Innoxel Lifesciences- Walk-In Interview for QC, QA, Manufacturing & Engineering on 22nd February 2026 @Vadodara
Date: 22nd February 2026 (Sunday)
Time: 10:00 AM to 4:00 PM
Venue: Innoxel Lifesciences Pvt. Ltd.Survey No. 534/1, Village: Kotambi, Near VCA Stadium, Tal: Waghodia, Vadodara, Gujarat
Quality Control (QC)
Department: Quality Control
Role: Chemist & Analysts (Analytical Method Validation, RM/PM)
Experience: 1–10 Years
Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm (Sterile USFDA Experience Preferred)
2. Sterile / Liquid Oral Manufacturing
Department: Sterile / Liquid Oral Manufacturing
Role: Operators & Supervisors (Skid Operation, Autoclave, Vial Washing, Tunnel, Filling)
Experience: 1–8 Years
Qualification:
ITI / Diploma (For Operators – Sterile USFDA Experience)
B.Pharm / M.Pharm (For Officers – Sterile USFDA Experience)
3. QC Micro
Department: QC Microbiology
Role: Microbiologists (EM & Analysts)
Experience: 1–8 Years
Qualification: B.Sc / M.Sc Micro (Sterile USFDA Experience Preferred)
4. Quality Assurance (QA)
Department: Quality Assurance
Role: Sr. Officer / Executive (Qualification, Validation, QMS, IPQA, Compliance)
Experience: 4–10 Years
Qualification: B.Pharm / M.Pharm (Sterile USFDA Experience Preferred)
5, Warehouse
Department: Warehouse
Role: Warehouse Operators / Officer
Experience: 1–8 Years
Qualification: ITI / B.Sc / B.Com (Sterile USFDA Experience Preferred)
6.Validation
Department: Validation
Role: Sr. Officer / Executive
Experience: 3–7 Years
Qualification: B.Pharm / M.Pharm (Sterile USFDA Experience Preferred)
7. Engineering (PM / HVAC / Utility)
Department: Engineering
Role: Technicians / Officers / Executive
Experience: 1–8 Years
Qualification: ITI (For Technicians)/ Diploma / B.E. (For Supervisory Staff)
8. Project Management (P.M.)
Department: Project Management
Role: Project Management
Experience: 2–4 Years
Qualification: M.Pharm with relevant experience in Injectables
9. Purchase
Department: Purchase
Role: Officers
Experience: 1–5 Years
Qualification: Any Graduate with Sterile USFDA Experience
