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A lembic Experience: From 2 to 6 year(s) Salary : ₹ Not Disclosed by Recruiter   Roles and Responsibilities Analytical method development development of all formulation dosage forms for domestic and ROW. Analytical method validation of all formulation dosage forms for domestic and ROW. Analytical method transfer of method developed in house as well as the products under contract manufacturing. Stability studies for all type of dosage forms/formulations for all the products under development in R&D. Carrying out all the analytical activities in compliance with the internal systems and safety guidelines. Role: Research Associate / Engineer Salary:  Not Disclosed by Recruiter Industry: Pharmaceutical & Life Sciences Functional Area: Research & Development Role Category: Pharmaceutical & Biotechnology Employment Type: Full Time, Permanent Key Skills 1. ADL 2. Analytical method development 2. Method Validation 3. HPLC 4. Stability Studies Education PG: M.Pharma in Any Specia

 Location: Haridwar Experience: 6 to 10 Years Job description Review of Quality Management systems like, Change controls, Deviations, Incidents and CAPA, OOS, OOT, Quality Risk Management, VMP, SMF, PQR, Cleaning validation, Product/ Mock Recalls, etc. Review of Quality Management Review Meetings observations and CAPA. Review BMR/BPR/PPQ/PQR/Hold time studies/ Technical agreements. To ensure the integrity of all data generated either manually or electronically. Review of SAP and other IT-related procedures. Review Sterile Injectable, Ophthalmic, Micro, Liquid, Ointments & OSD Operations. System, Operations, Practices & Documents Harmonization. Coordination with all sites Formulation for Compliance, Meeting & Trainings. Review the Sanitization & Hygiene practices & Formulation/ Sterile activities. Third-party, LL, RM/PM Vendor, Contract Testing Lab. Audits, Site Audits & compliance verification. Support for various regulatory and customer audits. Ensure all-time