Manufacturing Process Engineer job opportunity at Abbott.

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DateMore Than 30 Days Ago bot
Abbott Manufacturing Process Engineer
Experience: 13-years
Pattern: full-time
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degreeAssociate
loacation United States - Arizona - Scottsdale, United States Of America
loacation United States ..........United States Of America

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.       JOB DESCRIPTION: MAIN PURPOSE OF THE ROLE Experienced professional individual contributor that works under limited supervision. Applies subject matter knowledge in the area of Medical Device Manufacturing Process. Requires capacity to apply skills/knowledge within the context of specific needs or requirements. MAIN RESPONSIBILITIES   As the Experienced professional in the Medical Device Manufacturing Process Sub-Function, possesses well developed skills in implementing and maintaining high volume manufacturing processes. Serve as the primary process owner for several PCB manufacturing processes, including Solder, Epoxy Dispense, Wirebond, Underfill, Laser Processing, and Mechanical Routing. Establish and maintain robust, compliant, and validated processes that meet medical device manufacturing requirements. Develop and maintain process documentation , including work instructions, standard work, control plans, PFMEAs, and equipment settings. Conduct and document process capability analysis (Cp/Cpk) and implement actions to improve reliability and product performance. Own the lifecycle of process equipment: reflow ovens, dispensers, pick‑and‑place modules, wirebonders, underfill systems, lasers, mechanical routers, etc. Define equipment requirements, support vendor evaluations, lead installations, and oversee equipment validation (IQ/OQ/PQ). Collaborate with maintenance on PM schedules, calibration, uptime tracking, and tooling readiness. Evaluate and qualify all process materials, including solder paste, flux, epoxy/adhesives, underfill chemistries, wirebond materials, and cleaning solvents. Monitor daily yield, scrap, and defect trends; drive root cause investigation , CAPA activities, and long‑term corrective actions.  Services, troubleshoots, and solves engineering problems with processes or equipment already in operation. Generate and execute process validation protocols (IQ/OQ/PQ, PPQ) in alignment with medical device regulatory expectations. Provide manufacturability feedback to R&D on PCB layout, component spacing, bond pad design, solder joint access, and material compatibility. QUALIFICATIONS Education Associates Degree (± 13 years)             Experience/Background Minimum 1 year           The base pay for this position is $61,300.00 – $122,700.00 In specific locations, the pay range may vary from the range posted.       JOB FAMILY: Engineering       DIVISION: CRM Cardiac Rhythm Management          LOCATION: United States > Scottsdale : 8300 E. Pacesetter Way       ADDITIONAL LOCATIONS:       WORK SHIFT: Standard       TRAVEL: Yes, 10 % of the Time       MEDICAL SURVEILLANCE: Not Applicable       SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)       Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.       EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf       EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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