[Remote] Quality Control Analyst
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 testing and quality control activities in a regulated pharmaceutical or life sciences environment. The role assists with sample management, analytical testing, documentation, data review, instrument support, regulatory compliance, investigations, and audit readiness.
Responsibilities
- Laboratory Testing: Assist with routine testing and analysis of raw materials, in-process samples, finished products, and stability samples
- Sample Management: Support sample collection, preparation, labeling, tracking, and storage according to approved procedures
- Analytical Support: Assist with analytical techniques such as HPLC, GC, UV-Vis, FTIR, dissolution, pH, and titration , as applicable
- Documentation Management: Prepare and maintain laboratory notebooks, test records, worksheets, Certificates of Analysis, and other QC documentation
- Data Review: Assist with reviewing, recording, and verifying analytical data for accuracy, completeness, and compliance
- Instrument Support: Assist with laboratory instrument calibration, maintenance, troubleshooting, and qualification activities
- Regulatory Compliance: Ensure all QC activities follow cGMP, GDP, FDA , and applicable quality standards
- Investigation Support: Assist with OOS, OOT, deviations, root-cause analysis , and CAPA activities
- Cross-Functional Collaboration: Work with QA, Manufacturing, Validation, and other laboratory teams to support quality and testing requirements
- Audit Readiness: Maintain accurate and complete laboratory documentation to support internal and external audits and inspections
Skills
- Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Biotechnology, Microbiology, Life Sciences , or a related field
- Basic understanding of pharmaceutical or life sciences laboratory operations
- Familiarity with analytical testing techniques and laboratory equipment
- Understanding of cGMP, GDP, SOPs , and good laboratory documentation practices
- Strong analytical, problem-solving, and organizational skills
- Excellent written and verbal communication skills with strong attention to detail
- Fresh graduates and candidates with 0–2 years of relevant experience are encouraged to apply
- Basic knowledge of HPLC, GC, UV-Vis, FTIR, dissolution, pH, or titration is preferred
- Basic knowledge of OOS, deviations, CAPA , and quality investigation processes is preferred
Company Overview
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