Stellenbeschreibung:

Manager RA Regulatory Operations (Information Management) (m/f/d)

• Manages multiple, large and complex global regulatory submission projects.
• Develop and provide submission and contribute to the technical related regulatory strategy, intelligence and knowledge required to develop, register, and maintain global products.
• Contribute to strategic and technical input/support to drive implementation of global systems, tools and processes to support global development projects and/or marketed products.
• A seasoned, experienced professional with a full understanding of area of specialization; resolves a wide range of issues in creative ways.
• This job is the fully qualified, career-oriented, journey-level position .
• Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors.
• Demonstrates good judgment in selecting methods and techniques for obtaining solutions.
• Networks with senior internal and external personnel in own area of expertise.
• Contributes to many cost center goals and objectives; may contribute to service line goals -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)

Key performance indicators:

• Adherence to Sandoz policy and guidelines
• Project and stakeholder feedback


Work Experience:

• Cross Cultural Experience.
• Functional Breadth.
• Project Management.
• Operations Management and Execution.

Skills:

• Data Analysis.
• Documentation Management.
• Must-have: Veeva Vault RIM & GLORIA
• Project Management.
• Regulatory Compliance.

Languages :

Diversity and Inclusion

Division

SANDOZ

Business Unit

Development

Location

Germany

Site

Manager RA Regulatory Operations (Information Management) (m/f/d)

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NOTE / HINWEIS:

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