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Job Description Summary

The Quality Specialist is a key member of the site Quality Management System (QMS) team and will be responsible for supporting and sustaining core QMS processes, including Training, Internal Audits, Document Control, and the 3rd Party Calibration Program. This role helps ensure that our QMS complies with internal GE requirements as well as external standards (e.g., ISO 9001:2015/ISO 9001:2026) and customer expectations by effectively managing these QMS elements, the Quality Specialist will help ensure that processes, documentation, and employee competencies consistently meet GE’s quality goals and those of our customers and stakeholders.

Job Description

Essential Responsibilities

+ **QMS Training Program**

+ **Internal Audit Program**

+ **Document Control Program**

+ **Calibration Programs**

+ **Quality Control**

+ **Continuous Improvement**

QMS Training Program Support

+ Partner with the Lead Process Engineer to ensure the effectiveness and compliance of the training program as a key QMS process.

+ Maintain accurate training records for production employees in alignment with QMS and audit requirements.

+ Coordinate with employees, Team Leads, and Supervisors to keep training status current and compliant for their teams.

+ Ensure individual training plans are correctly completed and aligned with standard work and applicable procedures.

+ Update training plans in response to changes in processes, procedures, or standard work.

+ Organize and participate in meetings with HR and production supervisors to confirm training requirements are defined, met, documented, and closed in a timely manner.

+ Communicate changes to training requirements and training plans to production teams and supervisors.

+ Perform routine audits of the training program to verify that:

+ Training documentation is properly completed and submitted

+ Training records are accurately reflected in the training skills matrix

+ Training activities meet QMS and regulatory/customer requirements

Internal Audit Program Support

+ Plan and perform internal audits in accordance with the audit schedule and QMS procedures.

+ Collaborate with cross-functional Audit Teams to assess process conformity, identify nonconformities, and verify compliance with QMS requirements (e.g., ISO 9001:2015 and internal procedures).

+ Participate in cross-functional investigations to determine root causes of quality issues and audit findings.

+ Support the implementation and verification of corrective actions, including follow-up to confirm effectiveness and sustained improvement.

Document Control / QMS Documentation Support

+ Support the Lead Process Engineer in managing and maintaining the document control program as defined in the QMS.

+ Ensure production documents and procedures (e.g., work instructions, process standards, forms) accurately reflect current operations and QMS requirements.

+ Revise documentation in response to internal audit results, nonconformances, investigations, process changes, or QMS improvement initiatives.

+ Upload and route work instructions, procedures, training plans, and related documents in the document control system for review and approval.

+ Help ensure proper document revision control, availability of current versions at points of use, and timely removal of obsolete documents.

Calibration Program Support

+ Log equipment and instruments into the internal calibration tracking system in line with QMS and metrology requirements.

+ Work with the Process Engineer and 3rd party calibration supplier to ensure tools are:

+ Clean and in good working order

+ Calibrated on schedule

+ Properly labeled and fit for use

+ Help coordinate instruments that are calibrated internally, ensuring adherence to calibration procedures and intervals.

+ Collaborate with Industrial Engineering and other teams to ensure the correct tool is used for the correct application and that calibration requirements are defined and maintained within the QMS.

Quality Control Support

+ Support the implementation of quality control requirements defined in procedures, control plans, and work instructions.

+ Assist in monitoring key quality indicators (e.g., defect rates, rework, scrap, first-pass yield) and escalate trends or risks to the Quality and Operations teams.

+ Help review inspection records, test data, and production documentation for completeness, accuracy, and compliance with QMS and customer requirements.

+ Coordinate with production and quality teams to ensure inspection and test activities are performed as defined and properly documented.

+ Support the identification, documentation, and disposition of nonconforming product in accordance with QMS procedures.

+ Assist in verifying that corrective and preventive actions tied to quality issues are implemented and effective at the process level.

Continuous Improvement Support

+ Participate in continuous improvement activities related to QMS processes (e.g., training, internal audits, documentation, calibration, nonconformance handling).

+ Support structured problem-solving efforts (e.g., 5 Why, basic root cause analysis) to address audit findings, recurring nonconformances, and gaps in QMS processes.

+ Help identify opportunities to simplify and standardize QMS-related workflows while maintaining compliance (e.g., forms, templates, document routes, training records).

+ Assist in tracking and following up on QMS-related corrective and preventive actions (CAPAs) to ensure timely closure and sustained improvements.

+ Contribute to the development and updating of QMS metrics dashboards and visual management boards to increase visibility of quality and compliance performance.

+ Provide feedback from day-to-day QMS activities to support management reviews and site-level QMS improvement initiatives.

Required Qualifications

• Bachelor’s degree in a technical discipline or related field with a minimum of 2 years of experience as an internal auditor in a Production Quality Rolein a manufacturing environment **OR** High School Diploma (or GED) with a minimum of 4 years of experience in an industrial or manufacturing environment

• Minimum of 1 year of quality assurance or QMS-related experience

• ISO 9001:2015 Lead Auditor Certification

Desired Characteristics

• ISO 9001:2015 Internal Auditor Certification

• Experience working with quality management systems (e.g., internal audits, document control, CAPA, training, calibration, quality control)

• Strong oral and written communication skills; able to effectively communicate QMS and quality requirements across functions and levels

• Ability to work collaboratively in a team environment and build strong cross-functional relationships

• Strong attention to detail and thoroughness in executing QMS and quality control tasks

• Ability to adapt to changes in priorities and QMS requirements based on business needs or audit findings

• Comfortable working and communicating with employees at all levels of the organization

• Ability to independently prioritize and manage daily and weekly work within QMS timelines and audit schedules

+ Note: **To comply with US immigration and other legal requirements, it is necessary to specify the minimum number of years’ experience required for any role based within the USA.** **For roles outside of the USA, to ensure compliance with applicable legislation, the JDs should focus on the substantive level of experience required for the role and a minimum number of years should NOT be used.**

Additional Information

GE Vernova offers a great work environment, professional development, challenging careers, and competitive compensation. GE Vernova is an Equal Opportunity Employer (https://www.eeoc.gov/sites/default/files/2022-10/22-088\_EEOC\_KnowYourRights\_10\_20.pdf) . Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

GE Vernova will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).

**Relocation Assistance Provided:** No

For candidates applying to a U.S. based position, the pay range for this position is between $76,300.00 and $114,400.00. The Company pays a geographic differential of 110%, 120% or 130% of salary in certain areas. The specific pay offered may be influenced by a variety of factors, including the candidate’s experience, education, and skill set.

Bonus eligibility: ineligible.

This posting is expected to remain open for at least seven days after it was posted on January 19, 2026.

Available benefits include medical, dental, vision, and prescription drug coverage; access to Health Coach from GE Vernova, a 24/7 nurse-based resource; and access to the Employee Assistance Program, providing 24/7 confidential assessment, counseling and referral services. Retirement benefits include the GE Vernova Retirement Savings Plan, a tax-advantaged 401(k) savings opportunity with company matching contributions and company retirement contributions, as well as access to Fidelity resources and financial planning consultants. Other benefits include tuition assistance, adoption assistance, paid parental leave, disability benefits, life insurance, 12 paid holidays, and permissive time off.

GE Vernova Inc. or its affiliates (collectively or individually, “GE Vernova”) sponsor certain employee benefit plans or programs GE Vernova reserves the right to terminate, amend, suspend, replace, or modify its benefit plans and programs at any time and for any reason, in its sole discretion. No individual has a vested right to any benefit under a GE Vernova welfare benefit plan or program. This document does not create a contract of employment with any individual.

GE Vernova is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.