Responsible for quality of assigned new product introduction programs to ensure business objectives are met with regards to on time deliverables of program development while assuring compliance with local, divisional, and corporate policies and external agency regulations worldwide. Products include regulatory starting materials, Active Pharmaceutical Ingredients (API), and Drug Products produced by AbbVie plants or by third-party manufacturers, in Licensing relationships, or Co-Marketing relationships. Develop in concert with the appropriate regulatory strategies set forth by the governance processes. 

AbbVie Operations Quality Assurance is seeking a Product Quality Manager to lead quality deliverables for late-stage development and commercialization of Peptides, from registration through commercialization. We are seeking a highly motivated candidate with a proven track record of accomplishment in the field of peptide manufacturing development, to work in a multi-functional team environment at our North Chicago, IL location.

• Leads the development and implementation of global Product Quality Assurance strategy to support New Product Introduction (NPI) programs for the end-to-end commercial supply chain both at AbbVie plants as well as contract manufacturing facilities. Drives implementation of the Product Transfer Process. Primary driver for product quality risk management and compliance aspects of product development.   

• Acts as global quality lead to support regulatory submission by developing, reviewing and approving relevant module 3 documents. Works with Regulatory Affairs and coordinates with GMP manufacturing sites to prepare submissions and provides responses to agency submission deficiencies /questions in a timely manner.  Leads and manages pre-approval inspection readiness for the NPI programs.   Ensures regulatory approvals are obtained with no delays to market entries.

• Leads the selection of external manufacturing partners from Quality for NPI programs.  Leads the quality partner assessment and up skilling of the partners to meet AbbVie Operations’ expectation.  Partners with Quality Assurance audit team to qualify external manufacturing partners.   

• Communicates and negotiates with external manufacturing partner quality organization to maintain a consistent level of quality.  Provides quality oversight to maintain partner qualification for development and commercialization.   

• Supports the management of exception documents and Corrective and Preventive Actions. Coordinates input from technical groups to determine root cause and implement appropriate actions.  Serves as global quality representative at the change review board to drive/support global change plans needed for NPI programs. 

• Establishes and maintains relationships and open communication with cross functional groups to maintain roles and responsibilities and provides guidance on quality concerns.  Drives continuous improvement for NPI programs.