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Parexel

End-to-end clinical trials and regulatory consulting

Scientist 3 or Senior Scientist 1 Analytical Chemist - Drug Product

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeRahway, NJ, USANo salary listedIn-person

About the Job

Requirements

  • A B.S. or M.S. in Chemistry, Chemical Engineering, Biochemistry, Biology, or similar life sciences, with relevant experience in a GMP laboratory environment.
  • Hands-on experience with chromatographic analysis using UPLC, HPLC, and GC techniques, including method and instrument troubleshooting.
  • Adherence to Good Documentation Practices standards with accurate, compliant documentation.
  • General knowledge of separation science.
  • General understanding of analytical method development and method validation.
  • Hands-on experience with FTIR, Karl Fischer, and dissolution.
  • Computer, scientific, and organizational skills.
  • Oral and written communication skills and attention to detail.
  • Ability to multitask and manage multiple ongoing projects in parallel, including GMP release and stability testing, along with data processing, interpretation, and reporting.
  • Ability to work independently and as part of a team.

Responsibilities

  • Conduct analytical testing and analysis in a GMP laboratory environment, including GMP release and stability testing.
  • Process, interpret, and report data.

Desired Qualifications

  • Experience with Empower software.
  • Experience analyzing drug product and drug substance.

About the Company

Parexel

End-to-end clinical trials and regulatory consulting

Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.

Company size
10,001+
Company stage
Acquired
Total funding
$8.5B
Headquarters
Durham, NC
Founded
1982

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