Posted:20 hours ago|
Platform:
On-site
Full Time
Key Responsibilities:
· Maintain, review, and update QMS documentation (SOPs, Work Instructions, Records) to ensure accuracy and compliance.
· Lead coordination of internal audits and prepare comprehensive documentation for external audits.
· Support and sometimes lead training sessions, maintaining and updating training records.
· Conduct detailed QC checks and inspections independently, ensuring adherence to quality standards.
· Track, analyze, and follow-up on CAPA actions, driving timely closure.
· Manage supplier documentation and contribute to supplier quality management and risk assessment activities.
· Ensure robust document control and record retention in strict compliance with ISO 13485.
· Promote and enforce awareness of quality procedures across departments, offering guidance to junior team members.
Qualifications & Experience:
· Diploma or Bachelor's in Mechanical, Engineering, or related field.
· 4–5 years of experience in a quality or manufacturing environment (preferred).
· Strong knowledge of ISO 13485 and medical device regulations is an advantage.
Skills Required:
· Solid understanding of QMS principles and ISO standards.
· Excellent attention to detail and ability to maintain documentation accuracy.
· Strong organizational, analytical, and communication skills.
· Proficient in Microsoft Office (Word, Excel, Outlook).
· Ability to work independently, take ownership of tasks, and collaborate effectively within a team.
Job Types: Full-time, Permanent
Pay: ₹25,000.00 - ₹40,000.00 per month
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