Note: The job is a remote job and is open to candidates in USA. Virtue America is seeking an entry-level Quality Control Analyst to support laboratory testing and quality control activities in a GMP-regulated pharmaceutical or life sciences environment. The role involves analytical testing, laboratory documentation, investigations, instrument support, and collaboration with quality and manufacturing teams.
Responsibilities
- Perform routine testing of raw materials, in-process samples, and finished products
- Prepare samples, reagents, standards, and laboratory solutions
- Operate analytical instruments such as HPLC, GC, UV-Vis, FTIR, and pH meters
- Record and review laboratory data following GMP and Good Documentation Practices (GDP)
- Support laboratory investigations, including OOS , deviations, and CAPA activities
- Assist with instrument calibration, maintenance, and qualification
- Maintain laboratory documentation and ensure compliance with FDA and GMP requirements
- Collaborate with QA, Manufacturing, and Validation teams
- Support internal audits and inspection readiness activities
Skills
- • Bachelor's degree in Chemistry, Biochemistry, Biology, Microbiology, Pharmaceutical Sciences, Biotechnology, or a related Life Sciences field
- • 0–2 years of laboratory or Quality Control experience (internships/co-ops accepted)
- • Basic understanding of analytical laboratory techniques and GMP regulations
- • Strong analytical, communication, and documentation skills
- • Proficiency with Microsoft Office
- • Exposure to HPLC, GC, UV-Vis, FTIR, or dissolution testing
- • Familiarity with Empower, LabWare LIMS, OpenLab, or Chromeleon
- • Knowledge of GLP, GMP/cGMP, and Good Documentation Practices (GDP)
- • Internship or academic laboratory experience in pharmaceutical or life sciences industries
Company Overview
Company H1B Sponsorship