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 operations and product testing in a pharmaceutical or life sciences environment. The role involves performing analytical testing, reviewing data, maintaining laboratory documentation, supporting investigations and stability programs, and ensuring compliance with quality procedures.
Responsibilities
- QC Laboratory Operations: Perform routine laboratory activities according to approved methods, specifications, and SOPs
- Material Testing: Assist with testing of incoming raw materials, in-process materials, finished products, and stability samples
- Analytical Testing: Support physical, chemical, and instrumental analysis using techniques appropriate to the laboratory
- Laboratory Instruments: Operate and assist with routine maintenance, calibration, and troubleshooting of laboratory instruments
- Sample Preparation: Perform accurate sample weighing, dilution, preparation, labeling, and controlled sample handling
- Data Integrity: Record analytical results accurately and maintain complete, traceable laboratory records in accordance with ALCOA+ principles
- Results Review: Review test results against approved specifications and promptly communicate atypical or unexpected findings
- Investigation Support: Assist with OOS, OOT, deviations , laboratory errors, and root-cause investigations
- Documentation: Maintain laboratory notebooks, worksheets, test reports, logbooks, and Certificates of Analysis
- Compliance: Follow cGMP, GLP, GDP , laboratory safety requirements, and internal quality procedures
- Stability Program Support: Assist with sample pulls, testing schedules, and documentation for stability studies
- Cross-Functional Collaboration: Coordinate with QA, Manufacturing, R&D, Validation, and other laboratory teams to resolve quality-related issues
Skills
- Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Pharmacy, Biotechnology, Microbiology, Life Sciences , or a related field
- Basic understanding of pharmaceutical Quality Control laboratory practices
- Familiarity with analytical techniques such as HPLC, GC, UV-Vis, FTIR, dissolution, titration , or related laboratory methods
- Understanding of cGMP, GLP, GDP, SOPs , and laboratory safety practices
- Basic knowledge of OOS, OOT, deviations, CAPA , and laboratory investigations
- Strong analytical ability with excellent attention to detail and accuracy
- Good technical writing, documentation, and communication skills
- Ability to follow established procedures and maintain accurate laboratory records
- Fresh graduates and candidates with 0–2 years of relevant experience are encouraged to apply
- Awareness of data integrity and ALCOA+ principles is preferred
Benefits
- Remote work
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