Senores Pharmaceuticals – Walk-In for Technology Transfer | ADL | Regulatory Affairs Departments on 29th Mar’ 2026
Senores Pharmaceuticals – Walk-In for Technology Transfer | ADL | Regulatory Affairs Departments on 29th Mar’ 2026
Sai Manisha
March 25, 2026
Senores Pharmaceuticals Limited is a fast-growing pharmaceutical company focused on global regulated markets, including the US, EU, and ROW (Rest of World).
The company specializes in R&D, technology transfer, analytical development, and regulatory affairs, delivering high-quality pharmaceutical products that meet international regulatory standards.
Job Details Table
| Category |
Details |
| Company Name |
Senores Pharmaceuticals Ltd. |
| Job Type |
Walk-in Interview |
| Industry Type |
Pharmaceuticals |
| Location |
Ahmedabad |
| Work Area |
R&D Centre |
Walk-in Interview Details
| Details |
Information |
| Date |
29 March 2026 (Sunday) |
| Time |
10:00 AM – 3:00 PM |
| Venue |
Arrow House, SG Highway, Ahmedabad |
Department-wise Job Details
Technology Transfer (US Market)
| Position |
Experience |
Qualification |
Key Skills |
| Officer / Executive / Sr. Executive |
2 – 8 Years |
B.Pharm / M.Pharm |
Scale-up, Tech Transfer, Troubleshooting, ANDA |
| Executive – Documentation |
3 – 5 Years |
B.Pharm / M.Pharm |
BMR, Regulatory Documentation |
ADL (Analytical Development Lab – US Market)
| Position |
Experience |
Qualification |
Key Skills |
| Officer / Executive / Sr. Executive |
2 – 8 Years |
M.Pharm / M.Sc |
HPLC, GC, Dissolution, Method Development, Validation |
| Executive – Documentation |
3 – 5 Years |
B.Pharm / M.Pharm |
STPs, ICH Guidelines, Documentation |
Regulatory Affairs (US / EU / ROW)
| Position |
Experience |
Qualification |
Key Skills |
| Executive / Sr. Executive |
5 – 8 Years |
M.Pharm |
Lifecycle management, Regulatory compliance |
| Executive – PV / Documentation |
2 – 7 Years |
M.Pharm |
Pharmacovigilance, Dossier documentation, Due diligence |
Required Skills
| Skill Category |
Details |
| Technical Skills |
HPLC, GC, validation, tech transfer |
| Regulatory Knowledge |
ANDA, ICH, USFDA, EU guidelines |
| Documentation |
BMR, STP, dossier preparation |
| Analytical Skills |
Stability studies, troubleshooting |
| Soft Skills |
Communication, teamwork |
Educational Qualification
| Field |
Qualification |
| Pharma Roles |
B.Pharm / M.Pharm / M.Sc |
Role Highlights
| Aspect |
Summary |
| Level |
Mid-Level |
| Exposure |
US/EU regulated markets |
| Growth |
R&D / Regulatory career |
| Work Type |
Lab + documentation |
Contact Details
Why This Role is Valuable
- Opportunity to work in regulated markets (US/EU)
- Strong exposure to R&D, ADL, and Regulatory Affairs
- Career growth in pharma research & global compliance
- Hands-on experience with advanced analytical techniques
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About The Author
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