Walk-In Drive For Regulatory Affairs - FML Dept @ R&D Center (Hyderabad)

Walk-In Drive For Regulatory Affairs - FML Dept @ R&D Center (Hyderabad)

02 Oct
|
MSN Group
|
Hyderabad

02 Oct

MSN Group

Hyderabad

Walk-In Drive For Regulatory Affairs - FML Department in FML Division - MSN Laboratories, R&D; Center, Pashamylaram, Hyderabad on Friday 09.10.2026 ( Friday) .

Regulatory Affairs FML Department in FML Division , : ( Regulatory Affairs - FML Division ) Should have minimum of 02 to 10 years of experience in FML Regulatory Affairs

Job Title: Executive / Senior Executive / Jr Manager /Asst Manager

Experience: 02 to 10 years in FML RA field

Education: B Pharm M Pharm

Department : Regulatory Affairs - FML

Roles & Responsibilities :

- Collect documents from various departments to prepare regulatory submissions.
- Prepare regulatory submissions to relevant authorities.
- Prepare amendments, updates, and revisions to submissions.
- Conduct meetings with cross-functional teams (CFT) to address deficiencies received from regulatory authorities and customers.
- Draft responses to regulatory deficiencies and review comments.
- Update the database as per requirements.
- Prepare the applicant and restricted parts for Abbreviated Current Drug Applications (ANDAs).
- Compile dossiers in electronic Common Technical Document (eCTD) and Common Technical Document (CTD) formats for all relevant countries.
- Guide the CFT based on current requirements from regulatory authorities.
- Plan and allocate projects within the team.




- Assess proposed changes for approved products and finalize the submission category.
- Review and clear specifications, protocols, stability data, bio-waivers, etc.

Key Performance Indicators:

- Demonstrate in-depth knowledge of regulatory guidelines and requirements for each market.
- Ensure all submissions are cleared within the stipulated timeline.
- Provide actionable items to address regulatory queries and dossiers.

Required skills:

- Knowledge of RA Guidelines and Requirements
- Action Item for RA deficiency.

Cross-Functional Team Work

- Represent regulatory affairs at cross functional meetings and coordinate with R&D;, Production, Plant QA/QC and Marketing to efficiently and successfully complete regulatory activities
- Support plant teams in regulatory audits, liaison with domestic & export regulatory authority.
- Assess and approve change controls and update files accordingly

Interview Date : 09.10.2026 ( Friday) Department : Regulatory Affairs - FML Dept.

Experience : 02 to 10 Years

Position: Executive / Senior Executive / Jr Manager /Asst Manager

Work Location : MSN R&D; Center, Pashamylaram, Hyderabad

Interview Venue: MSN Laboratories, R&D; Center, Pashamylaram, Hyderabad on 09.10.2026 ( Friday)

📌 Walk-In Drive For Regulatory Affairs - FML Dept @ R&D Center (Hyderabad)
🏢 MSN Group
📍 Hyderabad

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