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Form of workJob Description
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 – 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. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description
The Senior Associate II of QA Regulatory will provide leadership and direction to the Quality Function within Operations. The primary responsibility is to ensure the effective implementation of Quality functions within their area, which encompasses Product Quality Assurance, Validation, Training, Regulatory Compliance, Quality Planning, Product Quality, and strategic initiatives. It is expected that the Sr. Quality Associate II will maintain superior quality standards while prioritizing efficiency in all aspects of their job. Don't miss the chance to join our team and demonstrate your expertise in the field of Quality Assurance. Take the next step in your career and apply today.
Responsibilities:
- Leads and influences peers and colleagues within the scope of their work.
- Responsible for various aspects of quality assurance related to products produced at the plant.
- Responsible for the effective organization, administration, and training within their functional area.
- Independently troubleshoot and resolve quality compliance issues.
- Provides regulatory and technical guidance to departments.
- Communicates with Management for Product Quality Review, Quality Initiatives, reports/memo, etc.
- Responsible for quality decisions related to their functional area to ensure compliance with AbbVie Quality Systems and cGMPs.
- Bachelor’s Degree required; preferably in Physical or Life Sciences, Pharmacy, or Engineering
- 8+ years of combined experience in Manufacturing, QA, RD in pharmaceutical, biologics, device or chemical industry
- Must be familiar with use of electronic document management and laboratory information management.
- Must also be familiar with Quality Systems as well as cGMP and other regulatory requirements.
- Strong communication Skills, both verbal and written
Additional Information
AbbVie 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.
