Job Details

Job Summary:

Regulatory Affairs (Snr) Manager - International/Row role – Switzerland. This is a newly created vacancy with the aim of developing this candidate into an Associate director with people and project management responsibility. Join one of the world’s leading companies in a proactive and exciting roll. In the first instance please call Theo Moore or Matt Greig on +44(0)207 801 3384 or +44 (0) 7918 195 166 or please send a full CV to Cv@advregulatory.com

Requirements:

Regulatory Affairs Snr Manager- International/Row Role – Switzerland – Join one of the worlds Leading Pharma Companies - Excellent salary, bonus and Package

 

Location: Switzerland, Basel, Zurich, Geneva

My Client:

My client is one of the worlds favorite pharmaceutical companies, with a well deserved reputation of innovation and successful product development.

They are extremely commercially focused and have placed a big emphasis on growth into International/RoW markets, so this is a key role within the regulatory affairs department.

This is a team of high achievers who are specialists within International/ROW markets, and now they are looking to expand the team with 2 new International/Row Regulatory (Snr) Managers.

You will be joining a very successful team , so you really need to be a forward thinking ambitious Regulatory professional to apply.

In the first instance please call Theo Moore or Matt Greig on +44(0)207 801 3384 or +44 (0) 79 18 195 166 or please send a full CV to Cv@advregulatory.com

The Role:

You will be tasked with providing regional strategic input and coordinating the development and registration of assigned projects ensuring alignment with the Global project strategy. This role will have high level Health Authority (HA) Interaction where you will be supporting Global Regulatory Leaders in HA negotiation.

Experience needed:

•Ideally you will have a Minimum 3-5 years experience of in international regulatory affairs, preferably some experience with Emerging Markets and an awareness of Drug development process and new development technologies
•Basic project management skills
•Assertive personality
 

Benefits: FULL RELOCATION, strong package, very low tax and a bonus.

TO APPLY
If you wish to apply for this role please click below, or send your CV with a covering note to cv@advregulatory.com quoting reference number noted above. Alternatively to have a confidential discussion about this or other potential roles or career options call Theo Moore or Matt Greig on +44 207 801 3384.

We work in the strictest of confidence and WILL NOT disclose any information to ANY third parties WITHOUT YOUR PRIOR CONSENT. For a confidential discussion call or apply today!

About ADV Regulatory
Advanced Regulatory has operating since 2004.
We are a recruitment business dedicated to the pharmaceutical industry, specialising in Regulatory Affairs, Quality Assurance, Clinical Development, Pharmacovigilance and Health Economics and Outcomes Research. We match professional candidates to the best permanent, contract and interim roles in the market.
Visit us at www.advregulatory.com

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