1 Quality Control
Qualification : M.Pharm / B.Pharm / M.Sc
Experience : 2-5 Years
Skills : QC HPLC/GC/GLP , Document Preparation
No.Of Vacancy : 15
2 ADL
Qualification : M.Pharm / B.Pharm / M.Sc
Experience : 2-5 Years
Skills : AMV/AMD
No.Of Vacancy : 04
3 Quality Assurance
Qualification : M.Pharm / B.Pharm
QMS / Stability Management - 2-5 Years
Vacancy : 08
IPQA - 10-12 Years
Vacancy : 01
Walk-In-Interview Date : 9th April 2024
Time : 9 AM - 2 PM
Venue : STALLION LABORATORIES PVT. LTD. Unit-II Plot No. D-4,5,6,17,18,19, Gallops Industrial Park II, Vasna Chacharwadi, Dist-Ahmedabad-382 110, Gujarat, India
Note :
Interested candidates should Walk-In for an Interview with a copy of latest resume, CTC Break-up & photo.
Working experience in USFDA approved facility shall considered only.
Candidate who cannot appear for the Walk in Interview may share their resume to aarti.oberol@stallionlabs.com
Candidate already appeared in last 06 months are not eligible for the interview
Contact : tel:+91 94093 09964
For its global operations, Stallion has three overseas offices—in Vietnam, Nigeria, and Angola and its headquarters in Ahmedabad, India.
Among the many therapeutic areas for which Stallion produces pharmaceuticals are antidiabetics, cardiovascular, urology, antibiotics (antibacterial, gastrointestinal, cough & cold, anxiolytics & antidepressants), analgesics (anti-inflammatory), nutritional supplements, antivirals, antifungals, anthelminthic, antiprotozoal, antimalarial, and antihistaminic).
Over 50 countries in South East Asia, Africa, Latin/Central America, and the CIS are home to Stallion's robust presence.
After the audit is completed and approved by the relevant authorities, the stallion is awarded ISO 9001-2015, WHO GMP, and GLP certifications (15 agencies approval).
According to the most recent SRA Guidelines, Stallion Laboratories Unit-II is a brand-new, ultra-modern facility that has already applied for clearance in SRA countries. It is intended for oral solid dosage forms.