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Qms Associate Jobs (NOW HIRING)

EKF DIAGNOSTICS INC

Quality Associate II - QMS

Boerne, TX · On-site

$28 - $37/hr

The Quality Associate II - Quality Management System (QMS) supports the development, maintenance, and continuous improvement of the QMS in alignment with ISO 13485, ISO 9001, FDA QMSR, MDSAP and ...

EKF DIAGNOSTICS INC

Quality Associate II - QMS

Boerne, TX · On-site

$28 - $37/hr

The Quality Associate II - Quality Management System (QMS) supports the development, maintenance, and continuous improvement of the QMS in alignment with ISO 13485, ISO 9001, FDA QMSR, MDSAP and ...

BSI Group

Associate QMS Auditor

Reston, VA

Associate Auditor Location: California, Texas, Illinois, Virginia, and Ohio About the Role: Are you ... Conduct audits across a wide range of industries, ensuring alignment with QMS (ISO 9001 and related ...

BSI Group

Associate QMS Auditor

Concord, NC

Associate Auditor Location: California, Texas, Illinois, Virginia, and Ohio About the Role: Are you ... Conduct audits across a wide range of industries, ensuring alignment with QMS (ISO 9001 and related ...

BSI Group

Associate QMS Auditor

Austin, TX

Associate Auditor Location: California, Texas, Illinois, Virginia, and Ohio About the Role: Are you ... Conduct audits across a wide range of industries, ensuring alignment with QMS (ISO 9001 and related ...

BSI Group

Associate QMS Auditor

San Jose, CA

Associate Auditor Location: California, Texas, Illinois, Virginia, and Ohio About the Role: Are you ... Conduct audits across a wide range of industries, ensuring alignment with QMS (ISO 9001 and related ...

BSI Group

Associate QMS Auditor

The Woodlands, TX

Associate Auditor Location: California, Texas, Illinois, Virginia, and Ohio About the Role: Are you ... Conduct audits across a wide range of industries, ensuring alignment with QMS (ISO 9001 and related ...

Takeuchi

QMS Coordinator

Moore, SC · On-site

$65K - $70K/yr

Maintain and administer the ISO 9001 Quality Management System (QMS) and related procedures ... Associate's or Bachelor's degree in Quality, Engineering, Business, or a related field, or ...

TAKEUCHI MFG U S LTD

QMS Coordinator

Moore, SC

$65K - $70K/yr

Maintain and administer the ISO 9001 Quality Management System (QMS) and related procedures ... Associate's or Bachelor's degree in Quality, Engineering, Business, or a related field, or ...

Algas-SDI International LLC

QMS Coordinator

Kent, WA · On-site

$75K - $92K/yr

Associate's degree or higher; Bachelor's preferred * 3+ years of experience in a QMS coordination, quality systems, or operations coordination role * Demonstrated experience with document control ...

Allred & Associates

Be Seen First

QMS Coordinator - Manufacturing

Elbridge, NY · On-site

$25 - $30/hr

High school diploma or equivalency; associate's degree or ISO 9001 Internal Auditor training ... maintain QMS documentation * Experience conducting internal audits and presenting findings to ...

Urgent

Allred & Associates

Be Seen First

QMS Coordinator - Manufacturing

Elbridge, NY · On-site

$25 - $30/hr

High school diploma or equivalency; associate's degree or ISO 9001 Internal Auditor training ... maintain QMS documentation * Experience conducting internal audits and presenting findings to ...

Urgent

Vertiv Group Corp.

Quality QMS Coordinator

Pelzer, SC · On-site

High school diploma or equivalent (Associate's degree in Quality, Engineering, or Manufacturing preferred) * 1-3 years of experience in a manufacturing quality or QMS role * Working knowledge of ...

PETOSKEY PLASTICS

QMS Manager

Hartford City, IN

... our customers, associates, and communities. If you are seeking a family-oriented company that ... Short- and Long-Term Disability The QMS Manager is responsible for coordinating the development ...

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How much do qms associate jobs pay per year?

As of Jun 14, 2026, the average yearly pay for qms associate in the United States is $141,209.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,000.00 and $212,500.00 per year, depending on experience, location, and employer.
What cities are hiring for Qms Associate jobs? Cities with the most Qms Associate job openings:
What are the most commonly searched types of Qms jobs? The most popular types of Qms jobs are:
What states have the most Qms Associate jobs? States with the most job openings for Qms Associate jobs include:
Qms Associate jobs near you
Infographic showing various Qms Associate job openings in the United States as of June 2026, with employment types broken down into 2% As Needed, 2% Full Time, 91% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $141,209 per year, or $67.9 per hour.

Quality Associate II - QMS

EKF Diagnostics Inc

Boerne, TX • On-site

Full-time

Posted 9 days ago

Job description

Job Type
Full-time
Description
SUMMARY OF POSITION:
The Quality Associate II - Quality Management System (QMS) supports the development, maintenance, and continuous improvement of the QMS in alignment with ISO 13485, ISO 9001, FDA QMSR, MDSAP and other applicable requirements. This role focuses on Corrective and Preventative Actions (CAPAs), internal audits, supporting external audits, training, batch release, supplier qualification and quality agreements, and QMS-level risk management. The position ensures the QMS remains compliant, effective, and inspection-ready.
ESSENTIAL FUNCTIONS, included but not limited to:
QMS Quality Oversight
  • Administer and maintain QMS processes including CAPAs, internal audits and training Standard Operating Procedures (SOPs).
  • Lead or support CAPA investigations, ensuring strong root-cause analysis, effectiveness checks, and timely closure.
  • Support internal audit planning, execution, reporting, and follow-up activities.
  • Support Quality Assurance (QA) Manager and QMS Documentation Lead with document control and change management activities, including SOPs, forms, labels, instructions for use (IFUs), and controlled templates.
  • Maintain and oversee the training management system.
  • Support QA review of the feedback and complaint handling activities, escalate to Regulatory as needed.
  • Perform quality review of supplier approval process, including risk assessments.
  • Support risk management activities (ISO 14971), as needed.
  • Perform trend analysis across QMS processes (CAPA, complaints, audits, training, etc.) and escalate trends.
  • Prepare reports for quality review board, management review, etc.
  • Support the training program by managing the training matrix, ensuring training assignments are accurate, current, and aligned with role requirements; monitor completion status and maintain compliant training records.

Batch Release
  • Review and approve batch records and final product documentation.
  • Ensure completeness, accuracy, and compliance of DHRs, COAs, and supporting documentation.

Documentation & Compliance
  • Ensure quality related documentation complies with ISO 13485, ISO 9001 and FDA 21 CFR 820 (QMSR), and other applicable requirements.
  • Support and participate in internal and external audits.
  • Ensure that batch reviews are conducted by personnel independent from the manufacturing, production or testing activities to ensure objective assessment and prevent conflicts of interest.
  • Support operations in ensuring their documentation complies with ISO 13485, ISO 9001 and FDA 21 CFR 820 (QMSR)
  • Draft, revise, and maintain SOPs, work instructions, forms, and controlled documents related to operations quality.
  • Support internal and external audits by providing quality records and participating in audit activities.

Training & Cross-Functional Support
  • Provide training on QMS, continuous improvements, Good Manufacturing Practice (GMP), Good Documentation Practices (GDP), and compliance requirements, as applicable.
  • Cross-train with the Quality team and provide support during peak workload periods.
  • Collaborate with Manufacturing, Procurement, Technical Support, Compliance (QC, RA) and other departments as applicable to ensure compliant operations.

OTHER FUNCTIONS:
  • Ensure compliance with safety regulations and procedures are implemented and followed; Maintain clean and safe work area.
  • Assist as needed in other areas of the Company where training requirements have been completed.
  • Perform other duties as assigned.

SUPERVISORY RESPONSIBILITIES:
  • None

TRAVEL:
  • 5% annually for supplier audits or cross-site activities.

Requirements
REQUIRED QUALIFICATIONS:
  • Bachelor's degree (B.A. /B.S.) from an accredited college or university in a science related field.
  • Legally authorized to work in the United States.
  • Three (3) years of quality experience in relation to medical devices or In vitro diagnostics devices.
  • Strong knowledge of various standards and regulations such as ISO 9001, ISO 13485, ISO 14971, Quality Management System Regulation (QMSR) (21 CFR Part 820).

PREFERRED QUALIFICATIONS:
  • Five (5) years proven quality experience in relation to In vitro diagnostics devices.
  • Knowledgeable supplier programs, CAPA, Internal Audits, Risk Management .
  • Knowledge of MDSAP.

BASIC SKILLS AND ABILITIES:
  • Project a positive company image by interacting with fellow employees, customers, and management in a cooperative, supportive, and courteous manner; displays a professional attitude.
  • Good computer skills including Microsoft Word, Excel, Outlook.
  • Detail oriented with a high level of accuracy, efficiency, and accountability.
  • Excellent organizational skills to meet goals and set priorities.
  • Proven ability to handle multiple projects and meet deadlines; work in a fast-paced environment.
  • Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm.
  • Initiative to offer new innovative ideas and improve processes.
  • Ability to work independently and as a member of various teams and committees.

REASONING ABILITIES:
  • Ability to define problems, collect data, establish facts, and draw valid conclusions.
  • Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
  • Must have strong analytical and planning skills sufficient to determine resources and time required to complete projects.

LANGUAGE SKILLS:
  • Good written and oral communication skills; with the ability to interface well with management, internal employees, FDA, notified bodies, and other international regulatory authorities.
  • Ability to read, analyze, and interpret general business periodicals, professional scientific and technical journals, technical procedures, financial reports, legal documents, and governmental regulations.
  • Ability to write reports, business correspondence, and procedure manuals.
  • Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community.

MATHEMATICAL SKILLS:
  • Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.
  • Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations.
  • Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis.

VISUAL ACUITY:
  • Close visual acuity to perform an activity such as preparing and analyzing data, transcribing, viewing a computer terminal, and reading.

PHYSICAL DEMANDS:
  • Must be able to wear and work in personnel protective equipment (PPE) as required.
  • Light physical activity performing non-strenuous daily activities of a primarily administrative nature.
  • Stationary position sitting for prolonged periods of time while utilizing standard office tools.
  • Constant repetitive motions that may include the wrists, hands and/or fingers to operate keyboard and mouse; dexterity and coordination necessary to handle files and single pieces of paper.
  • The ability to hear, understand, and distinguish speech.
  • Frequently communicate information and ideas with others to exchange information and understanding. Able to exchange accurate information in these situations.
  • Frequently lift and/or move up to 10 pounds, occasionally lift and/or move up to 25 pounds, and rarely lift and/or move up to 50 pounds.
  • Often move about inside the facility to access office machinery, correspond with other departments, attend meetings/training, etc.
  • Occasionally reaching for items above and below desk level.
  • Occasionally required to climb or balance; squat, stoop, kneel, crouch, or crawl, and smell.

ENVIRONMENT CONDITIONS:
  • Well lit, heated/air-conditioned indoor office setting with adequate ventilation.
  • The noise level in the work environment is low.
  • Periodic exposure to low temperatures in controlled refrigerators and/or freezers.
  • Some exposure to hazards or physical risks which require following basic safety precaution.

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