Quality Assurance Engineer

hace 6 días


Alajuela, Alajuela, Costa Rica Abbott A tiempo completo

Company Overview


Abbott is a global healthcare leader that helps people live more fulfilling lives in the areas of nutrition, diagnostics, and surgical and vascular products. We are seeking a highly skilled Quality Engineer to join our team in Costa Rica.


 


Job Summary


We offer an estimated salary of $80,000 - $120,000 per year, depending on experience. As a Quality Engineer at Abbott, you will play a key role in ensuring the quality and compliance of our medical devices and pharmaceuticals. You will work closely with cross-functional teams to develop and implement quality engineering methodologies and processes.


 


About the Role


You will be responsible for supporting technical and statistical investigations concerning optimization and compliance to specification. Additionally, you will provide support to lower-level engineering positions and own measuring process capability, process controls, and process validation efforts. You will also conduct NCMR Investigations, Calibration Out Of Tolerance (OOT) Investigations and Complaint Investigations (MA) related to manufacturing process.


 


Key Responsibilities


Support technical and statistical investigations concerning optimization and compliance to specification.


Provide support to lower-level engineering positions.


Own measuring process capability, process controls, and process validation efforts.


Conduct NCMR Investigations, Calibration Out Of Tolerance (OOT) Investigations and Complaint Investigations (MA) related to manufacturing process.


 


Requirements


To succeed in this role, you should have a Bachelor ́s Degree STEM (Science, Technology, Engineering (preferred), Math) (with equivalent experience in medical devices or pharmaceutical quality control). You should also have 4-6 years of experience in Quality or Engineering positions. Proficiency in computer applications (MS Excel, MS Word, MS PowerPoint) and knowledge of statistical/data analysis and report writing experience are required. Experience working on FDA, GMP, and ISO 13485 regulated environments is essential.


 


Preferred Qualifications


A Master's Degree in a position-related field is preferred. Experience with SAP and ASQ CQE / Six Sigma Blackbelt certification are also beneficial.



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