Natco Pharma Limited –Interviews for Production, Quality Control & Microbiology on 4th Feb’ 2024

Natco Pharma Limited –Interviews for Production, Quality Control & Microbiology on 4th Feb’ 2024

Job Opportunity at Natco Pharma Limited – Formulation Division

  • Department: Production, Quality Control & Microbiology
  • Experience: 2 to 6 years
  • Openings: 30
  • Qualification: Diploma / B.Sc / B.Pharm / M.Pharm / M.Sc
  • Position: Operator / Chemist / Officer / Executive
  • Work Location: Kothur (Near to Shadnagar)
  • Job Description:

    Production (Injectables):

    • Hands-on experience in Compounding, Auto Clave, Aseptic area Operations, Vial Washing, Filling, Optical Inspection of Injectable manufacturing.

    Quality Control (OSD & Injectables):

    • Hands-on experience in Raw Material, In-Process, Process Validation, GLP, Stability & Finished Product areas.

    Microbiology (OSD & Injectables):

    • Hands-on experience in MLT, BET, Waters & Sterility analysis, Media Preparation, Method Validations, and Environmental Monitoring activities.

    Interview Details:

    • Date: 04th February 2024 (Sunday)
    • Time: 09:00 AM to 02:00 PM
    • Venue: Natco Pharma Limited, Natco House, Road No. 2, Banjara Hills, Opp: A.P. Productivity Council of Hyderabad, Hyderabad, Telangana 500034.

    Requirements for Candidates:

    • Only candidates with Formulation experience and Regulatory exposure will be considered.
    • Interested & Relevant experienced candidates may walk-in to the mentioned address along with updated CV, Latest Increment letter, Pay slips, copies of Aadhar, Pan & Educational Certificates.

    Don’t miss this opportunity to join a dynamic team at Natco Pharma Limited and contribute to the advancement of the pharmaceutical industry.

Job Category: pharma
Job Type: Full Time
Job Location: Hyderabad

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ABHA

Abha is the Author  of pharmaceutical guidance, she is a pharmaceutical professional having more than 22 years of rich experience in pharmaceutical field. During her career, she works in the quality assurance department with multinational companies i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd. During his experience, she faces many regulatorily audits i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda, Kenya, Tanzania, Zimbabwe. She is currently leading a regulatory pharmaceutical company as a Head Quality. You can join him by Email, Facebook, Google+, Twitter, and YouTube