Associate Director Regulatory Policy

Almere (Sandoz)onsitedirector

Posted today · via Workday

About this role

Job Description Summary Join us, the future is ours to shape! Job Description Your Key Responsibilities: Your responsibilities include, but not limited to: Developing evidence-based policy positions for regulatory requirements for ethical and efficient development and manufacturing of generic and biosimilar medicines. Aligning Sandoz policy objectives and advocacy plans within Sandoz and within the trade association to shape emerging legislative proposals and regulatory guidelines of Health Authorities. Advocating for Sandoz policy objectives according to plans, e.g. via trade associations, conference presentations, publications, direct interactions with regulators and other relevant external stakeholders. Evaluating the impact of regulatory requirements.…

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What we'd score you on

reqspace match rubric

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1

Skills match

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2

Level fit

This role is director-level. We check your trajectory against it.

3

Domain experience

Your work in the role's domain matters more than your years total. We weight recent and direct experience.

4

Recency

A skill you used last quarter weighs more than one from five years ago. We grade on recency, not lifetime.

5

Location fit

This role is based in Almere (Sandoz). We weight your proximity and willingness to relocate.

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