Are you passionate about ensuring the safety and compliance of products in the market? Do you thrive in a fast-paced environment and enjoy staying up-to-date with changing regulations? If so, we have an exciting opportunity for you to join our team as a Regulatory Affairs Specialist at 3M. As a global leader in innovation and technology, 3M is committed to providing safe and effective products to our customers. To support this mission, we are seeking a highly skilled and detail-oriented individual to navigate complex regulatory requirements and drive our products to market. If you have a strong background in regulatory affairs and a desire to make a positive impact, we encourage you to apply today.
- Monitor and interpret changing regulations and standards related to the safety and compliance of products in the market.
- Develop and implement strategies to ensure 3M products meet all necessary regulatory requirements.
- Collaborate with cross-functional teams to ensure timely and accurate submission of regulatory documents and materials.
- Conduct thorough reviews of product labeling, packaging, and promotional materials to ensure compliance with regulatory standards.
- Maintain up-to-date knowledge of industry standards and best practices to inform product development and regulatory strategy.
- Communicate with regulatory agencies and respond to inquiries or requests for information.
- Develop and maintain relationships with key stakeholders, both internal and external, to support regulatory compliance and approvals.
- Conduct audits and assessments to ensure ongoing compliance with regulatory requirements.
- Participate in product development and launch activities to ensure all regulatory requirements are met.
- Prepare and submit necessary documentation for regulatory approvals and maintain accurate records.
- Monitor and investigate any potential safety issues or complaints related to products and take appropriate actions to address them.
- Provide guidance and support to other team members on regulatory compliance matters.
- Proactively identify and mitigate any potential risks related to regulatory compliance.
- Participate in industry conferences and events to stay informed and share knowledge and best practices.
- Continuously evaluate and improve internal processes and procedures related to regulatory affairs.
A Bachelor's Degree In A Relevant Field Such As Science, Engineering, Or Healthcare.
At Least 3 Years Of Experience In Regulatory Affairs, Preferably Within The Medical Device Or Pharmaceutical Industry.
Strong Knowledge Of Fda Regulations And International Regulatory Requirements.
Excellent Communication And Interpersonal Skills, With The Ability To Collaborate With Cross-Functional Teams.
Proven Track Record Of Successfully Managing Regulatory Submissions And Obtaining Approvals For New Products.
Quality Assurance
Project Management
Quality
Technical Writing
Global regulations
Government Relations
Product Testing
Compliance Management
Risk assessment
Regulatory analysis
Product Registration
Labeling Expertise
Communication
Conflict Resolution
Leadership
Time management
creativity
Attention to detail
Teamwork
Active Listening
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Regulatory Affairs Specialist in Maplewood, MN, USA is $60,000 - $100,000. This may vary depending on the specific company, experience level, and other factors.
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The 3M Company is an American multinational conglomerate corporation operating in the fields of industry, worker safety, US health care, and consumer goods.

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