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Staff Software Engineer
Toro TMS
Remote, United States
We are growing our fully remote Engineering team and looking for an entrepreneurial, product-minded Staff Software Engineer to join our team. The right person will be driven, curious, and…
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Reliability and Process Engineer
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Youngstown, OH
The Reliability and Process Engineer improves the reliability of critical equipment and tooling by eliminating chronic failures, reducing unplanned downtime, and mitigating the risk of…
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Software Quality Engineer
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- $77,000 to $104,000 USD / year
Zipliens is a leading lien resolution company that specializes in streamlining the lien process for personal injury law firms. Our work helps law firms operate more efficiently and helps…
Added 1 min ago
Packaging Engineer
Actalent
Warren, MI
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Mechanical Design Engineer
Actalent
Birmingham, MI
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Pre Production Engineer
Actalent
Lebanon, KY
Job Title: Pre-Production / Roll Forming EngineerJob DescriptionThe Pre-Production / Roll Forming Engineer utilizes advanced engineering, manufacturing process knowledge, and data analysis…
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Manufacturing Engineer
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- $33.6 to $40 USD / hour
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Mechanical Design Engineer
Actalent
Jeffersontown, KY
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Madison, AL
- $90,000 to $120,000 USD / year
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- $25 to $30 USD / hour
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Participate in hands-on project work, including design calculations, plan preparation, and field observations under the guidance of a licensed Professional Engineer.
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For Career Opportunities with CMU Medical Education Partners (CMEP), please read the following:
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EPTAM Plastics

Quality Engineer- 1st Shift

Lakeville, MN, United States

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Job details

Posting language: English

Original job description

EPTAM Precision Micro-Machining is looking for a Quality Engineer – 1st Shift to join our team in Lakeville, MN. Join us as we create medical devices that support our OEM partners in creating life-saving parts and positive outcomes for their patients. EPTAM Precision Micro-Machining in is a world-class manufacturer specializing in precision manufacturing of custom medical device components for original device manufacturers. We've established a strong reputation in providing custom implantable components across various medical sectors, including orthopedic, orthopedic spine, cardiovascular, vascular, endovascular, and pelvic health sectors. Our manufacturing operations support the Robot Assisted Surgery (RAS) and Minimally Invasive Surgery (MIS) industries, as OEM’s look for partners for the future of advanced interventions. Our facility, compliant with FDA and ISO 13485 standards, is celebrated for its high-quality system and standards. Our ingrained culture of quality, combined with seamless collaboration between Engineering, Quality, and Manufacturing Operations, allows us to deliver the very best to our employees, customers, and the world. EPTAM Solutions, our parent company with locations nationwide, is at the Heart of Manufacturing. We recognize our parts touch lives, and our teams assume this responsibility with vigor. Our minds never sleep. Join our incredible team at any one of our locations and reap the benefits of an employee focused company. We excel at what we do for our customers, our employees, and the world.

Benefits Include:

Professional Development/On the Job Training
Health and Wellness Benefits
Clean, Friendly, Safe work Environment
Recognition and Rewards Program
Tuition Re-imbursement
Competitive Pay/Merit Increases
401k w/ Company Match
Employee Assistance Program (EAP)

SHIFT DETAILS:

1st Shift Monday through Friday 6:00am to 2:30pm

POSITION SUMMARY: The Quality Engineer is primarily for the following:

Assisting with monitoring and maintaining the Quality Management System (QMS) to ensure compliance with ISO 13485 and 21 CFR part 820 (Quality System Regulation).
Providing focused, Quality Engineering support via communication to department managers of the Quality Management System including Complaint, CAPA, Risk Management, Supplier Quality and Document Control processes.

ESSENTIAL FUNCTIONS: Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

Ensure Quality Management System documentation and reporting of all Quality-related issues and projects are maintained.
Identify and support Quality Manager by executing plans and actions to achieve assigned quality goals.
Coordinate the tracking and closure of Quality issue-related documentation and Change Control related to RMA, NC, CAPA, and MRB System.
Support process owners and department managers/value stream leaders in methods of process improvement and process control related to RMA, NC, CAPA, and other Quality Management issues or concerns.
Monitor customer requests and ensure successful execution of customer-driven acceptance activities.
Develop, vet, and maintain inspection plans.
Draft IQ, OQ, and PQ protocols, execute validations within work cell(s), and write validation reports (IQ/OQ/PQ) for equipment and processes.
Measure components utilizing advanced measuring equipment (i.e., CMM, vision systems, etc.) and various hand gages such as calipers and micrometers.
Employees must be able to relate to other people beyond receiving instructions. Can get along with co-workers or peers and respond appropriately to feedback from a supervisor in a professional manner.

OTHER RESPONSIBILITIES:

Represent the company, as required, during customer, internal and ISO audits, as well as FDA inspections.
Support communication that ensures management and employee understanding of current Good Manufacturing Practices (cGMP).
Leverage industry practices and apply to internal systems and processes.
Ensure quality requirement flow down of customer purchase orders for products to be manufactured.
Identify quality system needs and convey same to Quality Manager for strategic planning and budgeting purposes.
Implement statistical process analysis on new and existing products as needed.
Identify, suggest, and lead changes to benefit the organization within the Quality System or Production.
Understand the sensitivity of the data handled by systems under your control and take appropriate measures to protect it.

EDUCATION AND EXPERIENCE:

EDUCATION: High School diploma or general education degree (GED). Bachelor’s degree with a major in a relevant technical field (STEM) preferred, but not required.
EXPERIENCE: 1+ year(s) relevant quality assurance experience or training, equivalent combinations or education and experience accepted OR demonstrated ability to execute the Essential Functions for this position. Internships and PT experience acceptable. Experience within a manufacturing, medical device company or other similarly regulated manufacturing environment preferred.
LICENSES, CERTIFICATIONS AND/ REGISTRATIONS: Industry recognized Quality certification(s) preferred, but not required.

ADP1550

1st Shift Monday through Friday 6:00am to 2:30pm

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