Hands on Experience in IPQA Manufacturing process and Engineering IPQA, AQA Micro, Documentation, Validations, Stability Management and Document review.
Ensure submission and approval of high-quality regulatory applications within planned timelines and Facilitate interactions with regulatory bodies on a regular basis for approvals.
In HPLC, GC, UV, IR, KF & Polarimeter etc. Zuventus Healthcare Ltd. is a dynamic and forward-thinking company that has achieved notable recognition in the healthcare industry and for medical contribution. In OSD manufacturing, packing & QMS
B.Pharm, BSc, MSc; Lincoln Pharmaceuticals Ltd., Ahmedabad based 40 years old, public limited having presence in 75 countries, 1700 registered products, own Manufacturing and R&D center and among indias top 70 pharma company.
B.Pharma/ M.Pharma Analysis/ M.Sc Analytical Chemistry; HPLC, IP, Stability, RM, FP, PM. Hetero Drugs is an Indian pharmaceutical company and the worlds largest producer of anti-retroviral drugs.
B.Pharm/ M.Pharm. BSC/MSC. Experience in analysis of RM, Finish, In Process, Stability samples by using instruments like HPLC, UV-visible spectrophotometer, dissolution apparatus, GC chromatography, IR spectrophotometer and AAS.
Daily routine analysis Wet lab and Instrument, Manage data records for the lab activities, Manage documentation of lab experiments, Co-ordinate with R&D for daily analysis.
Doctor of Pharmacy degree or Bachelors of Science degree in Pharmacy with one-year residency or fellowship or equivalent clinical experience. This Manager position will participate and lead in the direction, supervision, and provision of daily pharmacy operations in the Central Pharmacy in University Hospital over order verification, medication preparation and distribution across morning, afternoon, and midnights shifts.
Collaborates with BD and MSAT to ensure cross-functional alignment with platform process, equipment, raw materials, and, or automation for NLT one area ; Clearly understands, communicates, and manages differences in terms of documentation, sample handling, automation, cGMPs, etc. for different phases of the product life cycle.