Vacancy expired!
At Abbott, we're committed to helping people live their best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world in nutrition, diagnostics, medical devices and branded generic pharmaceuticals that create more possibilities for more people at all stages of life. Today, 99,000 of us are working to help people live not just longer, but better, in the more than 150 countries we serve.Manager Summary:Scope of work include:
Clinical Chemistry Analyzers
Engineering Design Changes
Investigation of Field/Customer Issues, Complaints
Returned Part Testing
Author test protocols and test records
Risk Assessments
Defect Tracking Investigations
Data mining and analysis
Process Design Plans
Part Evaluation/Ticket Trending
Functional Impact Assessment
Audit and Regulatory Supports
Summary:Proactively contributes to multiple moderate to complex projects and design changes in support of investigations. Resolves product problems and technical issues with minimal oversight across multiple system functions.Main Responsibilities:
Maintains adherence to Quality System - Implements and maintains the effectiveness of the quality system.
Design Control - Writes and executes moderately complex system related verification and or characterization protocols and data packages.
Applies moderately complex quantitative methods,analyzes data,evaluates results,forms conclusions and provides and implements improvements.
Risk Mitigation - Reviews technical risks and takes appropriate action.
Technical Investigation Support - May assist in developing FMEA for Risk Management.
Supports moderately complex investigations of system issues.
Collaborates across functional areas - Presents,delivers and interprets information amongst product team members,scientists,engineers,and other systems development personnel.
Works well with others in a collaborative,goal-driven environment.
Technical Leadership and Mentoring - May provide input into moderate to complex project and design plans and timelines.
May provide technical mentoring.
May participate in hiring process for system integration resources and provide input to System Integration Managers.
May provide feedback to expense monitoring.
Qualifications:Bachelor’s degree in Life or Physical Science,Bioengineering,Biomedical Engineering or closely related discipline is preferred. 2 years’ work related experience with degree or sufficient transferable experience to demonstrate functional equivalence to a degree. Knowledge of regulations and standards affecting IVDs and Biologics. Good Lab Practice, Good Manufacturing Practice, laboratory duties, PC Skills (Word, Excel, PowerPoint), Data representation.Preferred Qualifications:
Applicant can perform the following tasks with minimal oversight:
Experience in applying statistical data analysis to solve scientific or engineering problems
Experience in Root Cause analysis
Can write and execute moderately complex to complex test procedures
An Equal Opportunity EmployerAbbot welcomes and encourages diversity in our workforce.We provide reasonable accommodation to qualified individuals with disabilities.To request accommodation, please call 224-667-4913 or email corpjat@abbott.com
Vacancy expired!