Chemist - Quality Control

Position Summary

Responsibilities will include:

• Raise laboratory Change control, incidents, deviations and LI wherever applicable.
• Review of Instrument qualification and scheduled calibration planner.
• Ensure proper laboratory analysis as per MOA and current product specification.
• Ensure that the data generated is accurate, scientifically valid and compliant to the procedures and maintain the lab work as per Current Good Manufacturing Practice standards (cGMP) standards & NABL.
• To conduct sampling test as per Test Intimation sheet, fill up the sheet and attach supporting documents of testing and instrument report after completion of QC testing.
• Ensuring compliances to EHS policies, cGMP policies, data integrity policies and IT policies as per requirements
• To extract sample and pack the same for third party QC testing, send the sample along with specifications to the third party testing lab.
• Carry out sample analysis as per MOA.
• Operation and calibration of HPLC, GC- GC-HS, FTIR, UV, AAS, KF, AUTO TITRATOR, BALANCE and its trouble shooting.
• To maintain all record viz, consumption, Column, humidity, all instrument logbooks.
• Testing of all raw material sample, stability samples and finished product samples.
• Responsible for Wet analysis, Instrument analysis & Purified Water analysis and NABL accreditation certificate

Required Experience & Knowledge

Functional / Technical

Behavioral

Supervisory Responsibilities

• Yes
• Actylis is an Equal Opportunity Employer. Actylis US does not discriminate on the basis of race, religion, color, sex, gender identity or expression, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided based on qualifications, merit, and business need..