- Key Responsibilities: *
- Assist in maintaining and updating QMS documentation (SOPs, Work Instructions, Records).
- Help coordinate internal audits and prepare documentation for external audits.
- Support the training process by organizing sessions and maintaining training records.
- Perform basic QC checks and inspections under supervision.
- Assist with tracking and follow-up on CAPA actions.
- Help maintain supplier documentation and support risk management files.
- Ensure proper document control and record retention in compliance with ISO 13485.
- Promote awareness of quality procedures across departments.
**Qualifications & Experience: **
- Diploma or Bachelor s in Mechanical, Engineering, or related field.
- 1–2 years of experience in a quality or manufacturing environment (preferred).
- Familiarity with ISO 13485 and medical device regulations is an advantage.
Skills Required:
- Basic understanding of QMS principles and ISO standards.
- Positive attention to detail and documentation accuracy.
- Strong organizational and communication skills.
- Proficient in Microsoft Office (Word, Excel, Outlook).
- Ability to follow procedures and work collaboratively in a team.
Job Type: Full-time
Work Location: In person
📌 Quality Engineer -Implementing ISO 13485 (India)
🏢 International Industrial Springs
📍 India
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