Global Supply Chain QA Project Manager

Company Description

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 immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com. Follow @abbvie onX,Facebook,Instagram,YouTube,LinkedInandTik Tok.

Job Description

Purpose

Leads global projects and/or programs which support various strategic initiatives within the Quality System. Responsibilities include all aspects of end-to-end 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 cross-functional team to complete project milestones per established timeline. Leads meetings with cross-functional 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 cross-functional stakeholders at all levels of the organization to understand business needs and incorporate these into assigned project/program decisions.
• Manages end-to-end 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 cross-functional project teams with technical professionals in a global and/or complex, matrixed organization
• Strong oral and written communication, interpersonal, time management, influence, and problem-solving 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 ingood faith it will pay for this role at the time of this posting based on the job grade for this position. Individualcompensation paid within this range will depend on many factors including geographic location, and we may ultimatelypay 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/visioninsurance and 401(k) to eligible employees.
• This job is eligible to participate in our short-term incentive programs.
  
  
  

Note: No amount of payis considered to bewages 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 benefitsthat are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid andmay 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, serving our community and embracing diversity and inclusion. It is AbbVies policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

US & Puerto Rico only - to learn more, visithttps://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