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Introduction
This walk-in drive is a strong opportunity for candidates aiming to advance their career in a respected pharmaceutical environment. The roles offer learning, technical exposure and long-term career stability.
Company overview
pharma jobs continue to grow at Torrent Pharmaceuticals, one of India’s leading research-driven pharmaceutical companies. The organisation has strong global recognition for its quality systems, well-equipped labs and high-standard operational practices. Torrent’s facilities in Baddi operate with strict regulatory compliance and modern QC infrastructure. The company promotes innovation, disciplined processes and steady career development through professional training and supportive workplace values.
Job details
Job Title
Executive
Technical Assistant
Department
Quality Control (Formulation)
Salary
N/A
Requirements
Skills
Operation of QC instruments
Troubleshooting QC instruments
Handling OOS/OOT/Deviation
LCMS
HPLC
GC
UV
FTIR
Polarimeter
UV-Spectrophotometer
KF Apparatus
Method validation
Analysis of finished products
Stability samples
Raw materials
Packaging materials
Analytical method validation
Data interpretation
Troubleshooting
Solid oral dosage analysis
Quality process knowledge
Regulatory experience with ICH
USFDA, MHRA, ANVISA exposure
Qualification
M.Sc
B.Pharm
Experience
2 to 7 years
Vacancies
Not yet disclosed
Interview Details
Type
Walk-In Interview
Date and Time
23 November 2025
09:30 AM to 02:30 PM
Location/Platform
Torrent Pharmaceuticals Ltd
Near Baddi University
Village Bhud, Makhu Majra
Tehsil Baddi
District Solan, HP-173205
Documents Required
Updated Resume
One Passport Size Photograph
Latest Salary Slip
Education Certificates
ID Proof
How to Apply
Candidates can walk in directly with required documents or send their resume if unable to attend.
📧 shilpathakur@torrentpharma.com
📞 98055 08451
Arrive on time, dress professionally and carry all documents neatly organised. This is a good chance to join a reputed organisation offering growth and stability. pharma jobs like these provide strong exposure to analytical operations, validation processes and regulatory-driven QC standards.