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Senior Manager, Regulatory Affairs
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AbbVie

Senior Manager, Regulatory Affairs

Onsite Maidenhead, United Kingdom Full Time
Posted 5 hours ago
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powertofly approved What AbbVie Has to Offer:

Our work can—and does—have a tangible, lasting impact on millions of people. But it’s not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.

Job Details


Company Description

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.


Job Description

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.

Qualifications

  • 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

Additional Information

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 Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Company Details
AbbVie
 Chicago, IL, United States
Work at AbbVie

Together, we break through We believe the paths we take to achieving our breakthroughs matter. At AbbVie, every one of our 50,000 employees is a... Read more

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