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Qms Implementation Jobs in Texas (NOW HIRING)

Victaulic

Quality Manager - Fabrication

Justin, TX · On-site

Implement corrective action plans and monitor remediation effectiveness. * Conduct regular audits to ensure adherence to QMS and identify areas for improvement. * Foster a culture of quality ...

Kiewit

Engineering Quality Manager - OGC Engineering

Houston, TX · On-site

$120 - $150/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Oversee and lead the implementation of the Quality Management System (QMS) across the district, ensuring alignment with ISO 9000/9001, company standards, and industry regulations. * Develop and ...

Bureau Veritas

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Promote and support the application and implementation of systems and processes (e.g. QMS, Job Management System, Laboratory Information Management System) to improve quality, service, customer ...

Group CBS

Warehouse Manager

Irving, TX

Monitor warehouse performance metrics and implement continuous improvement initiatives. * Ensure compliance with OSHA regulations, ISO 9001/QMS standards, and company safety policies. * Safely ...

New

Bureau Veritas

Regional Quality Manager

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Promote and support the application and implementation of systems and processes (e.g. QMS, Job Management System, Laboratory Information Management System) to improve quality, service, customer ...

Panelmatic

Quality Manager

Conroe, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... QMS). This role requires cross-functional collaboration to support manufacturing excellence ... Develop, implement, manage and maintain all aspects of the Plant Quality Management System in ...

Panelmatic

Quality Manager

Conroe, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... QMS). This role requires cross-functional collaboration to support manufacturing excellence ... Develop, implement, manage and maintain all aspects of the Plant Quality Management System in ...

Panelmatic

Quality Manager

Conroe, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... QMS). This role requires cross-functional collaboration to support manufacturing excellence ... Develop, implement, manage and maintain all aspects of the Plant Quality Management System in ...

Rising Edge Group

Quality Control Manager

Dallas, TX · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... implementation of corrective actions * Continually develop and review inspection and test procedures * Ensure QMS processes are developed, maintained, and followed, as well as the development of ...

Randstad

Quality Control Officer

Austin, TX · On-site

$70K - $90K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

QMS & Document Control: Maintain procedures, work instructions, and records in alignment with ISO ... Implement and verify preventive actions for customer complaints logged by Inside Sales before ...

New

Yotta Energy

Senior Quality Engineer

Austin, TX · On-site

$83K - $113K/yr

Develop, implement, maintain, and audit the Quality Management System (QMS) * Ensure compliance with applicable ISO standards and customer requirements * Coordinate internal and external quality ...

Yotta Energy

Senior Quality Engineer

Austin, TX · On-site

$83K - $113K/yr

Develop, implement, maintain, and audit the Quality Management System (QMS) * Ensure compliance with applicable ISO standards and customer requirements * Coordinate internal and external quality ...

Novolex

Quality Manager

Dallas, TX · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Lead all internal, customer, and 3rd party audits for the QMS and SQF system * Communicate to relevant personnel all information essential to ensure the effective implementation of and maintenance of ...

Novolex

Quality Manager

Dallas, TX

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Lead all internal, customer, and 3rd party audits for the QMS and SQF system * Communicate to relevant personnel all information essential to ensure the effective implementation of and maintenance of ...

Novolex

Quality Manager

Dallas, TX

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Lead all internal, customer, and 3rd party audits for the QMS and SQF system * Communicate to relevant personnel all information essential to ensure the effective implementation of and maintenance of ...

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Qms Implementation information

What are the key skills and qualifications needed to thrive in the QMS implementation position, and why are they important?

To excel in QMS Implementation, you need a solid understanding of quality management principles, process improvement methodologies, and relevant industry standards, often grounded in experience with ISO 9001 or similar frameworks. Familiarity with QMS software platforms, audit tools, and certifications such as ISO Lead Auditor or Six Sigma are highly beneficial. Strong problem-solving abilities, attention to detail, and effective communication skills set outstanding professionals apart in this role. Mastering these skills is essential for ensuring that organizations achieve and maintain high-quality standards, operational efficiency, and continuous compliance.

Who is responsible for implementing QMS?

The responsibility for implementing a Quality Management System (QMS) typically falls to quality managers, QMS coordinators, or process owners within an organization. They oversee the development, documentation, and deployment of QMS procedures, often working with cross-functional teams and ensuring compliance with standards like ISO 9001. Effective implementation requires strong organizational skills and knowledge of quality management principles.

What are some typical challenges faced when implementing a quality management system (QMS)?

Implementing a QMS often involves managing resistance to change, harmonizing existing processes with new standards, and ensuring comprehensive documentation across teams. You may encounter challenges in gaining stakeholder buy-in, training staff on new procedures, and maintaining ongoing compliance under tight timelines. QMS Implementation roles require proactive problem-solving, clear communication, and the ability to foster collaboration across departments. Overcoming these challenges is key to embedding sustainable quality practices and achieving successful certification outcomes.

What is a QMS implementation?

A QMS Implementation job involves developing, deploying, and maintaining a Quality Management System (QMS) within an organization. This role ensures compliance with industry standards such as ISO 9001 and helps improve processes for efficiency and consistency. Responsibilities typically include documentation, training staff, conducting audits, and ensuring continuous improvement. The goal is to maintain high-quality standards, meet regulatory requirements, and enhance customer satisfaction. Professionals in this role need strong knowledge of quality principles, process management, and regulatory guidelines.

What are the most commonly searched types of Qms Implementation jobs in Texas?

The most popular types of Qms Implementation jobs in Texas are:

What are popular job titles related to Qms Implementation jobs in Texas?

For Qms Implementation jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Qms Implementation jobs in Texas look for?

The top searched job categories for Qms Implementation jobs in Texas are:

Qms Implementation jobs near you
Infographic showing various Qms Implementation job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 10% Part Time, and 3% Contract. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution.

Regulatory Affairs Specialist III (Plano, TX)

CEDENT

Plano, TX • On-site

Full-time

Re-posted 11 days ago

Job description

The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance in the design, manufacturing, and sales of medical devices (including Class I and II devices, software as a medical device, and de novo devices). The role includes obtaining and maintaining regulatory approvals, supporting quality management system (QMS) objectives, and ensuring adherence to applicable regulatory standards. Responsibilities (Specific tasks, duties, essential functions of the job) Regulatory Submissions and Compliance: Develop regulatory strategies to achieve market clearance in an effective and efficient manner Prepare, submit, and maintain product registrations, certifications, and approvals to meet US, EU and other regulatory requirements as applicable 510(k) and/or De Novo submissions for FDA Technical documentation for EU MDR compliance International product registration activities to meet business objectives Provide regulatory input to support product labeling Monitor new and changing regulatory requirements and ensure the business understands relevant impacts Lead corrective and preventive action (CAPA) efforts as assigned Product Development Support: Provide regulatory input throughout the product lifecycle, including design controls, to support regulatory submissions Change Control Management: Assess and document regulatory impacts of design changes, manufacturing changes, et al, including related updates to product registrations Audits and Inspections: Support and participate in internal and external audits and regulatory agency inspections QMS Support: Complete QMS training activities and provide regulatory expertise to continuous improvement activities Supporting Lean and Kaizen initiatives Comply with all company policies and procedures Assist with any other duties as assigned Qualifications (Experience and Education) Education: Bachelor of Science degree Experience: 5-7 years of regulatory affairs experience in medical device industry, preferably with respiratory devices.

Current experience leading multiple successful 510(k) clearances and CE marking is required, and experience with additional global regulatory pathways is preferred Technical Skills: Strong understanding of medical device product life cycle and regulatory requirements. In-depth knowledge of ISO 13485, FDA regulations (including 21 CFR Part 820), and EU MDR. Knowledge of ISO 14971 risk management for medical devices.

Proficiency in database systems and advanced Microsoft Excel skills for reporting and analysis. Understanding of continuous improvement principles. Personal Attributes: Strong verbal and written communication skills, with the ability to articulate complex technical issues clearly and effectively to cross-functional teams and regulatory bodies.

Strong analytical and critical thinking skills, with the ability to resolve complex complaints and implement long-term solutions. High level of attention to detail and accuracy, particularly when preparing regulatory submissions

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About Cedent

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CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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