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Job Location:
Monthly Salary:
Posted on:
30+ days ago
Vacancies:
1 Vacancy
Job Summary
Overview
The QC Analyst will execute laboratory testing and quality control activities within a GMP-regulated pharmaceutical manufacturing environment. The role ensures accurate analytical testing proper sample management equipment support and full compliance with cGxP and data integrity standards.
Key Responsibilities
- Perform analytical testing of API drug substance drug product finished product stability and packaging material samples
- Manage sample storage handling and documentation
- Ensure accurate and timely GMP-compliant documentation
- Support equipment maintenance calibration and qualification activities
- Maintain inspection readiness and adhere to SOPs GMP and HSE standards
- Participate in training retraining and continuous improvement initiatives
Requirements & Qualifications
Experience
- Prior experience in pharmaceutical QC laboratory environment
- Hands-on analytical testing experience
- Exposure to GMP documentation and data integrity practices
- Aseptic technique experience
Education
- Diploma / Apprenticeship as Laboratory Assistant or equivalent technical qualification
Technical Knowledge
- QC testing and sampling
- Knowledge of GMP/GxP standards
- Familiarity with laboratory equipment and quality systems
Skills & Competencies
- Detail-oriented and compliance-driven
- Strong documentation discipline
- Team-oriented and result-focused
- Able to work 12-hour rotating shifts
