Job Description

Roles & Responsibilities

• Monitor production processing through random quality audits.
• Perform and support quality inspections using proper equipment and techniques.
• Conduct statistical analysis on processes and report findings.
• Participate in problem-solving, root cause analysis, and corrective actions.
• Maintain accurate documentation of inspection results.
• Verify raw materials and outgoing products meet required specifications.
• Ensure production personnel follow correct procedures for quality checks.
• Support training of operators in QA procedures and measurement techniques.
• Develop and maintain quality procedures and work instructions.
• Audit compliance with quality management system standards.
• Generate and present quality reports (daily, weekly, monthly).
• Perform additional duties as directed by quality management.

Experience Required

• Minimum 3–5 years of experience as a lead, technician, or inspector in the medical device or pharmaceutical industry.
• Prior experience enforcing standard work instructions (SWI), SOPs, and product specifications.
• Hands-on experience with measuring equipment and statistical analysis tools.

Skills & Certifications

• Strong knowledge of GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices).
• Proficiency in Excel and data analysis.
• Strong mathematics and statistical analysis skills.
• Knowledge of quality criteria, inspection standards, and regulatory compliance.
• Ability to work independently with minimal supervision.
• Attention to detail and accuracy in documentation.

Eligibilities & qualifications

• Bachelor’s degree in Engineering, Life Sciences, or a related technical discipline (mandatory).
• Physical ability to perform job requirements, including lifting/carrying and prolonged standing/walking.
• Willingness to work in a manufacturing environment.

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