Job Description

for Quality Engineer - 1

:

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).

Candidate must be from a medical/Pharma background company with hands-on experience in ISO 13485 certification and compliance.

Familiarity with medical device regulations is an advantage.

Skills Required:

Basic understanding of QMS principles and ISO standards.

Good 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

Job Type: Permanent

Pay: ₹18,000.00 - ₹22,000.00 per month

Work Location: In person