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Monday, August 29, 2016

Sr. Executive / Executive/Research Associate/Manager Formulation Development - NDDS /Regulatory Affairs/Quality Control

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SrPosition / DesignationDepartmentNo. of
Opening
Location

1ManagerCQA

  • Implementation of Vendor Management System
  • Maintaining Vendor schedules and documents
  • Candidate should have Bulk Drugs / API facility experience
  • Should have experience of API / SM / Excipient Vendor Audit

hrd_matoda@intaspharma.com
2Matoda PlantClick to View
2Sr. Executive / ExecutiveCQA

  • Candidate should have Bulk Drugs / API facility experience
  • Should have experience of API / SM / Excipient Vendor Audit
hrd_matoda@intaspharma.com
1Matoda PlantClick to View
3Research AssociateFormulation Development - NDDS
  • Candidate should have experience in NDDS Product Development of Parenteral, Solid oral and Semi solid dosage forms for Regulated and Domestic Markets
  • Execution of Scale-up and Clinical Trial Batches for NDDS projects. Candidate should be competent for troubleshooting of the allotted projects
  • Responsible for exhibit / validation batches in co-ordination with process development lab
  • Should care for documentation and compilation of necessary regulatory submission data
  • Should have experience in technology transfer from R&D to manufacturing site
  • Monitoring stability of products during development and validation batches
  • Should co-ordinate with various functions like Analytical, QA, PDL & Plant etc.
sdwivedi@intaspharma.com
1AstronClick to View
4Senior Research ScientistRegulatory Affairs
  • Can initiate to collect, review & archive all technical information related to product registration for oral solid products in the Europe market. Person can take responsibility to coordinate with team members for dossier compilation, query responses activity and care of the assigned products for the EU countries
  • Acquaint the filling requirements for the veterinary oral solid drug products in the Europe market
  • Capable to provide the regulatory support to the various departments and regulatory system up gradation in context with the new regulatory requirements with respect to EU filling
  • Carry out activities associated with installing the dossier on web and its access by clients
  • Carry out additional activities related to the regulatory department as and when required
sdwivedi@intaspharma.com
3AstronClick to View
5Research AssociateR&D
  • Downstream Process Development and Protein Purification for Microbial and Mammalian Products
  • Understanding of Process characterization and QbD approach
  • Provide technical support for designing experiments and facilitating technology transfer activity to manufacturing
personnel_biotech@intaspharma.com
1BiopharmaClick to View
6Officer / Sr. Officer / ExecutiveQuality Control

  • Should be well-versed with operation of sophisticated instruments like HPLC, GC, AAS & UV Spectrophotometer
  • Should possess knowledge of GLP, GDP and various regulatory procedures
  • To perform method validation / method transfer
  • Knowledge of SAP will be an added advantage
prasenjit_das@intaspharma.com
4SEZClick to View


Send cv to:

hrd_matoda@intaspharma.com



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