Regulatory Affairs CMC, Associate Director

Lieu: United States - Redwood City

Fonction: Regulatory Affairs

Compagnie: Relypsa

Niveau de Séniorité: Director

Votre profil


Provide strategic regulatory support to internal brand, product and project teams.  
Pro-actively monitors the latest regulations, guidance, and actions from the FDA and competitors that may influence the landscape and assesses the potential impact on the regulatory and/or business strategy and planning.
Represent US regulatory and FDA perspectives within the Vifor global Regulatory Affairs teams. Work in close collaboration with Vifor global functions to integrate relevant aspects of US and global regulatory strategy.
Support regulatory aspects of submissions and communications with FDA by global regulatory staff for Vifor products.  
Manage timelines and resources to achieve stated objectives, ensuring tracking tools and regulatory databases are maintained in an up-to-date manner.


Provide strategic regulatory input on developmental and maintenance CMC projects
Ensure and lead proper FDA interactions on key CMC projects.
Oversee the preparation of CMC documents required by the FDA
Communicate with global RA colleagues and ensure the implementation of FDA CMC requirements within the organization.
Participate in the development of regulatory strategy and provide strategic input and regulatory advice to the project teams on both development program and lifecycle opportunities
Proactively identify project issues and implement appropriate regulatory strategies to mitigate risks
Develop and/or review regulatory documents to ensure that all submissions are of high quality
Interface with global Regulatory Affairs staff to provide input on US requirements or FDA processes
Support the preparation and conduct of Agency meetings as necessary to support regulatory filings and applications, including preparation and coordination of briefing packages
Develop and maintain current knowledge of US regulation and industry standards, and communicate requirements to others as needed.


The knowledge and skills necessary to perform the duties of this position are typically acquired through the following combination of education, experience, and knowledge, or the equivalent:
Minimum Requirements
- BS, BA in a relevant discipline, or BSN 
- Experience in regulatory xxx and in other areas of Regulatory Affairs
- At least 8 years in pharmaceutical or biotech industry in regulatory affairs
- Understanding of GMPs and GLPs; solid understanding of where to seek and how to interpret regulatory information.
- Strong and broad knowledge of CMC drug development
- Experience providing strategic CMC regulatory advice for the global development of products through all stages of development including pre-approval and marketed compounds 
- Proficiency in Microsoft Word, Excel, PowerPoint, and Adobe Acrobat and PRC software
Preferred Requirements
- MA/MS or PhD in life chemistry or chemical engineering, or PharmD preferred
- Experience in an international company with more than one marketed product

A propos de nous

Le groupe Vifor Pharma est une entreprise pharmaceutique internationale spécialisée. Son ambition est de devenir le leader mondial dans les domaines de la carence en fer, de la néphrologie et des traitements cardio-rénaux. L’entreprise est le partenaire de choix pour les médicaments et les solutions innovantes axées sur le patient. Le groupe Vifor Pharma aspire à aider les patients du monde entier atteints de maladies graves et chroniques à mener une vie meilleure et plus saine. La société développe, fabrique et commercialise des produits pharmaceutiques offrant des soins de précision aux patients. Le groupe Vifor Pharma occupe une position de premier plan dans toutes ses activités clés. Il se compose des entreprises suivantes: Vifor Pharma; Vifor Fresenius Medical Care Renal Pharma (sa société commune avec Fresenius Medical Care); et OM Pharma.

Le groupe Vifor Pharma a son siège en Suisse et est coté à la Bourse suisse (SIX Swiss Exchange, VIFN, ISIN: CH0364749348).

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