Quality Assurance Specialist - Medical Devices jobs at 3m in Brazil

The Impact You’ll Make in This Role:

As a Digital Shelf Specialist, you will manage the end-to-end syndication of product content to key e-commerce and channel partners. Your role will be essential in transforming complex product data into complete, accurate, and engaging digital content that supports online sales.

You will:

• Act as a project manager for the full syndication process, from collecting requirements to delivering enriched content.
• Collaborate with internal teams to source, validate, and complete product information.
• Leverage tools like Salsify, SAP Hybris, Adobe Assets, and retailer portals to ensure accurate data distribution.
• Monitor content performance, identify gaps, and continuously improve processes to enhance the digital shelf experience.

Your Skills and Expertise

• Bachelor’s degree (or equivalent) in Marketing, Business, Computer Science, or a related field.
• Experience in marketing, e-commerce or business-to-business (B2B) environments with a focus on product data and digital content.
• Proficiency in English (C2 level or higher), with excellent verbal and written communication skills.

Additional qualifications that could help you succeed even further in this role include:

• Strong project management and customer relationship skills.
• Experience working with GS1 (Global Standards 1) syndication and content distribution standards.
• Ability to interpret complex data requirements and communicate them clearly to technical and non-technical stakeholders.
• Familiarity with enterprise systems such as SAP, SAP Business Intelligence 4 (BI4), Global Enterprise Data Warehouse (GEDW), Celum, and/or other content management systems.
• High affinity for data quality and structured thinking.

Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly.

Please access the linked document by clicking select the country where you are applying for employment, and review. Before submitting your application, you will be asked to confirm your agreement with the terms.

Quality Assurance Specialist - Medical Devices, Sumaré/SP

AsQuality Assurance Specialistyou will play a key role for lead the Quality Management System (QMS) for 3M Medical Devices in accordance with ANVISA Good Manufacturing Practices – RDC 665/2022 (Brazilian Health Regulatory Agency) requirements in Sumaré/SP. In this role you will be ableleverage your broad knowledge and extensive experience to address complex situations and identify opportunities for process improvements. Your expertise will be crucial in maintaining high standards of quality and compliance, driving continuous improvement, and ensuring the successful commercialization of our medical devices in the Brazilian market.

The impact you will make in this role

• Ensure compliance with GoodManufacturing/StoragePractices and standard operating procedures.
• Maintain a robust Quality Management System (QMS) for 3M medical devices, aligned with local regulatory requirements and corporate guidelines. Ensure proper updates are made in alignment with area focal points and process releases.
• Ensure that global 3M Medical Devices policies impacting the Quality System are appropriately addressed by relevant QMS procedures.
• Oversee Corrective and Preventive Actions (CAPA).
• Lead internal and external audits.
• Ensure the correct application of the Change Management Process.
• Implement new standards, laws, requirements for the QMS (or customer)
• Ensure the training of new employees.
• Manage risk effectively.
• Provide technical advice to the legal representative regarding the characteristics of medical devices and ensure compliance with current regulations.

Your Skills and Expertise

To set you up for success in this role from day one, 3M is looking for candidates who must have the following qualifications:

• Bachelor’s degree in Pharmacy, Biology, Engineering, or a related field.
• Experience in a similar position with medical devices
• Advanced knowledge of quality management systems and post-marketing product surveillance activities.
• Knowledge of ANVISA quality requirements for medical devices, including good distribution and storage practices within the country.
• Knowledge of ISO 13485 requirements. Lead Auditor Certification is a differentiator.
• Ability to work cross-functionally on multiple projects, solve problems, and communicate issues effectively.
• Ability to execute project/program tasks with general supervision and minimal guidance.
• Fluency in English.

Additional qualifications that could help you succeed even further in this role include:

• Proficiency in Spanish.

Supporting Your Well-being

Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly.

Please access the linked document by clicking select the country where you are applying for employment, and review. Before submitting your application, you will be asked to confirm your agreement with the terms.