Description
Job Summary:
Professional responsible for developing and controlling operational procedures, supporting deviation investigations, and auditing quality documents.
Key Highlights:
1. Essential support in quality management and regulatory compliance.
2. Opportunity to develop skills in root cause analysis and action plans.
3. Collaboration in internal, external, and regulatory audits.
**Job Description:**
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\- Develop, review, and control operational procedures, forms, and work instructions; \- Support the opening and recording of non-conformities and change control; \- Assist in deviation investigations using root cause analysis tools; \- Assist in tracking action plans; \- Perform document verification of production orders, production records, and other Quality Management System documents; \- Monitor outstanding documentation issues with involved departments; \- Support internal, external, and regulatory audits.
**Mandatory Requirements:**
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Currently pursuing a Bachelor's degree in Pharmacy, Chemistry, Engineering, Biomedicine, Administration, or related fields.
6 months of experience
**Desirable Requirements:**
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* Organization;
* Good communication skills;
* Proactivity;
* Microsoft Office Suite.
**Employment Type:**
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CLT (Consolidation of Labor Laws)
**PwD (Persons with Disabilities):**
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NOT APPLICABLE
**Benefits:**
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Meal Voucher | Unimed Health Plan | Full Transportation Benefit | Life Insurance | Profit Sharing (PLR) | Attendance Program | Performance Bonus
**Work Location:**
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AIRELA FARMACEUTICA INDUSTRIA LTDA
**Working Hours:**
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7:30 AM to 5:18 PM