Stellenbeschreibung:

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

Join to apply for the Manager RA Regulatory Operations (Information Management) (m/f/d) role at Sandoz in Deutschland

Major accountabilities

• 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.

Key qualifications

• Cross Cultural Experience
• Managing Crises
• Functional Breadth
• Project Management
• Collaborating across boundaries
• Operations Management and Execution
• Data Analysis
• Documentation Management
• Must-have: Veeva Vault RIM & GLORIA
• Lifesciences
• Project Management
• Regulatory Compliance
• English

Why Sandoz?

Sandoz has an employee-first approach and prioritizes personal growth with access to Coursera and other learning platforms with more than 200,000 learning videos and 5,000+ courses. We offer company benefits including 30 days of annual leave, holiday allowance, rewards for special occasions, pension schemes and capital formation benefits, parental leave, and other offerings such as bike leasing.

Commitment to diversity & inclusion

We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Hiring decisions are based on qualifications, regardless of gender, ethnicity, religion, sexual orientation, age or disability. If you require accommodation, please let us know as a note on your CV.

Seniority level : Mid-Senior level

Employment type : Full-time

Job function : Legal

Industries : Pharmaceutical Manufacturing

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NOTE / HINWEIS:

EN: Please refer to Fuchsjobs for the source of your application

DE: Bitte erwähne Fuchsjobs, als Quelle Deiner Bewerbung