Manages supplier quality activities for pharmaceutical manufacturing, including low-risk investigations, supplier change controls, CAPA monitoring, audit follow-up, deviations, and quality performance metrics. Supports supplier quality initiatives, new product introductions, site improvement projects, and cross-functional collaboration while ensuring cGMP compliance and timely service across high-throughput manufacturing operations.
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
- Manage low risk investigations arising from materials nonconformity with cross functional team
- Manage low risk supplier change control with cross functional team
- Support performance measurements of the Supplier Quality Management business processes
- Manage Site CAPA systems and support monitoring program
- Coordinate 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
- Support and administration are provided timely 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
- Promote and follow safety work practices in the workplace
- Any other tasks as and when assigned by the Supplier Quality Supervisor
Operational Excellence - Project/New Product Introduction
- Support global supplier quality team initiatives or other site improvement projects e.g. New Product Introduction
- Support cross functional projects where necessary
- Bachelor’s degree in sciences (e.g. Biology, Chemistry), Pharmacy, or Engineering Degree or equivalent
- Minimum 2 years relevant work experience in cGMP Biotechnology/Pharmaceutical manufacturing industry is preferred.
- Knowledge in Supplier Quality Management and regulations is preferred.
- Experience in SAP, Trackwise are preferred
- Good communicator with experience with internal stakeholders 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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