Role at a glance
- Job function
-
Healthcare Healthcare Administration & Patient Services
- Salary
- Not Disclosed
- Location
- Zurich, Switzerland
- Employment
- Full-time
- Experience
- Experience within the pharmaceutical industry, preferably in Medical Affairs, Medical Operations, Medical Excellence, Quality Management, or Patient Services.
- Education
- Advanced degree in Life Sciences, Pharmacy, Medicine, or related field (PhD, PharmD, MD preferred).
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Role Summary
The Switzerland-based Medical Affairs Operations & Patient Services Manager supports Medical Affairs across the Central Europe cluster, with responsibility for operational excellence, medical quality and compliance, and patient support programs.
What You'll Do
- Lead initiatives to improve Medical Affairs processes, governance, efficiency, and compliance.
- Coordinate medical quality activities, including audits, inspections, CAPA management, and compliance monitoring.
- Establish and improve Patient Support Programs, overseeing compliant execution, vendors, and performance.
- Steward Medical Affairs data quality, analytics, and insights, and oversee quality systems and platforms.
- Coordinate cross-border processes, monitor operational performance, and develop reporting mechanisms.
Generated from the employer's posting. Verify important details before applying.
View full postingQualifications
Requires an advanced degree in Life Sciences, Pharmacy, Medicine, or a related field; pharmaceutical-industry experience; understanding of GxP, Medical Affairs compliance, and pharmaceutical regulations; experience with quality systems, audits, inspections, CAPAs, SOPs, vendors, analytics, and operational metrics; project management, stakeholder management, communication, collaboration, and presentation skills; knowledge of Medical Affairs systems or equivalent platforms; and fluent English.
Required
- Advanced degree in Life Sciences, Pharmacy, Medicine, or a related field.
- Experience within the pharmaceutical industry.
- Strong understanding of GxP, Medical Affairs compliance requirements, and pharmaceutical industry regulations.
- Experience managing quality systems, audits, inspections, CAPAs, SOPs, and compliance processes.
- Demonstrated project management expertise and ability to manage multiple complex initiatives simultaneously.
- Strong stakeholder management skills and ability to influence across functions and countries without direct authority.
- Experience managing external vendors and service providers.
- Experience utilizing analytics and operational metrics to drive business improvement.
Preferred
- Experience in Medical Affairs, Medical Operations, Medical Excellence, Quality Management, or Patient Services.
- PhD, PharmD, or MD.
- German, French, or Italian.
Original job description
Content provided by the employer
Original job description
Content provided by the employer
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
The Medical Affairs Operations & Patient Services Manager is a Switzerland-based role within Medical Affairs, reporting directly to the Cluster Medical Head, Central Europe. The position is responsible for driving operational excellence, medical quality, compliance oversight, patient support program management across the CH territory and across the cluster central europe for the cluster medical affairs team. The role plays a critical part in ensuring compliant, efficient, and innovative Medical Affairs processes while partnering closely with Medical Advisors, Quality Assurance, Ethics & Compliance, Regulatory Affairs, Pharmacovigilance, and Digital, Data & Technology teams.
How You Will Contribute
- Lead operational excellence initiatives across Medical Affairs, continuously improving processes, governance, efficiency, and compliance.
- Serve as the Medical Affairs focal point for medical quality activities, audits, inspections, CAPA management, and compliance monitoring.
- Partner with local, regional, and global stakeholders to implement harmonized and future-ready Medical Affairs processes.
- Establish, manage, and continuously improve Patient Support Programs (PSPs), ensuring compliant execution, vendor oversight, performance monitoring, and exceptional patient experience.
- Act as Medical Affairs Data Steward, driving data quality, analytics, and insights across Medical Affairs activities.
- Oversee Medical Affairs quality systems and platforms, including document, learning, and content management systems.
- Collaborate with Digital, Data & Technology teams to support digital health solutions and innovative patient engagement initiatives.
- Manage vendors and external partners supporting patient services, evidence generation, and medical operations activities.
- Drive a quality-focused culture by embedding continuous improvement, compliance, and best practices throughout Medical Affairs.
- Coordinate cross-border processes and ensure effective execution of activities requiring regional alignment and governance.
- Monitor operational performance metrics and develop reporting mechanisms that support decision-making and organizational improvement.
Skills and Qualifications
- Advanced degree in Life Sciences, Pharmacy, Medicine, or related field (PhD, PharmD, MD preferred).
- Experience within the pharmaceutical industry, preferably in Medical Affairs, Medical Operations, Medical Excellence, Quality Management, or Patient Services.
- Strong understanding of GxP, Medical Affairs compliance requirements, and pharmaceutical industry regulations.
- Experience managing quality systems, audits, inspections, CAPAs, SOPs, and compliance processes.
- Demonstrated project management expertise with the ability to manage multiple complex initiatives simultaneously.
- Strong stakeholder management skills with the ability to influence across functions and countries without direct authority.
- Experience managing external vendors and service providers.
- Data-driven mindset with experience utilizing analytics and operational metrics to drive business improvement.
- Knowledge of Medical Affairs systems such as TrackWise, PromoMats, MARV, DMS, LMS, or equivalent platforms.
- Strong communication, collaboration, and presentation skills.
- Fluent English required; German, French, or Italian considered an advantage.
What You Bring
As an experienced Medical Affairs professional, you thrive in a highly regulated and complex environment where operational excellence, compliance, and innovation must coexist. You are comfortable working independently while influencing diverse cross-functional stakeholders across the organization.
You possess a strong understanding of Medical Affairs operations, medical quality systems, evidence generation processes, and patient support programs. You use data and insights to identify opportunities, solve complex problems, and implement sustainable improvements.
You consistently demonstrate a patient-focused mindset, strong business acumen, and the ability to navigate ambiguity while maintaining the highest standards of quality, ethics, and compliance. You are recognized as a trusted partner who drives collaboration, enables execution, and contributes to Takeda's performance culture and enterprise-first mindset.
Why Join Us
This role offers a unique opportunity to shape the future of Medical Affairs operations within the Central Europe Cluster, driving impact across patient services, medical quality, operational excellence, evidence generation, and digital innovation while working directly with the Cluster Medical Leader Team
Locations
Zurich, SwitzerlandBase Salary Range:
CHF132,000.00 - CHF181,500.00
The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.
For information about our benefits, please click here.
Worker Type
EmployeeWorker Sub-Type
RegularTime Type
Full timeAbout the company
Takeda
Large Enterprise
Takeda is a global biopharmaceutical company headquartered in Tokyo, Japan, with a rich history spanning over 240 years. Specializing in the research, development, and commercialization of innovative medicines, Takeda focuses on therapeutic areas such as oncology, gastroenterology, neuroscience, and rare diseases. Committed to improving patient outcomes, the company harnesses advanced technologies and scientific expertise to deliver breakthrough therapies and enhance healthcare worldwide. Takeda's dedication to sustainability and social responsibility underscores its mission to strive towards better health for people and communities across the globe.