Global Labelling Operations Manager - Immunology

Company DescriptionAbbVie'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 at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job DescriptionJoin our Collaborative Global Labeling Team!The Global Labeling Operations Manager role (based in Lake County) is your chance to be part of a dynamic and inclusive team of GLO Managers. Reporting into the Section Manager, Global Labeling Operations, you'll work on the end-to-end labeling process of a diverse product portfolio, as part of a global strategic team. This exciting opportunity offers excellent growth potential. We offer a culturally inclusive environment that empowers you to reach your full potential!Please note that grades may differ from country to country. Qualifications

Bachelor’s degree in science, Engineering, Business or Supply Chain and minimum of 5 years' experience in Operations, Regulatory or Quality environment.

Equivalent successful industry experience (minimum 4 years) can be considered (see below for guidance).

Minimum of 4 - 6 years combined experience from totals: Quality/Regulatory – 2 years, Operations – 2 years, Pharmaceutical/Device Regulations – 2 years.

Experience and Skills

Proficiency in English (both written and oral)

Experience working effectively across different cultures, multiple functional areas and in complex matrix environments

Excellent written and oral communication skills with all levels of management and personnel

Demonstrated success in negotiating and problem-solving skills

Strong interpersonal and organizational skills

Excellent leadership skills and a proven ability to drive cross functional collaboration.

Understanding of Regulatory, Quality and Supply Chain aspects of labeling and impact of non-compliance

Knowledge of applicable regulations and standards affecting Pharmaceutical, Device, Device/Combo Products, specifically regulations and standards affecting the Packaging and Labeling Quality System

Strong project management skills including stakeholder management.

Self-motivated and strong focus on details and accuracy.

Additional InformationAbbVie 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 AbbVie’s 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, 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