Regulatory

Regulatory

Home to some of the world's most important international health institutions, as well as two of its largest pharmaceutical companies in Novartis and Roche, and with a number one ranking globally in terms of ease of doing business and innovation; Switzerland can truly lay claim to be a healthcare and life sciences powerhouse. Despite some of the highest operating costs of any country in the world, an increasing number of pharma companies are choosing to base their European and EMEA headquarters in Switzerland.

Regulatory affairs plays a crucial role in the pharmaceutical industry and is involved in all stages of drug development and also after drug approval and marketing. At any time, there are more than 300,000 clinical studies happening around the world. The process for bringing new pharmaceuticals to the market is prolonged due to regulation placed on the drugs sector to protect public safety. State regulations in Switzerland can lead to high administrative costs or preclude market access. However, at the same time, regulations can also promote competition and economy-friendly structures.

Under the Swiss regulatory approach, the drugs approvals process is quick and simple. Typically, it takes around 11 months to obtain a license from the country's medicines agency, Swissmedic, one of the fastest turnaround times in the world. Swissmedic is the national authorisation and supervisory authority for drugs and medical products. The agency ensures that only high-quality, safe and effective medical products are available in Switzerland, thus making an important contribution to the protection of human and animal health.

Our Zurich based consultants are specialists in their markets, recruiting top talent for the regulatory jobs market throughout Switzerland and Europe.

Regulatory Jobs

Regulatory Affairs Manager/Senior Manager
US$75 - US$95 per hour, Palo Alto

Manager, Regulatory Affairs A specialty pharmaceutical company is currently seeking a Manager Reg...

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Director/Senior Director Regulatory Affairs
Negotiable, United States of America

Director/Senior Director Regulatory Affairs A Clinical Stage biotechnology company that is focusi...

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RAQA Manager/Senior Manager
Negotiable, Seoul

My client is a global medical device company, headquartered in the US, specialising in Orthopaedi...

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Investigator Grant Manager
US$70 - US$85 per hour, California

**Remote Role** Job opportunity with a top biopharmaceutical company that is looking for an Inves...

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Manager Regulatory Affairs
Negotiable, Salt Lake City

Manager Regulatory Affairs Hybrid - Salt Lake City, Utah My leading pharmaceutical client is seek...

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Regulatory Affairs Specialist
Negotiable, United States of America

Regulatory Affairs Specialist (Remote) Are you a regulatory affairs specialist with expertise in ...

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Sr. Manager, Regulatory Affairs
Negotiable, New York

Are you a seasoned regulatory affairs professional with a background in generic pharmaceuticals a...

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[Pharma] REMOTE Regulatory Affairs Consultant, Strategy
US$105 - US$155 per hour, South San Francisco

Fully-Remote: Reg. Affairs Consultant Strategist We are a clinical stage biotech that aims to lea...

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Senior Director, Global Regulatory Affairs, Vaccines
Negotiable, Massachusetts

Title: Senior Director, Global Regulatory Affairs Summary: A world renowned leader in the pharmac...

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