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Amneal Pharmaceuticals Hiring for Quality Control (OSD)

Published on

Amneal Pharmaceuticals

0 – 10 years

Rajoda

B.Sc, M.Sc, B.Pharm, M.Pharm, Diploma, Degree

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Walk In Interview

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Amneal Pharmaceuticals, Inc. (NYSE: AMRX), a leading global pharmaceutical company with a team of over 7,500 dedicated colleagues, is committed to making healthy living possible. We achieve this through the development, manufacturing, and distribution of a diverse portfolio of more than 270 high-quality medicines. We are currently seeking talented and experienced professionals to join our growing team in Rajoda, Bavla, Ahmedabad.

Walk-in Interview for Quality Control – OSD (Oral Solid Dosage)

We invite qualified candidates to attend a walk-in interview for various Quality Control positions within our Oral Solid Dosage (OSD) department.

Date: Sunday, April 13th, 2025
Time: 9:00 AM to 1:00 PM
Location: Rajoda, Bavla, Ahmedabad

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Available Positions & Requirements:

Amneal Pharmaceuticals offers a variety of exciting career opportunities within our Quality Control department. Below are detailed descriptions of the open positions, their respective requirements, and essential skills:

1. Quality Control Supervisor:

  • Location: Rajoda
  • Qualification: M.Sc/B.Pharm/M.Pharm
  • Experience: 8-10 years of relevant experience in a regulated QC OSD pharmaceutical plant.
  • Key Responsibilities:
    • Supervise a team of 8-10 analysts per shift.
    • Ensure adherence to ALCOA (Attributable, Legible, Contemporaneous, Original, and Enduring) principles and service level agreements (SLAs).
    • Proficiency in operating and troubleshooting various laboratory instruments, including HPLC, UPLC, LCMS, GC, GCMS, and Dissolution apparatus.
    • Oversee method transfers and ensure regulatory compliance.
    • Prepare and review IQ/OQ (Installation Qualification/Operational Qualification) protocols and reports as per Standard Operating Procedures (SOPs).
    • Review various logs, methods, protocols, and reports to maintain data integrity.
    • Ensure compliance with Good Laboratory Practices (GLP) and Current Good Manufacturing Practices (cGMP) regulations.
    • Handle deviations, out-of-specification (OOS) results, and change controls.
    • Review records related to raw materials (RM), finished products (FP), packaging materials (PM), and stability testing utilizing various analytical techniques (UV, IR, HPLC, UPLC, GC, LCMS).
    • Ensure ALCOA adherence in all shift activities.

2. Quality Control In-House Engineer:

  • Location: Rajoda
  • Qualification: Diploma/Degree in Instrumentation & Control Engineering (ICE) or related field.
  • Experience: 0-3 years of experience.
  • Key Responsibilities: Responsibilities will depend on experience but may include instrument maintenance and troubleshooting, assisting with method validation, and supporting the QC team in maintaining laboratory equipment.

3. Quality Control Reviewer:

  • Location: Rajoda
  • Qualification: M.Sc/B.Pharm/M.Pharm
  • Experience: 8-10 years of relevant experience in a regulated QC OSD pharmaceutical plant.
  • Key Responsibilities: Thorough review of analytical data, documentation, and compliance records to ensure data integrity and regulatory compliance.

4. Quality Control Analyst:

  • Location: Rajoda & SEZ-Matoda
  • Qualification: M.Sc/B.Pharm/B.Sc
  • Experience: 2-5 years of relevant experience.
  • Key Responsibilities: Performing routine analytical testing, maintaining laboratory equipment, and adhering to SOPs and regulatory requirements.

5. Quality Control Technical Writer:

  • Location: Rajoda
  • Qualification: M.Sc/B.Pharm/B.Sc
  • Experience: 7-8 years of relevant experience.
  • Key Responsibilities: Preparing and reviewing SOPs, specifications, and technical documentation, ensuring clarity and compliance.

Essential Skills Across All Positions:

  • Strong regulatory and pharmacopeial knowledge.
  • Minimum 2 years of experience in documentation practices.
  • Basic knowledge of laboratory instruments (HPLC, GC, UV, KF).
  • Adherence to GLP/cGMP and regulatory compliance.
  • Ability to prepare SOPs, Standard Test Procedures (STPs), specifications, and change controls.

How to Apply:

Candidates who are able to attend the walk-in interview are encouraged to do so. Those unable to attend can submit their updated resume to one of the following email addresses:

  • aartig@amneal.com
  • manavg.patel@amneal.com
  • chandanid@amneal.com
  • jagdish.mathukiya@amneal.com

Important Disclaimer:

Beware of fraudulent job offers claiming to be from Amneal Pharmaceuticals Pvt. Ltd. or companies under the Amneal Group. Amneal will never send job offers from free email services (Gmail, Rediffmail, Yahoo Mail, Hotmail, etc.) nor request any fees or security deposits from job seekers. Amneal is not responsible for any actions taken based on employment offers not directly made by the company. Report any suspicious activity immediately.

Amneal Pharmaceuticals Hiring for Quality Control (OSD)