718 Clinical Quality jobs in the United Kingdom
Clinical Scientist/Quality Manager - Clinical Immunology Service - 81166Z25 - Grade 8
Posted today
Job Viewed
Job Description
Position Details
Clinical Immunology Service, School of Infection, Inflammation and Immunology, College of Medicine and Health
Location: University of Birmingham, Edgbaston, Birmingham UK
Full time starting salary is normally in the range £47,389 to £6,535 with potential progression once in post to 3,606
Grade: 8
Part Time (30 hours per week)
Fixed Term contract up to December 2026
Closing date: 12th October 2025
Our offer to you
People are at the heart of what we are and do.
The University of Birmingham is proud to have been a part of the City of Birmingham and the wider region for over 100 years, and we are equally proud to be recognised as a leading global university. We want to attract talented people from across the city and beyond, support them to succeed, and celebrate their success.
We are committed to helping the people who work here to develop through our sector-leading Birmingham Professional programme which provides all professional services staff with development opportunities and the encouragement to reach their full potential. With almost 5,000 professional services jobs in a wide-range of functions in Edgbaston and in our campus in Dubai, there are plenty of opportunities for you to be able to develop your career at the University.
We believe there is no such thing as a typical member of staff and that diversity is a source of strength that underpins the exchange of ideas, innovation, and debate. We warmly welcome people from all backgrounds and are committed to fostering an inclusive environment where diversity is at the heart of who and what we are, and how we work.
Supporting our people to achieve a healthy work/life balance is important both to our employees and to the success of the University and, depending on the role, we offer a variety of flexible working arrangements. We therefore welcome discussions on all forms of flexible working. In addition, you will receive a generous package of benefits including 40 days paid holiday a year, one paid day a year for volunteering, occupational sick pay, and a pension scheme. We also have three high quality subsidised day nurseries.
The University is situated in leafy Edgbaston and there are excellent transport links to our beautiful campus, including main bus routes and a train station on site. On campus we have a state-of-the-art sports centre with pool, shops, places to eat and drink, our own art gallery, museum and botanical gardens.
Find out more about the benefits of working for the University of Birmingham
Role Summary
As Quality Manager and a senior Health Care Scientist, the post holder will work closely with the Clinical Immunology Services (CIS) Director and senior leadership to ensure the delivery of a patient centred, quality driven, efficient and cost-effective service. The CIS provides a comprehensive Clinical Immunology diagnostics service to the West Midlands, regional services in lymphoma/leukaemia diagnosis and national services for neuro-immunology and myeloma reporting. Being situated within the University of Birmingham, the CIS also provides central trials analysis for a number of national and local research studies and has a strong track record in immunodiagnostic development.
The post holder will provide guidance and advice in all issues relating to quality within the laboratory. They will report to laboratory management on the functioning and effectiveness of the quality management system via management review, senior staff, general laboratory and quality management group meetings or on an ad hoc basis. The post holder will ensure the implementation, development and maintenance of a quality management system in order to provide service improvement via; ensuring conformity with ISO 15189 accreditation standards, liaising with accreditation bodies and keeping up to date with changes in standards. The post holder will have excellent communication and management skills and lead liaison with other Quality Managers and end-users to establish satisfaction. The post holder will take a lead role in document control and audit within the laboratory and educate, promote and encourage all staff to participate in QM.
The post holder will have significant expertise in the laboratory medicine and as part of the laboratory's senior management team, plan the activities and lead the development of the department. Operating with considerable autonomy, the post holder will supervise highly specialist clinical technical investigations including specialist assays, method and equipment evaluation/selection, research and development that incorporates medium to long term service development and enhancement.
The role is varied and includes the management of staff, provision and maintenance of services, and taking a lead role in the understanding and promotion of relevant health and safety requirements for medical laboratories. The role will include liaison with researchers to plan, cost, quality assure and deliver testing for translational research studies and clinical trials.
Main Duties
Senior leadership:
- As part of the laboratory's senior management team, plan the activities and lead the development of the department.
- Contribute to general departmental management by performing, subject to consultation, such tasks as delegated by the laboratory manager.
- Implement planned changes to the clinical technical service.
- Plan and prioritise the workload of the laboratory.
- Liaise with external agencies such as equipment manufacturers and engineers, suppliers of consumables.
- Meet commercial representatives on behalf of the CIS.
- Deputise for the laboratory manager at interdepartmental meetings, as required.
- Other duties appropriate to the grade.
Clinical:
- Prioritising, performing, interpreting, validating and authorizing specialist investigations according to standard operating procedures.
- Providing technical clinical advice to clinicians and other practitioners. This advice will include information relating to, for example, test selection, sample quality, and sample timing.
- Identify and communicate abnormal clinical results.
- Continue to develop a wide range of scientific expertise and skill and apply this to clinical problems, including the development of new methods, or improving existing ones for routine use, clinical trial work or research.
- Engage with end users to ensure their needs are met.
Technical:
- Perform appropriate specialist laboratory procedures and tasks that are consistent with the job holder's levels of specialist knowledge, skills and experience and take responsibility for the daily provision of the service.
- Be up to date with contemporary methods including any analytical equipment used in the section and lead in the procurement of such equipment as is deemed necessary for the service.
- Participate in equipment testing and adaptation as a function of service development.
- Assess suitability and urgency of pathology samples. Assign relevant tests and investigations.
- Ensure maintenance of equipment and stock control of consumables for the section.
- Supervise and train technical, clinical, research and medical staff as required.
- Monitor the performance of highly complex laboratory equipment and perform basic repairs in the event of malfunction.
Quality assurance:
- As part of the laboratory's senior management team take a lead role in supporting the quality manager to ensure departmental compliance with UKAS ISO15189.
- Together with senior colleagues take a leading role in ensuring the department's research activities are performed in accordance with GCLP and the requirements of MHRA.
- Supervise and trend internal and external quality control and actively participate in the laboratory quality assurance and risk management programmes.
- Report, investigate and document adverse events in accordance with departments risk management procedures.
- Provide documentation as a function of the department's accreditation with UKAS; for example, reviewing and updating standard operating procedures and documentation related to health and safety, competency, validation and verification.
- Participate in and plan laboratory audit processes.
Required Knowledge, Skills, Qualifications, Experience
Knowledge:
- In depth specialist knowledge of Immunology theory and practice particularly in relation clinical immunology diagnostics.
- Detailed understanding of immune assays including trouble-shooting processes.
- Detailed knowledge of quality management, especially in the context of the requirement of UKAS ISO15189.
- Detailed understanding of HSST / Clinical Scientist professional standards, ethics and proficiencies.
- Detailed understanding of health and safety matters related to medical laboratory science and familiarity with local, University and national legislation (e.g. Health and Safety at work Act).
- Detailed appreciation of the implications and requirements concerning the confidentiality of patient information (e.g. General Data Protection Regulations, Caldicott principles, etc).
Skills:
- Well-developed communication skills and the ability to communicate with staff and service users at all levels.
- Ability to direct and prioritise division of work for other staff (technical and clerical).
- Ability to motivate staff, promote good teamwork.
- Ability to recognise and resolve complex problems with specialised reporting.
- Responsibility for evaluation, interpretation and authorisation of patient results and training others in this process.
Qualifications:
- Science degree acceptable to ACB or equivalent qualification.
- State Registration with the Health and Care Professions Council or IBMS.
- MSc or equivalent qualification/experience required.
- Evidence of Continuing Professional Development in accordance with HCPC requirements.
Experience:
- Significant experience working as a Health Care Scientist specialising in immunological diagnosis and monitoring desirable.
- Experience in supervising small teams and taking responsibility for specific sections of the laboratory.
- Actively participate in CPD to maintain in depth specialist understanding of relevant aspects of work.
- Working with researchers to understand and deliver testing requirements for studies/clinical trials.
Planning and Organising
- The post holder will be self-motivated and proactive with the ability to work independently and as a team leader.
- The post holder will be expected to deputise for the laboratory manager when necessary.
- Responsibility for prioritising their own work, and that of others, when necessary, subject to departmental objectives and requirements.
- The ability to manage and prioritise a complex workload, often under pressure.
- Ability to offer a supportive approach to others in achieving objectives.
- Maintain an extremely flexible attitude to work to accommodate unplanned events.
Problem Solving and decision making
- The role holder will decide on the short term and long term priorities in their section of the laboratory.
- The role holder will decide which parts of the work are urgent and what must be reported urgently.
- The role holder will decide which methods used within the laboratory are appropriate after evaluation and quality control has been carried out.
- The role holder will decide if the results obtained are acceptable for release and if all quality control criteria have been met.
- The volume of sample provided from very sick patients, particularly children, is often limited. The role holder will be expected to decide on the best use of the sample to give the Consultant Immunologist the maximum requested information to aid diagnosis as quickly as possible.
- Participating in the selection/interviewing of staff with the BMS4 and making recommendations to HR.
- Arranging staffing cover, both planned, and in the event of staff absences.
- Recommending and/or implementing quality improvement measures.
- Identifying and referring results on sample investigations to medical staff.
Internal and External relationships
- Assist Laboratory Manager, Medical staff and other Scientists in the provision, maintenance and development of the service and standards of departmental quality and performance.
- Demonstrate excellent communication skills and the ability to contribute positively to discussions with staff at all levels both within and without the department.
- Ability to communicate results and deal with enquiries from laboratory and medical staff over sample requirements and results. This requires professionalism and attention to detail.
- Assist Laboratory Manager, Medical staff and Scientists in the provision, maintenance and development of the service and standards of departmental quality and performance.
- The role holder will liaise with clinicians in charge of individual patients to finalise arrangements for laboratory tests, provide detailed technical reports and information about which blood samples are appropriate for the tests to be carried out.
Develop and maintain good working relationships with all grades of staff from other hospitals and laboratories to whom a service is provided or where additional training is sourced.
Further particulars can be found here
Informal enquiries to Alex Richter, email:
View our staff values and behaviours here
We believe there is no such thing as a 'typical' member of University of Birmingham staff and that diversity in its many forms is a strength that underpins the exchange of ideas, innovation and debate at the heart of University life. We are committed to proactively addressing the barriers experienced by some groups in our community and are proud to hold Athena SWAN, Race Equality Charter and Disability Confident accreditations. We have an Equality Diversity and Inclusion Centre that focuses on continuously improving the University as a fair and inclusive place to work where everyone has the opportunity to succeed. We are also committed to sustainability, which is a key part of our strategy. You can find out more about our work to create a fairer university for everyone on our website .
Senior Quality Assurance Engineer - Medical Devices
Posted 10 days ago
Job Viewed
Job Description
Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS) in compliance with ISO 13485, FDA regulations (21 CFR Part 820), and other relevant international standards.
- Lead and participate in internal and external audits (e.g., FDA, Notified Bodies) and support regulatory inspections.
- Oversee the design, development, and validation of Quality Control processes and procedures.
- Review and approve product design specifications, risk management files, and validation protocols.
- Investigate product complaints, non-conformances, and CAPAs (Corrective and Preventive Actions), determining root causes and implementing effective solutions.
- Manage the change control process for product and process modifications.
- Develop and execute quality test plans and protocols for new product introductions and existing product improvements.
- Provide quality assurance support to R&D, manufacturing, and other cross-functional teams.
- Train and mentor junior QA personnel and contribute to the overall development of the quality team.
- Monitor industry best practices and regulatory changes, ensuring the QMS remains current and effective.
- Participate in supplier qualification and audits.
- Generate and analyze quality metrics to identify trends and areas for continuous improvement.
- Bachelor's degree in Engineering (Mechanical, Electrical, Biomedical), Science, or a related field.
- Minimum of 7 years of experience in Quality Assurance within the medical device industry.
- In-depth knowledge of ISO 13485 and FDA 21 CFR Part 820 is essential.
- Experience with risk management (ISO 14971) and design controls is required.
- Proven experience in conducting and leading internal audits and supporting external regulatory audits.
- Strong understanding of product development lifecycles and manufacturing processes in the medical device field.
- Excellent analytical, problem-solving, and critical thinking skills.
- Exceptional written and verbal communication skills, with the ability to document complex processes clearly and concisely.
- Proficiency in using QMS software and standard office productivity tools.
- Ability to work independently, manage priorities effectively, and collaborate with remote teams across different time zones.
- CQE (Certified Quality Engineer) or equivalent certification is a plus.
Senior Quality Assurance Engineer - Medical Devices
Posted 12 days ago
Job Viewed
Job Description
Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with ISO 13485 and relevant regulatory requirements (e.g., FDA 21 CFR Part 820).
- Conduct internal audits and support external audits by regulatory bodies and customers.
- Manage the non-conformance and CAPA (Corrective and Preventive Action) processes.
- Review and approve product design documentation, validation reports, and risk management files.
- Participate in risk management activities throughout the product lifecycle.
- Develop and deliver quality-related training to personnel.
- Monitor key quality metrics and provide regular reports to management.
- Collaborate with cross-functional teams (R&D, Manufacturing, Regulatory Affairs) to ensure quality is integrated into all stages of product development.
- Investigate product complaints and potential quality issues, recommending and implementing solutions.
- Stay current with evolving quality standards and regulatory landscapes.
Qualifications:
- Bachelor's degree in Engineering, Science, or a related field.
- Minimum of 5 years of experience in Quality Assurance within the medical device industry.
- In-depth knowledge of ISO 13485, FDA Quality System Regulation (QSR), and other relevant international standards.
- Proven experience in developing and managing QMS documentation.
- Strong understanding of design controls, risk management (ISO 14971), and validation processes.
- Excellent analytical, problem-solving, and root cause analysis skills.
- Exceptional attention to detail and organizational abilities.
- Strong written and verbal communication skills.
- Ability to work effectively both independently and as part of a remote team.
- Proficiency in quality management software and MS Office Suite.
Senior Quality Assurance Engineer - Medical Devices
Posted 14 days ago
Job Viewed
Job Description
Key Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with ISO 13485, FDA 21 CFR Part 820, and other relevant global regulations.
- Lead and participate in internal and external audits (regulatory bodies, Notified Bodies, customers).
- Manage and oversee CAPA (Corrective and Preventive Action) processes, including investigation, root cause analysis, and effectiveness checks.
- Review and approve Design History Files (DHFs), technical documentation, and risk management files (ISO 14971).
- Develop and execute validation and verification protocols for new products and processes.
- Conduct supplier quality audits and manage supplier qualification processes.
- Provide quality assurance support throughout the product lifecycle, from R&D to post-market surveillance.
- Train and mentor junior QA team members on quality systems and regulatory requirements.
- Monitor quality trends and identify opportunities for continuous improvement.
- Serve as a key point of contact for regulatory bodies and Notified Bodies during audits and inspections.
Qualifications:
- A Bachelor's degree in Engineering (Biomedical, Mechanical, Electrical), Science, or a related technical field.
- A minimum of 6 years of experience in Quality Assurance within the medical device industry.
- In-depth knowledge of ISO 13485, FDA 21 CFR Part 820, and other relevant medical device regulations.
- Proven experience with QMS implementation, maintenance, and auditing.
- Strong understanding of Design Controls, Risk Management (ISO 14971), and CAPA processes.
- Experience with validation and verification activities is essential.
- Excellent analytical, problem-solving, and decision-making skills.
- Strong written and verbal communication skills, with the ability to effectively communicate with regulatory bodies and internal stakeholders.
- Detail-oriented with a commitment to maintaining high quality standards.
- Ability to work effectively both independently and as part of a team.
Senior Quality Assurance Engineer - Medical Devices
Posted 15 days ago
Job Viewed
Job Description
Responsibilities:
- Develop, implement, and maintain the Quality Management System (QMS) in compliance with ISO 13485, FDA 21 CFR Part 820, and other relevant global regulations.
- Lead and participate in design control activities, including risk management (ISO 14971), verification, and validation planning and execution.
- Establish and manage product and process validation strategies.
- Conduct internal and external audits of suppliers and manufacturing processes.
- Investigate non-conformances, implement corrective and preventive actions (CAPA), and track their effectiveness.
- Review and approve design history files (DHFs), technical files, and regulatory submission documentation.
- Provide quality support to manufacturing operations, troubleshooting issues and driving continuous improvement.
- Manage post-market surveillance activities, including complaint handling and adverse event reporting.
- Train and mentor junior QA personnel.
- Stay abreast of evolving regulatory requirements and industry best practices.
- Minimum of 5 years of experience in Quality Assurance within the medical device industry.
- Thorough knowledge of ISO 13485, FDA 21 CFR Part 820, and other relevant medical device regulations.
- Experience with risk management processes (ISO 14971).
- Proven experience in developing and implementing CAPA systems.
- Strong understanding of design controls, validation processes (IQ, OQ, PQ), and change control.
- Experience with conducting internal and supplier audits.
- Excellent analytical, problem-solving, and decision-making skills.
- Strong written and verbal communication skills, with the ability to document and present findings clearly.
- Bachelor's degree in Engineering, Science, or a related field.
Senior Quality Assurance Manager (Medical Devices)
Posted 21 days ago
Job Viewed
Job Description
Key Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with relevant standards (e.g., ISO 13485, FDA 21 CFR Part 820).
- Oversee all aspects of quality assurance, including document control, CAPA management, internal audits, supplier quality, and regulatory compliance.
- Lead and mentor the QA team, fostering professional development and ensuring efficient operations.
- Prepare for and host regulatory inspections and audits from external bodies.
- Manage the risk management process, ensuring proactive identification and mitigation of quality-related risks.
- Collaborate with R&D, Manufacturing, and Operations to ensure quality is integrated into all product lifecycle stages.
- Establish and monitor key quality metrics (KPIs) and provide regular reports to senior management.
- Drive continuous improvement initiatives across the organization to enhance product quality and customer satisfaction.
- Ensure that all quality-related activities are documented thoroughly and accurately.
- Provide training and guidance to employees on quality standards and procedures.
- Stay abreast of evolving regulatory requirements and industry best practices in the medical device sector.
This role requires a minimum of 7 years of progressive experience in quality assurance within the medical device industry, with at least 3 years in a management capacity. A Bachelor's degree in a relevant scientific or technical field is required; an advanced degree is preferred. Exceptional leadership, communication, and problem-solving skills are essential. The ability to thrive in a remote, fast-paced environment, coupled with strong organizational and decision-making capabilities, is crucial. This is a unique opportunity to shape the quality strategy of a growing medical device company.
Senior Quality Assurance Engineer - Medical Devices
Posted 22 days ago
Job Viewed
Job Description
Be The First To Know
About the latest Clinical quality Jobs in United Kingdom !
Senior Quality Assurance Manager - Medical Devices
Posted 24 days ago
Job Viewed
Job Description
Key Responsibilities:
- Develop, implement, and maintain a comprehensive Quality Management System (QMS) in accordance with ISO 13485, FDA 21 CFR Part 820, and other relevant international standards.
- Oversee all quality assurance activities, including internal and external audits, CAPA management, change control, and document control.
- Ensure that all product development and manufacturing processes comply with regulatory requirements.
- Lead and mentor the QA team, fostering a culture of quality and continuous improvement.
- Manage supplier quality and conduct supplier audits to ensure compliance.
- Review and approve product documentation, including design history files (DHFs) and technical files.
- Investigate product complaints and non-conformances, implementing corrective and preventive actions.
- Prepare for and participate in regulatory inspections and audits.
- Stay informed about evolving regulatory requirements and industry best practices in the medical device sector.
- Contribute to strategic planning for quality and regulatory compliance initiatives.
- Manage product risk management activities.
Qualifications and Experience:
- Bachelor's degree in Engineering, Science, or a related field. A Master's degree is a plus.
- Minimum of 10 years of experience in Quality Assurance within the medical device industry.
- In-depth knowledge of ISO 13485, FDA Quality System Regulation (QSR), and other relevant global regulations.
- Proven experience in developing, implementing, and maintaining QMS.
- Strong experience in auditing, CAPA systems, and risk management.
- Demonstrated leadership and people management skills, with the ability to build and motivate a high-performing team.
- Excellent analytical, problem-solving, and decision-making abilities.
- Exceptional written and verbal communication skills, with the ability to interact effectively with regulatory bodies, suppliers, and internal stakeholders.
- Ability to work independently and manage priorities effectively in a remote environment.
- Experience with eQMS software is desirable.
This is a vital role that ensures the integrity and safety of our client's life-saving medical devices, offering the benefits of a fully remote position and the chance to lead quality initiatives. If you are a passionate and experienced QA professional, we encourage you to apply.
Design Quality Engineer - Medical Devices
Posted 1 day ago
Job Viewed
Job Description
Senior Design Quality Engineer - Medical Devices Falmouth, Cornwall £50,000 - £0,000 + Exceptional Benefits + Clear Path to Career Progression + Relocation Package
An innovative global medical device manufacturer is looking for a highly skilled Senior Design Quality Engineer to join its expanding R&D team based in Falmouth. This is a rare opportunity to play a pivotal role in the design, development, and delivery of life-changing medical technologies that truly make a difference.
As part of a collaborative and forward-thinking team, you'll work closely with internal and external partners to ensure products are designed, developed, and validated to the highest quality and regulatory standards. This role offers not only technical challenge but also strategic influence, with the chance to lead quality engineering initiatives across a diverse product portfolio.
What You'll Be Doing:
- Leading quality assurance activities during product design and development.
- Driving validation, verification and risk management processes.
- Leading and participating in design reviews and evaluations.
- Supporting CAPA, non-conformance resolution and continuous improvement initiatives.
- Engaging with suppliers to ensure quality requirements are met.
- Communicating complex technical information to stakeholders across the business.
What You'll Bring:
- A BSc/BEng in Electronics, Electrical Engineering, Robotics, Mechatronics, or a related field.
- At least 4 years of quality engineering experience, ideally within the medical device sector.
- Proven expertise in design control, product testing, and regulatory compliance.
- Familiarity with tools such as Altium Schematic Capture and design for manufacturing/assembly (DFMA).
- Strong leadership, project management, and interpersonal skills.
- A passion for quality and innovation with a keen eye for detail.
Why Join?
- Excellent salary: 0,000 - 0,000 per annum
- Outstanding benefits including generous holiday allowance, enhanced pension, and private healthcare.
- Career progression: Clear path toward leadership within a global organization.
- Purpose-driven work: Contribute to products that improve patient outcomes and change lives.
- Supportive environment: Work alongside experts in a positive, inclusive culture that values your growth.
If you're ready to take the next step in your career and want to be part of something truly meaningful, apply now to join a world-class team making a global impact.
Services advertised by Gold Group are those of an Agency and/or an Employment Business.
We will contact you within the next 14 days if you are selected for interview. For a copy of our privacy policy please visit our website.
Product Quality Engineer - Medical Devices
Posted 7 days ago
Job Viewed
Job Description
Product Quality Engineer – Medical Devices
Location: Kidlington
Salary: Highly Negotiable, Dependent on Experience
An exciting opportunity to join a growing medical imaging company developing cutting-edge 3D imaging technology. With commercialisation underway in the UK and US, we are expanding our manufacturing capability and seeking a Product Quality Engineer to strengthen the Quality & Regulatory Affairs team.
Role Overview
The Product Quality Engineer will plan, coordinate, and manage quality assurance and quality control activities across product development, manufacturing, and post-market. This includes developing DHF deliverables, supporting verification/validation, managing non-conformances and CAPAs, and providing compliance guidance to colleagues. The role plays a key part in ensuring adherence to ISO 13485, FDA 21 CFR 820 (transitioning to QMSR), and CE/510k requirements.
Key Responsibilities
- Lead and support quality engineering activities for medical, veterinary, and non-destructive testing systems.
- Contribute to design and manufacturing documentation, ensuring products can be effectively manufactured and tested.
- Oversee risk management planning, assessment, and reporting for new and modified products.
- Support design transfer, supplier qualification, and quality test method validation.
- Generate and maintain quality documentation, including SOPs, work instructions, and inspection procedures.
- Manage NCRs, CAPAs, and continuous improvement initiatives.
- Collaborate with R&D, suppliers, and manufacturing teams to embed quality throughout the lifecycle.
- Provide training and guidance on regulatory compliance and quality standards.
Qualifications & Skills
- Degree in Science or Engineering, or equivalent experience.
- Recognised Quality Management System qualification (e.g., ISO auditor) or similar experience.
- Strong knowledge of product development, manufacturing, and quality systems in regulated industries, ideally medical devices.
- Familiarity with standards such as ISO 13485, FDA QSR, risk management (FMEA), and medical device cybersecurity.
- Skilled in Lean/Six Sigma methods and tools such as Minitab, DOE, and SPC.
- Excellent planning, problem-solving, and communication skills, with the ability to work independently and collaboratively.
This is a great opportunity to join an innovative scale-up and directly contribute to the delivery of high-quality, safe, and effective products to market.