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Regulatory Affairs Manager, Development Products

Employer
NonStop Consulting
Location
Basel
Salary
Negotiable
Closing date
Jan 7, 2017

View more

Sector
Pharmaceutical, Regulatory Affairs
Contract Type
Employee
Hours
Full Time
Organization Type
Clinical Practice
Jobseeker Type
Professional

Job Details

Regulatory Affairs Manager/Senior Associate, development products, global HQ, EMA, strategic and hands on focus. Salary package competitive with Big Pharma, relocation help is available and most the team are ex-pats.

Want to join a new and growing division? Want to work in big pharma without all the restructuring? We are currently partnering with an expanding regulatory affairs team who are in the process of covering key submissions for products in early and late stage clinical. Specifically they are looking for regulatory affairs professional who can help take responsibilities for critical submissions for the EMA including DCP/CP submissions as well as CTA, HA interactions and life cycle maintenance activities. It is a great opportunity for someone who has done pre approval, who would like the chance to work in a growing team and to take steps up in regards to HA interactions and greater product ownership. If in principle you could be interested, then please reach out to me.

Key Responsibilities:

  • Leading submissions prior to MA for small molecule RX products
  • LCM activities for current portfolio
  • HA interactions and scientific advice
  • Close collaboration with global team

Key Requirements:

  • Life science degree
  • At least 3 years experience in regulatory affairs
  • Experience working with innovative pharma/biotech RX products with the EMA
  • Fluency in English

For a confidential discussion about regulatory affairs, or to apply, then send your CV to m.beedle@nonstop-recruitment.com or call me, Matt Beedle, Regulatory Affairs Consultant for Switzerland on +41435 080817. For regular job updates and market information please join the Switzerland regulatory affairs linked-in group. https://www.linkedin.com/groups/4550988

I am a specialist head hunter(recruiter) for regulatory affairs in the Pharmaceutical & Biotechnology industry. I offer a number of search options within the industry with a special focus on the Swiss regulatory affairs market as well as ATMP(Advanced Therapeutics) and biological regulatory professionals world wide. Please refer to ch.linkedin.com/in/regulatoryaffairsswitzerland for references.

Company

Our Consultants are trained to deliver an exceptional standard of recruitment services to clients across the life sciences, chemical, care, educations, technical, digital and finance industries. 

Our clients – and bottom line profits - tell us that we do a great many things very well. Complacency, however, is the last word you would associate with us. We work incredibly hard to deliver better and better results, based on stronger and stronger service delivery.  Which is why we believe the best is yet to come – for us, our clients and for the people who have what it takes to join us on the journey.

The result? We’re expanding (in the UK and across Europe and even to Boston, US) and continue to post impressive performances in all our niche sectors. 

Company info
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