Regulatory Affairs Teamlead – OM Pharma – Meyrin, GE

We are currently looking for an experienced Regulatory Affairs Team Lead who will lead key activities for EU, US and CH regions. You will be responsible for the definition and implementation of regulatory strategies based on the good knowledge and appropriate interpretation of guidelines and directives. Based in Geneva, you will report to the Head of Regulatory Affairs OM Pharma and your responsibilities will include:

  • Contribute to the definition and the implementation of regulatory strategies to expand the business (geographic expansion, new indications…) and support/maintain registrations
  • Coordinate life cycle activities / maintenance of existing product licenses
  • Coordinate dossiers submission according to the defined timelines (renewals, variations, responses to HA questions)
  • Ensure compliance of the portfolio with legal requirements
  • Conduct risk assessments and set-up mitigation plans
  • Cooperate with internal stakeholders to ensure alignment on strategies
  • Lead the EU, US and CH regions team (2 direct reports): be responsible for the management and development of staff by overseeing recruitment and training, evaluating performance, defining and assigning responsibilities, providing opportunities for career development

We are looking for a customer- and service-oriented person who brings experience in working with a wide variety of stakeholders across diverse teams both internally and with external partner companies. Furthermore, your profile meets the following criteria :

  • University Degree (PhD / MSc) in Life Sciences, Pharmaceutical Sciences or Medical
  • 10 years of experience in Regulatory Affairs, with a proven experience on US market (new registrations) and EU region (support to clinical trials activities)
  • Experience in people management and development
  • Ability to perform comprehensive gap assessments and build effective regulatory strategies (Good knowledge and appropriate interpretation of guidelines, directives etc…)
  • Self-assertion, creative and solution-oriented work approach
  • Strategic thinking and acting, entrepreneurship skills
  • Excellent communication and negotiation skills at all levels, diplomacy and respectful behavior
  • Good command of French and English both in oral and written conversation

You are a mature regulatory professional and describe yourself as a solution-oriented and flexible person, able to influence internal and external stakeholders. Your work is characterized by its accuracy, a proactive approach and you are able to work under pressure and to deal with tight deadlines. These skills will ensure your success in this role.

The Vifor Pharma Group
is a global specialty pharmaceuticals company. It aims to become the global leader in iron deficiency, nephrology and cardio-renal therapies. The company is the partner of choice for pharmaceuticals and innovative patient-focused solutions. Vifor Pharma Group strives to help patients around the world with severe and chronic diseases lead better, healthier lives. The company develops, manufactures and markets pharmaceutical products for precision patient care. Vifor Pharma Group holds a leading position in all its core business activities and consists of the following companies: Vifor Pharma; Vifor Fresenius Medical Care Renal Pharma (a joint company with Fresenius Medical Care); and OM Pharma.

Vifor Pharma Group is headquartered in Switzerland, and listed on the Swiss Stock Exchange (SIX Swiss Exchange, VIFN, ISIN: CH0364749348).

Location: Switzerland – Meyrin/Geneva

Function: Regulatory Affairs

Company: OM Pharma

Seniority Level: Senior Manager

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