Department: Quality Assurance - Formulation
Description: Should have relevant experience of Validation A IPQA activities in Solid Orate, Parenteral, Ophthalmic and Potent products manufacturing facility. Should have relevant experience of QMS document
Qualification: M.Sc, B.Pharm, M. Pharma
Experience: 0-8 Years
Department: Quality Assurance
Description: Should have relevant experience with QMS documents, validations. Qualifications for API manufacturing facility
Qualification: M.Sc, B.Pharm, M. Pharma
Experience: 0-8 Years
Department: Quality Control - Lab API and Formulation
Description: Should have experience of HPLC, OC, dissolutions apparatus, UV-vIsIble spectrometer, and have known for Solid Orals. Parenteral. Ophthalmic preparations, Potent products, and API products Tostlng.
Qualification: M.Sc, B.Sc
Experience: 0-8 Years
Department: Microbiology Lab - Formulation Sterile
Description: Should have experience of MLT, Environment Monitoring, water analysis. Autoclave. OHS, Vitek, Incubators and have knowledge of Solid Oral, Parenteral, Ophthalmic preparations, Potent products and API products
Qualification: M.Sc, B.Sc
Experience: 1-8 Years
Department: Development Quality Assurance (R&D)
Description: Review of Lab note book, review of Lab QMS system, review of technical package, development report, technology transfer of Solid Orals, Parenteral, Ophthalmic preparations, Potent products and API products
Qualification: M.Sc, B.Pharm, M. Pharma
Experience: 1-8 Years
Department: Production - API
Description: Should have Exposure of Hydrogenator. PP area, intermediate area, and SRP. Good sound knowledge of cGMP and Safety awareness.
Qualification: M.Sc. Chemistry /Chemical Engineering
Experience: 1-6 Years
Date: 10-11th February 2018
Time: 9:00 am to 6:00 pm
Venue: ROYAL ORCHID CENTRAL VAD00ARA
Near Shivajee Circle, Mujmahuda Road.
Akota. Vadodara. Gujarat. Info-390020
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