Regulatory Affairs - EU Submissions - Career Chance

Dec 07, 2017
Jan 06, 2018
169341 6
Emma Fleury
Jobseeker Type
Organization Type
Contract Type
Full Time

My client is a global pharmaceutical company, renowned for the production of drugs for several important therapeutic areas, like oncology, metabolic diseases, cardiology and neurology. He has recently opening new branches in East Europe, and for supporting his new projects he is currently looking for a new Regulatory Affairs Manager to join his team (m/w).

If you are an ambitious personality, ready to give an international kick off to your career, this is the right moment to join this company! They are namely producing new drugs and establish new markets, therefore you will get the chance to enhance your technical and scientific knowledge, as well as to prove your organization and communication skills, for getting the next step in your career development.

Your requirements:

  • 2+ Experience with regulatory submissions for European markets
  • Fluent English, written and spoken

Nice to have:

  • Experience with submission for the German market
  • Good command of German language, written and spoken

Starting Datum: ASAP

Contract Type: Permanent, full-time position

Location: Vienna area

Monthly Salary: 3.000 EUR gross, negotiable according to the experience

Feel interested in principle? You can pose me all questions you want!

Hereby my contact details: Ms Emma Fleury/ EMAIL / TEL 0049 892 109 33 63

If you want to apply, please send me your CV in World.doc Format by e-mail:

Check My Linkedin Profile:

If you are not interested, but you know someone who could like this or another job into the pharmaceutical industry, refer us! You could gain £200 in high street vouchers if we successfully manage to place your referrals.

NonStop Recruitment is a Swiss-headquartered, pan-European specialist recruitment consultancy. NonStop comprises a number of brands each covering a particular sector and with teams of consultants focusing on specific niches. NonStop offices across Europe provide licenced contract or labour leasing solutions, as well as permanent recruitment and executive search solutions. We are dedicated to fulfilling the expectations of our customers. Our unique in-house Quality Assurance function builds on and re-enforces a strong culture of ethics and customer service. For more information, see our website

Key Words

Regulatory Affairs, Research, Forschung, Maintenance, Compliance, Life Cycle Management, LCM, submission, Einreichung, Labelling, post- approval, change control, SOP, Standard Operative Process, Rare disease, seltene Krankheiten, Orphan drugs, Orphan-Arzneimittel, hematology, Hematologie, oncology, Onkologie, psychiatry, Psychiatrie, metabolic disease, metabolisches Syndrom, Diabetis, Cardiology, Cardiologie, Pulmonology, Pneumologie, Neurology, Neurologie, German, Deutsch, European, Europe, EMA, European Medicines Agency, Europäische Arzneimittel-Agentur, BfArm, Bundesinstitut für Arzneimittel und Medizinprodukte, English, Englisch, International, threatment, Behandlung, Niche products, Nischenprodukten