Quality Engineer
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Job Location:
Heredia - Costa Rica
Monthly Salary:
Not Disclosed
Posted on:
7 hours ago
Vacancies:
1 Vacancy
Job Summary
PURPOSE STATEMENT
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.
MAJOR RESPONSIBILITIES
Evaluate propose and implement medium 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 Medium Impact NCR.
Review and approve quality plans and First Article Plans related to the production process with low to medium 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 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. (5s) and comply with quality GOs 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 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 initiative
Qualifications :
EDUCATION
- Bachelors degree in Industrial Engineering Business Administrator or related career.
- Desirable CQE (CERTIFIED QUALITY ENGINEER certification) given by ASQ.
- B2 English proficiency.
EXPERIENCE
- Experience of at least 3 years as a quality supervisor/quality engineer in the medical industry.
- Experience in product transfer quality system validations and manufacturing new procedure definition risk assessment documentation development.
- Decision based on data analysis and Risk approach
- Intermediate Statistical Knowledge
Additional Information :
At AbbVie we are committed to cultivating a workplace culture that promotes inclusion diversity and personal growth. We recognize that our collective success is based on the individual well-being of our employees which is why we have designed a benefits package that considers every aspect of their lives.
- Enhanced Health and Wellness Coverage: Our administrative staff enjoys comprehensive medical and dental insurance ensuring peace of mind for you and your loved ones.
- Extended Vacation: We believe in the balance between work and personal life for our administrative team. Thats why we offer additional vacation days beyond legal requirements.
- Flexible Hybrid Work Model: For eligible positions within our administrative staff we have adopted a hybrid work scheme allowing the convenience of working from home two days a week.
- Life Insurance: Secure your familys future with our life insurance policy.
- Employee Assistance Program (EAP): Access professional support with our comprehensive EAP offering psychological legal and financial counseling.
- On-Site Health Services: Benefit from the convenience of having a company doctor and physical therapy services demonstrating our commitment to your health and well-being.
- Community and Social Engagement: Make a difference with a paid volunteer day allowing you to contribute to the community during company working hours.
- Special Leave Benefits: Celebrate your life achievements with extra leave days for marriage and enjoy your birthday with a day off.
- Employee Stock Purchase Plan: Participate in our companys success by purchasing shares at a special price exclusive to employees.
- Transportation and Meals subsidized.
- Solidary Association: Join a community focused on mutual help and enjoy the benefits that come with being a member.
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 & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Full-time
Key Skills
- APQP
- Quality Assurance
- Six Sigma
- ISO 9001
- PPAP
- Minitab
- Root cause Analysis
- ISO 13485
- Quality Systems
- Quality Management
- As9100
- Manufacturing
About Company
AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuro ... View more
