Titan Laboratories Pvt. Ltd., an integrated pharmaceutical company with a strong presence in domestic and international markets, is conducting a Walk-in Drive for Executive / Senior Executive – Regulatory Affairs positions. The company is looking for experienced Regulatory Affairs professionals with expertise in CTD/ACTD dossier preparation and ROW market submissions. This is an excellent opportunity for candidates seeking career growth in regulatory affairs within the pharmaceutical industry.
Job Details
| Particulars | Details |
|---|---|
| Company | Titan Laboratories Pvt. Ltd. |
| Job Role | Executive / Senior Executive – Regulatory Affairs |
| Department | Regulatory Affairs |
| Employment Type | Full-Time |
| Experience | 3–9 Years |
| Qualification | M.Sc., B.Pharm, M.Pharm |
| Work Location | Juinagar, Navi Mumbai |
Walk-in Interview Details
| Details | Information |
|---|---|
| Interview Date | 11th July 2026 (Saturday) |
| Interview Time | 9:30 AM – 4:30 PM |
| Interview Venue | Titan Laboratories Pvt. Ltd., Rupa Renaissance, Gate No. 7, Plot No. 207, Unit No. 401, Ground Floor, Turbhe MIDC Road, TTC Industrial Area, Juinagar, Navi Mumbai – 400705, Maharashtra |
Required Skills
- Prepare, compile, and review regulatory submissions for international markets.
- Prepare CTD/ACTD dossiers for Rest of World (ROW) markets.
- Ensure timely submission of dossiers and respond to regulatory queries.
- Coordinate with cross-functional teams for regulatory submissions and approvals.
- Liaise with regulatory authorities and internal stakeholders to resolve regulatory issues.
- Maintain accurate documentation of submissions and regulatory decisions.
- Organize and maintain regulatory files, records, and databases for assigned markets.
Desired Skills & Competencies
- In-depth knowledge of international regulatory markets and ICH guidelines.
- Strong understanding of regulatory submission processes and compliance requirements.
- Excellent organizational and documentation skills.
- Strong attention to detail.
- Good communication and coordination skills.
- Ability to work effectively with cross-functional teams.
Eligibility Criteria
| Criteria | Requirement |
|---|---|
| Qualification | M.Sc., B.Pharm, M.Pharm |
| Experience | 3–9 Years in Regulatory Affairs |
| Preferred Experience | CTD/ACTD dossier preparation and ROW market submissions |
Documents to Carry
- Updated Resume
- Aadhaar Card
- Latest Increment Letter with CTC Structure (if available)
- Last 3 Months’ Salary Slips
Contact Details
| Contact | Details |
|---|---|
| HR Contact Number | 022-67857000 |
| Email ID | dipika.m@titanpharma.com |
| Email ID | angha.d@titanpharma.com |
Why Join Titan Laboratories?
- Opportunity to work with a reputed integrated pharmaceutical organization.
- Exposure to global regulatory submissions and international markets.
- Career growth in Regulatory Affairs.
- Collaborative and quality-driven work environment.
- Work alongside experienced cross-functional teams in a regulated pharmaceutical setting.
Eligible candidates with relevant Regulatory Affairs experience are encouraged to attend the walk-in interview on 11th July 2026 with all the required documents. Candidates who are unable to attend may also share their updated resume with the HR team via the provided email addresses.
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