Lead supplier quality activities for a high-throughput cGMP manufacturing site: manage supplier investigations, change control, CAPA, supplier qualification, audits, and cross-functional projects while ensuring compliance and stakeholder communication.
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 DescriptionCompliance
- 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
- 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
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
AbbVie Singapore, Singapore, SGP Office
9 North Buona Vista Drive, Singapore, Singapore, Singapore, 138588
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