Incorporated in 1988, Stallion Laboratories is a leading pharmaceutical formulation manufacturer with a WHO GMP approved production facility and GLP qualified stringent quality control. We are known for our niche product formulations and a commitment to zero defect manufacturing and total quality management.
Contents
Job Description
QA Department
Designation: Executive – Officer
Education Qualification: M.Pharm / B.Pharm / M.Sc
Experience: 3 to 8 years
Roles: Validation/Qualification, Stability Management, Artwork/Documentation, APQR Preparation, Vendor Audit Documentation, AQA, IPQA
Production Department
Designation: Officer – Sr. Officer
Education: M.Pharm / B.Pharm
Experience: 2 to 5 years
Roles: Production-QMS, Coating
Packing Department
Designation: Officer
Education: M.Pharm / B.Pharm
Experience: 2 to 4 years
Roles: Primary, Secondary Packing
PPMC Department
Designation: Executive
Experience: 5 to 8 years
Engineering Department
Designation: Sr. Officer to Executive
Experience: 5 to 8 years
Roles: Plant Maintenance
ADL Department
Designation: Officer – Executive
Experience: 3 to 8 years
Roles: Documentation, AMV, AMD, Routine Analysis
Notes
- Eligibility: Only candidates with working experience in USFDA OSD facilities should apply.
- Documents to Bring: Latest resume, recent photo, salary structure, and last 3 months’ salary slips.
- Previous Applicants: Candidates who have appeared in interviews in the last 6 months are not eligible.
- Alternate Submission: If you cannot attend the walk-in, please email your resume to aarti.oberoi@stallionlabs.com and darshan.mistry@stallionlabs.com.
Event Details
Date: August 31, 2024
Time: 9:00 AM to 2:00 PM
Venue: Gallops Industrial Park – 2, Chachravadi Vasna, Matoda
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