QA

Bachelors degree in a science-related field such as Pharmacy, Chemistry, Biological Sciences, or related Life Sciences. GMP experience, with experience in pharmaceutical laboratory quality assurance, quality control, or laboratory operations in a dry product or solid oral dosage form environment. Lilly

ITI / Diploma for Operators (Sterile USFDA Exp.) B.Pharm / M.Pharm for Officer (Sterile USFDA Exp.)

QMS & Audit Compliance: Implementation and maintenance of QMS, document control, internal audits, audit preparation, inspection support and CAPA follow-up.

Responsible for all IPQA activities, Qualification of Equipment, QMS, Equipment Qualification, HVAC Qualification, DRA Documentation

Pharmacopoeial standards for Biosimilars. Development and Characterization of Biosimilars. Biotherapeutics: Regulatory landscape

Experience in analysis of Solid Oral - FP, Instrumentation, In-process or Stability. Experience of Analytical Method Validation. Experience of PMQC & Dissolution. 

Shodhana Laboratories is a pharmaceutical company specializing in Active Pharmaceutical Ingredients (APIs) and Intermediates. Established in 2000, they cater to both generic and custom requirements for well-known pharmaceutical brands

MSc / MPharm. in Pharmaceutical Chemistry, Analytical Chemistry,Chemistry, Pharmaceutical Analysis, Quality Assurance, or allied areas from a recognized University or equivalent.

B.Pharm / M.Pharm / M.Sc . Expertise in analysis on HPLC, GC, Assay, Dissolution. Method Validation Protocol creation and execution, Expertise in handling HPLC, ICPMS, GC etc. USV Private Limited