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Scientist Dissolution Jobs (NOW HIRING)

Scientist-II

Rahway, NJ · On-site

$111K/yr

Required Experience and Skills • The ideal applicant would have hands-on experience in GMP operations, advanced chromatographic separation science, spectroscopy analysis, dissolution testing, and ...

... including dissolution equipment * Conduct data analysis, interpretation, and technical ... scientific discipline * 4+ years of experience in a pharmaceutical or highly regulated QC ...

Associate Scientist Position Summary * Typical working hours are Monday - Friday 8 AM - 5 PM ... Methods and/or during compendial method evaluation for assay, impurities, dissolution etc. with ...

Scientist, R&D Analytical

Summit, NJ · On-site

$82K - $115K/yr

Scientist, R&D Analytical What we do At Kenvue, we realize the extraordinary power of everyday care ... Applied experience with HPLC, UPLC, GC, UV-Vis, FTIR, Dissolution, wet chemistry and compendial ...

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Scientist Dissolution information

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$37K

$91K

$160K

How much do scientist dissolution jobs pay per year?

As of Jun 5, 2026, the average yearly pay for scientist dissolution in the United States is $90,961.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,000.00 and $100,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Scientist Dissolution, and why are they important?

To thrive as a Scientist Dissolution, you need a solid background in pharmaceutical sciences, analytical chemistry, and experience with dissolution testing methodologies, typically backed by a relevant degree such as a BSc, MSc, or PhD. Proficiency in operating and troubleshooting dissolution apparatus (USP I/II), HPLC systems, and related data analysis software is essential, alongside familiarity with regulatory guidelines like USP and ICH. Attention to detail, critical thinking, and effective communication are important soft skills for designing experiments, interpreting results, and collaborating with cross-functional teams. These skills ensure the accurate evaluation of drug release profiles, compliance with industry standards, and the advancement of pharmaceutical product development.

What are some common challenges faced by a Scientist Dissolution when developing and optimizing dissolution methods for new pharmaceutical formulations?

As a Scientist Dissolution, one of the primary challenges involves developing robust and reproducible dissolution methods that accurately reflect the in vivo performance of new drug formulations. You may encounter variability due to complex drug properties, formulation differences, or equipment limitations. Collaborating closely with formulation scientists, analytical chemists, and regulatory teams is essential to troubleshoot issues, validate methods, and ensure compliance with regulatory guidelines. Staying current with technological advances and regulatory expectations is also important to overcome these challenges and deliver high-quality data.

What does a Scientist Dissolution do?

A Scientist Dissolution specializes in developing, validating, and performing dissolution tests, which measure the rate at which a drug is released from its dosage form (like tablets or capsules) into a solution. These tests are critical in pharmaceutical research and quality control to ensure consistent drug performance and bioavailability. The role involves designing studies, operating and maintaining dissolution test equipment, analyzing data, and preparing detailed reports to support regulatory submissions. Additionally, they may troubleshoot issues with formulations and collaborate with other scientists to optimize drug delivery systems.
Infographic showing various Scientist Dissolution job openings in the United States as of May 2026, with employment types broken down into 2% Internship, 12% As Needed, 21% Full Time, 62% Part Time, 2% Temporary, and 1% Contract. Highlights an 89% Physical, 8% Hybrid, and 3% Remote job distribution, with an average salary of $90,961 per year, or $43.7 per hour.
Data Reviewer-Senior Scientist, Quality Control

Data Reviewer-Senior Scientist, Quality Control

Amneal Pharmaceuticals

Piscataway, NJ • On-site

$85K - $105K/yr

Full-time

Medical, Retirement

Posted 21 days ago


Amneal Pharmaceuticals rating

7.3

Company rating: 7.3 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

56th of 71 rated pharmaceutical


Job description

Job Description
Description:
The Scientist 3 - QC is responsible to perform testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculate and report results on applicable specification documents, participate in method transfer activities within departments or between facilities or organizations. This role will also provide feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture.
Essential Functions:
  • Perform physical and chemical analysis of raw materials, in-process, and finished pharmaceutical products, including products on stability, according to written methods, material specification, and company policies as identified in standard operating procedures (SOPs). Comply with cGMps, SOPs, and STPs to avoid out-of-specification situation. Assure compliance with state and federal regulations.
  • Actively participate in any project work as and when assigned. Perform process validation and cleaning validation/verification testing on various drugs. Assist other scientists with analytical, instrument and software related problems as required.
  • Use sonic sifter, laser diffraction, Karl Fischer, UV-Vis spectrophotometer, Infra-red spectrophotometer, HPLC with UV detection as well as with conductivity detection, TLC, pH meter, and dissolution. Calibrate HPLC, Dissolution apparatus equipped with auto-sampler and /or in-line UV, pH meters, analytical balances, and Karl-Fischer titrator.
  • Document steps followed during analysis execution, calculate and report results. Actively participate in investigation of laboratory results.
  • Review laboratory analysis data for completeness, specification compliance, and compliance with company's written policies.
  • Report any abnormal findings to the Supervisor. As assigned, perform in-depth review of analytical records/reports to assure that calculations and other data are technically correct and compliant to relevant specifications.

Additional Responsibilities:
  • Assist the laboratory supervisor with handling non-routine special projects requiring activities such as out-of-specification investigations and out-of-alert limit investigations in the laboratory.
  • Ensure that expired chemicals and reference standards are removed from laboratory area.
  • Perform calibration of HPLC, GC, and other equipment as assigned by the supervisor.
  • Assist with hands-on training of newly hired Technicians or Scientists 1 and 2 levels.

Qualifications
Education:
  • Bachelors Degree (BA/BS) Chemistry or related science discipline - Required
  • Master Degree (MS/MA) Chemistry or related science discipline - Preferred

Experience:
  • 5 years or more in Bachelors Degree (BA/BS) -Testing of chemicals/pharmaceutical products
  • 3 years or more in Masters Degree (BA/BS) -Testing of chemicals/pharmaceutical products

Specialized Knowledge:
  • Must possess in-depth knowledge of analytical chemistry techniques, such as spectrophotometric, dissolution and drug release, chromatographic techniques (standalone or hypenated) and measuring physical parameters (viscosity, particle size or droplet size by laser diffraction, melting point by DSC, water content by TGA, identification by XRPD, and other techniques).
  • Must be able to follow compendial (USP/EP/BP/JP) procedures for analysis.
  • Must understand and apply cGMP requirements applicable to quality control laboratory.
  • Must have ability to apply advanced technical skills to troubleshoot and resolve complex analytical and instrument-related problems effectively and in a timely manner and report actions to the laboratory management in a timely manner.
  • Must be able to identify trends in analytical data.

The base salary for this position ranges from $85,000 to $105,000 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. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that help you enjoy your career alongside life's many other commitments and opportunities.
About Us
Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at accommodations@amneal.com. Requests will be handled confidentially and in accordance with applicable laws.