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(Sr.)Manager, CMC Regulatory Affair, R&D, Shanghai/Beijing @ Takeda

CNOnsiteFull-time
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About this role

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description

RESPONSIBILITIES:

• Develop and execute global regulatory strategies for assigned programs • Collaborate with regional counterparts to compile and align global regulatory strategies • Create and submit high-quality, compliant regulatory documents within defined timelines • Manage regulatory submissions and maintain compliance for assigned programs • Support health authority interactions and meetings related to assigned programs • Ensure accurate, up-to-date reporting of program status and milestones globally • Lead and mentor junior staff, enhancing team capabilities R&D Qualifications & Skills:

• Expertise in developing regulatory strategies and a deep understanding of CMC requirements • Proven ability to negotiate with and influence health authorities • Strong leadership skills, capable of managing and directing project teams • Effective at working across functions to align strategies and achieve objectives • Skilled in managing regulatory submissions and maintaining compliance • Excellent communication skills, able to clearly convey complex information • Proficient in mentoring and developing junior staff, enhancing team capabilities • Capable of identifying and mitigating risks in regulatory strategies and operations

Locations Shanghai, ChinaBeijing, China Worker Type Employee Worker Sub-Type Regular Time Type Full time

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