Monday, September 26, 2022

Intas Released Multiple Job Openings For B.Pharma,M.Pharm,MSc Graduates

 Intas Released Job Openings On 26/09/2022.Intas Experience spanning three decades in healthcare, with a wide range of formulations to meet the needs of ailing humanity, Intas Pharmaceuticals headquartered at Ahmedabad (India), is now a force to reckon with, in the global pharma horizon. With expertise in a range of formulations, from tablets to injectables to newer drug delivery systems, Intas is currently ranked 17th among the Indian Pharma majors..Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Intas Recruitment 2021 are provided below. Interested and eligible candidates can  submit application along with resume.


 

Vacancy Details:

Intas Recruiting B.Pharma,M.Pharm,M.Sc candidates with 03-08 Years Experience for Quality Analyst Position.Complete Details for the Quality Analyst as follows.

Important Details :

  • Location :Ahmedabad
  • No of Vacancies: 05
  • Details of Salary:NA
  • Opening date for online Application:26/09/2022
  • Mode of application :Online
  • How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps

Job Description/Skills Required

Qualification – Quality Assurance

  • Responsible for planning of periodic qualification planning, execution and report compilation.
  • Responsible for preparation and review of Qualification Protocols (IQ, OQ, PQ and RQ) and reports of process equipment like Manufacturing/Filtration vessel, Vial washing machine, Dehydrogenation Tunnel, Steam sterilizer, Lyophilized, Automatic Visual Inspection machine and facility used for aseptic formulations.
  • Responsible for Utility qualification (PW/WFI/Steam, Compressed Gases and HVAC system)
  • Responsible for review and execution of Temperature mapping study for Incubators, Cold Chambers, Stability Chambers, Processing and storage areas.
  • Responsible for protocol preparation, execution and review of Air flow visualization.
  • Responsible for review and execution of CIP and SIP qualification of processing equipment.
  • Responsible for protocol preparation, execution and review of Aseptic Process simulation.

Process & Cleaning Validation – Quality Assurance

  • Responsible for planning of periodic process validation planning, execution and report compilation.
  • Responsible for preparation, execution and review of process validation protocol, report and sampling.
  • Responsible for hold time study protocol preparation and report compilation.
  • Responsible for continuous process verification.
  • To prepare cleaning validation and cleaning verification matrixes, schedules, worst case assessment sheets, schedule tracking sheets for cleaning validation and cleaning verification.
  • Responsible for planning of periodic cleaning validation planning, execution and report compilation.
  • Responsible for Clean equipment hold time / Dirty equipment hold time study protocol preparation and report compilation.

Click here for Official notification and Apply