Quality Manager

Posted 2 Days Ago
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55426, Minneapolis, MN, USA
In-Office
100K-120K Annually
Mid level
Healthtech • Defense • Industrial • Manufacturing
The Role
Lead site quality assurance activities to maintain ISO and FDA regulatory compliance, manage audits, develop and train on QMS, perform root-cause analysis, maintain quality documentation (PFMEA, control plans), manage metrics, and support an ISO Class 8 cleanroom environment.
Summary Generated by Built In

Spectrum Plastics Group

The main responsibilities within the role of the Quality Assurance Manager will be to ensure the highest standards are met in accordance with regulatory requirements and/or stated standards (ISO & FDA); to continuously improve our quality reporting processes; to manage the team to ensure quality assurance results are maintained and produced in a timely manner; to control, review and challenge our quality associates on customer standards to ensure compliance by providing advice and support.

The ideal candidate will be required to read and interpret engineering drawings and quality specifications, to prepare quality inspection procedures and investigate and resolve quality problems; manage customer and third party quality audits as required; manage and/or perform direct internal quality audits; act as liaison with customers on quality issues; communicate company Quality Objectives to all employees; and work closely with all departments to build a Quality Team.

Key Responsibilities:

  • Responsible for site regulatory compliance
  • Ensure maintenance and implementation of Quality Systems and training
  • Act in conjunction with Plant Manager as technical contact on quality-related issues
  • Address customer concerns, applying root-cause analysis and problem-solving skills
  • Aid in development of suppliers and implementation of Quality Systems Documentation including training documentation and providing appropriate training
  • Lead audits by Third-Party Registrars/Customers
  • Fully support and work with all departments to ensure quality standards are upheld
  • Provide leadership within the daily QA activities and promote a Quality culture throughout the facility.
  • Support utilization of ISO and QMS systems cost-effectively
  • Utilize APQP/PPAP, process flow maps, FMEAs, control plans and measurement system evaluations to support Quality Standard requirements
  • Ensure Quality documentation is current with Corrective Actions (PFMEA, Control Plans, Flow Charts, etc)
  • Manage and report key Quality Performance Metrics
  • Work with other disciplines to ensure the integrity of an ISO Class 8 cleanroom
  • Promote company Core Values with key focus on Safety
  • Assist with other various duties as assigned by management
Qualifications
  • Must possess degree of Science or Business or similar, with 3-5 years’ experience in Quality Assurance in a manufacturing environment
  • Must have a thorough understanding and working knowledge of ISO 9001:2015 and ISO 13485:2016 standards.
  • Must be a certified Lead Auditor.
  • Must have experience managing third party regulatory and customer audits.
  • Must have thorough understanding of QA/QC theory, procedures and practices, including potential failure modes for company product lines
  • Must have basic understanding of manufacturing processes and operation systems
  • Must possess strong communication, presentation and analytical skills
  • Must have ability to negotiate and communicate successfully at all levels
  • Must possess strategic planning and development skills
  • Must have extensive knowledge of measuring/test equipment, gauging practices and capability of undertaking full GR&Rs
  • Must possess working knowledge of computers, software applications (at least: Word, Excel, Visio, Access and Outlook) and excellent reading/comprehension skills


Experience:

  • ISO Certification: 2 years (Preferred)
  • Quality Assurance: 3 years (Preferred)
  • Manufacturing: 3 years (Preferred)

Education:

  • Bachelor's (Preferred)

Skills Required

  • Degree in Science, Business, or similar
  • 3-5 years experience in Quality Assurance in a manufacturing environment
  • Thorough understanding and working knowledge of ISO 9001:2015 and ISO 13485:2016
  • Certified Lead Auditor
  • Experience managing third-party regulatory and customer audits
  • Thorough understanding of QA/QC theory, procedures and practices including failure modes
  • Basic understanding of manufacturing processes and operation systems
  • Strong communication, presentation and analytical skills
  • Ability to negotiate and communicate successfully at all levels
  • Strategic planning and development skills
  • Extensive knowledge of measuring/test equipment and gauging practices; capable of full GR&R studies
  • Working knowledge of computers and software applications (Word, Excel, Visio, Access, Outlook)
  • Experience with APQP/PPAP, process flow maps, FMEAs, control plans and measurement system evaluations
  • ISO Certification (2 years)
  • Quality Assurance (3 years)
  • Manufacturing experience (3 years)
  • Bachelor's degree

Spectrum Plastics Group Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Spectrum Plastics Group and has not been reviewed or approved by Spectrum Plastics Group.

  • Retirement Support A 401(k) match is included in the core package for full-time employees. This provides employer-backed retirement savings support beyond base pay.
  • Wellbeing & Lifestyle Benefits Paid Volunteer Time Off, wellness resources, an Employee Assistance Program, and employer‑paid life/short‑term/long‑term disability are part of the offering. These programs extend support for personal wellbeing and community involvement.
  • Healthcare Strength Health and dental coverage are available, with HSA options noted. The overall package is characterized as solid in multiple descriptions.

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The Company
HQ: Atlanta, GA
2,200 Employees
Year Founded: 1949

What We Do

Spectrum Plastics Group is a global leader in the design, development, and manufacturing of specialty medical components and devices, providing solutions from development through scaled manufacturing for medical and other demanding markets.

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