QUALITY ASSURANCE ENGINEER

DUTIES & RESPONSIBILITIES:

• Assist in preparing, organizing, and maintaining quality-related documents and records.
• Support the preparation and updating of SOPs, forms, checklists, and other quality documents.
• Assist in conducting quality checks and inspections as required.
• Monitor compliance with established procedures and quality requirements.
• Assist in documenting and investigating quality issues and non-conformities.
• Support Corrective and Preventive Action (CAPA) activities.
• Assist with internal audits and follow-up of audit findings.
• Coordinate with different departments regarding quality concerns and documentation.
• Prepare and maintain quality reports, monitoring sheets, and records.
• Assist in monitoring product and process quality.
• Help identify opportunities for process improvement and quality enhancement.
• Perform other Quality Assurance-related tasks as assigned.

QUALIFICATIONS:

• Bachelor’s Degree in Industrial Engineering, Chemical Engineering, Biomedical Engineering, Mechanical Engineering, or other related engineering courses.

• Experience in Quality Assurance, Quality Control, medical devices, healthcare, manufacturing, or a regulated industry is an advantage.

• Knowledge of Quality Management Systems (QMS) is an advantage.

• Familiarity with quality standards and regulatory requirements for medical devices is a plus.

• Proficient in MS Office, particularly MS Excel.

• Willing to learn and work in a regulated medical device environment.

WORK SCHEDULE:

• Monday - Thursday | 8:00AM - 6:00PM
• Friday | 8:00AM - 5:00PM