Analytical Chemist — GMP QC Lab (I–III)

Quagen Pharmaceuticals; West Caldwell (NJ); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Comprehensive benefits package

Job summary

A leading pharmaceutical manufacturer in New Jersey is seeking an Analytical Chemist to conduct a range of laboratory tests following GMP guidelines. The role requires a Bachelor's Degree in Science/Chemistry and 2-10 years of experience in a Quality Control Laboratory. Strong knowledge of analytical techniques and regulatory compliance is essential. This full-time position offers a comprehensive benefits package.

Qualifications

• Minimum 2-10 years of experience in a Quality Control Laboratory in a cGMP environment.
• Experience in the pharmaceutical industry preferred.
• Knowledge in Good Documentation practices and regulatory requirements.

Responsibilities

• Perform various physical and chemical tests per procedures and compendial monograph.
• Document all work clearly and accurately.
• Maintain appropriate laboratory records and logbooks.
• Comply with all regulatory and in-house requirements.
• Perform additional lab-related duties as assigned.

Skills

Analytical techniques (LC, GC, UV-Vis)

Good Documentation Practices

Knowledge of USP/FDA regulations

Education

Bachelor’s Degree in Science/Chemistry

Tools

Empower-3

QC instruments

Job description

A leading pharmaceutical manufacturer in New Jersey is seeking an Analytical Chemist to conduct a range of laboratory tests following GMP guidelines. The role requires a Bachelor's Degree in Science/Chemistry and 2-10 years of experience in a Quality Control Laboratory. Strong knowledge of analytical techniques and regulatory compliance is essential. This full-time position offers a comprehensive benefits package.