Cipla Ltd-Walk-in for Quality Control Department on 10th October 2024

Cipla Ltd-Walk-in for Quality Control Department on 10th October 2024

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At Cipla, we are committed to our purpose of “Caring for Life.” We are seeking passionate and skilled individuals to join our Quality Control team. If you have the right qualifications and experience, don’t miss this opportunity to be part of a leading pharmaceutical company.

Company Name: Cipla Ltd
Walk-in for: Team Member QC, Team Member QC (Micro)
Designation: Senior Executive

Job Description:

  • Review QC documents and raw data from instruments
  • Conduct lab rounds to ensure GLP compliance
  • Manage microbiological culture media
  • Perform microbiological testing of finished products and API
  • Monitor water and environmental conditions
  • Handle equipment validations and calibrations

Job Specifications:

  • Qualification: M.Sc. in Analytical Chemistry or Microbiology (Full Time)
  • Experience: 1-2 years of relevant experience
  • Candidates with over 60% marks will be considered for the interview

Note:

  • A written test may be part of the selection process
  • CV shortlisting will be based on company terms and conditions
  • The company reserves the right for evaluation processes

Walk-in Details:
Date: 10th October 2024 (Thursday)
Time: 9:30 AM – 12:00 PM

VENUE-Cipla Ltd,
D-22(Unit-3),MIDC, Kurkumbh, Tal: Daund, Dist. :Pune

JOB LOCATION Kurkumbh

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

Apply for this position

Allowed Type(s): .rtf

About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit 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. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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