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GRLI-0, Specialist License Management
A career at our company is an ongoing journey of discovery: our 60,300 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others
The Specialist Licence Management prepares dossiers and execute actions that support the license security and product compliance on the markets, and that meet company's and health authorities’ requirements. Encounter the challenges to enable representatives from all major disciplines involved to reach agreement on the license management strategy and approach.
Position will be working in a matrix organization, with extensive communication and collaboration with stakeholders from various functions within or outside Global Regulatory Affairs. The role will have to work on complex tasks and to propose solutions and strategies as part of their day to day work.
Who You Are:
Experience: Minimum 9 years of overall work experience in Pharma environment, Competent authority or Academia/R&D experience related to the role. Minimum 3 years of Regulatory affairs experience.
Degree in a Life Science, Medical, PharmD or related discipline (minimum MSc or equivalent degree), higher degree preferable (e.g. PhD in a scientific discipline)
Job Specific Competencies & Skills:
Ability to contribute to the dossier content and to perform content and quality review on regulatory documentation
Ability to develop and prepare successful regulatory strategies and dossiers
Experience in preparation and management of regulatory documentation, normally a full international submission (new product application) or large variations
Experience with life-cycle management activities in at least two regions (e.g. Europe, USA, International would be an asset)
Solid experience in Regulatory Affairs regulatory dossiers and regulatory procedures on a global scale, including submission/registrations types and related requirements
In Depth knowledge in Regulatory Affairs and experience of working in a global regulatory environment including exposure to registration procedures (CP, MRP, DCP, National etc.) and LCM strategies
Ability to review and interpret country specific and international regulatory guidelines, policies and regulations to generate submission ready deliverables as per request
Strong project management and documentation skills, proactive communication approach
Ability to execute appropriate risk assessment and mitigation in cooperation with line manager /team lead
Ability to provide Regulatory expertise into the planning and execution of projects and tasks
Ability to work within a matrix organisation, build relationships with internal or external stakeholder
Contributor level experience with Veeva Vault Registration module and EDMS RA applications
Excellent written and spoken communication skills and English language knowledge
Electronic City Phase 1 - Bangalore
We have several openings for License Management roles for various levels and profiles
Expectations and scope of responsibilities provided in this Job posting are for Specialist level
The exact designation to be offered will depend on applicants’ experience and knowledge confirmed during the screening process
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity. We believe that it drives excellence, innovation, and human progress. We care about our customers, patients, and our rich mix of people. This diversity strengthens our ability to lead in science and technology. We are committed to creating access and opportunities for all and empower you to fulfil your ambitions. Our diverse businesses offer various career moves to seek new horizons. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to bring their curiosity to life!