintain records as required by good laboratory practice Writes clear and technically correct reports with feedback from colleagues Liase with other departments and present technical information to team meetings Have awareness of change control procedures applicable to role Know and apply knowledge of health and safety procedures Responsible for own laboratory notebook and for the accuracy, quality and timeliness of experimental results Ensures that all work complies with the quality system Uses scientific and industry literature to broaden technical and theoretical understanding Highlights improvement opportunities to manager Consistently demonstrates recognised behaviours Basic Qualifications A Levels ( 16 years) STEM subjects desirable but not required Experience of working in a laboratory, scientific or technical environment or other relevant industry Experience of writing technical reports and presenting results Limited technical knowledge Good working knowledge of software packages such as Word, Excel, PowerPoint Randstad Business Support is acting as an Employment Business in relation to this vacancy.
Nov 08, 2026
Contractor
Role : Operations scientist Location : Witney Salary: 33,500 p.a Work hours : 37.5 hours a week Job type: 6 Months Client: Abbott Roles and Responsibilities Perform testing to protocol or procedure whilst adhering to good laboratory practice Develop protocols to accomplish goals Produce prototype product or communicate protoype requirements to support experiments. Utilise analytical instruments and train others in their operation Participate in experimental design discussions, identify variables that may impact experimental results Analyse data, evaluate results and form conclusions Prepares effective summaries of results and communicates these to wider team Compile and maintain records as required by good laboratory practice Writes clear and technically correct reports with feedback from colleagues Liase with other departments and present technical information to team meetings Have awareness of change control procedures applicable to role Know and apply knowledge of health and safety procedures Responsible for own laboratory notebook and for the accuracy, quality and timeliness of experimental results Ensures that all work complies with the quality system Uses scientific and industry literature to broaden technical and theoretical understanding Highlights improvement opportunities to manager Consistently demonstrates recognised behaviours Basic Qualifications A Levels ( 16 years) STEM subjects desirable but not required Experience of working in a laboratory, scientific or technical environment or other relevant industry Experience of writing technical reports and presenting results Limited technical knowledge Good working knowledge of software packages such as Word, Excel, PowerPoint Randstad Business Support is acting as an Employment Business in relation to this vacancy.
Associate Scientist 2 - Environmental Monitoring Support Location: Witney, Oxfordshire Salary / Rate: 31,000 per annum Contract Duration: 30 Weeks Department: Quality Assurance / Laboratory Operations About the Role We are seeking a detail-oriented and compliant Associate Scientist to join our team in Witney on a 30-week contract basis. In this role, you will provide vital operational, laboratory, and administrative support for site Environmental Monitoring (EM) programmes. You will play a central role in maintaining a fully compliant Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) environment through accurate sample collection, rigorous data management, trend analysis, and inspection-ready record keeping. Key Accountabilities & Responsibilities Environmental Monitoring Operations Perform routine environmental monitoring activities, sample collection, labeling, and processing in strict accordance with approved protocols. Support data trending and assist senior team members with investigations into out-of-trend environmental monitoring results. Ensure monitoring equipment, testing materials, and consumables are properly maintained, stocked, and prepared for use. Adhere strictly to GLP and GMP requirements across all monitoring duties. Documentation & Record Management Maintain clear, accurate, and up-to-date batch records, laboratory logbooks, worksheets, and controlled documentation. Review environmental monitoring records for accuracy and completeness to ensure an inspection-ready state. Collate, scan, file, archive, and retrieve paper and electronic laboratory records in line with site retention procedures. Assist with periodic document updates and policy reviews as assigned. Data Management & Reporting Input, verify, and maintain monitoring data within electronic quality management systems and databases. Compile operational data for routine compliance summaries, technical reports, and team presentations. Identify data trends or discrepancies and communicate findings clearly to line management. Quality, Safety & Administrative Support Maintain full compliance with site Quality Systems, standard operating procedures (SOPs), and EHS (Environmental Health & Safety) regulations. Support internal audits, regulatory inspections, and continuous improvement initiatives by preparing required documentation. Provide day-to-day departmental support, including stock inventory control, order raising, and activity scheduling. Key Requirements & Experience Technical Knowledge: Working knowledge of Good Manufacturing Practice (GMP) or Good Laboratory Practice (GLP) principles within a regulated manufacturing or laboratory environment. Systems Proficiency: Strong computer literacy, including MS Office (Excel, Word, PowerPoint) and familiarity with electronic quality or database systems. Data Integrity & Precision: Outstanding attention to detail with strong record-keeping, trend analysis, and document review skills. Organization & Collaboration: Excellent time management skills with the ability to prioritize routine sampling tasks, work effectively in cross-functional teams, and follow strict protocols consistently. Why Apply? This contract position offers a great opportunity to gain hands-on quality and environmental monitoring experience within a highly regulated manufacturing site, developing core skills in GMP compliance, data integrity, and laboratory operations. Randstad Business Support is acting as an Employment Business in relation to this vacancy.
Nov 08, 2026
Seasonal
Associate Scientist 2 - Environmental Monitoring Support Location: Witney, Oxfordshire Salary / Rate: 31,000 per annum Contract Duration: 30 Weeks Department: Quality Assurance / Laboratory Operations About the Role We are seeking a detail-oriented and compliant Associate Scientist to join our team in Witney on a 30-week contract basis. In this role, you will provide vital operational, laboratory, and administrative support for site Environmental Monitoring (EM) programmes. You will play a central role in maintaining a fully compliant Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) environment through accurate sample collection, rigorous data management, trend analysis, and inspection-ready record keeping. Key Accountabilities & Responsibilities Environmental Monitoring Operations Perform routine environmental monitoring activities, sample collection, labeling, and processing in strict accordance with approved protocols. Support data trending and assist senior team members with investigations into out-of-trend environmental monitoring results. Ensure monitoring equipment, testing materials, and consumables are properly maintained, stocked, and prepared for use. Adhere strictly to GLP and GMP requirements across all monitoring duties. Documentation & Record Management Maintain clear, accurate, and up-to-date batch records, laboratory logbooks, worksheets, and controlled documentation. Review environmental monitoring records for accuracy and completeness to ensure an inspection-ready state. Collate, scan, file, archive, and retrieve paper and electronic laboratory records in line with site retention procedures. Assist with periodic document updates and policy reviews as assigned. Data Management & Reporting Input, verify, and maintain monitoring data within electronic quality management systems and databases. Compile operational data for routine compliance summaries, technical reports, and team presentations. Identify data trends or discrepancies and communicate findings clearly to line management. Quality, Safety & Administrative Support Maintain full compliance with site Quality Systems, standard operating procedures (SOPs), and EHS (Environmental Health & Safety) regulations. Support internal audits, regulatory inspections, and continuous improvement initiatives by preparing required documentation. Provide day-to-day departmental support, including stock inventory control, order raising, and activity scheduling. Key Requirements & Experience Technical Knowledge: Working knowledge of Good Manufacturing Practice (GMP) or Good Laboratory Practice (GLP) principles within a regulated manufacturing or laboratory environment. Systems Proficiency: Strong computer literacy, including MS Office (Excel, Word, PowerPoint) and familiarity with electronic quality or database systems. Data Integrity & Precision: Outstanding attention to detail with strong record-keeping, trend analysis, and document review skills. Organization & Collaboration: Excellent time management skills with the ability to prioritize routine sampling tasks, work effectively in cross-functional teams, and follow strict protocols consistently. Why Apply? This contract position offers a great opportunity to gain hands-on quality and environmental monitoring experience within a highly regulated manufacturing site, developing core skills in GMP compliance, data integrity, and laboratory operations. Randstad Business Support is acting as an Employment Business in relation to this vacancy.
