Description
Develop documentation for the Quality Management System;
Analyze customer complaints and nonconformities;
Schedule, plan, and convene critical review meetings and change control meetings;
Prepare critical reviews to support corrective action decisions;
Monitor new product registrations and maintenance with ANVISA, which may be handled by a third-party company;
Develop and review instructions related to departments;
Perform product registration/data entry in SAP according to ANVISA approval;
Conduct training relevant to the quality area;
Assist with technical documentation clearance for export products;
Monitor external audits and inspections;
Monitor label approval for packaging in accordance with current regulations;
Maintain departmental organization;
Comply with company policies and standards;
Other duties inherent to the position.
Qualifications and Specific Knowledge:
Education in Quality Management, Pharmacy, Engineering, or related fields.
Mandatory: Quality tools, nonconforming products, document and record control, internal audits, RDC 665:2022, ISO 13485:2016; ISO 9001, knowledge of quality management routines and risk management, fluent English.
Employment Type: CLT
Working Hours: Monday to Friday, from 7:00 AM to 4:48 PM
Location: Cajuru neighborhood - Curitiba - PR
Salary: To be negotiated
Position Type: Full-time, permanent CLT
Compensation: R$2.500,00 - R$2.600,00 per month
Benefits:
* Medical assistance
* Dental assistance
* Commercial agreements and discounts
* Life insurance
* Meal allowance
* Transportation allowance
Experience:
* Quality Management Documentation (Mandatory)
Workplace: On-site