Gujarat

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

Posses a degree in Pharmacy or a diploma in Pharmacy of a recognized university, or an equivalent educational qualification and must have registered his, her name with the Gujarat Pharmacy council. A candidate possessing knowledge of Computer in a additional qualification.

B.Pharmacy from a recognized institute OR 10+2 with science stream Physics, Chemistry, Biology from a recognized Board And Approved Diploma in Pharmacy from an Institute recognized by the pharmacy council of India and registered as pharmacist under the pharmacy Act 1948.

M.Sc. in Chemical, Physical sciences Organic, Inorganic, Physical, Applied Chemistry and Scholars who are selected through National Eligibility Tests including CSIR-UGC NET including lectureship and GATE, or Selection through National level examinations conducted by Central Government Departments and their agencies and institutions such as DST, DBT, DAE, DOS, DRDO, MoE, ICAR, IMCR, IIT, IISc, IISER, NISER etc.

SCIENCES, PHARMACY GRADUATES B.SC, M.SC, B. PHARM, M. PHARM WITH 0 TO 3 YEARS EXPERIENCES IN ANY OF QA FUNCTION VALIDATION, IPQA, QMS, COMPLIANCE, DQA, LAB QA OF A FORMULATION - STERILE, NON STERILE DOSAGE

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. 

B.Pharma / M.Pharma/ B.Sc / M.Sc. (Organic Chemistry / Analytical Chemistry); experience in injectable manufacturing, Aseptic area operations, Packing, Visual inspection, QMS activities. relevant functional experience in OSD manufacturing and Packing operations / QMS activities

Analytical method validation of different methodology. Dissolution Method Development and validation. Validation and method development protocol and report preparation.

Stallion Laboratories incorporated in 1988 as an integrated private sector Pharmaceutical Formulation Manufacturer, has acquired an unmatched record of managing niche product in formulations with a WHO GMP approved production facility and GLP qualified stringent quality control.