Senior Manager, Regulatory Affairs
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Maidenhead, ENGLAND
- Research & Development
- Hybrid
- Full-time
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
To expedite approval of all regulatory submissions for company products in accordance with agreed business priorities and to provide strategic regulatory advice of all matters relevant to the business.
Responsibilities
- Develop and implement overall regulatory strategy for assigned region to ensure local best practice to meet global requirements.
- Develop external environment strategy to drive business goals on velocity of registration.
- Monitor regulatory environment to ensure awareness and communication both locally and globally on technical issues, best practice and environmental trends for registration.
- Minimize risk to business operations by ensuring compliance of all activities to regulatory standards.
- Build and maintain strategic relationships with relevant Head Office and Regional personnel to maximize data and information exchange for business planning.
- Direct regulatory staff to ensure their professional development and achieve company objectives in the area.
- University Degree in pharmacy or appropriate scientific discipline.
- Minimum 10 years regulatory experience in industry.
- Excellent leadership skills.
- Excellent communication skills at all levels.
- Excellent influencing skills
- Stakeholder management
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.
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https://www.abbvie.com/join-us/reasonable-accommodations.html
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Pay Range: $
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Where We Work
Role is primarily site- or office-based but can occasionally be performed remotely. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.