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 at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Purpose Statement: 

Support all API manufacturing activities to deliver to the business production plan, while meeting quality and safety compliance. Identify and drive production productivity improvement through yield improvement, waste and cycle-time reduction.

Major Responsibilities:

• Accountable for the continuous improvement activities/initiative for the manufacturing department.
• Develop and enhance capacity model, implement programs and reporting to improve production efficiency.
• Liaise with Tech Ops and Engineering to ensure the design of appropriate process fit in order to facilitate the introduction of new products.
• Work with all the support function to facilitate any trouble shooting activities resulting in timely closure of investigation and CAPA.
• Communicate effectively company policies, objectives and results as appropriate.
• Ensure accountability and commitment in achieving the goals of continuous improvement of EHS performance and maintaining legal compliance through active participation in AbbVie EHS programs.
• Review and update manufacturing documentations to meet cGMP and safety compliance.
• Identify areas for process, operator training and operational streamlining. Be involved in continuous Improvement (CI) projects.
• Oversee in all troubleshooting activities in processing issues, deviations and coordinating with other functions when require immediate and preventive actions.

• Bachelor Degree in Engineering (Chemical/ Pharmaceutical Engineering) or equivalent technical Degree. Master Degree desired but not required.
• Minimum of 5 years of pharmaceutical manufacturing experience.
• Able to work comfortably in 12-hour rotating shift (Day/Night)
• Ability to quickly know products and processes in order to assess performance issues.
• Demonstrates the highest levels of integrity and a strong work ethic.
• Proficiency in Delta V and MES 
• Good knowledge of GxP requirements and regulations.
• Good level of decision making and problem solving.
• Good planning and scheduling skills.
• Good communication skills both verbal and written.
• Good interpersonal skills. 

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