Amneal walk-in Manufacturing & QC

Amneal walk-in Manufacturing & QC

Amneal Pharmaceuticals ITI, B.Pharm Vacancies – Ahmedabad

Amneal Pharmaceuticals hiring ITI, B.Pharm, M.Sc candidates for multiple Manufacturing & QC vacancies at Ahmedabad.

Amneal Pharmaceuticals is conducting a walk-in interview at its SEZ Matoda facility in Ahmedabad for experienced professionals in pharmaceutical manufacturing and quality control. This hiring drive targets candidates with hands-on exposure to regulated OSD plants who are seeking stable, long-term careers with a globally recognized pharmaceutical company. With strong systems, advanced technology, and international compliance standards, this opportunity is well-suited for professionals looking to deepen their expertise in high-quality pharmaceutical production and quality assurance.

Company Overview

Amneal Pharmaceuticals, Inc. (NYSE: AMRX) is a global pharmaceutical company with a strong footprint across development, manufacturing, and distribution of high-quality medicines. With a workforce of over 7,500 professionals worldwide, Amneal supports healthcare systems through a diversified portfolio of more than 270 pharmaceutical products spanning generics, specialty medicines, and complex dosage forms.

The company operates USFDA and other globally regulated manufacturing facilities and follows stringent GMP, data integrity, and quality compliance frameworks. Amneal’s focus on operational excellence, patient safety, and affordable healthcare has positioned it as a trusted name in the pharmaceutical manufacturing and quality control domain.

Job Role & Responsibilities

Manufacturing Department (OSD – Regulated Plant)

Selected candidates in the manufacturing department will be responsible for executing core production activities for oral solid dosage forms in compliance with cGMP and regulatory requirements.

Key responsibilities include:

  • Operation and supervision of granulation, compression, coating, capsule filling, and bottle packing processes
  • Hands-on handling of RMG, FBE, FETTE compression machines, auto coaters, and bottle packing lines
  • Ensuring adherence to batch manufacturing records and SOPs
  • Monitoring critical process parameters during manufacturing
  • Maintaining equipment cleanliness, calibration, and compliance
  • Supporting audits, inspections, and continuous improvement initiatives
  • Working with track and trace systems for serialized packaging operations

This role contributes directly to consistent product quality, regulatory compliance, and uninterrupted supply of essential medicines.

Quality Control Department

Quality Control professionals will play a critical role in ensuring product safety, efficacy, and compliance through analytical testing and documentation.

Key responsibilities include:

  • Routine analysis of raw materials, in-process samples, and finished products
  • Performing analytical tests such as assay, dissolution, content uniformity (CU), blend uniformity (BU), and related substances
  • Independent handling of instruments including HPLC, GC, UV, UPLC, FTIR, KF titrator, and PSD analyzers
  • Preparation and review of analytical records and reports
  • Compliance with data integrity, GMP, and laboratory safety requirements
  • Supporting regulatory audits and investigations

This position is ideal for professionals seeking long-term careers in pharmaceutical quality control within regulated manufacturing environments.

Eligibility / Qualifications

Educational Qualifications

  • ITI
  • Diploma (Pharmaceutical / Technical)
  • B.Sc
  • M.Sc
  • B.Pharm

Relevant courses include Pharmaceutics, Pharmaceutical Analysis, Industrial Pharmacy, Analytical Chemistry, Organic Chemistry, Microbiology, Quality Assurance, Pharmaceutical Technology, and related life sciences disciplines.

Experience Requirements

  • Manufacturing & Quality Control: 2 to 6 years

Candidates must have prior experience working in regulated OSD pharmaceutical plants with exposure to GMP-compliant operations.

Designations Offered

  • Officer
  • Executive

Final designation will be based on experience, skill level, and interview assessment.

Location & Salary

  • Job Location: SEZ Matoda, Ahmedabad, Gujarat
  • Interview Venue: Amneal Pharmaceuticals, SEZ Matoda, Ahmedabad

Salary will be competitive and aligned with industry standards. Compensation will be determined based on qualifications, experience, technical exposure, and current CTC.

Walk-In Interview Details

  • Date: 30th January 2026 (Friday)
  • Time: 10:00 AM to 12:00 PM
  • Venue: Amneal Pharmaceuticals, SEZ Matoda, Ahmedabad

Candidates should carry updated resumes, educational certificates, experience letters, and valid identification. Early arrival is recommended.

Application Process

Candidates unable to attend the walk-in interview may share their resumes via email:

Official website: https://www.amneal.com

Why Build Your Career at Amneal Pharmaceuticals

  • USFDA and globally regulated manufacturing environment
  • Exposure to advanced pharmaceutical manufacturing and analytical technologies
  • Strong focus on GMP, data integrity, and quality systems
  • Stable organization with global career opportunities
  • Direct contribution to affordable, high-quality healthcare solutions

Important Disclaimer

Beware of fake job offers claiming to be from Amneal Pharmaceuticals or companies under the Amneal Group. Amneal does not send job offers from free email services and does not charge any recruitment fees or security deposits. Employment offers are made only through official company channels. Candidates are advised to remain vigilant and report suspicious activities.

FAQs

Who can attend this walk-in interview?

Candidates with ITI, Diploma, B.Sc, M.Sc, or B.Pharm qualifications and 2 to 6 years of experience in regulated OSD plants can attend.

Is this opportunity open to freshers?

No. This hiring drive is strictly for experienced candidates.

What type of manufacturing exposure is required?

Experience in granulation, compression, coating, capsule filling, and bottle packing with regulated equipment is required.

What analytical instruments should QC candidates be familiar with?

HPLC, GC, UV, UPLC, FTIR, KF titrator, and PSD analyzers.

Is salary negotiable?

Salary will be finalized based on experience, skill set, and current compensation.

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Summary Table

Company Amneal Pharmaceuticals, Inc.
Vacancies Officer, Executive (Manufacturing & Quality Control)
Required Education ITI, Diploma, B.Sc, M.Sc, B.Pharm
Experience 2 to 6 years
Amneal walk-in Manufacturing & QC
Amneal walk-in Manufacturing & QC

To apply for this job email your details to chandanid@amneal.com


You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

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