Senior Cleaning Validation Analytical Chemist (GMP)

Parexel; Dover (DE); On-site; USD 95,000 - 125,000; Full time

Job summary

Parexel is seeking a Scientist III - Cleaning Validation Analytical Chemist to join as a full-time employee of Parexel FSP on a long-term assignment onsite at a client location in Rahway, NJ. The role emphasizes hands-on analytical work in GMP environments and strict adherence to ALCOA documentation principles.

The ideal candidate has BS or MS in chemistry with relevant hands-on experience and will perform data interpretation, reporting, and preparation of GMP documentation, while ensuring safe

Qualifications

• BS in chemistry or a closely related field with at least 3-5 years of hands-on research experience.
• MS in analytical chemistry or a closely related field with at least 1-2 years of hands-on research experience.

Responsibilities

• Support cleaning validation and cleaning verification analysis for GMP manufacturing areas.
• Conduct raw materials release testing using many methodologies and techniques in a GMP laboratory.
• Data interpretation, processing, and reporting.
• Prepare GMP documentation including analytical reports and certification of analyses.
• Responsible for following safe laboratory practices and for maintaining the work area in a clean, orderly and safe manner.

Skills

Chromatographic analysis (UPLC/HPLC/GC

Separations science

Computer & data analysis

Communication

Organization

GMP ALCOA documentation

Analytical method development

Education

BS in chemistry or related field

MS in analytical chemistry or related field

Tools

Empower chromatographic software

FTIR

UV/VIS

Job description

Parexel is seeking a Scientist III - Cleaning Validation Analytical Chemist to join as a full-time employee of Parexel FSP on a long-term assignment onsite at a client location in Rahway, NJ. The role emphasizes hands-on analytical work in GMP environments and strict adherence to ALCOA documentation principles.

The ideal candidate has BS or MS in chemistry with relevant hands-on experience and will perform data interpretation, reporting, and preparation of GMP documentation, while ensuring safe