Senior Analytical Chemist - Drug Product (Scientist III) - Onsite

Parexel; Juneau (AK); On-site; USD 90,000 - 120,000; Full time

Job summary

Parexel is hiring a Scientist 3 - Analytical Chemist (Drug Product) for a full-time, long-term assignment onsite at a client location in Rahway, NJ. This role requires a B.S./M.S. in a life sciences field and experience in a GMP laboratory environment.

Responsibilities include chromatographic analysis (UPLC/HPLC/GC), method development/validation, and GMP release testing. Strong documentation, communication, and organizational skills are essential, with the ability to work independently or as

Qualifications

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

Responsibilities

• Hands-on experience with chromatographic analysis using various UPLC, HPLC and GC techniques, including method and instrument troubleshooting.
• Adheres to GDP standards and ALCOA+ principles in lab notebook documentation.
• General knowledge of separations science.
• Analytical method development and method validation.
• Hands-on experience with FTIR, KF and Dissolution.
• Strong computer, scientific, and organizational skills.
• Excellent communication (oral and written) and attention to detail.
• Ability to multi-task and manage multiple projects including GMP release and stability testing.

Skills

Chromatography

GDP/ALCOA+ docs

Separation science

Method development

FTIR / KF / Dissolution

Data reporting

Communication

Project multitasking

Independent/Teamwork

Education

B.S./M.S. in Chemistry

Tools

FTIR

Karl Fischer (KF)

Dissolution

UPLC/HPLC/GC instrumentation

Job description

Parexel is hiring a Scientist 3 - Analytical Chemist (Drug Product) for a full-time, long-term assignment onsite at a client location in Rahway, NJ. This role requires a B.S./M.S. in a life sciences field and experience in a GMP laboratory environment.

Responsibilities include chromatographic analysis (UPLC/HPLC/GC), method development/validation, and GMP release testing. Strong documentation, communication, and organizational skills are essential, with the ability to work independently or as