Expert Regulatory Affairs (m/f/d)
Responsibilities
- Preparation and submission of registration dossiers to CDSCO
- Communication with local authorities and agencies
- Preparation of clinical trials incl. ethics committee submissions
- Handling of variations and follow-ups
- Strategic adaptation of EU approvals for the Indian market
Profile
- Experience with Indian regulations (CDSCO, Drugs and Cosmetics Act, MDR 2017)
- Knowledge of medical device regulations
- Hands-on mindset and creativity in regulatory strategy
- Fluent in English (negotiation level)
- German and/or Polish: nice to have
Benefits
- Creative and free work at an international company
About Hays
With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.
Staffing process for freelance specialists
- Analysis of qualifications
- Telephone or personal interview
- Contact with customers
- Contract with Hays
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1. Analysis of qualifications
We carry out a detailed analysis of your technical qualifications on the basis of your CV, your application documents and your profile.
Contact at Hays
+ 49 621 1788-4297© Copyright Hays plc, . Das Wort HAYS, die H-Symbole, „Hays Working for your tomorrow" und „Powering the world of work" sowie damit verbundene Logos und Illustrationen sind eingetragene Markenzeichen der Hays PLC. Die H-Symbole sind Originaldesigns, die in vielen Ländern geschützt sind. Alle Rechte vorbehalten.