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.

Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.

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 student debt program and FreeU 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.

The Opportunity

This position supports the Cardiac Rhythm Management division.

As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats.

This individual will work with supervisors, engineers, technicians, and operators to address problems and opportunities identified on manufacturing lines. He or she will be accountable for quality, safety, product output and yield initiatives, as well as providing line support on a daily basis.

What You’ll Work On

Responsible for daily support to manufacturing activities in order to meet established goals for safety, quality, yield, and attainment.
Maintains systems that monitor key performance indicators, such as yield, nonconforming material, and attainment. If indicators show an adverse trend, works with the functional team to plan and implement appropriate changes.
Works with Operations support team (supervisor, engineers, operators, technicians) to investigate potential non-conformances, determine initial bracketing and product containment, and support generation of non-conforming material reports, if needed.
Responsible for product/process knowledge and understanding of basic cause-and-effect of line and process changes. Understands potential risk related to product nonconformance. Has knowledge of product requirements and specifications.
Understands clear criteria of conforming/ non-conforming product and the test/inspection methods used for verifying product conformance.
Maintains manufacturing documentation such as process instructions, test & inspection methods, and form packets and updates through change control process as needed.
Investigates adverse trends in line performance and reports findings. Prepares and communicates recommendations and action plans.
Leads root cause analysis efforts for basic/simple manufacturing events, utilizing DMAIC model and A3s. Supports CAPA investigations with data gathering and analysis as needed.
Assists in ideation and implementation of new fixturing and tooling for manufacturing line
Supports validation activities for new or updated equipment or processes, including writing of qualification protocols/reports, equipment specifications, and preventative maintenance procedures.
Supports maintenance technicians in equipment availability issues. Reviews equipment work order completion and performs product impact analysis to release equipment for manufacturing use.
Assists in the training of Operations and Maintenance personnel
Owns Out-of-Tolerance reports for manufacturing equipment and works with Quality Engineering to determining product impact.
Assists with Manufacturing Investigation of adverse product events in the field.
Complies with all regulations and standards for Quality, Environment, Health, Safety and Energy (EHS&E) Global Policies, Abbott Engineering Standards, and other governance areas as applicable.

Requirements

EDUCATION AND EXPERIENCE YOU’LL BRING

Bachelors Degree or relevant experience
0-3 years of experience

Preferred Requirements

Up to 3 years of experience, both overall and any industry-specific experience.
Knowledge and proficiency in the application and principles of Manufacturing & Process Engineering.
Ability to effectively communicate cross-functionally to assist in resolving Quality/Engineering issues.
Excellent written, verbal and interpersonal communication skills.
Knowledge of common office applications: Word, PowerPoint, Excel.
Ability to interact effectively with all employee job levels.
Multitasks, prioritizes and meets deadlines in timely manner. Strong organizational and follow-up skills, as well as attention to detail.
Basic understanding of materials, product design, product testing.
Preferred: basic understanding and knowledge of statistics, GD&T, tolerance stack up analysis, Statistical Process Control “SPC”, fundamentals of Design of Experiments “DOE” and problem solving methodologies
Preferred: familiar with the use of various inspections tools including but not limited to: pin gauge, caliper, micrometer, snap gauge, drop gauge, block gauge, optical comparator, vision system, etc.
Preferred: experience working in a medical device manufacturing environment such as: extrusion, injection molding, laser cutting, cleaning, passivation, electropolishing, assembly, bonding, packaging, testing, inspection methods, and others.
Preferred: experience working in a broader enterprise/cross-division business unit model preferred. Ability to work in a highly matrixed and geographically diverse business environment. Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
Preferred: experience use of statistical software (ex: Minitab, JMP), six sigma training and/or certification, use of Solidworks (or similar CAD software), MS project, Verification & Validation activities, basic understanding of FDA, Good Manufacturing Practice “GMP” and ISO guidelines.
Ability to travel approximately 5%, including internationally(If required)

Apply Now

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com

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/Abbottand on Twitter @AbbottNews and @AbbottGlobal

The base pay for this position is $72,100.00 – $114,700.00. In specific locations, the pay range may vary from the range posted.

Abbott

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