Amneal Pharmaceuticals

Scientist, Formulation R&D

Amneal Pharmaceuticals • $117K — $120K *
Piscataway, NJ 08854In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
Today
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Job Overview by Ladders

Qualifications

  • Master's degree in Pharmacy, Chemistry, Pharmaceutics, or related field is required.
  • Minimum of 12 months of experience in formulation R&D or related position.
  • Familiarity with oral solid dosage forms such as tablets and capsules.
  • Experience in conducting pre-formulation studies and excipient compatibility assessments.
  • Understanding of ICH guidelines and regulatory requirements for product development.

Responsibilities

  • Develop and optimize oral solid dosage formulations such as tablets and capsules.
  • Conduct pre-formulation studies and assess excipient compatibility.
  • Support analytical method development and validation for assays and stability tests.
  • Design and execute stability studies in compliance with ICH guidelines.
  • Troubleshoot formulation and analytical issues during development and scale-up.
  • Collaborate with manufacturing and quality teams for technology transfer.
  • Prepare technical reports and support regulatory submissions including ANDA/CTD.

Benefits

  • Health, dental, and vision insurance.
  • Retirement savings plan options.
  • Paid time off and holidays.
  • Professional development and training opportunities.
Full Job Description
Job Description

Scientist, Formulation R&D: Develop and optimize formulations for oral solid dosage forms (tablets, capsules, and modified release products). Conducting pre-formulation studies, excipient compatibility assessments, and dissolution profiling. Supporting analytical method development and validation for assay, dissolution, and stability- indicating methods. Design and execute stability studies as per ICH guidelines to establish product shelf life. Perform troubleshooting of formulation and analytical issues during development and scale-up. Collaborate with manufacturing and quality teams for pilot-scale and commercial-scale technology transfer. Prepare technical reports, development documents, and regulatory submission support (ANDA/CTD). Ensure strict adherence to cGMP, GLP, and regulatory requirements throughout the development process.

Qualifications

Requirements: Must have at least a Master's degree in Pharmacy or Chemistry or Pharmaceutics, or related field. Must have 12 months of experience in the position or in a related position.

Salary: $117K - $120K per annum.

Hours: 40 hrs/wk 8:30am - 5:30pm

Location: Piscataway, NJ

About Amneal Pharmaceuticals

Amneal Pharmaceuticals, Inc. is an integrated specialty pharmaceutical company powered by a robust U.S. generics business and a growing branded business. Together, our team is working to build one of the most dynamic pharmaceutical companies in our rapidly changing industry. Today’s healthcare environment requires a new approach and new ideas. While staying true to our reputation for quality, service and value, we are reinventing our processes, our playbook and our creative partnerships. Our goal is simple: to be a healthy, growing company that endures for decades and that is an indispensable partner to the healthcare providers and patients we serve. Amneal is headquartered in Bridgewater, New Jersey.
Learn more about Amneal Pharmaceuticals
Size
7,000 employees
Market Cap
$616.6 million
Industry
Pharmaceuticals & Biotech
Net Income
$91 million
5 Year Trend
+20.5%
Revenue
$1.9 billion
NASDAQ
AMRX
* Ladders Estimates

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