
Regulatory Affairs Officer
3 weeks ago
This role is for one of the Weekday's clients
Salary range: Rs Rs ie INR 3-8 LPA)
Min Experience: 3 years
Location: India, Hyderabad
JobType: full-time
Requirements
Key Responsibilities:
Drug Master Files (DMF):
- Prepare, compile, and review US DMFs (Type II), EU ASMFs, and other region-specific dossiers.
- Manage lifecycle activities such as updates, deficiency responses, and annual reports.
- Collaborate with internal teams to gather technical documents for submissions.
Regulatory Documentation & Submissions:
- Compile CTD/eCTD dossiers for global regulatory submissions (USFDA, EDQM, WHO, TGA, etc.).
- Ensure adherence to current international regulatory guidelines and standards.
- Maintain accurate records, document control systems, and submission archives.
Cross-Functional Collaboration:
- Coordinate with QA, QC, R&D, and Production teams for necessary documentation and technical inputs.
- Support preparation and review of product specifications, stability data, and Certificates of Analysis (COAs).
Audits & Inspections:
- Provide assistance during regulatory audits and inspections by international authorities and clients.
- Address regulatory queries and observations in a timely manner.
Regulatory Intelligence:
- Monitor and interpret updates in global regulatory guidelines (USFDA, EMA, ICH, etc.).
- Provide inputs on regulatory strategies, product classification, and compliance requirements.
Required Skills & Qualifications:
- Bachelor's or Master's degree in Pharmacy, Life Sciences, or a related field.
- 3-7 years of experience in Regulatory Affairs, preferably in pharmaceuticals, nutraceuticals, or herbal formulations.
- Strong understanding of DMF/ASMF preparation and submission processes.
- Familiarity with global regulatory frameworks (USFDA, EMA, TGA, WHO, etc.).
- Excellent documentation, communication, and organizational skills.
- High attention to detail with the ability to manage deadlines effectively
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