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ROLE OVERVIEW \n Are you passionate about ensuring the highest standards in quality and compliance? A leading organisation in the industry is seeking a dedicated Quality Assurance Officer to join their dynamic team in Oxfordshire. This role offers the chance to make a significant impact on the quality processes and systems at a key time for this Biopharmaceutical business. \n KEY DUTIES AND RESPONSIBILITIES: \n Your duties as the Quality Assurance Officer will be varied; however, the key duties and responsibilities are as follows: \n 1. Overseeing and maintaining the quality management system to ensure compliance with industry standards. \n 2. Conducting internal audits and inspections to identify areas for improvement. \n 3. Collaborating with cross-functional teams to implement corrective and preventive actions. \n 4. Providing training and guidance on quality assurance processes and best practices. \n 5. Previous experince working with Assay's \n ROLE REQUIREMENTS: \n To be successful in your application to this exciting role as the Quality Assurance Officer, we are looking to identify the following on your profile and past history: \n 1. Relevant degree in a scientific or technical discipline. \n 2. Proven industry experience in quality assurance within a Sterile environment \n 3. A working knowledge and practical experience with quality management systems and regulatory requirements. \n This role is perfect for someone who thrives in a detail-oriented environment and is committed to upholding the highest standards of quality. If you have a keen eye for detail, strong analytical skills, and a proactive approach to problem-solving, this position will provide you with a challenging and rewarding career path. \n Take the next step in your career and apply now to become a Quality Assurance Officer in Oxford. Your expertise will be instrumental in driving quality excellence within the organisation. \n Key Words: Quality Assurance / QA Officer / Quality Management / Compliance / Internal Audits / Regulatory Standards / Preventive Actions / Quality Systems / Oxford / United Kingdom \n Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.

ROLE OVERVIEW \n We are currently looking for a Quality Assurance Officer II to join a leading biotech/pharmaceutical organisation based in a collaborative and innovative environment. This is an exciting opportunity for a skilled QA professional to contribute to the development, implementation, and maintenance of essential quality systems that ensure compliance and product integrity. \n In this role, you will play a pivotal part in supporting batch reviews, managing quality investigations, and driving continuous improvement initiatives. You will work closely with cross-functional teams, external vendors, and regulatory bodies to uphold the highest standards of GMP compliance and assist in audit preparations and execution. \n KEY DUTIES AND RESPONSIBILITIES \n Your duties as the Quality Assurance Officer II will be varied however the key duties and responsibilities are as follows: \n\n • Provide guidance and coordination in the development, implementation, and maintenance of Quality Assurance systems and activities.\n, • Manage batch review and final quality review activities supporting QP release and prioritisation.\n, • Drive improvement of GMP compliance, Change Controls, Deviations, and CAPA systems.\n, • Lead thorough root cause investigations and quality improvement activities.\n, • As the QA Officer II, you will review and approve SOPs, validation documents, GMP records, and other quality documentation.\n\n ROLE REQUIREMENTS \n To be successful in your application to this exciting role as the QA Officer II we are looking to identify the following on your profile and past history: \n\n • Experience of Assays\n, • Proven extensive experience (5+ years) working within quality within a pharmaceutical environment.\n, • Experienced working within Aseptic manufacturing environments\n\n WHAT’S IN IT FOR YOU? \n Joining our client offers the opportunity to work at the forefront of biotech and pharmaceutical manufacturing, supporting critical quality functions, and developing your expertise in a dynamic industry setting. You will be part of a collaborative team committed to excellence and continuous improvement, with access to ongoing training and development. \n Key Words: Quality Assurance / GMP / Regulatory Compliance / Batch Review / Root Cause Investigation / CAPA / Audit / Risk Management / Vendor Oversight / Process Improvement \n "Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career".

Location: Oxfordshire (Hybrid – 60% Office / 40% Home) Job Type: Full-time Salary: Competitive DOE \n The Opportunity \n An exciting opportunity has arisen for an ambitious and commercially minded Strategic Business Development Lead to join an innovative technology organisation. This is a unique role combining strategic business development, stakeholder engagement, project leadership and marketing, making it ideal for someone who enjoys building relationships, driving growth and turning ideas into successful outcomes. \n Working closely with senior leadership, you will help identify and develop new business opportunities, manage strategic projects and strengthen relationships across government, education, commercial and technical sectors. You'll also play a key role in shaping marketing initiatives, supporting business strategy and delivering projects that improve operational efficiency through emerging technologies. \n Key Responsibilities \n\n • Identify, develop and secure new strategic business opportunities.\n, • Build and manage relationships with key stakeholders across government, education, commercial and technical organisations.\n, • Develop account plans and growth strategies to achieve business objectives.\n, • Lead strategic discussions and convert ideas into clear, actionable plans.\n, • Manage strategic projects, timelines and stakeholder communications.\n, • Coordinate product demonstrations, presentations, meetings and industry events.\n, • Support the development and delivery of marketing campaigns, communications and events.\n, • Analyse business processes and identify opportunities for automation and continuous improvement.\n, • Track pipeline activity, project progress and business performance, providing regular reports to senior leadership.\n, • Collaborate across multiple departments to ensure business priorities are delivered effectively.\n\n We're looking for someone who is: \n\n • Experienced in business development, strategic partnerships or commercial relationship management.\n, • Comfortable engaging with senior stakeholders and decision-makers.\n, • Highly organised, proactive and able to manage multiple priorities.\n, • A confident communicator with strong presentation and negotiation skills.\n, • Commercially aware with excellent analytical and problem-solving abilities.\n, • Experienced in project management and cross-functional collaboration.\n, • Self-motivated and able to work independently while contributing to a wider team.\n\n Desirable Experience \n\n • Degree or equivalent experience in a STEM subject such as Engineering, Computer Science, Mathematics or Physics.\n, • Experience within technology, software, engineering, education or scientific sectors.\n, • Understanding of digital technologies, software development or AI.\n, • Experience delivering strategic marketing initiatives.\n, • Leadership or mentoring experience.\n, • Knowledge of CRM systems and project management tools.\n\n What's on Offer \n\n • Hybrid working (60% office / 40% home)\n, • Opportunity to work on high-profile strategic projects\n, • Collaborative and innovative working environment\n, • Career development within a growing technology business\n, • Competitive salary and benefits package\n\n Our client is an equal opportunities employer and welcomes applications from all suitably qualified candidates regardless of age, disability, gender identity, marital status, race, religion or belief, sex or sexual orientation.

Position: Mechanical Technician Department: Cryobitz Manufacturing Location: Witney Salary: competitive Role Purpose We are seeking a skilled, practical technician to manufacture and assemble high-quality cryogenic products, including transfer lines, LN2 traps, vacuum-insulated components and associated assemblies. This is a hands-on role with a strong emphasis on precision welding, soldering, brazing, and mechanical assembly. The successful candidate will produce neat, accurate and carefully to engineering drawings and defined quality standards. Key Responsibilities Assemble bespoke cryogenic systems from engineering drawings and build information. Fit pipework, valves, vacuum components, flanges and mechanical assemblies. Perform vacuum and helium leak testing of components and assemblies. Prepare, clean and handle components for high and ultra-high vacuum (UHV) applications. Maintain high standards of cleanliness throughout assembly and prevent contamination of vacuum-critical components. Complete mechanical fitting, drilling, tapping and general assembly work. Occasionally operate manual mills and lathes for simple machining and modification work. Follow route cards, drawings, Standard Work Instructions and manufacturing instructions. Complete and record required checks during assembly. Identify, investigate and resolve build problems, escalating issues where required. Carry out rework and modifications when required. Essential Skills and Experience Previous mechanical assembly, engineering or manufacturing experience. Strong practical and mechanical skills. Ability to read and work from engineering drawings. Good problem-solving skills and the ability to identify practical solutions to build issues. Excellent attention to detail and a high standard of workmanship. Ability to work to strict cleanliness standards. Experience using hand tools and workshop equipment. Ability to follow documented processes and instructions. Able to work independently and take responsibility for the quality of completed work. Good communication and teamwork skills. Desirable Skills & Experience Experience handling and assembling components for high vacuum or ultra-high vacuum (UHV) applications . Understanding of UHV cleanliness, contamination control and appropriate component handling.. Vacuum and helium leak testing. Cryogenic or high-vacuum equipment. Stainless steel pipework and fittings. Swagelok or similar compression fittings. Manual milling and turning. Precision mechanical assembly. Scientific, laboratory or specialist engineering equipment. Omega is acting as an Employment Agency in relation to this vacancy. Omega does not charge candidates any recruitment or job-seeking fees at any stage of the hiring process. TPBN1_UKTJ

Position: Mechanical Engineering Technician Location: Witney, Oxfordshire Job Type: Permanent / Onsite My client, a specialist manufacturing business are on the hunt for an experienced Mechanical Engineering Technician to join their team! Role and Responsibilities – Mechanical Engineering Technician In this role, you will be assembling complex components and products for the scientific industry in line with tight tolerances and customer demand. Other responsibilities include: Troubleshooting – identifying, documenting, resolving and reporting technical issues during the assembly process Actively work with the D.O. to improve products and increase efficiency of assembly processes. Quality control and inspection – Conducting visual inspections to ensure products meet quality and specifications throughout the assembly process Experience or Qualifications – Mechanical Engineering Technician NVQ or HNC Qualified in Engineering field Previous experience in assembly ideally within a scientific environment Experience working to tight tolerances Welding, Soldering and Fabrication experience (desirable) Benefits – Mechanical Engineering Technician 25 Days + Bank Holidays Private Health Care Options Early Finish Fridays Overtime Available Candidates who currently are a Mechanical Engineering Technician, Assembly Technician, Engineering Technician or Mechanical Assembler may be suitable for this position. For more information regarding this Mechanical Engineering Technician role please contact Ben Herd on 01453 829523 or Omega Resource Group is acting as an Employment Agency in relation to this vacancy. Omega Resource Group is an employment agency specialising in opportunities at all levels within the Engineering, Aerospace, Automotive, Electronics, Defence, Scientific, Oil & Gas, Construction and Manufacturing sectors. For details of other opportunities available within your chosen field please visit our website Omega is acting as an Employment Agency in relation to this vacancy. Omega does not charge candidates any recruitment or job-seeking fees at any stage of the hiring process. TPBN1_UKTJ

Experience or Qualifications – Sales & Customer Support Admin (Part Time) Previous experience in a similar admin role (ideally within a fast paced environment) Strong customer service background Experience using SAGE 200 or similar ERP software (desirable) Understanding of scientific or engin

Abbott Diabetes Care in Witney is seeking a System Project Lead to drive global system initiatives that support clinical studies, data management and scientific activities. You will collaborate with Clinical Affairs teams in the UK and US, plus Business Systems and external partners, to translate business needs into practical technology solutions. You will lead end-to-end projects, simplify processes, improve data handling, and enable effective collaboration while ensuring privacy, #J-18808-Ljbffr

Abbott is seeking an Analytical Chemistry leader at our Witney site to steer a growing laboratory responsible for release, stability testing, and lifecycle management of combination products. You will guide a team of analysts, ensure regulatory compliance, and drive continuous improvement in a GMP-regulated environment. The role combines scientific leadership with operational management and strategic influence, offering the opportunity to scale capabilities as product volumes grow within #J-18808-Ljbffr

JOB DESCRIPTION:Senior Manager, Design TransferLocation: Witney Abbott is about the power of health. For more than 135 years, Abbott has been helping people reach their potential, because better health allows people and communities to achieve more. Joining us, you can shape your career as you shape the future of healthcare. With a diverse, global network serving customers in more than 160 countries, we create new solutions across the spectrum of health, around the world, for all stages of life. Whether it's next-generation diagnostics, life-changing devices, science-based nutrition, or breakthrough medical technologies, we are advancing some of the most innovative healthcare solutions availabletoday. ABOUT OUR DIABETES CARE DIVISION: World Leader in Glucose Monitoring, Abbott Diabetes Care designs, develops and manufactures leading-edge glucose monitoring systems for use in both home and hospital settings. Our technologies are transforming the way people manage diabetes, including the revolutionary FreeStyle Libre portfolio, which has helped redefine glucose monitoring for millions of users around the world. Through continued investment in innovation, manufacturing excellence and world-class quality systems, Abbott Diabetes Care remains at the forefront of healthcare technology, delivering solutions that help people live healthier, fuller lives. THE OPPORTUNITY: At Abbott Diabetes Care, our technologies are transforming the lives of millions of people living with diabetes worldwide. As our portfolio continues to expand across the FreeStyle Libre family, Blood Glucose Monitoring Systems, medical device combination products and emerging digital health technologies, we have an exciting opportunity for a Senior Manager, Design Transfer to join our Quality organisation. In this highly visible leadership role, you will be responsible for overseeing the design transfer of products that will reach more than 15 million customers globally and support a business delivering in excess of $10 billion in revenue over the next five years. You will lead the successful transfer of new product introductions, design changes, validation activities and quality processes from Research & Development into manufacturing operations across Abbott sites and external manufacturing partners. Working at the intersection of Quality, Operations, Engineering, Regulatory Affairs and R&D, you will play a critical role in bringing innovative healthcare technologies to market while ensuring compliance with global regulatory requirements and Abbott quality standards. Key responsibilities include: Leading the strategy, planning and execution of design transfer activities for new products, product changes and manufacturing improvements. Driving the commercialization of innovative diabetes care technologies from development into global manufacturing operations. Partnering with cross-functional and cross-site stakeholders to ensure successful product launches and business continuity. Ensuring compliance with Abbott Quality Systems and external regulatory requirements, including FDA and ISO standards. Supporting the selection and onboarding of Abbott and external manufacturing sites for product transfers. Leading validation strategies, including process validation, test method validation and manufacturing qualification activities. Driving continuous improvement initiatives to enhance product quality, operational performance and regulatory compliance. Providing leadership, coaching and technical guidance across quality engineering and project teams. Acting as a key subject matter expert during regulatory inspections and quality audits. Managing risk through the application of tools such as DFMEA, PFMEA, Fault Tree Analysis and other risk management methodologies. This is a unique opportunity to influence the future of Abbott's Diabetes Care business while leading global initiatives that directly impact products used by millions of people every day. ABOUT YOU: We're looking for an experienced quality and design transfer leader with a passion for innovation, collaboration and delivering excellence in a highly regulated environment. To be successful, you will bring: A Bachelor's degree in a scientific, engineering or related discipline. Progressive experience within the medical device industry. Leadership or management experience. Strong knowledge of medical device regulations and quality systems, including FDA regulations, ISO 13485 and risk management principles. Extensive experience in product development lifecycles, design controls, design transfer, process validation and change management. Proven experience leading complex cross-functional projects across multiple sites and stakeholders. Strong understanding of manufacturing processes, quality systems and product commercialization activities. Excellent communication, relationship-building and stakeholder management skills. The ability to influence at all levels of the organisation and drive results in a fast-paced global environment. Experience working with contract manufacturers, large-scale product transfers and global supply chains would be highly advantageous. WHAT WE OFFER: This is an opportunity to take on a strategic leadership role within one of the world's leading medical technology organisations. You will work alongside talented colleagues across Quality, R&D, Operations and Regulatory Affairs while helping to bring life-changing healthcare technologies to patients around the world. Abbott offers a benefits platform that provides security to you and your family. As you'd expect from an innovative global healthcare company, we offer a competitive salary, bonus opportunity, a class-leading defined contribution pension scheme, private healthcare, life assurance, flexible benefits and extensive opportunities for professional development and career progression. At Abbott, you'll be empowered to make a meaningful difference while developing your leadership career within a business that is shaping the future of healthcare.The base pay for this position isN/AIn specific locations, the pay range may vary from the range posted. #J-18808-Ljbffr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutrition and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutrition and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Abbott is the global leader in Diabetes Care with the number one continuous glucose monitor worldwide. We are delivering breakthroughs for people living with diabetes through the highest level of accuracy in our unmatched sensing technology. Today, more than 7 million people globally rely on the FreeStyle Libre system to help manage their diabetes. As a Statistics & Analysis Manager, you will provide both technical and people leadership across Clinical and R&D projects within Abbott's Diabetes Care business. Leading a team of statisticians and analysts, you will be responsible for shaping statistical strategy, allocating resources across a diverse project portfolio, and ensuring the delivery of high-quality analysis projects that support product development, clinical evidence portfolio, regulatory submissions and business decision-making. This is a key leadership role where you will build capability within the team, develop talent, and foster a high-performance culture while ensuring statistical excellence across the organisation. • Lead and coordinate statistical support across Clinical and R&D programmes, ensuring quality, consistency and compliance., • Manage, coach and develop a team of statisticians and analysts, providing guidance, feedback and career development support., • Drive team performance through effective goal setting, performance management and development planning., • Allocate and manage statistical resources across multiple projects, balancing priorities and business needs., • Support new product development through robust experimental design, data analysis and interpretation., • Ensure analyses, reports and sampling plans meet internal standards, regulatory requirements and industry best practice., • Provide statistical and clinical input into regulatory submissions and interactions with regulatory bodies., • Partner with cross-functional stakeholders to influence strategy and support critical business decisions., • Identify opportunities for continuous improvement within statistical methodologies, processes and team capability., • Contribute to recruitment, onboarding and succession planning activities to support the continued growth of the statistics function., • Degree qualified in Statistics, Mathematics or a related technical discipline., • Proven experience leading and managing technical teams, including responsibility for performance management, coaching, mentoring and employee development., • Demonstrated people leadership experience, with a track record of building, developing and retaining high-performing teams., • Strong expertise in statistics, analysis and performance measurement gained within a commercial, scientific or technical environment., • Experience managing multiple priorities and delivering results through a team., • Excellent communication and stakeholder management skills, with the ability to influence decision-making and communicate complex technical concepts to both technical and non-technical audiences., • Experience working within a regulated or operationally complex environment, such as medical devices, pharmaceuticals, healthcare or manufacturing, is advantageous., • Experience using SAS or other statistical analysis software is advantageous., • Competitive compensation package., • Structured development and career progression opportunities., • The opportunity to lead and develop a talented statistical team., • The chance to make a meaningful impact on innovative technologies that improve the lives of millions of people living with diabetes worldwide. #J-18808-Ljbffr

This is a highly visible specialist role, providing GMP expertise across the business to support the manufacture of life-changing healthcare products. As a recognised subject matter expert, you will work closely with Quality, Operations, Engineering and other cross-functional teams to ensure compliance with regulatory requirements, quality standards and Abbott procedures. You'll play a key role in supporting quality initiatives, driving continuous improvement and providing guidance on GMP requirements across complex projects and business activities. This position offers the opportunity to influence quality culture, support operational excellence and contribute directly to maintaining the highest standards of product quality and patient safety., • Providing expert guidance on Good Manufacturing Practice (GMP) requirements and expectations., • Supporting the implementation and maintenance of effective quality systems and compliance processes., • Partnering with cross-functional teams to ensure GMP requirements are embedded within manufacturing and operational activities., • Leading or supporting complex quality and compliance projects across the business., • Identifying opportunities for process improvement and implementing effective solutions., • Supporting internal and external audits, inspections and compliance activities., • Driving continuous improvement initiatives that enhance product quality, compliance and operational performance., • Acting as a trusted quality resource, providing coaching and support to colleagues across the organisation. We're looking for a quality professional who combines strong GMP knowledge with excellent communication and problem-solving skills., An Associate's Degree or equivalent qualification in a relevant scientific, technical or engineering discipline., • In-depth knowledge of Good Manufacturing Practices (GMP) and quality systems within a regulated industry., • Experience supporting quality and compliance activities in a manufacturing environment., • The ability to manage complex projects and deliver results across multiple stakeholders., • Strong analytical and problem-solving skills with a continuous improvement mindset., • Excellent communication and influencing skills, with the ability to build effective working relationships across all levels of the organisation., • A proactive approach and the ability to work independently while collaborating effectively within cross-functional teams., • Experience within the medical device, pharmaceutical or other regulated manufacturing industries would be advantageous. Abbott is about the power of health. For more than 135 years, Abbott has been helping people reach their potential, because better health allows people and communities to achieve more. Joining us, you can shape your career as you shape the future of healthcare. With a diverse, global network serving customers in more than 160 countries, we create new solutions across the spectrum of health, around the world, for all stages of life. Whether it's next-generation diagnostics, life-changing devices, science-based nutrition, or breakthrough medical technologies, we are advancing some of the most innovative healthcare solutions available today. This is a fantastic opportunity to join a global healthcare leader and develop your career within a quality-focused organisation committed to improving lives around the world. Abbott offers a benefits platform that provides security to you and your family. As you'd expect from an innovative global healthcare company, we offer a competitive salary, bonus opportunity, a class-leading defined contribution pension scheme, private healthcare, life assurance, flexible benefits and excellent opportunities for professional growth and development. At Abbott, you'll have the chance to work alongside talented colleagues, contribute to meaningful healthcare innovations and make a real difference to patients worldwide. #J-18808-Ljbffr

Reporting to the Testing and Analytical Manager, you will lead the Analytical Chemistry laboratory responsible for supporting the release, stability testing, and lifecycle management of innovative combination products that integrate both pharmaceutical and medical device components. The laboratory will play a critical role in ensuring the quality, compliance, and timely release of products used by millions of people worldwide Initially leading a growing team, you will have responsibility for building, developing, and scaling the organisation as product volumes increase. This role offers a unique combination of scientific leadership, operational management, and strategic influence. You will be the site's analytical chemistry authority, providing technical direction while ensuring robust laboratory operations, regulatory compliance, and continuous improvement., • Ensure timely execution of product release, stability, and investigative testing, • Plan and prioritise workloads to meet business and regulatory commitments, • Maintain compliance with GMP, ISO 13485, and global regulatory requirements, • Lead complex investigations, including OOS, OOT, and deviation management, • Serve as the analytical chemistry subject matter expert for HPLC assay and impurity testing, Dissolution testing, Total drug content analysis, Method troubleshooting and problem solving, • Support method development, transfer, validation, and lifecycle management activities, • Provide technical guidance to Quality, Manufacturing, Regulatory Affairs, and R&D teams, • Develop long-term laboratory capability and technology strategies, • Lead laboratory modernisation and continuous improvement initiatives, • Support new product introduction and combination product programmes, • Represent the site during audits, inspections, and divisional technical forums, • Degree in Analytical Chemistry, Pharmaceutical Sciences, or a related scientific discipline, • Significant experience leading teams within a GMP-regulated analytical laboratory, • Strong technical expertise in analytical chemistry techniques, including HPLC and dissolution testing, • Experience supporting analytical method validation, transfer and life cycle management, • Strong understanding of GMP, data integrity, and regulated laboratory environments, • Proven ability to lead, coach, and develop technical teams, • Excellent problem-solving, communication and stakeholder management skills, • Experience supporting pharmaceutical, medical device, or combination product testing programmes, • Understanding of regulatory requirements applicable to drug-device combination products, • Knowledge of ICH analytical validation requirementsExperience supporting regulatory inspections and audits, • MSc or PhD in Analytical Chemistry, Pharmaceutical Sciences, or a related discipline, • Experience supporting new product introductions and technology transfer activitiesundefined, • You may already have experience working with combination products or drug-device systems and understand the unique analytical, quality, and regulatory challenges these products present. However, we also welcome applications from experienced analytical chemistry leaders from pharmaceutical, medical device, biotechnology, or related regulated industries who are eager to develop expertise in this exciting and growing area Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries., This role offers the opportunity to lead a critical function supporting the release of innovative products that improve lives globally. You will have the chance to build and shape a high-performing analytical team, influence technical strategy, and contribute to the future of combination product development at Abbott. • Competitive compensation and benefits package, • Structured development and career growth opportunities, • A collaborative, innovative environment with real impact on patient outcomes #J-18808-Ljbffr

Position: Mechanical Technician Department: Cryobitz Manufacturing Location: Witney Salary: competitive We are seeking a skilled, practical technician to manufacture and assemble high-quality cryogenic products, including transfer lines, LN traps, vacuum-insulated components and associated assemblies. This is a hands-on role with a strong emphasis on precision welding, soldering, brazing, and mechanical assembly. The successful candidate will produce neat, accurate and carefully to engineering drawings and defined quality standards. • Assemble bespoke cryogenic systems from engineering drawings and build information., • Fit pipework, valves, vacuum components, flanges and mechanical assemblies., • Perform vacuum and helium leak testing of components and assemblies., • Prepare, clean and handle components for high and ultra-high vacuum (UHV) applications., • Maintain high standards of cleanliness throughout assembly and prevent contamination of vacuum-critical components., • Complete mechanical fitting, drilling, tapping and general assembly work., • Occasionally operate manual mills and lathes for simple machining and modification work., • Follow route cards, drawings, Standard Work Instructions and manufacturing instructions., • Complete and record required checks during assembly., • Identify, investigate and resolve build problems, escalating issues where required., • Carry out rework and modifications when required., • Previous mechanical assembly, engineering or manufacturing experience., • Strong practical and mechanical skills., • Ability to read and work from engineering drawings., • Good problem-solving skills and the ability to identify practical solutions to build issues., • Excellent attention to detail and a high standard of workmanship., • Ability to work to strict cleanliness standards., • Experience using hand tools and workshop equipment., • Ability to follow documented processes and instructions. Able to work independently and take responsibility for the quality of completed work. Good communication and teamwork skills. • Experience handling and assembling components for high vacuum or ultra-high vacuum (UHV) applications., • Understanding of UHV cleanliness, contamination control and appropriate component handling.., • Vacuum and helium leak testing., • Cryogenic or high-vacuum equipment., • Stainless steel pipework and fittings., • Swagelok or similar compression fittings., • Manual milling and turning., • Precision mechanical assembly., • Scientific, laboratory or specialist engineering equipment. #J-18808-Ljbffr

System Project Lead Location: Witney Drive global systems innovation that supports life‑changing healthcare technologies. Abbott Diabetes Care At Abbott, we're committed to helping people live healthier lives through breakthrough technologies and innovative healthcare solutions. As the world leader in glucose monitoring, Abbott Diabetes Care develops products such as FreeStyle Libre, transforming the way people manage diabetes around the world. We have an exciting opportunity for a System Project Lead to join our Clinical Affairs team. This is a highly visible global role that will lead the development, implementation, and continuous improvement of systems that support clinical studies, scientific research, and data management activities across Abbott Diabetes Care. Working closely with Clinical Affairs teams in both the UK and US, as well as Business Systems teams and external partners, you will act as a key link between business needs and technology solutions. You will be responsible for identifying opportunities to improve processes, introducing new systems and capabilities, and ensuring existing platforms continue to meet the evolving needs of the organisation. • Lead system‑related projects from concept through to implementation, collaborating with stakeholders to gather requirements, evaluate solutions, manage vendors, and ensure successful deployment., • Play a critical role in helping Clinical Affairs teams operate more efficiently by simplifying processes, improving data management, and enabling effective collaboration across global teams., • Work closely with Clinical Affairs subject matter experts to develop and optimise systems that support clinical studies and scientific activities, while ensuring all solutions remain compliant with data privacy, cybersecurity, validation, and regulatory requirements., • Support the development of reporting tools, dashboards, and visualisations that provide valuable business insights and improve decision‑making., • Drive the adoption of new technologies through training, support, and ongoing engagement with stakeholders., • Continually assess opportunities for process improvement and innovation, ensuring Clinical Affairs has the systems and capabilities needed to support future business growth. We are looking for a proactive and collaborative systems professional with experience in project management, business systems, systems implementation, or process improvement. You will be comfortable working across multiple functions and geographies, managing competing priorities, and translating complex business requirements into practical and effective technology solutions. You will have a degree in Business Systems, Information Systems, Computer Science, or a related discipline, or equivalent experience, together with strong communication, stakeholder management, and problem‑solving skills. Experience using project management tools such as Microsoft Project is essential. Experience within Clinical Research, Medical Devices, Healthcare, Life Sciences, or another regulated industry would be advantageous, but is not essential. Most importantly, you will bring a passion for technology, continuous improvement, and delivering solutions that create meaningful business impact. • Competitive salary, • Defined contribution pension scheme, • Private healthcare, • Life assurance, • Flexible benefits programme, • Opportunities for professional development The base pay for this position is N/A. In specific locations, the pay range may vary from the range posted. • Job Family: Medical & Scientific Affairs, • Division: ADC Diabetes Care, • Location: United Kingdom > Witney : Production Facility, • Additional Locations: (none specified), • Work Shift: Standard, • Travel: Yes, 5 % of the Time, • Medical Surveillance: Not Applicable, • Significant Work Activities: Not Applicable Abbott is about the power of health. For more than 135 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions — across the spectrum of health, around the world, for all stages of life. Whether it’s next‑generation diagnostics, life‑changing devices, science‑based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health. The people of Abbott come to work each day with relentless energy, enthusiasm and a promise to enhance the health and well‑being of millions of people. They push the boundaries to help manage and treat some of life’s greatest health challenges. We invite you to explore opportunities at Abbott, to see if your talents and career aspirations may fit with our openings. An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce. Follow Us: Facebook LinkedIn YouTube Twitter #J-18808-Ljbffr

Abbott is about the power of health. For more than 135 years, Abbott has been helping people reach their potential, because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions across the spectrum of health, around the world, for all stages of life. Whether its next-generation diagnostics, life-changing devices, science-based nutrition, or breakthrough medical technologies, we are advancing some of the most innovative healthcare solutions available today. World Leader in Glucose Monitoring, Abbott Diabetes Care designs, develops and manufactures leading-edge glucose monitoring systems for use in both home and hospital settings. Our technologies are transforming the way people manage diabetes, including the revolutionary FreeStyle Libre portfolio, which has helped redefine glucose monitoring for millions of users around the world. Through continued investment in innovation, manufacturing excellence and world-class quality systems, Abbott Diabetes Care remains at the forefront of healthcare technology, delivering solutions that help people live healthier, fuller lives. This is a highly visible specialist role, providing GMP expertise across the business to support the manufacture of life-changing healthcare products. As a recognised subject matter expert, you will work closely with Quality, Operations, Engineering and other cross-functional teams to ensure compliance with regulatory requirements, quality standards and Abbott procedures. You'll play a key role in supporting quality initiatives, driving continuous improvement and providing guidance on GMP requirements across complex projects and business activities. This position offers the opportunity to influence quality culture, support operational excellence and contribute directly to maintaining the highest standards of product quality and patient safety. • Providing expert guidance on Good Manufacturing Practice (GMP) requirements and expectations., • Supporting the implementation and maintenance of effective quality systems and compliance processes., • Partnering with cross-functional teams to ensure GMP requirements are embedded within manufacturing and operational activities., • Leading or supporting complex quality and compliance projects across the business., • Identifying opportunities for process improvement and implementing effective solutions., • Supporting internal and external audits, inspections and compliance activities., • Driving continuous improvement initiatives that enhance product quality, compliance and operational performance., • Acting as a trusted quality resource, providing coaching and support to colleagues across the organisation. We're looking for a quality professional who combines strong GMP knowledge with excellent communication and problem-solving skills. To be successful, you will have: • An Associate's Degree or equivalent qualification in a relevant scientific, technical or engineering discipline., • In-depth knowledge of Good Manufacturing Practices (GMP) and quality systems within a regulated industry., • Experience supporting quality and compliance activities in a manufacturing environment., • The ability to manage complex projects and deliver results across multiple stakeholders., • Strong analytical and problem-solving skills with a continuous improvement mindset., • Excellent communication and influencing skills, with the ability to build effective working relationships across all levels of the organisation., • A proactive approach and the ability to work independently while collaborating effectively within cross-functional teams., • Experience within the medical device, pharmaceutical or other regulated manufacturing industries would be advantageous. This is a fantastic opportunity to join a global healthcare leader and develop your career within a quality-focused organisation committed to improving lives around the world. Abbott offers a benefits platform that provides security to you and your family. As you'd expect from an innovative global healthcare company, we offer a competitive salary, bonus opportunity, a class-leading defined contribution pension scheme, private healthcare, life assurance, flexible benefits and excellent opportunities for professional growth and development. At Abbott, you'll have the chance to work alongside talented colleagues, contribute to meaningful healthcare innovations and make a real difference to patients worldwide. The base pay for this position is N/A. In specific locations, the pay range may vary from the range posted. Operations Quality DIVISION: ADC Diabetes Care LOCATION: United Kingdom > Witney : Range Road ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Yes, 5 % of the Time MEDICAL SURVEILLANCE: Not Applicable SIGNIFICANT WORK ACTIVITIES: Not Applicable Abbott is about the power of health. For more than 135 years, Abbott has been helping people reach their potential because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions across the spectrum of health, around the world, for all stages of life. Whether it's next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health. The people of Abbott come to work each day with relentless energy, enthusiasm and a promise to enhance the health and well-being of millions of people. They push the boundaries to help manage and treat some of life’s greatest health challenges. We invite you to explore opportunities at Abbott, to see if your talents and career aspirations may fit with our openings. An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce. Follow Us: Facebook LinkedIn YouTube Twitter #J-18808-Ljbffr

We have an exciting opportunity for an experienced Test Method Validation Specialist to join our Technical Services team in the role of Operations Scientist II, supporting technical product release at Witney, West Oxfordshire. In this role you will be integral for the transfer of scientific test methods from R&D to Operations, including leading validation activities in our product release laboratory. Day-to-day, you will support the test method requirements for the transfer of product from R&D to Operations. You will: • Create validation documents, including plans, protocols and reports., • Oversee Test Method Validation activities for the sensor release laboratory., • Provide process development and characterisation support for new sensor test methods., • Support sensor release laboratory operational requirements., • Have knowledge of change control procedures and processes., • Work cross functionally to support the transfer of test method from R&D., • Ensure adherence to industry standards and regulatory guidelines., • Encourage open technical exchange with other departments / projects., • Actively identify improvement opportunities., • Present technical information to team meetings, • Consistently demonstrates recognised behaviours. To be successful, you will have a minimum of Bachelor's degree in a scientific or Engineering discipline, and will bring prior experience of test method development and validation with a preference for candidates with test method validation experience. You must have excellent attention to detail skills, a logical and methodical approach to problem solving, the ability to prioritise and manage projects, and the flexibility to adapt to changing circumstances or new demands. A lot of your work will involve cross-functional teams, so you'll also need the communication and inter-personal skills to be able to build relationships with colleagues in various departments across the business. Good IT skills including Excel and PowerPoint are also required for this role. With a track record of innovation and development, Abbott Diabetes Care designs, develops and manufactures leading-edge glucose monitoring systems, for use in both home and hospital settings. We have a Global Centre of Excellence for Medical Devices based in Witney, Oxfordshire. The site manufactures significant volumes of test strips annually and has also been instrumental in the research, development and manufacture of the next generation FreeStyle Libre Flash Glucose Monitoring System, launched in September 2014., Abbott offers a benefits platform that provides security to you and your family. As you'd expect from an innovative global health care company, we offer a competitive range of benefits including excellent salaries, a class-leading defined contribution pension scheme, private healthcare, life assurance, subsidized canteen and a flexible benefits scheme. Here at Witney, we also like to help our employees live life to the fullest, and therefore we offer a range of optional initiatives for you to get involved in, including local community STEM outreach, yoga and more! #J-18808-Ljbffr

Abbott is about the power of health. For more than 130 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions — across the spectrum of health, around the world, for all stages of life. Location : Witney Abbott is about the power of health. For more than 130 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions — across the spectrum of health, around the world, for all stages of life. Whether it’s next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health. World Leader in Glucose Monitoring, Abbott Diabetes Care designs, develops and manufactures glucose monitoring systems for use in both home and hospital settings. We have a Centre of Excellence in Witney for the development and manufacture of electrodes and biosensors used by patients and healthcare professionals for the day-to-day management of diabetes. The site has been instrumental in the research, development and manufacture of the FreeStyle Libre Flash Glucose Monitoring System as well as exciting developments in the Libre family including FreeStyle Libre 2, FreeStyle Libre 3 and the Libre Sense system. We are passionate about doing work that improves the quality of people’s lives. We’re hiring a Senior Specialist Regulatory Affairs to join the EMEAP regulatory affairs team, which is growing to meet the demands of the business and to support a strong product pipeline. You will be responsible for a portfolio of cutting-edge medical devices & IVDs, leading regulatory activities for new product introductions and significant on-market changes for the Europe, Middle East, Africa and Pakistan (EMEAP) region. You will work as part of a global team, to develop, lead and implement strategies that will ensure the timely introduction of new products onto the international market in a fast-paced environment. You will coordinate and oversee preparation of complete and scientifically sound regulatory submissions and lead interactions with the Notified Body and country regulatory contacts to facilitate the regulatory submission review process to ensure a timely approval process. • Formulate, develop and lead business critical regulatory strategies for the EMEAP region., • Act as the regulatory subject matter expert in design control projects, assessing changes and managing roll out programs for existing products and new launches., • Become a technical expert in ADC devices and support interactions with EU Notified Body/UK Approved Body, as well as competent authorities, as required, • Manage the creation and development of EU & UK Technical files in accordance with MDR 2017/745, IVDR 2017/746 and other application regulations., • Provide coaching and mentoring to more junior team members, • Identify and implement process improvements and efficiencies per the global regulatory affairs strategy. Bachelor’s degree or equivalent preferably in a Scientific discipline e.g. Chemistry, life Sciences, Biology. • Knowledge of MDR 2017/745 Regulations and ISO13485 is essential, additionally, knowledge of IVDR 2017/746 is preferred, • Experience within a medical device or healthcare manufacturing industry in a regulatory or quality role., • Experience of Technical File creation and maintenance, as well as post market changes, • Experience of working with Notified Bodies and/ or other regulatory bodies, • You need to have excellent written and oral communication skills necessary to be able to produce succinct reports and documentation and to effectively communicate with other departments, managers and external regulatory organizations. In addition to a competitive salary, Abbott offers a highly attractive benefits package which includes a defined-contribution pension scheme, a share ownership scheme, private healthcare, life assurance, and a flexible benefits scheme which you can tailor to your own requirements. #J-18808-Ljbffr

JOB DESCRIPTION: About Abbott Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life‑changing technologies spans diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. About Abbott’s Diabetes Care Team Abbott is the global leader in Diabetes Care, providing innovative solutions to help people manage their health with confidence. Our world‑leading sensing technology supports millions of people globally, enabling better, more informed decisions every day. The Opportunity This is a rare opportunity to lead and shape a strategically important analytical chemistry function within one of Abbott's largest global manufacturing sites. Reporting to the Testing and Analytical Manager, you will lead the Analytical Chemistry laboratory responsible for supporting the release, stability testing, and lifecycle management of innovative combination products that integrate both pharmaceutical and medical device components. The laboratory will play a critical role in ensuring the quality, compliance, and timely release of products used by millions of people worldwide Initially leading a growing team, you will have responsibility for building, developing, and scaling the organisation as product volumes increase. This role offers a unique combination of scientific leadership, operational management, and strategic influence. You will be the site's analytical chemistry authority, providing technical direction while ensuring robust laboratory operations, regulatory compliance, and continuous improvement. • Lead a High-Performing Analytical Laboratory, • Provide leadership, coaching, and development for analysts, scientists, and laboratory supervisors, • Build a culture focused on safety, quality, accountability, and continuous improvement, • Manage resource planning to support current operations and future growth, • Drive laboratory performance through effective KPI management and operational excellence, • Deliver Critical Product Release and Stability Testing, • Ensure timely execution of product release, stability, and investigative testing, • Plan and prioritise workloads to meet business and regulatory commitments, • Maintain compliance with GMP, ISO 13485, and global regulatory requirements, • Lead complex investigations, including OOS, OOT, and deviation management, • Provide Technical Leadership, • Serve as the analytical chemistry subject matter expert for HPLC assay and impurity testing, Dissolution testing, Total drug content analysis, Method troubleshooting and problem solving, • Support method development, transfer, validation, and lifecycle management activities, • Provide technical guidance to Quality, Manufacturing, Regulatory Affairs, and R&D teams, • Shape the Future, • Develop long-term laboratory capability and technology strategies, • Lead laboratory modernisation and continuous improvement initiatives, • Support new product introduction and combination product programmes, • Represent the site during audits, inspections, and divisional technical forums, • Essential Degree in Analytical Chemistry, Pharmaceutical Sciences, Chemistry, or a related scientific discipline, • Significant experience leading teams within a GMP-regulated analytical laboratory, • Strong technical expertise in analytical chemistry techniques, including HPLC and dissolution testing, • Experience supporting analytical method validation, transfer and life cycle management, • Strong understanding of GMP, data integrity, and regulated laboratory environments, • Proven ability to lead, coach, and develop technical teams, • Excellent problem-solving, communication and stakeholder management skills, • Highly Desirable Experience supporting pharmaceutical, medical device, or combination product testing programmes, • Understanding of regulatory requirements applicable to drug-device combination products, • Knowledge of ICH analytical validation requirements, • Experience supporting regulatory inspections and audits, • MSc or PhD in Analytical Chemistry, Pharmaceutical Sciences, or a related discipline, • Experience supporting new product introductions and technology transfer activities You may already have experience working with combination products or drug-device systems and understand the unique analytical, quality, and regulatory challenges these products present. However, we also welcome applications from experienced analytical chemistry leaders from pharmaceutical, medical device, biotechnology, or related regulated industries who are eager to develop expertise in this exciting and growing area. • Competitive compensation and benefits package, • Structured development and career growth opportunities, • A collaborative, innovative environment with real impact on patient outcomes The base pay for this position is N/A In specific locations, the pay range may vary from the range posted. JOB FAMILY: Manufacturing DIVISION: ADC Diabetes Care LOCATION: United Kingdom > Witney : Production Facility ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Yes, 10 % of the Time MEDICAL SURVEILLANCE: Not Applicable SIGNIFICANT WORK ACTIVITIES: Not Applicable Abbott is about the power of health. For more than 135 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions — ... An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce. Follow Us: Facebook LinkedIn YouTube Twitter #J-18808-Ljbffr