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Full Time Bioequivalence Jobs (NOW HIRING)

Granules Pharmaceuticals

Biochemist

Chantilly, VA · On-site

$69K - $73K/yr

Job Type Full-time Description Granules Pharmaceuticals Inc., (GPI) is a subsidiary of Granules ... and bioequivalence studies using cGMP/cGLP, Empower, Titration, HPLC, dissolution * Perform ...

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As of Aug 31, 2026, the average yearly pay for full time bioequivalence in the United States is $127,248.00, according to ZipRecruiter salary data. Most workers in this role earn between $112,000.00 and $142,500.00 per year, depending on experience, location, and employer.

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Infographic showing various Full Time Bioequivalence job openings in the United States as of August 2026, with employment types broken down into 86% Full Time, 7% Temporary, and 7% Contract. Highlights an 93% Physical, and 7% Remote job distribution, with an average salary of $127,248 per year, or $61.2 per hour.

Biochemist

Chantilly, VA • On-site

Granules Pharmaceuticals
See more jobs at Granules Pharmaceuticalsexternal

$69K - $73K/yr

Full-time

Re-posted yesterday

Job description

Job Type
Full-time
Description
Granules Pharmaceuticals Inc., (GPI) is a subsidiary of Granules India LTD. Over the past 34 years, we have worked towards strengthening our core and we are currently the 10th fastest growing generic pharma company in the US! With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule dosage form, orally disintegrating modified release tablets (XR, MR, ER), modified release suspension and controlled substances capabilities in an abuse deterrent technology platform.
We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to give customers reliable and affordable options.
Responsibilities include but not limited to:
  • Analyze bio-availability and bioequivalency of pharmaceutical products using HPLC, UV-Vis, GC, FTIR
  • Perform routine release tests of raw materials and finished products using OOS/OOT and LIMS
  • Perform in-vivo dissolution test related to the biopharmaceutic characteristics of the drug substance and bioequivalence studies using cGMP/cGLP, Empower, Titration, HPLC, dissolution
  • Perform solubility studies of drug substances as per Bio-Pharmaceutics classification system (BCS) in accordance with FDA regulations
  • Conduct and coordinate elemental impurities study for Pharmaceutical Products as per ICH guidance;
  • Interpret test results and established specifications and control limits to ensure appropriateness of data for release; Analyze biochemical results

Submit résumé referencing job code ASY001 to HR, Granules Pharmaceuticals, Inc., 3701 Concorde Parkway, Chantilly, VA 20151
Requirements
Educational Requirements:
Must have a Bachelor's degree in Biochemistry, Chemistry, or Biotechnology plus 2 years experience in Quality Control within a Pharmaceutical Manufacturing company.
Skills Requirements:
Working knowledge in HPLC, UV-Vis, FTIR, OOS/OOT, Dissolution, Titration, cGMP, LIMS
Salary Description
$69,564~$73,000/year

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