Senior Supplier Quality Manager
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Shanghai, Shanghai
- Operations
- On-Site
- Full-time
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.
The Supplier Quality Manager performs a key function in the Quality relationship building, QA oversight and issue resolution with suppliers/TPMs in support of AbbVie’s commercial and pipeline supply chains. The individual will work collaboratively across Technical, Manufacturing, Quality, Product Support and Research and Development teams in direct support of supplier management. In this role, the supplier quality manager is the primary quality contact to specific strategic supplier partners. This individual will be responsible for assuring investigations, CAPAs, change management, and audit readiness meet agency and Abbvie expectations. The individual will provide on site supplier support and upskilling to ensure the key suppliers are improving quality performance and ready for agency inspections.
- Build and maintain strong relationships with regional suppliers to support AbbVie’s pipeline and on market product portfolio.
- Assure authenticity of commercial and pipeline product supply chains by performing on-site visits with suppliers to verify business operations and potential areas of improvement.
- Conduct quality business reviews with identified suppliers to assure customer interface of necessary communication to support new product launches.
- Drive remediation efforts with suppliers including PAI readiness and issue resolution.
- Leverage technical expertise to assist in issue resolution at suppliers including investigation review and CAPA planning.
- Ensure all quality expectations related to suppliers in New Product Introductions (NPI) are met.
- Participate in process validation campaigns at Suppliers and provide validation overviews to Quality Business unit.
- Execute audit readiness and upskilling at suppliers in preparation to external and internal quality audits
- Coordinate remediation efforts when poor audit performance is identified at EU suppliers.
- Bachelor's degree, preferably in Chemistry or Engineering
- 15+ years of overall experience in Quality and or Manufacturing with specialist or supervisor experience
- Good problem solving and analytical skills
- Good verbal and written communication skills in English
- Good interpersonal relations / communications skills
- Knowledge of quality / compliance management as well as regulations and standards affecting API, Bulk Drug or Finished goods manufacturing.
- Prior experience in analytical labs, manufacturing environment and managing supplier compliance desired.
- Able to travel up to 30 – 50 % of the time.
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.
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Pay Range: $
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Where We Work
Role is exclusively performed at a site or office and onsite presence is required. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.