Medtronic

Quality Engineer II

Medtronic$82K — $90K *
Manufacturing & Automotive
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • High School Diploma or equivalent required
  • 4-year degree in Business, Quality, Engineering or related preferred
  • 2-3 years' experience in a Quality role, ideally in biomedical, automotive, or aerospace
  • Ability to read and interpret engineering drawings
  • Proficient in Microsoft Office
  • Strong written and verbal communication skills

Responsibilities

  • Establish process control plans including capability studies and Gage R&R studies
  • Provide quality documentation to manufacturing floor
  • Monitor production processes for conformity to quality standards
  • Participate in Advance Product Quality Planning (APQP)
  • Prepare and submit Production Part Approval Process (PPAP) packages
  • Develop and implement SPC activities and techniques
  • Conduct Layered Process Audits (LPA) as per the plan

Benefits

  • Health and Safety Standards for a safe work environment
  • Continuous improvement and Lean methodologies are encouraged
  • Opportunity for hands-on experience on the manufacturing floor
  • Occasional involvement in cross-functional audits
  • Sustainable work hours, with a typical Monday to Friday schedule
  • Exposure to various operations disciplines including Manufacturing and Quality
Full Job Description
Description

The Quality Engineer assists in the implementation and maintenance of all quality system requirements, including customer concerns and visits, gauging, process control plans, supplier issues, and customer specific requirements.

Key Responsibilities
• Establish and implement process control plans to include capability studies, gage repeatability and reproducibility (Gage R&R) studies.
• Provide quality related documents to the manufacturing floor, including control plans, control cards, visual aids and work instructions.
• Monitor production floor processes for conformance to control plans and customer requirements which includes fit, function, reliability, durability and reappearance criteria.
• Participate in Advance Product Quality Planning (APQP).
• Prepare and submit Production Part Approval Process (PPAP) packages ensuring all elements are met per customer requirements.
• Develop and implementation of SPC activities, including originating objectives, goals and time tables, and implementing new techniques as they become available.
• Perform capability studies on new jobs and in other situations where they are needed.
• Participates in and performs Layered Process Audits (LPA) per plan.
• Ensures Housekeeping and Health & Safety Standards are maintained.
• Complies with policies and procedures pertaining to facility or divisional adopted standards such as ISO and ITAR.
• Utilizes the concepts of continuous improvement including Lean.
• May, on occasion, be required to perform duties other than those specified in this description.

Education:
• High School Diploma or equivalent required.
• 4-year College or University Degree in Business, Quality, Engineering or related field preferred.
• 2 - 3 years' experience in a Quality related role, preferably in the biomedical, automotive or aerospace industry.

Skills Required:
• Ability to solve complex problems and exercise judgment based on the analysis of multiple sources of information.
• Ability to read and interpret engineering drawings and specifications.
• Ability to support and/or lead root cause analysis, disciplined problem-solving and decision-making processes.
• Proven leadership, interpersonal skills and personal development skills.
• Experience in a variety of basic operation disciplines: Manufacturing, Quality, Process / Tooling and Shop Floor Supervision.
• Proficient in Microsoft Office.
• Excellent written and verbal communication skills.
• Experience supporting internal or supplier audits is a plus.

Work Environment:

Office setting

Manufacturing floor environments

Controlled temperature environments

Expected Hours of Work This is a Full-Time Salary/Hourly position required to work Monday through Friday, with occasional weekends.

Travel:

Up to 10%

Pay Range

$82,000.00 Annually to $90,000.00 Annually

About Medtronic

Medtronic plc is an Irish-domiciled multinational medical device company that develops and manufactures medical device technologies and therapies to treat chronic diseases worldwide. Medtronic was founded in 1949 in Minneapolis, Minnesota, as a medical equipment repair shop. Today, the company operates in more than 160 countries and employs over 90,000 people. Medtronic's primary products include implantable pacemakers and defibrillators, insulin pumps, spinal and neurostimulation devices, surgical tools, and patient monitoring systems. The company is committed to improving patient outcomes and expanding access to healthcare through innovative medical technologies.
Learn more about Medtronic
Size
95,000 employees
Market Cap
$102.7 billion
Industry
Net Income
$2.8 billion
Founded
1949
5 Year Trend
+1.3%
Revenue
$27.9 billion
NASDAQ

Similar Jobs

More Jobs at Medtronic

  • Medtronic
    Quality Engineer II
    $82K — $90K *
    Shirley, MA 01464 (Middlesex County)
    Manufacturing & Automotive
    In-Person
  • Quality Engineer II
    $82K — $90K *
    Poway, CA 92064 (San Diego County)
    Manufacturing & Automotive
    In-Person

More Manufacturing & Automotive Jobs

Find similar Quality Engineer II jobs: