[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 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

Company Overview

Company H1B Sponsorship