Chroma Technology

Quality Systems Engineer

Chroma Technology • $70K — $95K *
Manufacturing & Automotive
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • BS degree in science, business, or equivalent experience
  • 3+ years of experience with ISO 9001:2015 Quality Management Systems
  • Knowledge of quality management processes and ISO standards
  • Familiarity with standard business processes such as sales, quoting, and customer service
  • Strong analytical and problem-solving skills
  • Experience in training others on processes and procedures
  • Excellent communication skills with stakeholders

Responsibilities

  • Maintain and enhance the quality management system for compliance
  • Plan, execute, and document internal audits
  • Act as the lead contact for audits from customers and third parties
  • Administer continuous improvement and corrective action projects
  • Ensure effective document control and management
  • Develop and present QMS training programs
  • Lead management review meetings with quality metrics analysis

Benefits

  • Medical, Dental and Vision Insurance
  • 401K plan
  • 80 hours of sick/personal time and vacation
  • Education Assistance
  • Wellness reimbursement
Full Job Description
Quality Systems Engineer

Onsite or Hybrid - Bellows Falls, VT

Job Summary/Objective:

The Quality Systems Engineer owns the company's Quality Management System and quality compliance processes, ensuring they remain effective, audit-ready, and aligned with applicable standards and customer requirements. This role works across the organization to ensure customer quality issues are effectively addressed and drive sustainable corrective action. The Quality Systems Engineer also provides leadership on continuous improvement projects spanning both manufacturing operations and business processes.

Primary Responsibilities and Essential Functions:

  • Maintain and improve the quality management system to ensure compliance with applicable standards and customer requirements
  • Plan and execute the internal audit program: develop the audit schedule, conduct process and system audits, document findings, and drive closure of nonconformances
  • Serve as a lead point of contact for customer, registrar, and third-party audits; coordinate audit responses and follow-up actions
  • Administer and lead continuous improvement or CAPA projects: assign, track, and verify actions to closure, and drive the use of structured problem-solving methodologies across the organization
  • Ensure the functionality of the document control system, including creation, revision, approval, and obsolescence of controlled documents
  • Develop and deliver QMS training, including onboarding employees on quality system procedures and identifying quality training needed
  • Chair management review, including preparation of quality metrics, trend analysis, lead meeting and discussion and follow-up on action items.
  • Support supplier quality system development, including supplier evaluations, supplier corrective action requests (SCARs), and supplier onboarding
  • Lead risk-based thinking activities within the QMS, including process risk assessments and mitigation planning
  • Review customer agreements and quality requirement documents to identify quality system obligations; flow down customer-specific requirements into QMS processes, procedures, and control plans
  • Support change management by evaluating the QMS impact of process, product, organizational changes and customer requirements
  • Analyze quality data to identify trends and prioritize improvement projects
  • Facilitate cross-functional problem-solving teams to resolve internal nonconformances, quality escapes, and recurring process issues.
  • Provide oversight of the nonconforming material process across production, customer returns, and incoming inspection, including identification, segregation, disposition.
  • Provides backup support for processing customer returns as needed
  • Provide leadership and guidance on Manufacturing and Business process improvement projects in support of quality initiatives
  • Serve as the primary resource for day-to-day quality questions and special situations across the organization; exercise independent judgment to resolve issues within established quality system requirements and escalate complex or high-risk matters to the Manufacturing and Quality Engineering Manager


Required Education, Experience, and Eligibility Qualifications:

  • BS degree in science, business, or equivalent experience
  • 3+ years working within a Quality Management System compliant with ISO 9001:2015, including QMS administration and internal/external auditing.
  • Demonstrated knowledge and leadership experience of quality management processes, process documentation, and ISO standards
  • Familiarity with standard business processes and business process reengineering: Sales, quoting, product development, Customer service, inventory and order management, shipping, procurement, quality assurance
  • Strong analytical/problem solving skills and ability to use statistical tools and techniques
  • Demonstrable experience training others in process and procedures
  • Ability to communicate effectively and professionally with co-workers, customers, and suppliers
  • Demonstrated ability to lead and be part of multidisciplinary teams
  • Self-directed and detail-oriented with the ability to multitask


Compensation and Benefits
  • Pay Range $70,000 - $95,000
  • Medical, Dental and Vision Insurance
  • 401K
  • 80 Hours Sick/Personal Time and 80 Hours Vacation
  • Education Assistance and Wellness Reimbursement


Please note that the compensation offered to the selected candidate will be based on a variety of factors, including but not limited to experience, skills, education, and internal equity. As such, applicants should not expect to receive the maximum of the posted range.

Please visit our career page at www.chroma.com to review the full job description, summary of benefits, and to apply online.

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