Quality Assurance Executive
3 weeks ago
To handle all activities related quality management system, Quality Assurance & regulatory affairs for ISO 9001 & 13485, 93/42/EEC Directive including
- Technical files making & updating including risk management, clinical evaluation, post market surveillance, quality plan, ESRs, etc.
- Fulfilment of regulatory requirements related to EC directive, various Govt. tenders & registration of overseas.
- Follow up of local regulatory & drugs requirements.
- Validation
- machines, processes, clean rooms, material & sterilization.
- Organizing internal & external audits including notified bodies audits related to quality management system & CE and follow up of non-closure reports.
- Dealing in customer complaints, investigating, root cause analysis and replying, vigilance reporting & recall.
- MRM- Organizing & follow up actions from previous meetings.
- Review & modification in all the SOPs & manuals.
- Master list of records
- Establishment & updating.
- Master list of documents
- Establishment & updating.
- Deviations
- Follow up & records
- Corrective & preventive actions
- Corrections, implementations & maintenance.
- Calibration of equipment and machines of production & quality control.
- Handling out the pre-dispatch inspections of shipments by the outside agencies and certification bodies.
- Training
- Planning & Imparting
**Requirements**:
- Work experience should be minimum 1-2 years in medical devices manufacturing.
- Excellent computer skills
- Goal Oriented
- Strong communication skills, including the ability to explain and teach methodologies
- Understanding of manufacturing methods and quality standards
- A confident and determined approach
- Excellent organizational & time management skills
- Team player
**Salary**: ₹25,000.00 - ₹30,000.00 per month
Schedule:
- Day shift
Supplemental pay types:
- Yearly bonus
**Education**:
- Bachelor's (preferred)
**Experience**:
- total work: 4 years (preferred)
**Speak with the employer**
+91 8130384348
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