Senior Supplier Quality Engineer

Posted Yesterday
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Maple Grove, MN, USA
In-Office
Senior level
Healthtech
The Role
Leads supplier quality activities for medical device materials and components, including supplier selection, qualification, audits, performance monitoring, change notifications, SCARs, testing, CAPAs, nonconformances, and quality metrics. Owns supplier-related quality system processes and supports internal and external audits. Partners across engineering, manufacturing, supply chain, and quality teams while providing technical leadership and potentially supervising employees.
Summary Generated by Built In

This role is responsible for partnering with development, manufacturing, supply chain, and quality teams to assess, onboard, and qualify new material and component suppliers and monitor continued supplier performance. The supplier quality engineer is the primary liaison to Nextern suppliers to facilitate communication related to quality of supplied materials, change notifications, performance assessments/audits, and resulting actions as applicable. All engineering functions are responsible for compliance with the Quality System and relevant regulations and standards, continuous improvement, and as needed, professional interaction with Nextern Customers.


Requirements

DUTIES AND RESPONSIBILITIES:

· Partners with development and supply chain teams to initiate new and monitor existing suppliers

· Assess purchased material and supplier characteristics to determine supplier categorization

· Initiate, populate, and maintain supplier files to ensure traceable supplier control

· Ensure supplier and supplied part documentation meets business and program requirements

· Receive, initiate, and assess supplier change notifications. Coordinate with SMEs as necessary

· Initiate and assign ownership for Supplier Corrective Action Requests (SCARs)

· Coordinate and execute, as applicable, material and component testing in support of material qualification

· Define and establish monitoring requirements/plans for receiving inspection and supplier data

· Compile, analyze, and present supplier specific performance metrics for project design and management reviews

· Initiate, investigate, and coordinate SME support as necessary to process supplied part NCs & CAPAs

· Owner of Quality System processes for supplier selection, qualification, and monitoring

· Proactively identify redundancy and opportunities for efficiency in Quality System requirements

· Review and approve changes for supplied parts to ensure adequate supplier data/linkage

· Support external and internal audits as Subject Matter Expert (SME) for owned QMS processes

· Plan and lead supplier audits and support supplier monitoring audits, as necessary

· Other duties as assigned

SUPERVISORY RESPONSIBILITIES:

This job may have supervisory/management responsibilities. Where supervisory responsibilities are relevant:

· Carries out supervisory responsibilities in accordance with the organization's policies and applicable laws

· Interviews, hires, and trains employee(s). Manages employee(s) work direction, resource load, review/appraisal, and career development. Addresses and support resolution of employee complaints/issues.

QUALIFICATIONS:

· Bachelor's Degree (BS) in life science discipline or equivalent combination of education and experience.

· 10+ years of experience in medical device Quality function, or 5+ years of experience in a Supplier Quality/Supplier Engineering role

· Experience working in quality systems as defined in 21 CFR 820 and ISO 13485

· BSI (or equivalent) ISO 13485 Lead Auditor certification

· Understanding of ISO 14971 and application of risk management to supplier qualification

· Demonstrated technical expertise and leadership in quality

· High attention to detail, organization, and accuracy

· Instinctual capability for creative thinking and proposing novel solutions

· Strong ability to communicate (written and verbally) within and across disciplines and organization structures

· Demonstrated use of quality tools and methodologies (e.g. nonconformance, CAPAs, root cause analysis, etc..)

· Familiarity with statistical software, such as Minitab, preferred

· Experience with Product Lifecycle Management (PLM) software (e.g Windchill, Agile, Propel)

· Intermediate to advanced proficiency with MS Office Suit (Word, Excel, PowerPoint, Project, Outlook)


Benefits
  • Health Care Plan (Medical, Dental & Vision)
  • Retirement Plan with Company Match
  • Paid Time Off, Personal Days, AND Birthday Holiday!
  • Lifetime Membership Subsidy and Wellness Resources
  • Life Insurance (Basic, Voluntary & AD&D)
  • Family Leave (Maternity, Paternity)
  • Short-Term & Long-Term Disability
  • Taco Thursdays!!!

Nextern is an equal opportunity employer. We encourage applications from candidates of all backgrounds and experiences, and we are committed to fostering an inclusive and diverse workplace. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Skills Required

  • Bachelor’s degree in a life science discipline or equivalent combination of education and experience
  • 10 or more years of experience in a medical device quality function, or 5 or more years in a supplier quality or supplier engineering role
  • Experience with quality systems defined by 21 CFR 820 and ISO 13485
  • BSI or equivalent ISO 13485 Lead Auditor certification
  • Understanding of ISO 14971 and risk management application to supplier qualification
  • Demonstrated technical expertise and leadership in quality
  • High attention to detail, organization, and accuracy
  • Creative thinking and ability to propose novel solutions
  • Strong written and verbal communication skills across disciplines and organizational structures
  • Experience using quality tools and methodologies, including nonconformance management, CAPAs, and root cause analysis
  • Familiarity with statistical software such as Minitab
  • Experience with Product Lifecycle Management software such as Windchill, Agile, or Propel
  • Intermediate to advanced proficiency with Microsoft Office Suite, including Word, Excel, PowerPoint, Project, and Outlook
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The Company
HQ: Saint Paul, MN
172 Employees
Year Founded: 2000

What We Do

Nextern collaborates with innovators, clinicians, and device partners to create, iterate, optimize and manufacture best-in-class medical devices. We bring an unmatched core competence in medical device product design and development through manufacturing as a leverageable asset to collaborators like you, who are focused on accelerating the commercial side of the business.​

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