Are you a skilled professional in Drug Regulatory Affairs with 2 to 8 years of experience? We have an exciting opportunity for you! Theon Pharma is urgently hiring for the position of Drug Regulatory Affairs Executive to join our dynamic team in Nalagarh. If you have expertise in CTD, ACTD, Dossier Preparation, and Row Market, this could be the perfect role for you.
About Theon Pharma
Theon Pharma is a leading name in the pharmaceutical industry, committed to delivering high-quality healthcare solutions. We specialize in regulatory compliance, drug development, and market authorization, ensuring our products meet global standards. Join us to be a part of a team that values innovation, professionalism, and excellence.
Job Details
- Position: Drug Regulatory Affairs Executive
- Experience: 2 to 8 years
- Location: Nalagarh
- Key Skills Required:
- CTD (Common Technical Document)
- ACTD (ASEAN Common Technical Dossier)
- Dossier Preparation
- Row Market Knowledge
Key Responsibilities
As a Drug Regulatory Affairs Executive, your primary responsibilities will include:
- Preparing, reviewing, and submitting regulatory documents such as CTD and ACTD.
- Ensuring compliance with global regulatory requirements for drug approval.
- Coordinating with cross-functional teams for dossier preparation and submission.
- Managing regulatory submissions for Row Markets.
- Keeping abreast of changes in regulatory guidelines and ensuring adherence.
- Liaising with regulatory authorities to address queries and facilitate approvals.
Desired Skills and Qualifications
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or a related field.
- 2 to 8 years of experience in Drug Regulatory Affairs.
- Proficiency in CTD, ACTD, and dossier preparation.
- Strong understanding of Row Market regulations.
- Excellent communication and interpersonal skills.
- Attention to detail and ability to work under tight deadlines.
