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 X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
The Affiliate Sr. QA Manager is responsible for providing leadership and oversight of Quality Compliance matters at an operational and regulatory complex commercial entity or multiple commercial entities in support of the quality system requirements associated with: pharmaceutical products, medical devices, combination products and biologics. Specific areas include Storage and Distribution, Product Complaints, potential quality events/product shortage execution, Supplier Controls, Product Quality Review, Risk Management, Agency inspections/internal audits, Lab Controls, CAPA, and overall Quality Manual requirements. This position will ensure that all product, process, or system related quality activities supporting the business from receipt through shipment of final product are in compliance with Corporate, governmental, and local regulations.
Responsible for the integration and support of quality regulations: drug, biologics, device and/or combination products driving the design of effective quality systems, procedures and/or processes within cross functional teams to ensure compliance as well as efficiency throughout our quality systems.
Bachelor’s Degree in Chemistry, Pharmacy, Biology, or other technical/scientific area.
Minimum of 10 years experience in quality assurance, quality control, operations, regulatory or relevant experience. Min 5 years Management experience.
Knowledge and familiarity with product, process, and both internal and external customer requirements and regulations.
Knowledge of QA systems and GxP compliance requirements including regulations and standards affecting device, biologics and pharmaceutical products.
Strong influencing, motivational, interpersonal and relationship building skills with staff and at all levels.
Ability to make operational and business decisions with minimal direction.
Excellent written and oral communication skills. Proficiency in English.
Ability to think strategically and enterprise wide to ensure compliance and business needs are met or exceeded.
Negotiation skills, effective collaboration and ability to anticipate needs and requirements, managing matrix teams.
Strong computer skills and knowledge of enterprise systems such as SolTraqs, Attache and Attache Pro.
Knowledge of the Local Sanitary Regulation (Good Manufacturing Practices and Sanitary Regulation as a Sanitary Responsible).
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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