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AR&D Chemist

Job in Woodbridge Township, Middlesex County, New Jersey, 07095, USA
Listing for: Quagen Pharmaceuticals
Full Time position
Listed on 2026-09-30
Job specializations:
  • Pharmaceutical
  • Healthcare
Salary/Wage Range or Industry Benchmark: 55000 - 75000 USD Yearly USD 55000.00 75000.00 YEAR
Job Description & How to Apply Below

We are seeking a highly motivated and detail-oriented Entry-Level AR&D Chemist to join our growing pharmaceutical research and development team. This role is responsible for supporting analytical method development, validation, and testing activities for drug substances and drug products in a pharmaceutical development environment. This role requires a strong foundation in analytical chemistry, attention to detail, and the ability to work collaboratively with cross-functional teams while following cGMP requirements.

Key Responsibilities
  • Perform routine and non-routine analysis of APIs, excipients, and finished dosage forms using analytical techniques such as HPLC, UPLC, GC, Dissolution, UV, FTIR, KF, and other laboratory instrumentation.
  • Assist senior scientist in method validation and verification activities following approved protocols and current ICH guidelines.
  • Support senior scientists in the development, optimization, and transfer of analytical methods.
  • Perform stability sample testing, record results, and support stability studies and data trending activities.
  • Maintain accurate laboratory notebooks, test records, analytical reports, and electronic data in compliance with cGMP and data integrity requirements.
  • Adhere to laboratory procedures, standard operating procedures (SOPs) and applicable regulatory requirements.
  • Perform other duties assigned commensurate with position.
Qualifications
  • Education: Bachelor’s (B.S.) or Master’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Pharmacy, or related scientific discipline.
  • Experience: 0–2 years of experience in a pharmaceutical AD/QC laboratory or regulated laboratory environment.
  • Basic understanding of cGMP, GLP, laboratory documentation, and data integrity principles.
  • Strong problem-solving, organizational, and communication skills.
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