Manufacturing/Process Engineer II

About the company

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve today's serious health problems and address tomorrow's medical challenges. We strive to have a remarkable impact on people's lives in several key therapeutic areas, such as immunology, oncology, and neuroscience, and in the products and services of our Allergan Aesthetics portfolio. For more information about AbbVie, visit us at http://www.abbvie.com/. Follow @abbvie on LinkedIn, Facebook, Instagram, X, and YouTube.

Your tasks

Efficiently manage resources, product control, and implementation of improvements, adding value to all production processes, according to the standards, quality, and safety regulations defined by the company, to achieve the fulfillment of the goals and objectives established for the manufacturing area.

• Collaborate in the control of in-process products on all production lines under charge, in order to ensure compliance with priorities and identify possible constraints.
• Ensure production line results in order to control compliance with the Production Plan.
• Evaluate and implement changes in procedures, catalogs, First Article, First Shipment First Article, among other improvement opportunities in the production process to ensure they are carried out in an agile and appropriate manner to achieve operational cost reduction.
• Provide support to production lines in order to clarify procedures and evaluate the technique applied in the execution of the task, so as to avoid deviations in quality system requirements.
• Provide support in managing production capacity in order to agree on production commitments with the logistics department.
• Provide support during external or internal audit processes required by the regulatory body.
• Participation in improvement teams focused on Conversion Loss/SWAT and Operating Supplies. Leading improvement teams and achieving the goals proposed by the department.
• In case of deviations from procedures in the areas under charge, the event must be investigated and preventive and corrective actions must be identified in order to eliminate the root cause of these.
• Ensure the timely availability of retained material according to the company's quality system.
• Provide support in Human Resources in order to contribute to induction processes, job changes, among other cases that arise in the area under charge.
• Ensure the motivation of the employees under charge, ensuring that behaviors that promote the AbbVie culture are reinforced and recognized in a timely manner, both formally and informally.
• Guarantee compliance with corporate and legal EHS requirements through adherence to internal policy and procedures. Likewise, guarantee compliance through the adoption of strategies, internal controls, communication, and necessary training.
• Continuously improve EHS results through leadership, commitment, and active participation in all EHS-related initiatives.
• Execute all other functions inherent to the position and those assigned by the immediate supervisor, in order to utilize the area's resources in the best possible way.

Requirements

Education and Experience

• Bachelor's degree in Industrial Engineering, Industrial Production Engineering, Chemical Engineering, Industrial Chemistry, or 80% progress in the degree and at least one year of experience in the Medical Industry.
• Intermediate English.

Other Professional Skills

• Knowledge of GMP´s, Lean Manufacturing, Six sigma, Quality Auditor is desirable.

Other

Additional Information 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, and people with disabilities.