Analytical Scientist - QC & Stability Testing

Artech Information System LLC; East Hanover (NJ); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading IT Staffing Company in New Jersey is seeking a Quality Control Analyst responsible for routine QC Stability testing and analytical data verification. Candidates must possess at least 3 years of experience in a cGMP laboratory and a degree in analytical chemistry. Proficiency in HPLC, GC, and other analytical tools is essential. This role demands excellent organizational and communication skills, adhering to FDA and cGMP regulations while ensuring good documentation practices.

Qualifications

• Minimum of 3 years' experience in a cGMP laboratory.
• Knowledge of stability regulation and its application in the industry.
• Familiarity with FDA, DEA, and EPA regulations.
• Ability to follow good documentation practices.

Responsibilities

• Perform routine QC Stability testing of finished dosage forms.
• Verify and validate US CPO Quality Control data.
• Ensure compliance with established QC procedures.
• Independently troubleshoot analytical and instrument problems.

Skills

cGMP laboratory experience

HPLC

GC

UV/VIS

Dissolution testing

Excellent communication

Excellent organizational skills

Analytical data interpretation

Education

Degree in analytical chemistry

Tools

LIMS

Job description

A leading IT Staffing Company in New Jersey is seeking a Quality Control Analyst responsible for routine QC Stability testing and analytical data verification. Candidates must possess at least 3 years of experience in a cGMP laboratory and a degree in analytical chemistry. Proficiency in HPLC, GC, and other analytical tools is essential. This role demands excellent organizational and communication skills, adhering to FDA and cGMP regulations while ensuring good documentation practices.