Pharma QC Analyst - HPLC & Stability Testing

PSG Global Solutions; Summit (NJ); On-site; USD 60,000 - 85,000; Full time

Job summary

A leading talent management firm is seeking candidates for a laboratory role in Summit, New Jersey. The responsibilities include assisting with laboratory analysis for clinical release and routine stability testing, conducting analytical experiments and documenting lab work following compliance protocols. Ideal candidates should possess a BS/MS in Chemistry and have 2-4 years of cGMP/GLP experience, alongside skills in HPLC and teamwork. This position represents an excellent opportunity for career advancement in a dynamic environment.

Qualifications

• Minimum 2-4 years recent cGMP/GLP pharmaceutical laboratory experience.
• Experience with HPLC, dissolution, FT-IR, UV/Vis spectrophotometry, KF.
• Able to work well in a team environment to achieve results.

Responsibilities

• Assist with laboratory analysis for clinical release and routine stability testing.
• Conduct testing independently and assist other analysts in analytical testing.
• Document laboratory work in compliance with GLP/cGMP requirements.

Skills

HPLC

Dissolution

Scientific judgment

Team collaboration

Analytical testing

Education

BS/MS in Chemistry or relevant discipline

Tools

UV/Vis spectrophotometry

FT-IR

Karl Fischer

Job description

A leading talent management firm is seeking candidates for a laboratory role in Summit, New Jersey. The responsibilities include assisting with laboratory analysis for clinical release and routine stability testing, conducting analytical experiments and documenting lab work following compliance protocols. Ideal candidates should possess a BS/MS in Chemistry and have 2-4 years of cGMP/GLP experience, alongside skills in HPLC and teamwork. This position represents an excellent opportunity for career advancement in a dynamic environment.