Onsite Analytical Chemist (Drug Substance Analysis) - GMP

Parexel; Carson City (NV); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Full benefits

Sick time

401K

Paid holidays

Paid time off

Job summary

Parexel is seeking a Scientist 3 - Analytical Chemist (Drug Substance Analysis) to join a long-term Parexel FSP assignment onsite at a client in Rahway, NJ. The role covers routine stability testing, SOP writing, and method development in a GMP lab.

You will analyze samples using UPLC/HPLC/GC, uphold GDP standards, document precisely, and collaborate across teams to ensure quality data supporting late-stage drug product development.

Qualifications

• B.S./M.S. in Chemistry, Chemical Engineering, Biochemistry, Biology or similar life sciences and relevant years of experience in a GMP laboratory environment.
• B.S. with 3-5 years of experience; M.S. with 1-2 years of experience

Responsibilities

• Perform routine and stability sample analysis
• SOP authoring and maintenance
• Support method development and validation activities
• Ensure compliant documentation and GDP standards
• Collaborate with team to troubleshoot analytical issues
• Work independently and in a team to manage multiple projects

Skills

Chromatographic analysis

GDP/GMP documentation

Method development

FTIR/KF/Dissolution

Data interpretation

Communication skills

Time management

Empower software

Team collaboration

Education

Bachelor's/Master's in Chemistry or related

Tools

UPLC/HPLC/GC instruments

FTIR

KF

Dissolution tester

Job description

Parexel is seeking a Scientist 3 - Analytical Chemist (Drug Substance Analysis) to join a long-term Parexel FSP assignment onsite at a client in Rahway, NJ. The role covers routine stability testing, SOP writing, and method development in a GMP lab.

You will analyze samples using UPLC/HPLC/GC, uphold GDP standards, document precisely, and collaborate across teams to ensure quality data supporting late-stage drug product development.