Global Supply Chain QA Project Manager

Purpose

Leads global projects and/or programs which support various strategic initiatives within the Quality System. Responsibilities include all aspects of endtoend project and/or program management within specific area of expertise. Actively collaborates with manufacturing sites external manufacturing regulatory supply chain product quality compliance and other global functions in order to successfully deliver objectives. Provides regular updates and recommendations to senior leadership in order to drive an effective Quality System.

Responsibilities

• Develops project timelines deliverables conducts research analysis monitors project status and provides expertise for global projects/programs supporting strategic global Quality initiatives
• Actively collaborates with crossfunctional team to complete project milestones per established timeline. Leads meetings with crossfunctional partners.
• Utilizes expertise within GxP to review various types of content such as external regulations or governing documents and provide recommendations.
• May create and manage project/program tasks within quality software system.
• Builds and maintains collaborative partnerships with crossfunctional stakeholders at all levels of the organization to understand business needs and incorporate these into assigned project/program decisions.
• Manages endtoend lifecycle of project/program including driving team accountability addressing project risks driving effective decision making.
• Creates and continuously improves meaningful metrics to demonstrate effectiveness and performance of assigned project/program.
• Monitors changes in external regulations and project manages changes to internal processes accordingly.
• Effectively delivers project or program status updates and recommendations for future strategic initiatives to senior leadership

Qualifications :

Qualifications

• Bachelors degree in Science/Engineering/Business Management or equivalent technical work experience
• 5 years of relevant Quality experience in a GMP pharmaceutical biologics and/or medical device manufacturing environment
• Strong understanding of cGxPs regulatory inspections regulatory documents global regulations and standards
• Experience in Project Management and leading crossfunctional project teams with technical professionals in a global and/or complex matrixed organization
• Strong oral and written communication interpersonal time management influence and problemsolving skills
• Proficient in the use of standard software applications including Office 365

Additional Information :

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: 

• The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location and we may ultimately pay more or less than the posted range. This range may be modified in the future.

• We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees.

• This job is eligible to participate in our shortterm incentive programs. 

Note: No amount of pay is considered to be wages or compensation until such amount is earned vested and determinable. The amount and availability of any bonus commission incentive benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Companys sole and absolute discretion consistent with applicable law. 

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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Work :

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