29d ago
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Scientist, Quality Control

United StatesUnited States·Piscatawaymid
OtherQuality Control
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Quick Summary

Key Responsibilities

Stays abreast of new developments in analytical technologies. Contributes to improvement in laboratory operations to increase efficiency and GMP compliance.

Requirements Summary

Performs analysis and release of active pharmaceutical ingredients, excipients, in-process materials, and finished drug products to support the formulation development team,

Technical Tools
OtherQuality Control

The Scientist-2 is a mid-level analytical scientist opportunity supporting the analytical development of pharmaceutical oral dosage form. The individual in this capacity performs analytical methods qualifications/validations, analyzes active pharmaceutical ingredients, excipients, and finished dosage forms using appropriate analytical methods and maintains/qualifies analytical equipment.

  • Performs analysis and release of active pharmaceutical ingredients, excipients, in-process materials, and finished drug products to support the formulation development team, maintaining full compliance with all applicable US FDA - cGMP regulations and internal SOPs.
  • Develops and optimizes new and existing analytical methods for qualification and release testing of products. Develops stability indicating methods and performs methods validation.
  • Provides timely responses to all internal and external inquiries.
  • Ensures deadlines are met for product development schedules, and checks that technical and compliance requirements are met.
  • Evaluates, recommends, and implements new analytical technologies and instrumentation for testing.
  • Assists with training other members of the analytical development team.

Responsibilities

~1 min read
  • →Stays abreast of new developments in analytical technologies. Contributes to improvement in laboratory operations to increase efficiency and GMP compliance.
  • Bachelors Degree (BA/BS) Chemistry or related science - Required
  • Master Degree (MS/MA) Chemistry or related science - Preferred
  • 3 years or more in pharmaceutical experience (with Bachelor's Degree)
  • 1 year or more in pharmaceutical experience (with Master's Degree)
  • Broad knowledge of modern analytical equipment and techniques.
  • Extensive experience in cGMP laboratory testing. Hands-on experience with HPLC, GC, TLC, and MS.
  • Methods development experience.
  • Experience writing the standard operating procedures (SOPs) and test methods.

 

The base salary for this position ranges from $75,000 to $90,000 per year. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, with this position within the first 12 months. Amneal ranges reflect the Company’s good faith estimate of what Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, experience, geographic location and other relevant skills. 

Location & Eligibility

Where is the job
Piscataway, United States
On-site at the office
Who can apply
US

About this job

Who can apply
United States
Posted
29 days ago
Employer
has 288 open jobs on Jobera.

Listing Details

Posted
September 16, 2026
First seen
September 25, 2026
Last seen
October 15, 2026

Posting Health

Days active
19
Repost count
1
Trust Level
26%
Scored at
October 15, 2026

Signal breakdown

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Scientist, Quality Control