Regulatory Affairs Consultant - OTC pharmaceuticals URGENT
- Employer
- NonStop Consulting
- Location
- Brussels
- Salary
- Negotiable
- Closing date
- Jul 9, 2019
View more
- Sector
- Science, Life Sciences, Anatomy/Physiology
- Contract Type
- Employee
- Hours
- Full Time
- Organization Type
- Corporate
Job Details
My client is a leader in consumer healthcare, currently searching for a new Benelux RA contractor with a speciality in OTC / Cosmetics.
Their portfolio is very broad, filled with products ranging from heartburn relief to migraines but also condoms and wax strips.
Being a leader in their industry, they naturally have their own Research & Development team which means you will be working with exciting and new products on a regular basis.
They are currently looking for an experienced consultant with expertise in FAHMP submission for medicinal products, preferably OTC. For a couple of months (up to 6m but possibly more).
It will mostly involve variations, renewals, new submissions, closing phase with FAMHP, preparing local documents, regulatory feedback to GRA, PQR, etc.
Key expertise will be knowledge in advertising of OTC medicines for public & HCP's in Belgium. If you have this or know someone who does, call me yesterday! (or today, I can compromise).
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.
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