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Assistant Manager / Deputy Manager - IPQA
full-timeAhmedabad

Summary

Location

Ahmedabad

Type

full-time

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About this role

Description:

This role ensures GMP and GxP compliance in dispensing, manufacturing, and packaging. Responsibilities include machine and area clearance, product sampling, in-process checks, batch record reviews, and raw material verification. The position also involves approving packaging details, reviewing environmental and calibration records, managing change controls and deviations, and ensuring proper labelling and document archiving.


Essential Functions:

  • To perform Machine and area clearance during dispensing, manufacturing, and packaging operation.
  • To perform sampling of blend, finished product, reserve sample, stability sample, hold time samples and other in process samples and tmanage sampling aids.
  • To carry out in process checks, AQL and ANSI Sampling as per respective documents viz. protocol, BMR, BPR, SOPs and other GxP documents.
  • Review of Master BMR, SOPs, Batch Record Review and Batch Release, Shop floor management.
  • To ensure GMP practices at manufacturing shop floor.
  • To verify raw material dispensing activity.
  • To approve batch coding details during packaging operation.
  • Review of executed batch records and release for next processing stage.
  • Preparation and review of CPV data trend.
  • To perform impact assessment of breakdown memo.
  • To initiate change control, unplanned and planned deviation wherever required.
  • To review area, equipment, and cleaning log and tensure proper labelling.
  • To review environmental monitoring record, calibration records and executed Batch Manufacturing and packaging Records and respective electronic records.
  • To perform calibration of IPQA instruments.
  • To ensure appropriate labelling during manufacturing and packaging. Storage, handling and dispensing of printed packing materials.
  • To review and approve packaging artworks, proofs, and shade cards.
  • To archive executed documents like BMR, BPR, Hold time Protocol etc..
  • To review and approve the Quality Notification (Viz Change control and Deviation) during Batch Manufacturing/packaging.

    Additional Responsibilities:
  • To monitor and record the environmental condition of label control room.
  • To prepare and revise functional SOPs, wherever required.
  • Activities other than defined in the Job Responsibility are to be done, as per the requirement of HOD, by following HODS instructions and guidance. 

Skills: 

  • In-Process Checks & Monitoring - Advanced
  • Batch Record Review - Advanced
  • Compliance and Regulatory Knowledge - Advanced
  • Internal Audits and Inspections - Advanced
  • Document and Record Review - Advanced
  • Line Clearance & Batch Record Review - Advanced
  • Process Deviation Identification & Handling - Advanced
  • Audit & Regulatory Inspection Readiness (USFDA, EMA, MHRA, EUGMP,WHO) - Intermediate
  • Risk Assessment & Change Control - Mastery

Monitors production processes in real-time to ensure compliance with specifications and GMP - Intermediate

Other facts

Tech stack
In-Process Checks & Monitoring,Batch Record Review,Compliance and Regulatory Knowledge,Internal Audits and Inspections,Document and Record Review,Line Clearance & Batch Record Review,Process Deviation Identification & Handling,Audit & Regulatory Inspection Readiness,Risk Assessment & Change Control,Monitors Production Processes

About Amneal

Amneal Pharmaceuticals, Inc. (NASDAQ: AMRX) is guided by a simple belief: essential medicines should be accessible to everyone. What began as a promise to deliver high-quality, affordable medicines has evolved into a diversified portfolio spanning complex generics and injectables, biosimilars, and specialty medicines, including more than 290 products, with scale and capabilities that help reach patients across the healthcare system while combining world-class precision with a deep sense of personal responsibility for every dose we deliver.

Content is for informational purposes only and 3rd party content does not reflect Amneal’s opinions.

Amneal has the right to remove comments that violate another’s copyright or intellectual property, mention an Amneal product, use profanity or are defamatory, promote and solicit for third-party sites, initiatives, or products, or are factually inaccurate or misleading or spam.

Amneal recommends that you consult with your healthcare provider regarding personal health matters. To report a product complaint or adverse event related to an Amneal product, contact Drug Safety at 877-835-5472, option 3 or [email protected]. If you are currently experiencing a life-threatening event, please immediately contact 911.

Team size: 5,001-10,000 employees
LinkedIn: Visit
Industry: Pharmaceutical Manufacturing
Founding Year: 2002

What you'll do

  • The Assistant Manager/Deputy Manager - IPQA is responsible for ensuring GMP and GxP compliance during dispensing, manufacturing, and packaging operations. Key tasks include machine clearance, product sampling, batch record reviews, and managing change controls.

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Frequently Asked Questions

What does a Assistant Manager / Deputy Manager - IPQA do at Amneal?

As a Assistant Manager / Deputy Manager - IPQA at Amneal, you will: the Assistant Manager/Deputy Manager - IPQA is responsible for ensuring GMP and GxP compliance during dispensing, manufacturing, and packaging operations. Key tasks include machine clearance, product sampling, batch record reviews, and managing change controls..

Why join Amneal as a Assistant Manager / Deputy Manager - IPQA?

Amneal is a leading Pharmaceutical Manufacturing company.

Is the Assistant Manager / Deputy Manager - IPQA position at Amneal remote?

The Assistant Manager / Deputy Manager - IPQA position at Amneal is based in Ahmedabad, Gujarat, India. Contact the company through Clera for specific work arrangement details.

How do I apply for the Assistant Manager / Deputy Manager - IPQA position at Amneal?

You can apply for the Assistant Manager / Deputy Manager - IPQA position at Amneal directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Amneal on their website.