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

Job Description

Operational and Technical

Drive initiatives to enhance operational processes and equipment performance, aiming to achieve the highest standards of manufacturing excellence.Lead thorough investigations into non-conformance incidents, developing comprehensive reports on issues related to quality and Environment, Health, and Safety (EHS) observed during manufacturing or batch reviews.Proactively monitor existing processes and equipment to identify opportunities for improvement and implement effective solutions.Provide strategic input and recommendations on operational improvements that align with business targets and contribute to overall manufacturing success.Review and contribute to the development of batch-related recipes (such as those in POMS and DeltaV), manual operations procedures, and additional manufacturing documentation to ensure accuracy and efficiency.Offer expert input or review the design of batch and cleaning manufacturing recipes within the Distributed Control System (DCS).Lead and manage digitalization projects that align with and support the company's strategic business objectives, enhancing automation and efficiency.Conduct training sessions for operators on processes and procedures, ensuring compliance and proficiency in operational practices.

Safety

Adheres to safe work environment in accordance with regulatory and global/local EHS policies.Leads/participates in safety risks assessments or participates in process hazard analysis as an operations representative (PHA).

Quality

Actively resolve batch related document errors in a timely manner.Communicates all events/issues effectively with relevant stakeholders.Provide inputs for investigation – impact assessment and appropriate CAPA.Ensures overall plant upkeep during the shift and ensuring plant is always in audit ready mode.

Schedule

Oversees deliverables ahead, anticipates complexities and prevents potential delays. Ensures processes are running as per planned schedule with minimal delays. Highlights effectively to shift supervisor if delays are expected.
Qualifications
Degree in Chemical Engineering/Chemistry or equivalent technical related diploma is required.At least 3 - 4 years of experience in working in a GMP manufacturing environment is preferred.Familiar with DeltaV and MES system.Yellow Belt certification would be preferred.
Additional Information

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 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