Senior Manager, Regulatory Affairs CMC (Onsite Hybrid) - AbbVie
North Chicago, IL
About the Job
We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio
For more information about AbbVie, please visit us at www.abbvie.com
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Job Description The Senior Manager Regulatory Affairs, Chemistry, Manufacturing and Controls (CMC) works with internal and external partners to deliver products to patients
Prepares CMC regulatory strategies that enable first pass approvals
Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new marketing applications and supplements/variations
Builds and maintains relationships within the Regulatory Affairs functional areas, Operations and Research & Development (R&D) organizations
Represents CMC on teams such as product development, Global Regulatory Product Teams and Operations brand teams to negotiate, influence, and provide strategic advice
Responsibilities: + Prepares CMC regulatory product strategies
Prepares and manages regulatory submissions, including new applications and amendments, renewals annual reports, supplements and variations 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
+ Responds to global regulatory information requests
+ Develops strategies for CMC agency meetings, manages preparation for agency meetings, and manages content of pre-meeting submissions
+ Manages products and change control with an understanding of regulations and company policies and procedures
Analyzes and approves manufacturing change requests
+ Represents CMC regulatory affairs on teams such as the product development, Global Regulatory Product Teams and Operations brand teams, for assigned projects; negotiates with and influences team members with support of management to maximize chances for first pass approval of regulatory submissions
+ Stays abreast of regulatory procedures and changes in regulatory climate
Analyzes legislation, regulation and guidance, provides analysis to the organization + Develops, implements, and documents policies and procedures within the regulatory affairs department
Participates in initiatives internal to RA CMC
Represents CMC regulatory affairs on project initiatives with other functional areas to drive efficiencies across the company
Qualifications + Required Education: Bachelor’s Degree in Pharmacy, Chemistry, Biology or Pharmacology, Engineering or related subject
+ Preferred Education: Relevant advanced degree preferred
Certification a plus
+ Required Experience: 8 years pharmaceutical experience + Preferred Experience: 10 years pharmaceutical experience including 5-plus years in regulatory affairs or 5-plus years in Discovery, R&D, or Manufacturing
+ Experience developing and implementing successful global regulatory strategies
+ Experience working in a complex and matrix environment
+ Strong oral and written communication skills
+ Note: Higher education may compensate for years of experience Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: + The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position
Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range
This range may be modified in the future. + 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 short-term incentive programs
+ This job is eligible to participate in our long-term incentive programs Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable
The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion
It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status
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