Kyowa Kirin is a global specialty pharmaceutical company that leverages advanced biotechnologies to develop innovative medicines for challenging diseases. Focusing on oncology, immunotherapy, rare diseases, and neurology, the company operates in North America with offices in Princeton, NJ; Toronto, Canada; and La Jolla, CA. Known for its collaborative culture prioritizing innovation, diversity, integrity, and 'wa,' Kyowa Kirin fosters an environment where expertise and ideas are shared to drive significant advancements in patient care.
Open Positions
Medical Affairs Operations Lead
Relevant scientific degree or certification, significant industry experience, project management skills, and line management experience
Global Labelling Strategist - Associate Director
Bachelor's degree, 5+ years experience in pharmaceutical industry, good leadership and communication skills
HR Operations Specialist DACH
Completed Bachelor's degree, funded experience in HR, fluent German and English knowledge
Manager, R&D QA, Global Audit, Inspections and R&D Quality
Bachelor's degree required, 3+ years of experience in GCP/GLP Quality Assurance, and strong knowledge of regulatory requirements
Patient Journey Manager - Erfurt, Göttingen, Minden
University degree, several years of sales experience, excellent communication and analytical skills
Scientific Relations Manager
Scientific background, experience in pharmaceutical industry, excellent language skills, digital experience, and extensive knowledge of health systems
Global Director, Data Architecture
Bachelor's degree in computer science, Engineering, or a related field; Master's degree preferred. Proven experience in designing and implementing target Enterprise data and information architectures for global organisations
Global ICT Business Partner (Regulatory Affairs & Pharmacovigilance)
Bachelor's degree, strong computer science background, experience in pharmaceutical R&D technology support, and operational support background
Patient Journey Manager - Oldenburg, Bremen, Bremerhaven, Lüneburg
Regulatory Affairs Associate - Based in GALASHIELS
Life science qualification with experience in pharmaceutical regulatory affairs, ability to travel, flexibility of working hours, and good communication and organisational skills
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