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Зона ответственности описана чётко: управление системой качества охватывает производство и поставки клиентам в развивающемся бизнесе автоматизации для клеточной терапии. При оценке важно учесть обязательную работу на площадке рядом с Кембриджем.
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Понятная рольПерспективная сфераСильный пакет льготРабота на площадке
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Quality Manager (Biotech): Owning and improving the Quality Management System for robotic and automated cell-therapy manufacturing systems delivered to customers with an accent on ISO 9001 compliance, supplier quality, audits, and regulatory requirements. Focus on leading quality investigations, managing CAPA and non-conformances, supporting system verification and customer handover, and embedding practical quality processes across engineering and manufacturing.
Location: Cambridge, England, United Kingdom; based at Melbourn Science Park, approximately 10 miles south of Cambridge.
Company
Cellular Origins develops the Constellation platform, combining robotics, automation and bioprocess equipment to scale cell-therapy manufacturing.
What you will do
Own and continually improve the Quality Management System while maintaining ISO 9001 standards.
Support quality across system development, manufacturing, verification, deployment and customer handover.
Work with customers on quality and regulatory requirements and support customer audits.
Manage supplier quality through audits, issue resolution and continuous improvement.
Lead quality investigations, non-conformance management, and corrective and preventive actions.
Embed practical quality processes and provide training, guidance and mentoring across engineering, manufacturing and delivery.
Requirements
STEM degree or equivalent relevant experience.
Quality management experience in a technical development and manufacturing environment.
Experience supporting the manufacture, verification, commissioning or delivery of complex systems to customers.
Strong knowledge of QMS management and ISO 9001 standards.
Understanding of quality and regulatory requirements in regulated manufacturing environments, including awareness of GMP.
Experience managing customer and supplier audits, non-conformances and continuous improvement.
Strong communication, collaboration and stakeholder management skills, with the ability to influence and support teams.
Pragmatic, hands-on approach to quality and the ability to balance technical, customer and commercial priorities.
Culture & Benefits
Entrepreneurial and collaborative environment with modern office, laboratory and engineering spaces.
Annual bonus, 25 days of holiday and an employer pension contribution of 10% of salary.
Private medical insurance for employees and dependants.
Enhanced family-friendly leave and life insurance worth six times salary.
Subsidised lunches, electric car leasing, cycle-to-work scheme and season ticket loan.
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