
CSV Manager
Bengaluru, KarnatakaAt Takeda, we are guided by our purpose of creating better health for people and a brighter future for the world. Every corporate function plays a role in making sure we — as a Takeda team — can discover and deliver life-transforming treatments, guided by our commitment to patients, our people and the planet.
People join Takeda because they share in our purpose. And they stay because we’re committed to an inclusive, safe and empowering work environment that offers exceptional experiences and opportunities for everyone to pursue their own ambitions.
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Job Description
The Future Begins Here
At Takeda, we are leading digital evolution and global transformation. By building innovative solutions and future-ready capabilities, we are meeting the need of patients, our people, and the planet.
Bengaluru, the city, which is India’s epicenter of Innovation, has been selected to be home to Takeda’s recently launched Innovation Capability Center. We invite you to join our digital transformation journey. In this role, you will have the opportunity to boost your skills and become the heart of an innovative engine that is contributing to global impact and improvement.
At Takeda’s ICC we Unite in Diversity
Takeda is committed to creating an inclusive and collaborative workplace, where individuals are recognized for their backgrounds and abilities they bring to our company. We are continuously improving our collaborators journey in Takeda, and we welcome applications from all qualified candidates. Here, you will feel welcomed, respected, and valued as an important contributor to our diverse team.
About the role:
The Digital Risk and Compliance, Manager is responsible for managing the global information security risk program across the organization. This individual will work directly with business leaders to understand security and risk issues, oversee risk management and assessment efforts, and develop effective remediation programs.
About the Role
We are seeking a seasoned Validation Manager with deep expertise in Computer System Validation (CSV) and a strong background in Software as a Medical Device (SaMD). This role is critical to ensuring our digital health platforms meet global regulatory standards and deliver safe, effective, and compliant solutions.
Key Responsibilities
- Lead CSV activities for systems supporting SaMD and SiMD, ensuring compliance with GxP and data integrity standards.
- Expertise in global regulatory compliance related to SaMD/SiMD, including 21 CFR Part 11, 21 CFR Part 820, FDA SaMD guidelines, and ISO 13485.
- Proven ability to validate commercial software platforms, focusing on data integrity, scalability, and GxP compliance.
- Hands-on experience with real-world evidence platforms, ensuring accurate system validation and patient outcomes enablement.
- Deep understanding of system integration and interoperability testing for digital health and connected devices.
- Strong experience in cross-functional collaboration to validate SaMD/SiMD and align SaMD processes with commercial objectives and market realities.
- Plan, draft, and maintain validation documentation, including validation plans and specification documentation , Validation Summary Report.
- Develop testing protocols such as Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
- Execute validation tests and compile comprehensive phase reports.
- Evaluate and address validation risks associated with system changes, updates, or implementations.
- Collaborate with external system providers during implementation, ensuring alignment with validation requirements and quality standards.
- Act as a subject matter expert Medical Device Regulation (MDR) 2017/745 and the In Vitro Diagnostic Regulation (IVDR) 2017/746 (EU), Validation of CSV supporting SaMD
- Maintain detailed and up-to-date validation documentation in compliance with regulatory standards and industry best practices.
- Investigate deviations, discrepancies, or non-conformances encountered during validation activities and ensure corrective actions are appropriately implemented.
- Provide training and mentorship to team members and stakeholders regarding validation processes, protocols, and best practices.
- Serve as a go-to expert for validation-related challenges and initiatives.
- Stay informed of industry developments, evolving regulations, and emerging technologies related to validation processes and systems.
- Continuously integrate improvements and ensure alignment with regulatory guidelines.
Qualifications
- 8-10 years of experience in a similar role
- Bachelor's degree in a relevant field (e.g., Computer Science, Engineering, Life Sciences).
- Proven experience validating systems in regulated environments, especially those supporting SaMD.
- Strong knowledge of:
- 21 CFR Part 11, 21 CFR Part 820
- FDA SaMD guidelines
- ISO 13485, EU MDR 2017/745, EU IVDR 2017/746
- Hands-on experience with:
- Real-world evidence platforms
- Data integrity and scalability validation
- System interoperability testing
- Strong analytical and problem-solving skills.
- Excellent communication and teamwork abilities.
- Attention to detail and a commitment to quality.
Skills and Experience:
- Experience with AI/ML-enabled SaMD.
- Familiarity with cybersecurity and privacy compliance in medical software.
- Exposure to global regulatory submissions and lifecycle management.
- Must have experience working in agile environment and use of modern quality tools ( e.g. ( JIRA, Confluence, Qtest, etc)
- Working knowledge of Validations supporting SAMD
- Experience working with virtual teams on a global basis
- In depth knowledge of GxP regulations( such as from FDA, EMA, etc) related to SAMD, IT Systems
- Ability to lead teams in the correct interpretation of regulations
- Good oral and written communications skills, business acumen with problem solving and analytical skills
WHAT TAKEDA CAN OFFER YOU:
- Takeda is certified as a Top Employer, not only in India, but also globally. No investment we make pays greater dividends than taking good care of our people.
- At Takeda, you take the lead on building and shaping your own career.
- Joining the ICC in Bengaluru will give you access to high-end technology, continuous training and a diverse and inclusive network of colleagues who will support your career growth.
Benefits:
It is our priority to provide competitive compensation and a benefit package that bridges your personal life with your professional career. Amongst our benefits are:
- Competitive Salary + Performance Annual Bonus
- Flexible work environment, including hybrid working
- Comprehensive Healthcare Insurance Plans for self, spouse, and children
- Group Term Life Insurance and Group Accident Insurance programs
- Employee Assistance Program
- Broad Variety of learning platforms
- Diversity, Equity, and Inclusion Programs
- Reimbursements – Home Internet & Mobile Phone
- Employee Referral Program
- Leaves – Paternity Leave (4 Weeks) , Maternity Leave (up to 26 weeks), Bereavement Leave (5 calendar days)
About ICC in Takeda
- Takeda is leading a digital revolution. We’re not just transforming our company; we’re improving the lives of millions of patients who rely on our medicines every day.
- As an organization, we are committed to our cloud-driven business transformation and believe the ICCs are the catalysts of change for our global organization.
#Li-Hybrid
Locations
IND - BengaluruWorker Type
EmployeeWorker Sub-Type
RegularTime Type
Full timeSuccess profile
What makes a successful team member within Corporate at Takeda?
- Collaborative
- Strategic
- Insightful
- Results driven
- Goal-oriented
- Achiever
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Impact across generations Partnership brings together world-leading plasma companies to focus on developing and delivering a hyperimmune immunoglobulin in the global fight against COVID-19.
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Takeda Scoops Global Top Employers® Award Takeda Pharmaceutical Company Limited today announced it has become part of a select group of only 15 to receive Top Global Employer® status for 2024.
Working at Takeda
-
Inclusion
Here, you will feel welcomed, respected, and valued as a vital contributor to our global team. -
Collaboration
A strong, borderless team, we strive together towards our priorities and inspiring mission. -
Innovation
Bold initiatives, continuous improvement, and creativity are at the heart of how we bring scientific breakthroughs from the lab to patients. -
Top Workplace
Recognized for our culture and way of working, we’re one of only 17 companies to receive Top Global Employer® status for 2024. -
Work-Life
Our people-first mission extends beyond patients to include their families, communities, and our own Takeda family. -
Empowerment
Through trust and respect, you will have genuine support from leaders, managers, and colleagues to do your best work.
We're Steadfast In Our Commitment to Four Key Imperatives
Patient
Responsibly translate science into highly innovative medicines and accelerate access to improve lives worldwide.
People
Create an exceptional people experience.
Planet
Protect our planet.
Data & Digital
Transform Takeda into the most trusted, data-driven, outcomes-based biopharmaceutical company.
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