Posted:1 day ago|
Platform:
Work from Office
Full Time
Role & responsibilities To maintain the QA documents in compliance state and ensure they are all time ready for internal and external audits. Preparation and review of SOPs. To act as training coordinator and oversee implementation & compliance of training matrix. To maintain the vendor approval document. Daily issuance and retrieval of records of other departments. To maintain records of change control, deviations, CAPA, incidents logs, OOS, OOT. To prepare and maintain calibration and validation schedules of equipments as per VMP. Upkeep and follow-up for new product licenses. To prepare APR, trends. Prepare and review of BMR and analytical reports. Upkeep of retain samples and controls samples and their records. To maintain GMP in the plant and identify problem areas and report to Head-Quality. Line clearance in dispensing and production area. To perform in-process sampling, testing and document the observations. To handle IPQA activity in warehouse and production area.
Stellar Formulations
Upload Resume
Drag or click to upload
Your data is secure with us, protected by advanced encryption.
Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.
We have sent an OTP to your contact. Please enter it below to verify.
Instantly access job listings, apply easily, and track applications.
Pharmaceutical Manufacturing
51-200 Employees
5 Jobs
Key People
Savli, Vadodara
0.5 - 3.0 Lacs P.A.
Bengaluru
4.25 - 9.25 Lacs P.A.
5.5 - 7.0 Lacs P.A.
6.0 - 24.0 Lacs P.A.
0.5 - 0.5 Lacs P.A.
Medak, Telangana
7.0 - 10.0 Lacs P.A.
10.0 - 19.0 Lacs P.A.
Gurugram, Delhi / NCR
10.0 - 20.0 Lacs P.A.
Hyderabad
1.0 - 4.75 Lacs P.A.
Experience: Not specified
Salary: Not disclosed
