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 114000 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 pickandplace 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 longterm 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
$61300.00 $122700.00
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: EEO is the Law link - Espanol: Experience:
IC