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Requirement For Agm-qa(ipqa) @ Hetero

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 Requirement For Agm-qa(ipqa)

Job Description

Roles and Responsibilities


  • Performing In-process Quality checks (IPQA) at production and verification of production activities as per standard procedures and cGMP.
  • Review of completed and On-line Batch production Records.
  • Reviewing of new Batch production Records.
  • Review of online BMR and BPR before dispatch.
  • Review/Checking of dispatch labels/ containers/ packing against packing list.
  • Performing line clearance during production change over.
  • Monitoring of validations such as: Cleaning validation and Process validation.
  • Fulfill the documentation requirements and co- ordinate with external audits and internal audits.
  • Documentation system Issue, Retrieval and control of Documents.
  • Verifying the production equipment, records and their calibration.
  • Monitoring the production block and pharma area cleanliness daily.
  • Monitoring of process activity as per batch manufacturing record/ batch packing records.
  • Ensuring online entries of BMR, log books, discrepancies to be rectified immediately.
  • Ensuring status board are updated as per the activity.
  • Implementation of all c GMP systems in manufacturing facility.

Job Location: HETERO LABS LIMITED, SEZ, Nakkapalli, Visakhapatnam Dist


Interested candidates send their CV to pr*******v@he********s.com


please mention subject as " IPQA-HEAD"


Regards

PRASANTH-HR

Talent Acquisition


,

Employement Category:

Employement Type: Full time
Industry: Pharma / Biotech
Role Category: Sales / BD
Functional Area: Not Applicable
Role/Responsibilies: Requirement For Agm-qa(ipqa)

Contact Details:

Company: Hetero
Location(s): Visakhapatnam

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Hetero

Company ProfileHetero Drugs LimitedM/s. Hetero Drugs Ltd is one of the Largest Pharmaceutical Company in India.

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