Associate Engineer Product Development at Abbott Pediatrics

St. Paul, Minnesota, United States -

Full Time

Start Date

Immediate

Expiry Date

31 May, 26

Salary

101300.0

Posted On

02 Mar, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Engineering Support, Process Improvement, Technical Problem Solving, Product Development, Dimensioning, Tolerance Evaluations, Electrical Analysis, Troubleshooting, Corrective Action, Configuration Control, Engineering Test Reports, Engineering Change Papers, Operator Procedures, Process Validation, Quality Management Systems, Regulatory Compliance

Industry

Hospitals and Health Care

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 115,000 colleagues serve people in more than 160 countries. MAIN PURPOSE OF THE ROLE Working under general supervision, is responsible for providing engineering support to device manufacturing operations. Develops and implements efficient, cost-effective process improvements. Work requires the application of theoretical principles and creative/analytical techniques typically acquired in a recognized four-year or more academic course of study. Applies engineering and scientific principles to the evaluation and solution of technical problems. Exercises an appropriate level of technical judgment in planning, organizing, performing and coordinating product development engineering assignments. Performs engineering studies. Stays abreast of and communicates technical advancements to colleagues and associates. Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness. MAIN RESPONSIBILITIES • Provides engineering support for existing operations • May perform dimensioning and tolerance evaluations of components, drawings and tooling • May perform electrical analysis of failed components or devices for troubleshooting and corrective action purposes • Oversees device configuration control and modifies the configuration as required • Writes Engineering Test Reports (ETR’s), memos, Engineering Change Papers, creates travelers, and develops written operator procedures • Performs process validations on equipment and processes as required. • Resolves and/or facilities the resolution of problems including identifying causes to prevent re-occurrence • 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. QUALIFICATIONS Education Education Level Major/Field of Study or Equivalent Bachelors Degree (± 16 years) Electrical/mechanical engineering, material science, or related engineering field. An equivalent combination of education and work experience Experience/Background Experience Details Minimum 1 year Relevant design and manufacturing work experience as related to medical devices. Demonstrated ability to analyze and evaluate technologically complex devices. 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. Ability to leverage and/or engage others to accomplish projects. • Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization. Multitasks, prioritizes and meets deadlines in timely manner. Strong organizational and follow-up skills, as well as attention to detail. Ability to travel approximately 5%, including internationally. The base pay for this position is $50,700.00 – $101,300.00. In specific locations, the pay range may vary from the range posted.

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Responsibilities

The role involves providing engineering support to device manufacturing operations, including developing and implementing efficient, cost-effective process improvements. Responsibilities include performing engineering studies, overseeing configuration control, writing technical documentation, and performing process validations as required.