Description
Job Summary:
Responsible for ensuring compliance with Good Manufacturing Practices (GMP), managing technical documentation, and qualifying suppliers and personnel.
Key Highlights:
1. Technical documentation and report management
2. Supplier and service provider qualification
3. Training of new employees
Perform duties related to adherence to Good Manufacturing Practices, release of finished products for sale, management, updating, and archiving of technical documentation, reports, licenses, and other related items; verify process compliance; train new employees; and qualify suppliers and service providers in accordance with quality and safety technical standards and procedures.
Base Salary: R$ 3.700,00 per month
Meal Allowance: R$ 300,00 \- no payroll deduction;
Lunch Voucher: R$ 27,50
Transportation Voucher: 6% payroll deduction
Equipped cafeteria with refrigerator and microwave;
Coffee break hours;
Unimed Health Plan
Tuition Assistance
Day Off
Requirements: Completed Bachelor's degree in Pharmacy, Chemical Engineering, or related fields.
Desirable: Specialization in Quality Management, Postgraduate degree, or MBA in related fields.
Certifications: Lead Auditor, Yellow Belt (Lean Manufacturing)
Language: Basic English
Working Hours:
Monday to Thursday: 07:30 AM to 5:30 PM (1-hour break)
Friday: 07:30 AM to 4:30 PM (1-hour break).
Job Type: Full-time, Permanent CLT contract
Compensation: Starting at R$3.700,00 per month
Benefits:
* Fuel allowance
* Education allowance
* Commercial partnership agreements and discounts
* Free parking
* Meal voucher
* Transportation voucher
Education:
* Completed higher education (Mandatory)
Experience:
* Quality assurance (Mandatory)
License/Certification:
* Lead Auditor, Yellow Belt (Lean Manufacturing) (Mandatory)
Work Location: On-site