- 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
- 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
- Creative and free work at an international company
Ihr Kontakt
Referenznummer
832126/1
Kontakt aufnehmen
Telefon:+ 49 621 1788-4297
E-Mail: positionen@hays.de
Anstellungsart
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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.
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