[MedTech] Business Unit Regulatory Affairs Manager, Regulatory Affairs (CSS Group)
Key Responsibility
- Project Management for all project in the team. Make RA strategy for new product introduction to drive our business.
- Take action to inquiry and/or instruction from Health Authority as a representative from Business Unit Regulatory Affairs in J&JKK.
- Execute action related regulatory compliance by having preventive and avoidance action doing risk analysis and management in RA part
- Assist the group member as a first-line manager, to plan and evaluate performance.
- Mentor, coach, train and develop the direct reports. Evaluate performance and provide opportunities for growth.
- Communicate with all stakeholders including commercial and OpCo related RA matters in the team.
- Contribute to RA organizational action as DRI or SME for assigned project
- Contributes to development of team budget and implements cost controls.
At Johnson & Johnson,?we believe health is everything. Our strength in healthcare innovation empowers us to build a?world where complex diseases are prevented, treated, and cured,?where treatments are smarter and less invasive, and?solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.
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