What are the responsibilities and job description for the Regulatory Affairs position at Katalyst Healthcares & Life Sciences?
Responsibilities :
requirements:
- Works with RA Manager and Platform Leaders to ensure timely execution of regulatory strategies with business objectives and customer results
- Assesses regulatory pathways for new products, product modifications or product conversions; develops regulatory strategies and planning for submissions or support of customers' regulatory submissions
- Partners with and supports Pharma customers in securing timely development, submissions, addressing health authority questions and regulatory drug-device combination products approvals
- Performs regulatory impact assessment of changes linked to the field of expertise and assigned platform
- Liaises with cross-functional and cross company teams to meet customer needs in driving new drug delivery solutions for global markets
- Develops and maintains knowledge & awareness on assigned fields of expertise: identify applicable regulations and standards, perform regulatory intelligence/watch, educate appropriate contact partners
- Identifies and communicates potential risks and mitigations associated with regulatory strategies to partners
- Support to customers for regulatory advice and registration of their products and interact as necessary with the U.S. regulatory agencies and EU Notified Bodies
- Reviews and/or approves product marketing claims and communication, Advertising/promotional materials, and labeling
- Conduct trainings on regulatory issues for staff and for business stakeholders (e.g., Platform, R&D, Marketing and Pharma Partners)
- Participates in internal/external trade, professional, and standards development organizations
- Manages multiple projects with minimal supervision
requirements:
- Knowledge in medical devices regulation registration requirements and pathways (variations, renewals, supplements), in the US and EU markets. Pharmaceutical experience is a plus.
- Understanding of product development cycle and quality management systems
- Experience in meeting with, making presentations to, and negotiating with leadership and/or regulators
- Ability to use your time productively and efficiently (structured and self-organized with strong project management skills)
- Ability to resolve problems and to make appropriate regulatory decisions under pressure
- Ability to adapt, multitask and respond quickly in a rapidly changing and often ambiguous environment, Strong team player.
- Ability to drive and maintain favorable customer experience and customer-centricity (internal & external)
- B.S. or B.A. degree in a technical field (e.g., engineering, biology, chemistry). Advanced degree preferred.
- Minimum five years of directly related professional experience (Regulatory) in increasingly responsible positions in the medical device, biologic, or pharmaceutical fields
- Demonstrated project management, negotiation, influencing and communication skills.
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