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Remote Iso Trainer Jobs in California (NOW HIRING)

Diality

Clinical Research Associate

Irvine, CA · Remote

$120K - $135K/yr

... ISO 14155, ICH-GCP). This position plays a key role in supporting research projects at Diality ... Perform remote monitoring activities such as source data verification (SDV) and data entry checks ...

Vercel

GRC Analyst

San Francisco, CA · On-site +1

$134K - $202K/yr

... ISO 27001, SOC 2, HIPAA, PCI DSS, and more. Your role will be instrumental in ensuring that our ... You will report to the Head of GRC and will be located ((remote, onsite, hybrid)). Think you may ...

Kargo

Network Security Engineer

San Francisco, CA · On-site +1

$123K - $168K/yr

Configure and maintain firewalls, VPNs, network segmentation, NAC, and secure remote access ... Support compliance initiatives (SOC 2, ISO 27001, NIST, etc.). * Develop security policies ...

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Remote Iso Trainer information

What is a Remote ISO Trainer?

A Remote ISO Trainer is a professional who provides training on ISO (International Organization for Standardization) standards, such as ISO 9001, ISO 14001, or ISO 27001, through online platforms rather than in-person sessions. They help organizations and individuals understand and implement ISO requirements to improve quality, safety, or security management systems. Training is delivered via webinars, virtual workshops, and digital resources, making it accessible regardless of geographic location. Remote ISO Trainers typically customize their content to suit the specific needs of their audience and may also assist with preparing for ISO certification audits.

How does a Remote ISO Trainer effectively engage and assess trainees without in-person interaction?

As a Remote ISO Trainer, leveraging interactive tools like video conferencing platforms, virtual whiteboards, and online quizzes is essential to keep trainees engaged. Frequent check-ins, breakout sessions, and real-time feedback help replicate in-person dynamics and ensure understanding. Trainers must also be adept at recognizing non-verbal cues through digital means and providing individual support when needed. Regular assessment through assignments and online evaluations ensures that all participants meet ISO standards, even in a remote setting.

What are the key skills and qualifications needed to thrive as a Remote ISO Trainer, and why are they important?

To thrive as a Remote ISO Trainer, you need in-depth knowledge of ISO standards, auditing processes, and training methodologies, typically supported by a relevant degree and ISO Lead Auditor certification. Familiarity with virtual training platforms, learning management systems (LMS), and document management tools is crucial. Excellent communication, adaptability, and the ability to engage and motivate remote learners are standout soft skills in this role. These skills ensure effective training delivery, compliance with ISO standards, and successful learner outcomes across diverse, distributed teams.

What is the difference between Remote Iso Trainer vs Remote Quality Assurance Specialist?

AspectRemote Iso TrainerRemote Quality Assurance Specialist
CertificationsISO training certifications, quality management certificationsISO standards, quality assurance certifications
Work EnvironmentConducts remote training sessions, develops training materialsReviews processes, audits, and ensures compliance remotely
Industry UsageUsed in manufacturing, healthcare, and tech sectors for employee trainingUsed across industries to maintain product/service quality standards

The Remote Iso Trainer primarily focuses on delivering ISO compliance training and developing educational materials remotely. In contrast, the Remote Quality Assurance Specialist concentrates on monitoring, auditing, and ensuring quality standards are met across processes. Both roles require knowledge of ISO standards and quality management but differ in their core responsibilities and daily activities.

What are the most commonly searched types of Iso Trainer jobs in California?

The most popular types of Iso Trainer jobs in California are:

What are popular job titles related to Remote Iso Trainer jobs in California?

For Remote Iso Trainer jobs in California, the most frequently searched job titles are:

What job categories do people searching Remote Iso Trainer jobs in California look for?

The top searched job categories for Remote Iso Trainer jobs in California are:

What cities in California are hiring for Remote Iso Trainer jobs?

Cities in California with the most Remote Iso Trainer job openings:

Remote Iso Trainer jobs near you
Infographic showing various Remote Iso Trainer job openings in California as of August 2026, with employment types broken down into 58% Full Time, and 42% Contract. Highlights an 100% Remote job distribution.

Sr. Quality Assurance Engineer (ISO 13485)

Prismatik

Irvine, CA • On-site, Remote

$99K - $120K/yr

Full-time

Posted 19 days ago

Job description

We're looking for a Sr. QA Engineer to help build quality into every stage of our medical device development and manufacturing. You'll have broad ownership across quality engineering, risk management, CAPA, validation, and our Quality Management System. Working closely with cross-functional teams, you'll solve complex quality challenges, support new products and processes, and help ensure what we build meets the highest standards for safety, performance, and compliance.

Essential Functions:
  • Ensure compliance with applicable regulatory standards, including FDA 21 CFR Part 820, ISO 13485, MDSAP, and EU MDR.
  • Lead and support CAPA investigations, non-conformance management, and root cause analysis using tools such as 8D, Fishbone, and 5 Whys.
  • Own and continuously improve elements of the Quality Management System (QMS), including document control, internal audits, supplier quality, and change control.
  • Collaborate cross-functionally with R&D, Manufacturing, and Regulatory Affairs to support design control, risk management (ISO 14971), and product development lifecycle activities.
  • Lead internal and supplier audits, and support external audits and inspections (e.g., FDA, Notified Bodies).
  • Participate in validation activities (IQ/OQ/PQ) for processes, equipment, and software used in manufacturing and quality operations.
  • Develop, monitor, and analyze quality metrics to identify trends, drive continuous improvement, and ensure effectiveness of corrective actions.
  • Provide quality engineering support to Quality Control, including guidance on inspection methods, metrology, and measurement system capability.
  • Conduct and document investigations of NCRs, complaints, and deviations, providing effective and sustainable corrective and preventive actions based on engineering analysis.
  • Lead and mentor junior engineers, fostering technical growth and reinforcing a culture of quality and compliance.
  • Integrate ISO 14971 risk management and IEC 62366 usability engineering activities within Glidewell/Prismatik processes.
  • Ensure organizational compliance with the QMS through ongoing training, education, and internal communication.
  • Collaborate with Manufacturing and Engineering to coordinate pilot production, process validations, and risk analyses for new products and processes.
  • Ensure calibration and preventive maintenance systems meet compliance and operational requirements.
  • Identify and implement process optimizations using Lean and Six Sigma methodologies to improve manufacturability, reduce risk, and enhance efficiency.
  • Identify opportunities for design or re-design of equipment, tools, and fixtures to improve manufacturing processes and product quality.
  • Perform other related duties and special projects as assigned by management.
Minimum Qualifications:
  • Bachelor's degree in Engineering, Science, or a related technical field.
  • Minimum of 5 years of experience in Quality Assurance or Quality Engineering within the medical device industry, or equivalent education and experience demonstrating comparable skills and knowledge.
  • Strong working knowledge of FDA regulations, ISO 13485, and other applicable international quality standards.
  • Hands-on experience with risk management (ISO 14971), design controls, and validation methodologies.
  • Proven analytical, problem-solving, and communication skills.
  • Proficiency in quality and statistical analysis tools such as Minitab or equivalent software.
  • Demonstrated project management experience.
  • Certified Quality Engineer (CQE), Certified Quality Auditor (CQA), or Six Sigma certification, preferred.
  • Experience with combination products or Class I/II medical devices, preferred.
  • Familiarity with EU MDR and UDI regulatory requirements, preferred.
Pay range: $99,000 - $120,000/yr.
Exact compensation may vary based on skills and experience.
This role is fully onsite at our Irvine, CA campus. Remote or hybrid arrangements are not available.
Employment Type: full-time

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