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 atwww.abbvie.com. Follow @abbvie onLinkedIn,Facebook,Instagram,XandYouTube.

Responsible for managing and implementing quality compliance programs and measures to ensure AbbVie medicines and ingredients are safe, effective, and of appropriate quality. Initiates and leads high impact, global, cross-functional projects as response to complex large scale external compliance standard updates and changes. Benchmarks and participates in industry interest organizations, representing AbbVies interests, and influences regulation modification and establishment when possible.

Responsibilities:

Owns external compliance standard updates, from identification of the change through assessment and implementation for assigned scope

Manages the assessment and implementation of compliance related changes according to official timelines, acting as the event owner in the corporate Quality Management System

Actively follows up with Subject Matter Experts (SMEs), such as QA and R&D site contacts, as well as Quality COE leads, to ensure the implementation of changes are completed in a timely manner, including initiating the Document Change Control (DCC) process and updating impacted documents

Provides interpretation quality compliance standards to functional areas such as Regulatory, QA, R&D, Manufacturing

Leads the generation of metrics to monitor the performance of compliance

Leads complex cross-functional initiatives or projects to address or implement compliance

Proactively represents AbbVie's interests with applicable external industry interest groups and organizations

Serves as the AbbVie point of contact for external parties related to compliance and communicates to them any comments, questions, or issues from internal SMEs. Leads alignment activities between external and internal stakeholders.

• Bachelors Degree in Chemistry, Pharmacy, Biology, Microbiology, Engineering, or other technical/scientific area required
• 6+ years in quality assurance and/or quality system oversight required.
• Experienced in the use of standard software applications including Office 365
• Strong interpersonal, verbal, and written communication skills, effective facilitation and collaboration with stakeholders (including sites or cross-functional teams)
• High level of competence, confidence, and credibility for interaction with stakeholders
• Proficient organization, planning, and project management skills
• Ability to demonstrate high level of independence and decision making, anticipate program scope and deliverable changes, and effectively communicate issues with management
• Strong analytical skillsets, detailed and quality oriented, and with great judgment and integrity
• Ability to provide strategic direction and support for problem solving
• Must demonstrate effective performance to prevent legal or regulatory vulnerabilities which would result in product recall or governmental seizure for lack of compliance to requirements

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

• The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at the timeofthis posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographic location,andwemay ultimatelypay more or less than the posted range. This range may be modified in thefuture.

• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.

• This job is eligible to participate in our short-term incentiveprograms.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.The amount and availability of anybonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employee remains in the Company's soleandabsolutediscretion unless and until paid andmay be modified at the Companys sole and absolute discretion, consistent withapplicable law.

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, visithttps://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