Abbott
Overview
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio spans diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Working at Abbott: You can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with a high employer contribution. Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit — an affordable path to getting a bachelor’s degree. A company recognized as a great place to work in dozens of countries and named one of the most admired companies in the world by Fortune. A company recognized as one of the best big companies to work for, and as the best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
This position works on site at our Carlsbad, CA location in the Cardiometabolic Division in Abbott Rapid Diagnostics. Our diagnostic solutions are used in hospitals, laboratories, and clinics around the globe. The information derived from our tests, instruments, and informatics systems informs patient care decisions for conditions ranging from heart attacks to blood disorders to infectious diseases and cancers.
What You’ll Work On
This position is responsible for developing and maintaining quality engineering methodologies and providing quality engineering support within new product development, manufacturing, or system/services support.
In Addition
Identify, review, and implement effective process control systems to support development, qualification, and ongoing manufacturing of products to meet or exceed internal and external requirements. Perform risk assessments across functions (e.g., FMEA, change management, and issue investigation/resolution). Lead in the review and/or implementation of assurances, process controls, and CAPA systems to meet or exceed requirements. Assist in the review, development, and execution of streamlined business systems to identify and resolve quality issues. Apply sound, systematic problem-solving methodologies to identify, prioritize, communicate, and resolve quality issues. Document experiment plans and results, including protocol writing and reports. Draft and review CTQ parameters and specifications. Lead the investigation, resolution, and prevention of product and process non-conformances. Participate in or lead teams supporting quality disciplines, decisions, and practices (e.g., represent the Quality function as a Core Team Member).
Requirements
Required Qualifications
Bachelor’s degree in Science, Engineering or a closely related discipline More than 2 years of Engineering experience and demonstrated use of quality tools/methodologies Solid communication and interpersonal skills Project management and leadership skills, including the ability to lead multi-departmental project teams and resolve quality-related issues in a timely and effective manner Advanced computer skills, including statistical/data analysis and report writing Prior medical device experience preferred Experience implementing product and process improvement methodologies (e.g., Six Sigma and Lean Manufacturing). ASQ CQE or other certifications preferred Experience working in a broader enterprise/cross-division model preferred in a highly matrixed and geographically diverse environment Ability to work in a team or as an individual contributor in a fast-paced, changing environment Strong verbal and written communications with ability to communicate at multiple levels Multitasks, prioritizes, and meets deadlines in a timely manner Strong organizational and follow-up skills, with attention to detail
Preferred Qualifications
Experience reviewing validation and transfer activities related to documentation control processes ASQ CQE or other certifications preferred Experience with Change management and Non-Conformance/CAPA
Apply Now
Learn more about health and wellness benefits: www.abbottbenefits.com Follow your career aspirations to Abbott for diverse opportunities. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews. The base pay for this position is $79,500.00 – $138,700.00. Pay range may vary by location.
Job Details
Seniority level: Entry level Employment type: Full-time Job function: Quality Assurance Industries: Hospitals and Health Care
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Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio spans diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Working at Abbott: You can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with a high employer contribution. Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit — an affordable path to getting a bachelor’s degree. A company recognized as a great place to work in dozens of countries and named one of the most admired companies in the world by Fortune. A company recognized as one of the best big companies to work for, and as the best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
This position works on site at our Carlsbad, CA location in the Cardiometabolic Division in Abbott Rapid Diagnostics. Our diagnostic solutions are used in hospitals, laboratories, and clinics around the globe. The information derived from our tests, instruments, and informatics systems informs patient care decisions for conditions ranging from heart attacks to blood disorders to infectious diseases and cancers.
What You’ll Work On
This position is responsible for developing and maintaining quality engineering methodologies and providing quality engineering support within new product development, manufacturing, or system/services support.
In Addition
Identify, review, and implement effective process control systems to support development, qualification, and ongoing manufacturing of products to meet or exceed internal and external requirements. Perform risk assessments across functions (e.g., FMEA, change management, and issue investigation/resolution). Lead in the review and/or implementation of assurances, process controls, and CAPA systems to meet or exceed requirements. Assist in the review, development, and execution of streamlined business systems to identify and resolve quality issues. Apply sound, systematic problem-solving methodologies to identify, prioritize, communicate, and resolve quality issues. Document experiment plans and results, including protocol writing and reports. Draft and review CTQ parameters and specifications. Lead the investigation, resolution, and prevention of product and process non-conformances. Participate in or lead teams supporting quality disciplines, decisions, and practices (e.g., represent the Quality function as a Core Team Member).
Requirements
Required Qualifications
Bachelor’s degree in Science, Engineering or a closely related discipline More than 2 years of Engineering experience and demonstrated use of quality tools/methodologies Solid communication and interpersonal skills Project management and leadership skills, including the ability to lead multi-departmental project teams and resolve quality-related issues in a timely and effective manner Advanced computer skills, including statistical/data analysis and report writing Prior medical device experience preferred Experience implementing product and process improvement methodologies (e.g., Six Sigma and Lean Manufacturing). ASQ CQE or other certifications preferred Experience working in a broader enterprise/cross-division model preferred in a highly matrixed and geographically diverse environment Ability to work in a team or as an individual contributor in a fast-paced, changing environment Strong verbal and written communications with ability to communicate at multiple levels Multitasks, prioritizes, and meets deadlines in a timely manner Strong organizational and follow-up skills, with attention to detail
Preferred Qualifications
Experience reviewing validation and transfer activities related to documentation control processes ASQ CQE or other certifications preferred Experience with Change management and Non-Conformance/CAPA
Apply Now
Learn more about health and wellness benefits: www.abbottbenefits.com Follow your career aspirations to Abbott for diverse opportunities. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews. The base pay for this position is $79,500.00 – $138,700.00. Pay range may vary by location.
Job Details
Seniority level: Entry level Employment type: Full-time Job function: Quality Assurance Industries: Hospitals and Health Care
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