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

We are now recruiting a Senior Manager, Product Quality Neurotoxin for our diverse Team. 

Reporting to the Product Quality Director, you will be responsible for quality of assigned products and near commercial Neurotoxin Pipeline Products to ensure business objectives are met with regards to on time delivery of product while assuring compliance to local, divisional, and corporate policies and external agency regulations worldwide. Products under your remit include regulatory starting materials, Active Pharmaceutical Ingredients (API), Intermediates, and Drug Products produced by AbbVie plants or by third-party manufacturers, In Licensing relationships, or Co-Marketing relationships. You will act as the primary quality representative for the global supply chain pertaining to manufacturing business relationships and build and maintain relationships with IME Operations, Supplier Quality Management, Commercial QA, Global Supply Chain, Domestic and International AbbVie Plants and Affiliates, Regulatory Affairs, R&D, and S&T to ensure alignment on strategic initiatives.

Are you intrigued? Do you want to learn more?
A snapshot of your key responsibilities would be:

Direct cross-functional team member to achieve on-time quality deliverables, high customer value, and high quality product to meet patient demands. Ensures delivery of quality elements needed to facilitate lifecycle management that provide products directly to distribution centers, or to AbbVie domestic and International plants for further packaging and/or testing.

Product Quality contact for Post Marketing Quality Assurance with end-to-end understanding and management of customer complaints across the various nodes within AbbVie. Routine complaint trending and analysis.
Product Quality Assurance contact for Global Change control system, including Quality Assessment of changes, and oversight of all global changes. Chair of the gCRB.
Develops Global Product Quality Assurance strategies and implements agreed strategies to support relevant products produced at AbbVie plants.
Reviews, approves and opens necessary Quality System Management records in a timely manner to maintain a high level of product compliance. Supports the management of exception documents and CAPA where relevant.
Makes key decisions on product quality, compliance and regulatory conformance issues and elevates medium and high-risk events to AbbVie management.
Ensures alignment of Quality and Technical Agreements with the legal contracts and that the commitments of the same agreements are being fulfilled.
Core team member or lead of strategic programs; including Brand Teams, New Product
Introductions, Product Transfers, Global Strategic Initiatives.
Influences the decision making process to ensure quality requirements are included when improvement initiatives take place.

Qualifications

Education & Experience 

Bachelor’s Degree in relevant Life Science or other Technical area required.
Technical or Analytical background required for problem resolution with technical, quality, product and or engineering related issues.
Minimum of 5+ in Quality Assurance Operations Management, Regulatory, Operations, or Technical Support in a pharmaceutical setting. Required regulatory inspection experience with direct interaction with regulatory inspectors. Direct Plant experience in a pharmaceutical setting with a minimum of 5 years preferred.
Knowledge and a comprehensive understanding of some biological and/or pharmaceuticals.

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

Recruitment Fraud Alert

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AbbVie will never request sensitive personal information (such as bank account details, social security numbers, or payment of any kind) during the recruitment process.
If you suspect you have received a fraudulent offer or communication claiming to be from AbbVie, please do not respond, open any attachments, or click on any hyperlinks.

If you have any questions or concerns regarding the authenticity of a communication alleged to have been made by or on behalf of AbbVie, please contact us immediately.

Protect yourself by verifying job offers and communications. Your safety is important to us.

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.