Job Responsibility:
1. To ensure that GLPs followed in the laboratory.
2. To establish, develop, validate testing Procedures.
3. To Prepare protocols, reports and monitor samples of Method validation and
Method Development.
To perform the calibration of instrument/equipment. To ensure that instruments and
equipment are calibrated as per given schedule and records are maintained accordingly.
To perform analysis for Raw material, finish products and stability samples.
To ensure that samples are analysed in time and results are conveyed to
department head or reviewer as per requirement and as per the procedure.
To maintain documentation for Regulatory Submission
Maintaining of SOP as per regulatory requirements and periodically reviewed.
To ensure all record are maintained as per the procedures.
Any other work assigned by the superiors.
To prepare Method of analysis (MOA) and Specification and any other
documents of new drug product.
To perform Method transfer to Department.
Qualification :
B. Pharm / M. Pharm
Experience : 2-3 Years
Job Location :Vadodara
- Experience2 - 7 Years
- No. of Openings2
- EducationB.Pharma, B.Sc, M.Pharma, M.Sc
- RoleAdl Officer
- Industry TypeHospitals / Medical / Healthcare Equipments
- Gender[ Male / Female ]
- Job CountryIndia
- Job TypeWork from Office
- Face interview locationPragnesh Makwana SR.HR RECRUITER Mob. No. : 9033075122 E-mail - Id : rect1@saigroupbrd.com