Company 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 X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

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.

Responsible for the management and oversight of a large team or multiple teams including hiring, setting performance expectations, providing performance feedback, development of staff and handling of personnel issues. Ensuring adequate resources and appropriate training to effectively support and meet changing business and compliance needs.Establish training requirements and maintenance of a diverse and agile cross trained and effective team to ensure business continuity and compliance. Lead and oversee support activities related to product actions in the affiliate. Assure key metrics are being monitored and met to ensure compliance and to drive continuous improvement including review of procedures and process to identify areas of opportunity.Partner with stakeholders across the enterprise to gain a better understanding of processes external to QA to determine best steps forward.Responsible for partnering and overseeing support activities related to product actions in the affiliate. Oversee coordination and investigation of key quality systems (ie. CAPA, product complaints) ensuring KPIs are being met.Perform assessments to determine compliance to processes, procedures and regulations to identify potential gaps and mitigate and implement improvements. Support internal and external quality inspections and audits including reporting, response to observations and tracking of action plans.Quality management of supplier qualification program including performance monitoring for key suppliers, QTA management and assessments.Provide guidance and oversight for all activities governed by Good Storage and Distribution Practices including monitoring of controlled temperature and cold chain shipments.Represent affiliate QA in regional, global and cross functional teams, projects and programs, as appropriate.In addition to the previous responsibilities and in agreement with the local Law, as a Sanitary Responsible, is responsible to ensure compliance with the Law and other applicable provisions, in accordance with local Good Manufacturing Practices and General Health Law, as well as attend the verification visits made by the health authorities and authorized third parties, responding in a timely manner to any observation and / or requirement requested by the Health Authority.As a Sanitary Responsible, is responsible for the quality of the product, together with the highest authority of the organization and is responsible for ensuring that a Quality Management System is in place.
Qualifications

Bachelor’s Degree in Chemistry, Pharmacy, Biology, 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)

Additional Information

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.

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:

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