Analytical Chemist (Drug Product) – GMP & Stability Expert

Parexel

Honolulu (HI)

On-site

USD 80,000 - 110,000

Full time

14 days+
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Benefits offered by this job

Full benefits
Sick time
401K
Paid holidays
Paid time off

Job summary

Parexel is seeking a Scientist 2 or 3 - Analytical Chemist (Drug Product) for a full-time, onsite role with a client in Rahway, NJ. The position requires a BS/MS in chemistry or related fields and experience with GMP analyses using HPLC/UPLC and data interpretation.

Strong communication and project-management skills are essential as you support stability testing and method development. You will contribute to SOP authoring, data integrity, and continuous improvement in a compliance-driven lab

Qualifications

  • Experience with GMP analysis using HPLC/UPLC including assay/impurity/etc., troubleshooting and data processing interpretation/analysis
  • Strong computer, scientific, and organizational skills
  • Clear communicator who speaks up about problems and improvement ideas
  • Able to manage multiple ongoing projects
  • Ability to work independently and as part of a team
  • Self-motivation, efficiency, adaptability, and a positive attitude

Responsibilities

  • Perform routine and stability sample analysis.
  • Author SOPs and contribute to method validation.
  • Support continuous improvement and technology development for optimized lab operations.
  • Contribute to robust analytical methods and high-quality stability data for late-stage product development.

Skills

GMP analysis
HPLC/UPLC
Troubleshooting
Data interpretation
Sample management
Communication
Project management
Independence
Team collaboration
Self-motivation

Education

B.S./M.S. in Chemistry, Biochemistry, Engineering, or related discipline

Tools

Empower software

Job description

Parexel is seeking a Scientist 2 or 3 - Analytical Chemist (Drug Product) for a full-time, onsite role with a client in Rahway, NJ. The position requires a BS/MS in chemistry or related fields and experience with GMP analyses using HPLC/UPLC and data interpretation.

Strong communication and project-management skills are essential as you support stability testing and method development. You will contribute to SOP authoring, data integrity, and continuous improvement in a compliance-driven lab

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