Analytical Chemist II/III - Drug Product, GMP/HPLC, Rahway

Parexel; Pierre (SD); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Full benefits

Sick time

401K

Paid holidays

Paid time off

Job summary

Parexel FSP is seeking a Scientist 2 or 3 - Analytical Chemist (Drug Product) to join a full-time, long-term assignment onsite in Rahway, NJ. You will contribute to stability testing, analytical method validation, and SOP generation in a regulated lab environment.

The ideal candidate has GMP/HPLC/UPLC experience, strong data interpretation skills, and the ability to manage multiple projects while collaborating closely with cross-functional teams.

Qualifications

• Experience with GMP analysis using HPLC/UPLC including assay/impurity
• Routine testing, data integrity assessments, investigative report authoring, and/or sample management
• Strong computer, scientific, and organizational skills
• Clear communicator who speaks up about problems and improvements
• 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

• In the drug product registration stability testing lab, perform routine and stability sample analysis
• SOP authoring and day-to-day problem solving
• Contribute to new technologies and continuous improvement for lab operations
• Apply analytical characterization techniques to drive robust, high-quality stability data

Skills

GMP analysis

HPLC/UPLC

Data processing & interpretation

Clear communicator

Project management

Independent work

Self-motivation & adaptability

Education

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

Tools

Empower software

Job description

Parexel FSP is seeking a Scientist 2 or 3 - Analytical Chemist (Drug Product) to join a full-time, long-term assignment onsite in Rahway, NJ. You will contribute to stability testing, analytical method validation, and SOP generation in a regulated lab environment.

The ideal candidate has GMP/HPLC/UPLC experience, strong data interpretation skills, and the ability to manage multiple projects while collaborating closely with cross-functional teams.