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Job Opportunity for Regulatory Affairs at Troikaa Pharma



Job Opportunity for Regulatory Affair's at Troikaa Pharma

Troikaa Pharma is a leading company with the remarkable ability to constantly innovate through creative Imagination. Our NODS brands Dynapar AQ and Dynapar QPS are path breaking & have revolutionised pain care. These innovative products are backed by strong global patents. Continuous focus on innovation and an unwavering commitment to quality has helped Troikaa establish itself both in domestic and international markets. The company is driven by a visionary leadership and a strong multicultural workforce representing more than 85 countries. It’s state-of-the-art manufacturing facilities located at Thol, Dehradun and Sanand are accredited by global authorities including WHO, PIC/S, ANVISA Brazil, INVIMA, Europe Market & several other regulatory authorities.

Interview For - Europe Market & ROW

Looking stability and longevity of your current & previous assignment with good exposure in Corporate Regulatory Affair.

Sr. Executive / Asst. Manager / Dy. Manager
Expected M.Pharma by education with 5 to 10 years experience in Europe Market for Dossier compilation, review & submission (DCP/MRP) for new products in target countries. Should have knowledge of eCTD software.
CTC - 6 to 12 LPA

Officer & Executive
Expected M.Pharm by education with 2-5 years experience in ROW Market for Dossier compilation, review & submission.
 CTC - 3.50 to 5.50 LPA

Interested candidates may upload their CV on below given link

Registration Link

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