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

Compliance

Responsible for medium risk investigations arising from materials nonconformity with cross functional team
Responsible for medium risk supplier change control with cross functional team
Manage performance measurements of the Supplier Quality Management business processes
Accountable for the site approved Supplier Listing is compliance with cGMP requirement
Accountable for Site Supplier qualification Program
Responsible for Site CAPA systems and monitoring program
Ensure timely resolution of site supplier quality issues (such as deviations), audit assessments and subsequent follow-up actions
Ensure compliance with applicable AbbVie policies, processes and procedures, contributing to the execution of strategies and oversight of Supplier Quality programs
Ensure timely execution for all supplier related quality activities to the high throughput multi products plants with 24/7 operations while maintaining customer satisfaction service level
Maintain high levels of Customer satisfaction by positively managing internal and external relationships
Site's key representative for global COE forums and responsible for ensuring that information is cascaded timely and accurately to relevant stakeholders by driving actions/communication as required
Promote and follow safety work practices in the workplace

Operational Excellence - Project/New Product Introduction

Manage global supplier quality team initiatives or other site improvement projects, e.g., New Product Introduction.
Manage Global CAPA system improvement initiatives, e.g., One Track implementation.
Support cross functional projects where necessary

Qualifications

Minimum 6 years relevant work experience in cGMP Biotechnology/Pharmaceutical manufacturing industry is preferred.
Knowledge in Supplier Quality Management and regulations is preferred.
Experience in SAP and TrackWise are preferred
Effective communicator with experience with internal and external stakeholders is required.
Good Problem-Solving skills is required
Highly Motivated, Independent, Organized and Growth mindset.
Able to be a team player and collaborate with different departments and all levels of the organization
Agile and able to respond to business urgent requests
Microsoft office skills

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

Senior Supplier Quality Assurance Specialist