Senior Manager, International Commercial Review & Ops

Takeda Pharmaceutical; Zürich; On-site; CHF 141,000 - 194,000; Full time

Job summary

Takeda Pharmaceutical Co. in Zurich, Switzerland, seeks a Senior Manager for the Commercial Material Review Process (CMRP). Lead CMRP operations, drive platform improvements, and coordinate training across global teams to ensure efficient, compliant reviews.

Role requires 3+ years in business or pharma with strong project management, cross-functional collaboration, and facilitation skills within a global regulatory context. Full-time on-site role with competitive base salary.

Qualifications

• Bachelor’s Degree or equivalent with 3+ years general business experience.
• 2+ years direct experience coordinating advertising and promotional processes.
• Experience in the pharmaceutical industry.
• Experience working with cross-functional groups to achieve goals.
• Project management experience and MS Office proficiency.
• Facilitation skills to align cross-functional stakeholders.

Responsibilities

• Lead CMRP operations and coordinate review processes.
• Partner with GRA A&P Excellence to optimize PromoMats capabilities and user experience.
• Drive continuous improvement to simplify ways of working and increase efficiency.
• Develop and communicate CMRP performance insights and trends.
• Ensure training and change activities align with evolving processes and systems.
• Build cross-functional partnerships across stakeholders to advance excellence.

Skills

Project management

Cross-functional collaboration

Microsoft Office

Facilitation skills

Pharmaceutical industry experience

Education

Bachelor’s Degree

High School Diploma

Job description

Takeda Pharmaceutical Co. in Zurich, Switzerland, seeks a Senior Manager for the Commercial Material Review Process (CMRP). Lead CMRP operations, drive platform improvements, and coordinate training across global teams to ensure efficient, compliant reviews.

Role requires 3+ years in business or pharma with strong project management, cross-functional collaboration, and facilitation skills within a global regulatory context. Full-time on-site role with competitive base salary.