We are currently looking for a QA Associate to join a leading pharmaceutical company on a 9 month contract.
Quality & Compliance Support: Documentation Review: Perform detailed, real-time review of manufacturing and laboratory documentation, ensuring accuracy, completeness, and adherence to regulatory standards.
Contribute to a state of audit readiness by actively participating in quality system improvements and continuous improvement initiatives.
Compliance Issue Management: Utilize in-depth GMP and QMS knowledge to manage and escalate major and critical quality issues, including deviations and CAPAs.
Serve as a quality liaison for key stakeholders across manufacturing, technical operations, and supply chain teams.
Training & Best Practice Promotion: Mentor team members on cGMP principles and best documentation practices, supporting a culture of compliance and proactive quality.
Strong knowledge of GMP and pharmaceutical quality systems
Proficient in documentation review and risk-based decision making
High attention to detail with accurate data entry skills
Excellent organizational, planning, and time-management abilities
IT literate (MS Office; familiarity with databases)
Working knowledge of deviations, CAPAs, and quality investigations
Involvement in continuous improvement or pharmaceutical quality system (PQS) enhancement projects