Regulatory Affairs Manager

3 weeks ago

Raleigh, North Carolina, United States Michael Page Full time
Room For Growth Pays up to $155k About Our Client

Join a leading company in the CPG industry, committed to innovation, quality, and compliance.

Job Description

Regulatory Compliance: Ensure all CPG products comply with local, national, and international regulations. Stay up-to-date with evolving regulatory requirements and assess their impact on current and future products.Regulatory Submissions: Prepare, review, and submit regulatory documents to relevant authorities, including product registrations, amendments, and renewals. Manage interactions with regulatory agencies to facilitate the approval process.Labeling and Documentation: Ensure product labeling, packaging, and advertising materials are compliant with regulatory standards. Maintain accurate and up-to-date regulatory documentation, including dossiers, technical files, and regulatory submissions.Cross-functional Collaboration: Work closely with R&D, Quality Assurance, Legal, and Marketing teams to ensure regulatory compliance across all functions. Provide regulatory guidance during the product development process and support cross-functional teams in understanding regulatory requirements.Risk Management: Identify potential regulatory risks and develop strategies to mitigate them. Lead the development and implementation of regulatory policies and procedures within the company.Regulatory Intelligence: Monitor and analyze changes in CPG regulations, including FDA, EU TPD, and other relevant global standards. Provide regular updates to senior management and advise on the implications for the business.Training and Education: Develop and deliver training programs on regulatory requirements and best practices for internal teams. Ensure continuous improvement in regulatory knowledge and awareness across the organization.External Relations: Build and maintain relationships with regulatory authorities, industry associations, and other external stakeholders. Represent the company in regulatory forums and contribute to industry discussions on regulatory issues.

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.

The Successful Applicant

Bachelor's degree in Regulatory Affairs, Life Sciences, Chemistry, or a related field. Advanced degree preferred.Minimum of 5-7 years of experience in regulatory affairs within an FDA regulated industry or a closely related field.In-depth knowledge of global CPG regulations, including FDA, EU TPD, and other relevant standards.Strong experience in regulatory submissions and interactions with regulatory agencies.Excellent communication skills, with the ability to effectively convey complex regulatory information to internal and external stakeholders.Proven ability to manage multiple projects and priorities in a fast-paced environment.Detail-oriented with strong analytical and problem-solving skills.Ability to work independently and as part of a cross-functional team.Familiarity with electronic nicotine delivery systems (ENDS) and related regulatory requirements.Knowledge of regulatory software and database management tools.

What's on Offer Salary up to $155k, plus bonusComprehensive health and wellness benefitsEmployee Stock Purchasing ProgramProfessional development opportunitiesCollaborative and inclusive work environmentMonthly travel

This role is a hybrid opportunity and will be on-site 50% of the time during a two week period.

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