5+

Good exposure require in IPQA - Sterile, Qualification Sterile & OSD & Documentation Cell. Finished, AMV & Stability Section, knowledge of Instrument - HPLC. GC. Preferably know-how of Chromeleon Software.

RPG Life Sciences, a part of RPG Enterprises, is an integrated pharmaceutical company operating in the domestic and international markets in the Branded Formulations, Global Generics and Synthetic APIs space. The company is a research based, pharmaceutical company, producing a wide range of quality, affordable medicines.

Looking for candidates with relevant experience in Injectable regulated manufacturing plant. M.Pharm, B.Pharm, M.Sc, B.Sc, ITI, Diploma.

Oversee daily QC laboratory operations, ensuring compliance with cGMP, FDA, and other regulatory requirements. Validate, and implement analytical methods, including HPLC and plate-based assays as well as General assays. Ensure accurate and timely testing of raw materials, packaging materials, in-process samples, and finished products.

Injectable, parenteral, sterile manufacturing experience is a must Aseptic behaviour, Knowledge of GDP, GMP, ALCOA, Vial and Bag filling machine.

Deep understanding of Pharma GMP testing industry and the testing requirements of Method Development and Validation, Trace analysis Nitrosamine, Elemental, Genotoxic, Related substances E&L Testing & Packaging testing.

Support Formulation R&D in arranging the materials for development, optimization, confirmatory and exhibit batches which are under development in Hyderabad surround locations. API samples, Impurities, Working standards support for Formulation development stage.

B.Pharm/ M.Pharm / M.Sc; Hiring for SEZ 1 OSD Manufacturing Unit, Ahmedabad. IPQA / equipment qualification /QA QMS; Granulation, IGL, Compression, Coating, Wurster coating, Capsule filling

M.Sc. / M.Pharm, Technically competent on analytical method development and Validation of complex products like liposomes, transdermal, long acting injectable, suspensions, Nano particles, Microspheres, topicals and peptides. Responsible for developing, establishing, and validating analytical testing methodologies, transfer; ensure all analytical testing activities are in compliance with applicable regulatory guidance.