Mylan Laboratories Limited (A Viatris Company) Walk-in On 10th Feb 2024 Bsc,Msc,bpharm,Mpharm

Mylan is a global healthcare company focused on making high quality medicines available to everyone who needs them. Our heritage of being a provider of generic pharmaceuticals goes back to our founding in West Virginia in 1961. Today, we are passionate champions for better health around the world with a platform unmatched in the industry. We have one of the broadest and most diverse portfolios, with more than 7,500 marketed products that include prescription generic and brand-name medicines, and consumer healthcare products. 

Vacancy details:

  • Department: Officer – IPQA ( OSD & Injectable )/QC
  • Qualification: B.Sc in Any Specialization, B.Pharma in Any Specialization/M.Pharma in Any Specialization, MS/M.Sc(Science) in Any Specialization
  • Experienced: 1 – 6 years
  • Salary: ₹Not Disclosed

Job Description: Greetings from Mylan Laboratories Limited  !!

Important Details :

  • Location: Ahmedabad
  • Post of date:08/02/2024
  • Selection Process: The selection will be on the basis of Interview.
  • Mode of Interview: Face To Face Interview
  • Interview Rounds of Interview: HR

Walkin Interview Details:

Date:10th February

Time:9.30 AM – 4.00 PM

Venue: Mylan Laboratories Limited (A Viatris Company) Plot no 20/21, PHARMEZ, Sarkhej-Bavla NH 8A, Nr. Vill. Matoda, Dist. Ahmedabad, Gujarat-382213 Direct: +91.02717.681625

Contact – Nitu Singh ( 02717681625 )

Role & responsibilities

1) Verification for Dispensing of API.

2) Line clearance at respective stage

.3) PPM verification for autoclaving, CIP-SIP of Manufacturing Vessels.

4) Sampling at intermediate and finished product stage.

5) Inprocess test (IPQC test).

6) Review of audit trail report.

7) Review of logbook

8) Review of sterilization cycles i.e. Leak test, Bowie dick, Load cycles, CIP-SIP cycles of vessels.

9) Review of Batch Record stage wise i.e. Dispensing, Mixing, Autoclaving, Vial Washing & Depyrogenation, Filling & Sealing, Terminal Sterilization, Visual Inspection, Vial Labelling and Packaging.

10) Review of daily environmental monitoring.

11) Review of filter and filter integrity report.

12) Calibration & daily verification of respective IPQA instrument.

13) AQL sampling & testing.

14) Withdrawal of control samples.15) Annual verification of control samples.

16) Verification of vial rejection generated during process and packaging.

17) Issuance and verification of visual inspection qualification kit.

18) Review of visual inspector’s qualification report.

19) Performing and verification of in-process challenge test at packaging stage.

20) Execution of process validation sampling as per protocol

.21) Execution of cleaning validation sampling as per protocol

.22) Breakdown maintanance verification in SAP.

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