QUALITY ASSURANCE ENGINEER

Variance Trading Corporation; Quezon City; On-site; PHP 300,000 - 420,000; Full time

Job summary

Variance Trading Corporation in Metro Manila is seeking a Quality Assurance professional to help maintain compliance and document control in a regulated medical device environment.

You will assist with quality records, SOPs, CAPA, and internal audits, coordinating with departments to ensure quality standards are met. Candidates should have an engineering degree, familiarity with QMS, and strong MS Office skills.

Qualifications

• Bachelor’s degree in engineering or related field within QA context.
• Experience in Quality Assurance/Quality Control in regulated environments.
• Familiarity with Quality Management Systems (QMS) and medical device standards is a plus.
• Proficient in MS Office, especially MS Excel.

Responsibilities

• Assist in preparing, organizing, and maintaining quality 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 CAPA activities.
• Assist with internal audits and follow-up of audit findings.
• Coordinate with 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 QA-related tasks as assigned.

Skills

Quality awareness

Attention to detail

Education

Engineering degree (Industrial/Chemical/Biomedical/Mechanical)

Tools

MS Excel

MS Office

Job description

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