About the role
In this position, you will conduct inspections and audits on medical devices to ensure they meet quality standards and regulatory requirements. Your attention to detail and understanding of quality assurance processes will be critical in this role. This part-time position suits professionals looking for flexible work arrangements while contributing to healthcare product safety.
You will be responsible for reviewing production processes, documenting findings, and participating in corrective action discussions. Our client values quality and safety, offering a collaborative environment where your expertise in quality assurance can shine.
What you'll do
- Conduct quality inspections of medical devices.
- Document and report compliance issues.
- Participate in continuous improvement initiatives.
- Review production processes and provide feedback.
What you'll need
- Degree in engineering or related field.
- 2-5 years of experience in quality assurance.
- Knowledge of ISO standards.
Skills
Strong analytical skills.
Attention to detail.
Familiarity with quality assurance tools.
Good to have
Experience in medical device industry.
Knowledge of regulatory compliance.
Benefits
- Flexible part-time schedule.
- Professional growth opportunities.
- Collaborative team environment.
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
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Questions about this job
What does the role entail?
You will inspect medical devices for quality compliance and conduct audits.
What qualifications do I need?
A background in quality assurance or engineering, with relevant experience.
Is this a full-time or part-time position?
This is a part-time onsite role.
What is the salary for this position?
The salary ranges from INR 25,000 to INR 45,000 per month.
Listing last updated