Trainee
finecure · Rudrapur
- Experience0–1 yrs
- SalaryNot disclosed
- Work modeonsite
- Levelfresher
- Posted8 Aug 2026
About finecure
finecure is hiring in Rudrapur in pharma biotech. This role looks for around 0+ years of experience.
Skills
- GMP
- in-process quality assurance
- qualification
- validation
- sampling
- document review
- SOP compliance
The role
A pharmaceutical quality professional at a pharmaceutical manufacturing company prepares GMP documentation and manages in-process quality assurance, qualification, and validation activities. The role performs sampling, document review, SOP compliance, and schedule tracking.
Full job description
Job Description:
To prepare and revise functional Standard Operating Procedure/s, where ever required.
To prepare protocols, reports and other GMP documents.
To perform IPQA task such as line clearance, sampling, document review and log book review
Handling over the shift base charge for continued operations.
To perform sampling and dispensing of RM/PM and solvent materials at warehouse.
To track all approved schedule/s and dates in which they are due for their next review like calibration schedule, preventive maintenance schedule, qualification schedule.
To involve in qualification (FAT/IQ/OQ/PQ/CQ/RQ) and validation (Process, Bulk hold, cleaning, stability, Dirty Equipment Hold, Cleaned equipment hold) activity while execution.
To monitor SOP compliance, identify gap analysis and report to superior.