Prepares device regulatory product strategies with limited supervision.
Prepares regulatory submissions, including new applications and amendments, renewals, annual reports, supplements and variations under limited supervision and responds to regulatory information.
Analyzes and interprets information that impacts regulatory decisions. Seeks expert advice and technical support as required for strategies and submissions
Reviews and revises regulatory submissions to effectively present data and strategy to regulatory agencies under limited supervision
Develops strategies for device meetings, manages preparation for agency meetings and manages content of pre-meeting submissions under limited supervision
Manages products and change control with an understanding of regulations and company policies and procedures with limited supervision. Analyzes and approves manufacturing change requests with limited supervision.
Stays abreast of regulatory procedures and changes in the regulatory climate. Analyzes legislation, regulation and guidance and provides analysis to the organization under limited supervision
Develops, implements, and documents policies and procedures within the regulatory affairs department under supervision of manager. Participates in initiatives internal to RA.
Significant Work Activities: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required
Required Education: Bachelor's degree in pharmacy, biology, chemistry, pharmacology, engineering or related subject
Required Experience: 6 years pharmaceutical or industry related experience. 3-5 years in quality systems or cross-functional project management. Preferred Experience: 6 years pharmaceutical experience including 5 years in regulatory affairs or 5 years in Discovery, R&D, or Manufacturing
Knowledge of the ISO/CE process and global product registration process. Experience with eCTD tools and EDMS applications.
Knowledge of global regulatory intelligence and policy to analyze external regulatory trends and internal compliance trends to drive proactive initiatives to ensure compliance for Device/Combination Products.
Understanding of device/combination product regulations
Experience working in a complex and matrix environment
Strong oral and written communication skills
Ability to travel up to [15] % of time
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our long-term incentive programs.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Ric
Benefits
Dental insuranceVision insurance401(k)Paid time offPerformance bonus
Additional Information
The Manager, Regulatory Affairs Device , works with internal and external partners to deliver products to patients. Prepares device regulatory strategies that enable first pass approvals under limited management supervision. Develops and manages content strategy for global regulatory submissions, including INDs/CTAs and amendments, new market applications and supplements/variations with limited management supervision. Build and maintain relationships within the Regulatory Affairs functional areas and the Operations and Research & Development (R&D) organizations. Represents RA Device on product development and life-cycle management teams to negotiate, influence, and provide strategic advice to peers in RA, R&D, and Operations.
Abbvie · North Chicago, IL