Regulatory Affairs Specialist at 3M

São Paulo, São Paulo, Brazil -

Full Time

Start Date

Immediate

Expiry Date

09 May, 26

Salary

0.0

Posted On

08 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Regulatory Affairs, Medical Devices, English Proficiency, Communication Skills, Organizational Skills, Attention to Detail, Cross-Functional Collaboration, Audit Participation, Global Strategy, Market Access, Cosmetic Regulatory Experience, Microsoft Office Proficiency, Curiosity, Creativity, Compliance, Product Licensing

Industry

Industrial Machinery Manufacturing

Description

3M has a long-standing reputation as a company committed to innovation. We provide the freedom to explore and encourage curiosity and creativity. We gain new insight from diverse thinking, and take risks on new ideas. Here, you can apply your talent in bold ways that matter. Job Description: Regulatory Affairs Specialist Collaborate with Innovative 3Mers Around the World Choosing where to start and grow your career has a major impact on your professional and personal life, so it’s equally important you know that the company that you choose to work at, and its leaders, will support and guide you. With a wide variety of people, global locations, technologies and products, 3M is a place where you can collaborate with other curious, creative 3Mers. The Impact You’ll Make in this Role As a Regulatory Affairs Specialist you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative people around the world. The person hired for this position in the 3M Consumer Healthcare Business within Consumer Business Group will make an impact by: • Serving as Functional Subject Matter Expert • Lead/coordinate medical device and cosmetic regulatory affairs for part of the US designed portfolio • Coordinate communication and compliance globally • Support international requests • Support new product introductions and existing product changes • Conduct global regulatory assessments and partner to determine global strategy • Participate in audits; champion compliance • Support product licenses, establishment licenses, etc • Ensure market access and right to operate Your Skills and Expertise To set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications: • Bachelor’s degree or higher (completed and verified prior to start) from an accredited institution • Experience in Regulatory Affairs in Medical Devices • Advanced English Speaking and Writing Competency Additional qualifications that could help you succeed even further in this role include: • Advanced Degree • Regulatory Affairs Certificate (RAC) • Medical Device Regulatory Affairs experience with FDA • EU Medical Device Regulation experience • Ability to interface with regulatory agencies and support audits • Demonstrated communication skills, must be able to summarize and articulate technical/regulatory information to diverse audiences both verbally and in writing in English • Cosmetic Regulatory Experience • Ability to work cross functionally across a global organization • Excellent organizational skills, attention to detail • Ability to work with different cultures and cross functional teams • Experience leading programs without significant oversite • Proficient in Microsoft Office Tools Work location: • Work location: This role follows an on-site working model, requiring the employee to work at least four days a week at the Sumaré, Brazil site. • Flex hours to accommodate USA team time zone • Travel: May include up to 5% domestic/international • Relocation: Not authorized Supporting Your Well-being 3M offers many programs to help you live your best life – both physically and financially. To ensure competitive pay and benefits, 3M regularly benchmarks with other companies that are comparable in size and scope. Chat with Max For assistance with searching through our current job openings or for more information about all things 3M, visit Max, our virtual recruiting assistant on 3M.com/careers. Grade: T4 Learn more about 3M’s creative solutions to the world’s problems at www.3M.com or on Instagram, Facebook, and LinkedIn @3M. A 3M é um empregador que oferece oportunidades iguais à todos. A 3M não discriminará nenhum candidato baseado em sua raça, cor, idade, religião, gênero, orientação sexual, identidade ou expressão de gênero, nacionalidade ou deficiência. Safety is a core value at 3M. All employees are expected to contribute to a strong Environmental Health and Safety (EHS) culture by following safety policies, identifying hazards, and engaging in continuous improvement. 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. 3M Global Terms of Use and Privacy Statement Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at 3M are conditioned on your acceptance and compliance with these terms. Please access the linked document by clicking here, 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. At 3M we apply science in collaborative ways to improve lives daily as our employees connect with customers all around the world. Learn more about 3M's creative solutions to global challenges at www.3M.com or on Twitter @3M or @3MNews.

Responsibilities

As a Regulatory Affairs Specialist, you will serve as a Functional Subject Matter Expert and lead medical device and cosmetic regulatory affairs for part of the US designed portfolio. You will also coordinate communication and compliance globally and support new product introductions and existing product changes.