QA or RA Executive
Job Description:
Job Description:
1. Responsible for Overall QA activities & to look after QMS compliance in accordance with ISO 13485/cGMP.
2. Preparation & Up-gradation of SOP, Specifications
3. Maintain the Records of BMR, BPR, Batch Inspection Documents
4. Maintaining Document & Record Control
5. Preparation & Up-gradation of Routine Validation Protocol & Reports.
6. Handling CAPA, Non- Conformance & Deviations
7. Require understanding on QA & Regulatory activities in medical device industry
8. oversee the risk management process and related activities.
QA for MDR (MEDICAL DEVICE RULES) / ISO13485
COMPULSORY
Key Skills :
Company Profile
It is an ISO 13485 Certified manufacturer specializing in development of innovative medical devices critical to Gastroenterology, Urology and Interventional Radiology.
Based in Surat, we thrive to offer technological advancements in the industry to improve the quality of healthcare standards globally.
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- Interested candidates are requested to apply for this job.
- Recruiters will evaluate your candidature and will get in touch with you.