Posted: 3 weeks ago
Openings: 1
Applicants: 5+
Job Description
We are hiring an IPQA Officer for a medical device manufacturing company.
The candidate will be responsible for in-process quality assurance and documentation activities.
Key Responsibilities
- Ensure proper document control and documentation management.
- Maintain QMS as per ISO 9001, ISO 15378, and ISO 13485 standards.
- Perform sampling, testing, documentation, and evaluation of data.
- Conduct line clearance and in-process checks in production area.
- Review receipt of materials from warehouse to production.
- Review batch processing records and ensure compliance.
- Coordinate with production and quality teams for QA activities.
- Ensure adherence to SOPs and quality standards.
Required Skills
- Experience in IPQA or quality assurance activities.
- Knowledge of ISO 9001, ISO 15378, and ISO 13485.
- Good understanding of documentation and QMS systems.
- Knowledge of line clearance and in-process inspection.
- Attention to detail and analytical skills.
- Good communication and coordination abilities.
| Role | IPQA Officer |
| Industry Type | Medical Device |
| Department | Quality Assurance / IPQA |
| Employment Type | Full Time |
Education
UG: Any Graduate
PG: Any Postgraduate
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