Quality Control Systems Specialist

United StatesUnited States·Bryanmid
Quality Control SpecialistLaboratory & Life Sciences
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Overview

Summary The Quality Control Systems Specialist is responsible for administering and improving quality system processes to ensure compliance with customer, regulatory, engineering,

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Quality Control SpecialistLaboratory & Life Sciences

The Quality Control Systems Specialist is responsible for administering and improving quality system processes to ensure compliance with customer, regulatory, engineering, and industry requirements. This position independently evaluates contractual, technical, and regulatory requirements; determines quality documentation and compliance strategies; assesses documentation and quality-system risks; and provides guidance to cross-functional teams regarding quality and compliance obligations.

The Quality Control Systems Specialist serves as a key resource to Quality, Engineering, Manufacturing, and Supply Chain functions by interpreting customer and industry requirements, administering quality-system processes, identifying compliance risks, recommending corrective actions, and supporting continuous improvement initiatives. Success in this role requires sound judgment, strong analytical skills, and the ability to make independent decisions regarding quality documentation, compliance requirements, and quality-system effectiveness.

Responsibilities

~2 min read
  • →Analyze customer drawings, specifications, purchase orders, contracts, and technical requirements to determine required certifications, inspection records, test reports, and other objective quality evidence (OQE), and identify documentation necessary to demonstrate compliance with contractual and regulatory requirements.
  • →Interpret applicable military, NAVSEA, ASTM, ASME, customer, and other industry specifications and independently determine documentation, inspection, testing, and compliance requirements necessary to satisfy contractual and regulatory obligations.
  • →Develop and maintain customer compliance matrices by interpreting customer requirements and determining the appropriate quality records, certifications, and objective evidence necessary to demonstrate compliance.
  • →Develop, review, and approve customer data books and documentation packages to ensure contractual, technical, and regulatory requirements have been satisfied.
  • →Serve as a quality documentation resource for customers by interpreting compliance requirements, resolving documentation issues, and providing guidance regarding quality deliverables.
  • →Administer quality records management and retention systems to ensure compliance with customer, regulatory, legal, and company requirements.
  • →Administer and evaluate the effectiveness of the calibration program for inspection, measuring, and test equipment to ensure quality-system compliance and minimize operational risk.
  • →Monitor NCR and CAPA activities, evaluate trends and recurring issues, and recommend corrective and preventive actions to improve quality-system effectiveness.
  • →Analyze quality-related issues, recommend solutions, and facilitate resolution through collaboration with internal and external stakeholders.
  • →Develop, revise, implement, and periodically evaluate quality procedures, forms, controls, and continuous improvement initiatives.
  • →Ensure adherence to applicable customer requirements, industry standards, regulations, and company procedures.
  • →Coordinate third-party certification activities, determine required documentation, and resolve documentation issues that may impact certification acceptance.
  • →Evaluate inspection requirements, coordinate NDE activities, and determine quality documentation necessary to demonstrate compliance with applicable specifications and customer requirements.
  • Strong attention to detail and organizational skills.
  • Ability to read and interpret engineering drawings, specifications, purchase orders, and customer requirements.
  • Ability to review and correlate material certifications, inspection records, test reports, NDE reports, and other objective quality evidence (OQE) to documented requirements.
  • Demonstrated analytical, risk assessment, problem-solving, and decision-making abilities.
  • Strong written and verbal communication skills.
  • Proficient in Microsoft Office applications, particularly Excel, Word, and Outlook.
  • Ability to manage multiple projects and priorities in a fast-paced manufacturing environment.
  • Ability to independently evaluate compliance requirements, prioritize competing demands, and exercise sound judgment in resolving quality-system issues.
  • Knowledge of quality management systems and quality documentation principles.
  • Familiarity with military, NAVSEA, ASTM, ASME, AWS, DNV, or other industry standards preferred.
  • Experience working with compliance matrices, data books, manufacturing record books, or customer quality deliverables preferred.
  • Knowledge of manufacturing, machining, fabrication, welding, NDE, or subsea/oil and gas equipment preferred.
  • Ability to exercise discretion and independent judgment in interpreting quality requirements, evaluating compliance risks, and recommending corrective actions.
  • Associate degree in Quality, Engineering Technology, Manufacturing Technology, Industrial Technology, Business Administration, or related field; or an equivalent combination of education and relevant quality systems experience.

Preferred

  • Bachelor's degree in Quality Management, Engineering Technology, Manufacturing, Industrial Technology, Business Administration, or a related discipline.
  • Equivalent combinations of education, training, and relevant experience will be considered.
  • 3+ years of experience in quality systems, quality assurance, regulatory compliance, manufacturing quality, supplier quality, audit administration, or related quality-focused roles in an industrial or manufacturing environment.

Preferred

  • 5+ years of experience administering quality systems, evaluating compliance requirements, supporting audit programs, or leading quality documentation and compliance activities within a manufacturing environment.
  • Experience interpreting engineering drawings, technical specifications, customer requirements, and regulatory standards to determine documentation, inspection, testing, and compliance requirements.
  • Experience developing, reviewing, or approving quality data books, manufacturing record packages, and customer compliance documentation in support of contractual and regulatory requirements.
  • Experience interpreting and applying military, defense, customer-specific, or other highly regulated quality and compliance requirements.

About FET
FET (Forum Energy Technologies, Inc.) is a global company, serving the crude oil, natural gas, and renewable energy industries. FET is headquartered in Houston, TX with quality manufacturing, efficient distribution, and service facilities conveniently located to support the major energy-producing regions of the world. Forum’s products and services range from the underwater reservoir to the refinery, from the sea floor to the above ground transportation line. We pride ourselves on giving you a comprehensive offering of solutions to maximize your operations and improve your bottom line. Our customers are our partners and we work with them to solve their ever-changing challenges.

FET is an Equal Opportunity Employer. FET does not discriminate on the basis of race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected under federal, state, or local law. All employment decisions and practices at FET are subject to the foregoing non-discrimination provisions and are based solely on merit, competence, performance, and business needs at the time.

FET participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. FET participa en E-Verify y proporcionará al gobierno federal la información de su Formulario I-9 para confirmar que usted está autorizado para trabajar en los EE.UU..

As part of our hiring process, we may use technology, including AI-enabled tools, to help review and assess applications based on job-related criteria. All hiring decisions are made by our recruitment team and hiring managers.

Location & Eligibility

Where is the job
Bryan, United States
On-site at the office
Who can apply
US

About this job

Who can apply
United States
Posted
Today
Employer
has 85 open jobs on Jobera in 5 countries.

Listing Details

Posted
October 28, 2026
First seen
October 28, 2026
Last seen
October 28, 2026

Posting Health

Days active
0
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0
Trust Level
56%
Scored at
October 28, 2026

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Quality Control Systems Specialist