QC

Exposure to injectable manufacturing, in-process checks, manpower handling, GMP documentation, machine breakdown & troubleshooting, audit compliance.

Candidate should have good exposure on analysis of FG / RM / Stability / PM samples using various QC instruments (LCMS/HPLC/GC/Dissolution, Malvern 3000 etc). Candidate with exposure of L1MS will be preferred.

Intas is one of the leading multinational pharmaceutical formulation development manufacturing and marketing companies in the world.

Biological E. Limited invites both experienced professionals and fresh diploma holders, as well as graduates and self-driven individuals, to join its Speciality Injectables Business located in Shamirpet, Hyderabad

Production & Packing - ITI / Diploma / B.Sc. Quality Control - M.Sc (Chemistry)/ B. Pharma Quality Assurance - B. Pharma, M. Pharma

Exp in handling QC instruments, GLP, QMS, Documentation, AMV, HPLC, Stablity Analysis, reviewer, URS / SOP / Protocols / STPs preparation.

Planning of AMT, AMV, API verification & Review, overall GLP maintaining & compliance, Preparation of MOA and protocols, Coordination for TT & AMV, Must have knowledge of cGMP, GLP

Monitor on-floor QA activities, in-process checks, and documentation accuracy. Maintain control over qualifications, preventive maintenance, and calibration reviews.

Require Analyst/ Reviewer with experience of API analysis using for Wet lab/ Stability / Inprocess Lab & Micro lab instruments like UV, Autotitrator, Muffer Furnance, IR, Potentiometer, Karlfisher, pH meter etc.