Job Description
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and 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 high employer contribution
Tuition reimbursement, the Freedom 2 Save (https://www.abbott.com/corpnewsroom/strategy-and-strength/tackling-student-debt-for-our-employees.html)
student debt program and FreeU (https://www.abbott.com/corpnewsroom/strategy-and-strength/college-degree-for-free-its-possible-with-freeu.html)
education benefit - an affordable and convenient path to getting a bachelor's degree.
A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
This position works out of our St. Paul, MN location in the Electrophysiology division. In Abbott?s Electrophysiology (EP) business, we're advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives.
As the Sr. Engineer, you will provide development support as a part of a multidisciplinary product development team, overseeing projects throughout concept to launch in all phases of Design Controls with focus on medical electrical systems. You will be a key contributor to the design, development and testing activities for complex medical devices.
We're looking for:
Critical thinkers : People who challenge status quo and work to find just the right solutions.
Collaborators : Partners who listen to ideas, share thoughts, and work together to move the business forward.
Problem Solvers : People who can take on complex problems and apply first principles and sound technical practices.
Communicators
:
People who can communicate project progress, data analysis and conclusions effectively across a broad set of stakeholder.
Responsible
:
People who own their deliverables and activities and see things through to completion. People who take personal accountability for end results.
What You'll Work On
Lead and implement complex development projects including quality improvement initiatives.
Sets strategies for cross-functional teams and drives towards compliant and efficient solutions to complex problems.
Execute on Holistic & Strategic Design Verification/Validation Strategies with emphasis on:
Technical analysis of requirements, specifications, and control strategy
Efficient and cost-effective execution of validation and verification
Alignment of design outputs to production and process controls
Proper verification techniques including inspection, demonstration, test, etc.
Lead design characterization activities for development projects
Influence design and verification decisions through use of applied statistics.
Support design test and inspection method development, and lead method validation activities.
Ensure DHF content integrity, completeness, and regulatory / standards compliance; collaboratively communicating & resolving gaps.
Support and ensure internal & external audit responses and on-time product re-certifications.
Support and ensure the establishment of objective, measurable, discrete, and verifiable customer and product requirements.
Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
Performs other related duties and responsibilities, on occasion, as assigned.
Qualifications
Bachelor level degree in Engineering or Technical Field; advanced degree / Biomedical Engineering / Electrical Engineering / Computer Science preferred.
5-8+ years Engineering experience with new product development
Working knowledge on design verification and design validation techniques.
Working knowledge of applied statistics, sampling strategies, and design of experiments, including statistical software tools such as Minitab.
Strong organizational and follow-up skills, as well as attention to detail
Ability to collaborate on-site on a regular basis.
Ability to travel approximately 10%, including internationally.
Knowledge of FDA, IEC 60601, GMP, ISO 13485, and ISO 14971
Prior medical device experience preferred
Apply Now (https://www.jobs.abbott/us/en)
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:
www.abbottbenefits.com (http://www.abbottbenefits.com/pages/candidate.aspx)
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. 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 and @AbbottGlobal.
The base pay for this position is $75,300.00 - $150,700.00. In specific locations, the pay range may vary from the range posted.
An Equal Opportunity Employer
Abbot 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
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and 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 high employer contribution
Tuition reimbursement, the Freedom 2 Save (https://www.abbott.com/corpnewsroom/strategy-and-strength/tackling-student-debt-for-our-employees.html)
student debt program and FreeU (https://www.abbott.com/corpnewsroom/strategy-and-strength/college-degree-for-free-its-possible-with-freeu.html)
education benefit - an affordable and convenient path to getting a bachelor's degree.
A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
This position works out of our St. Paul, MN location in the Electrophysiology division. In Abbott?s Electrophysiology (EP) business, we're advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives.
As the Sr. Engineer, you will provide development support as a part of a multidisciplinary product development team, overseeing projects throughout concept to launch in all phases of Design Controls with focus on medical electrical systems. You will be a key contributor to the design, development and testing activities for complex medical devices.
We're looking for:
Critical thinkers : People who challenge status quo and work to find just the right solutions.
Collaborators : Partners who listen to ideas, share thoughts, and work together to move the business forward.
Problem Solvers : People who can take on complex problems and apply first principles and sound technical practices.
Communicators
:
People who can communicate project progress, data analysis and conclusions effectively across a broad set of stakeholder.
Responsible
:
People who own their deliverables and activities and see things through to completion. People who take personal accountability for end results.
What You'll Work On
Lead and implement complex development projects including quality improvement initiatives.
Sets strategies for cross-functional teams and drives towards compliant and efficient solutions to complex problems.
Execute on Holistic & Strategic Design Verification/Validation Strategies with emphasis on:
Technical analysis of requirements, specifications, and control strategy
Efficient and cost-effective execution of validation and verification
Alignment of design outputs to production and process controls
Proper verification techniques including inspection, demonstration, test, etc.
Lead design characterization activities for development projects
Influence design and verification decisions through use of applied statistics.
Support design test and inspection method development, and lead method validation activities.
Ensure DHF content integrity, completeness, and regulatory / standards compliance; collaboratively communicating & resolving gaps.
Support and ensure internal & external audit responses and on-time product re-certifications.
Support and ensure the establishment of objective, measurable, discrete, and verifiable customer and product requirements.
Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
Performs other related duties and responsibilities, on occasion, as assigned.
Qualifications
Bachelor level degree in Engineering or Technical Field; advanced degree / Biomedical Engineering / Electrical Engineering / Computer Science preferred.
5-8+ years Engineering experience with new product development
Working knowledge on design verification and design validation techniques.
Working knowledge of applied statistics, sampling strategies, and design of experiments, including statistical software tools such as Minitab.
Strong organizational and follow-up skills, as well as attention to detail
Ability to collaborate on-site on a regular basis.
Ability to travel approximately 10%, including internationally.
Knowledge of FDA, IEC 60601, GMP, ISO 13485, and ISO 14971
Prior medical device experience preferred
Apply Now (https://www.jobs.abbott/us/en)
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:
www.abbottbenefits.com (http://www.abbottbenefits.com/pages/candidate.aspx)
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. 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 and @AbbottGlobal.
The base pay for this position is $75,300.00 - $150,700.00. In specific locations, the pay range may vary from the range posted.
An Equal Opportunity Employer
Abbot 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
Key skill Required
- HTML
- Applied Statistics
- Data Analysis
- Quality Management
- Accountability
- Analysis
- Attention to Detail
- Audit
- Biomedical Engineering
- Career Development
- Characterization
- Collaboration
- Compliance
- Computer Science
- Demonstration
- Design
- Development
- Development Support
- Electrical Engineering
- Electrophysiology
- Environmental
- Environmental Management
- Healthcare
- Influence
- ISO 13485
- ISO 14971
- Management
- Management Systems
- Medical Device
- Method Development
- Method Validation
- Minitab
- Multidisciplinary
- Personal Accountability
- Product Development
- Quality Improvement
- Regulatory Requirements
- Reimbursement
- Sampling
- Science
- Security
- Standards Compliance
- Statistical Software
- Statistics
- Strategic Design
- Strategy
- Validation
- International