Job Overview
-
Date PostedMay 25, 2023
-
Location (State / UT)
-
Expiration dateAugust 30, 2024
-
Experience1 Year, 6 Years
-
GenderAny
-
Desired QualificationBachelor Degree, Master’s Degree
Job Description
Roles and Responsibilities:
- Ensure that the products are manufactured as per the cGMP.
- Maintain documentation as per regulatory authorities’ requirements like change control, and deviations.
- Highlight technical problems and take corrective actions.
- Maintain safety practices
Desired Candidate Profile:
- Should have experience in manufacturing of Semisoliddosage form and should have FDA audit exposure
- Experienced in Handling critical equipment like reactor, centrifuge, blender, sifter, multi-mill, etc.
Qualification: B.Tech/B.E. in Chemical, MS/M.Sc(Science) in Chemistry
Work Location; Vadodara
Walk-In Details:
Date & Time: 28 May , 9.30 AM – 3.30 PM
Venue:
Hotel Sarovar Residency Boisar
Tarapur Road, MIDC Rd, Near MPCB Office,
Boisar, Maharashtra 401504
Contact: Himanshu Jani