Job Description

About Us

Propack Technologies is a Pharmaceutical Machine Manufacturer that has been supplying Process equipment & systems for Pharmaceutical, Bioprocessing & Cosmetic industries. With a strong commitment to quality, efficiency, and customer satisfaction, we have built a reputation for delivering high-performance packaging systems and services across domestic and international markets.

We are looking for a detail-oriented QA/QC Documentation Engineer with at least 1 year of experience in managing technical and quality-related documentation. The candidate will be responsible for maintaining accurate records, preparing quality documents, supporting audits, and ensuring compliance with internal and external quality standards.

Key Responsibilities

Prepare, maintain, and update QA/QC documents, SOPs, checklists, and reports. Organize and manage documents related to equipment manufacturing, inspection, and testing. Handle document approval processes and maintain document master lists. Assist in preparing quality-related documents such as FAT, SAT, IQ/OQ, calibration reports, etc. Ensure all documentation meets internal quality standards and customer requirements. Assist QA/QC engineers in preparing inspection reports and quality records. Provide documentation support during internal and external audits. Maintain detailed records of non-conformities, corrective actions, and preventive action reports. Ensure all quality-related records are properly stored and accessible.

Required Skills:

Strong knowledge of QA/QC documentation processes. Basic understanding of mechanical components and engineering drawings. Proficiency in MS Office (Excel, Word, ). Attention to detail and strong organizational skills. Good communication and coordination abilities. Familiarity with SOP writing and audit documentation.
Job Type: Full-time

Education:

Bachelor's (Required)
Work Location: In person