Heredia, Costa Rica (On-Site) · Posted 1 day ago
Job Function Other
Job Type Full-Time

About this role

ICompany Description

About AbbVie

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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

Ensure that our product is functional and safe for the end customer by understanding, developing and
applying quality control systems, as well as analyzing, proposing and implementing improvement of
quality and manufacturing processes, thinking about improving defects in a timely and efficient manner
  • Evaluate, propose and implement high complexity improvements in processes in the process
    quality area, seeking to strengthen processes while improving their efficiency, guided and advised
    by the area manager .
  • Search for solutions to problems identified in the areas of manufacturing and process quality
    through the application of Lean tools.
  • Support assigned root cause investigations (NCRs), as well as the development of action plans and
    the implementation of corresponding actions, during the established period of time. Review and
    Approve documents for High Impact NCR.
  • Develop and establish new processes and procedures from a quality perspective based on the Risk system evaluation, be part of the process and product transfer projects from the planning stage to its operationalization with high understanding of the ISO standard and other regulations.
  • Coach and train colleagues to achieve a high performance team following the department's
    purpose, as well as make high-impact decisions evaluating the risk in the absence of the manager
  • Review and approve quality plans and First Article Plans related to the production process with low to high complexity, as well as propose changes to PFMEAs, this for those projects where you are assigned as a Quality representative.
  • Perform reviews to OT Core System documents as well as validation/qualification protocols (IQ,
    PPQ, IOQ, IO, PR, etc.) where assigned as a quality representative complex and advance system.
  • Provide support to key company projects, including definition and implementation of controls
    aimed at ensuring product quality.
  • Ensure the order and cleanliness of the areas under your responsibility. (5's) and comply with
    quality GO's in the corresponding period.
  • Do the other functions inherent to the position and those assigned by your immediate manager.
  • Meet compliance with corporate and legal EHS requirements, by complying with internal policy and procedures. In addition, ensure compliance through the adoption of necessary strategies, internal controls, communication and training.
  • Continuously maintain EHS results through leadership, commitment and participation in all EHS-related initiatives.


Qualifications

Education:
  • Bachelors degree in Industrial Engineering Bussiness Administrator or related career.
  • Desirable CQE (CERTIFIED QUALITY ENGINEER certification) given by ASQ.
  • Intermediate/advanced English proficiency.

Experience:
  • Experience of at least 3-5 years as a quality
    supervisor/quality engineer in the medical
    industry.
  • Plus: Experience in product transfer, quality
    system, validations and manufacturing, new
    procedure definition, risk assessment
    documentation development.

Skills:
  • Critical thinking
  • Focus on excellence
  • Open and authentic
  • Project management
  • Communication
  • Decision based on data analysis and Risk
    approach
  • Advance Statistical Knowledge


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/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.htmlI
Job ID: 86675732

About the company

AbbVie
We are AbbVie. A global Fortune 500 biopharmaceutical company creating life-changing medicines and first-in-kind solutions that make a real difference in people’s lives. Our 50,000+ employees across geographies, disciplines, and therapeutic areas put impact at the core of every decision. With over $50B invested in R&D since our founding in 2013, we’re always focused on helping people and communities thrive for generations to come. Our work can—and does—have a tangible, lasting impact on millions of people. But it’s n…
View full profile & all jobs

Jobs you may like

AbbVie
(Senior) Software Validation Engineer - Quality...
Ludwigshafen, Germany (on-site)
AbbVie
Quality Senior Manager
North Chicago, IL, United States (on-site)
AbbVie
Associate Engineer, Quality Systems
North Chicago, IL, United States (on-site)
AbbVie
Engineer, Quality
Tempe, AZ, United States (on-site)