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Iso Rep Jobs in Florida (NOW HIRING)

atrion

Quality Engineering Manager

Davie, FL · On-site

Act as assistant to the Management Representative during regulatory and customer audits. * Develop ... ISO 13485 Lead Auditor * Lean Six Sigma Green Belt or Black Belt * Working knowledge of IEC 60601 ...

ARTHREX

Biocompatibility Specialist II

Naples, FL · On-site

Actively represent Arthrex and the medical device industry through active involvement in international standards committees such as AAMI, ISO, and SOT; * Manage the appropriate maintenance, review ...

grupoSky

Be Seen First

Promoter / Sales Representative

Miami, FL · On-site

$35 - $50/hr

Represent brand at activations in mall or retail sites * Engage with customers and support on-site ... ISO 9001:2015 certification since 2011.

Arthrex

Biocompatibility Specialist II

Naples, FL · On-site

Actively represent Arthrex and the medical device industry through active involvement in international standards committees such as AAMI, ISO, and SOT; * Manage the appropriate maintenance, review ...

TSE Industries Inc

WHK Quality Engineer

Clearwater, FL · On-site

$80K - $100K/yr

... with cGMP practices, ISO 13485 requirements and local government and company procedures. The ... The requirements listed below are representative of the knowledge, skill, and/or ability required.

TSE Industries Inc

WHK Manufacturing Engineer

Clearwater, FL · On-site

$64K - $83K/yr

Work with Quality to ensure all systems are in compliance with ISO 13485. Implement new processes ... The requirements listed below are representative of the knowledge, skill, and/or ability required.

Kavaliro

Associate Quality Engineer

Orlando, FL · On-site

$35 - $40/hr

Working knowledge of ISO 9001 standards, with Internal Auditor certification preferred. Prior ... company representative. Job Requirements On-Site By using best practices and optimal employee ...

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Iso Rep information

What is an ISO Rep?

ISO Reps, or Independent Sales Organization Representatives, are professionals who act as intermediaries between merchants and payment processors or banks. Their main role is to help businesses set up merchant accounts so they can accept credit and debit card payments. ISO Reps often provide guidance on payment solutions, negotiate rates, and offer customer support. They may work independently or as part of a larger organization, and they play a critical role in helping businesses navigate the complex world of payment processing.

What are the key skills and qualifications needed to thrive as an ISO Rep?

To succeed as an ISO Rep (Independent Sales Organization Representative), you need strong sales acumen, knowledge of merchant services, and experience in payment processing, often supported by a background in finance or business. Familiarity with CRM systems, payment gateways, and industry compliance certifications like PCI DSS is typically required. Exceptional interpersonal skills, negotiation abilities, and resilience are vital for building client relationships and closing deals. These skills enable ISO Reps to effectively acquire new merchants, navigate complex payment solutions, and maintain compliance in a competitive industry.

What are some common challenges faced by ISO Reps when managing merchant accounts, and how can they be addressed?

ISO Representatives often encounter challenges such as handling complex merchant onboarding processes, addressing technical concerns with payment terminals, and ensuring compliance with industry regulations. Effective communication with both merchants and internal support teams is essential for resolving issues quickly. Staying updated on the latest payment technologies and regulatory changes can help ISO Reps proactively support their clients and build long-lasting relationships.

What is the difference between Iso Rep vs Product Specialist?

AspectIso RepProduct Specialist
Required CredentialsISO certifications, technical knowledgeProduct knowledge, certifications may vary
Work EnvironmentManufacturing, quality assuranceSales, marketing, technical support
Employer & Industry UsageManufacturing, industrial sectorsConsumer goods, technology, manufacturing
Common Search & ComparisonYesYes

The Iso Rep primarily focuses on ensuring compliance with ISO standards and quality assurance within manufacturing environments. In contrast, a Product Specialist concentrates on product knowledge, sales support, and customer engagement. While both roles require technical understanding, Iso Reps are more involved in quality processes, whereas Product Specialists focus on product promotion and customer relations.

What are popular job titles related to Iso Rep jobs in Florida?

For Iso Rep jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Iso Rep jobs in Florida look for?

The top searched job categories for Iso Rep jobs in Florida are:

Iso Rep jobs near you
Infographic showing various Iso Rep job openings in Florida as of August 2026, with employment types broken down into 88% Full Time, 5% Part Time, 5% Contract, and 2% Nights. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution.

Quality Engineering Manager

atrion

Davie, FL • On-site

Full-time

Re-posted 26 days ago

Job description

JD534-016: 

Position:

Manager, Quality Engineering

Department:

Reports To:

Vice President, Quality Assurance & Regulatory Affairs

FLSA Status:

JD Number:

JD534-016

Revision:

A

Summary:

Manages the Quality Engineering team to support new product development, process quality, CAPA, post-market compliance, supplier management, project management, internal & external auditing, and risk management activities with respect to global regulatory requirements and MDSAP (FDA, ISO, EU MDR, ANVISA, MHLW, and TGA). 

 

 

General Duties and Responsibilities:

 

  • Ensure the ongoing integrity, adequacy, and appropriateness of the Quality Management System and associated processes.  
  • Provide technical support, leadership and quality guidance to multi-functional teams, including Quality, Regulatory, R&D, Operations, Engineering, and Marketing.
  • Select, develop, and evaluate Quality Engineering staff to support all aspects of design and manufacturing quality.
  • Act as assistant to the Management Representative during regulatory and customer audits.
  • Develop and implement and improve efficient quality systems processes. 
  • Utilize project management strategy at a department level to successfully execute multiple projects with competing resources and prioritization. 
  • Establish and maintain quality metrics and utilizes KPIs to drive improvements.
  • Manage the CAPA program (to include Complaints, SCARs, NCMRs, Audit Non-Conformances and Corrective & Preventive Action projects).  Ensure thorough investigations and implement effective corrective actions to prevent recurring issues.
  • Utilize root cause analysis and statistical techniques for complex problem solving of technical product and manufacturing issues.  
  • Ensure a high level of supplier quality through effective supplier evaluation, approval, and monitoring processes.  Collaborate with internal supply chain and external suppliers to drive continual improvement of supplier quality. 
  • Develop and maintain FMEAs, Controls Plans, and SOPs to identify and mitigate risks. 
  • Support the development and validation of new products and production lines.  
  • Write, review, and approve documents (SOPs, Protocols, Reports, and ECOs) pertaining to key quality system elements affecting product quality.
  • Apply basic risk management principles to all aspects of the quality system.

 

Qualifications:

Required

  • Technical Engineering or Science degree at the Bachelor level or above.
  • 8+ years of quality engineering experience in a highly regulated industry.
  • 3+ years managing team members with varied backgrounds, experience, and technical capabilities.
  • Excellent working knowledge of medical device regulations and industry standards pertaining to manufacturing (FDA 21 CFR Part 820, ISO 13485, EU MDR (2017/745), the Medical Device Single Audit Program (MDSAP), and ISO 14971), IEC 60601.. 
  • Demonstrated project management skills, including the ability to prioritize and manage multiple project workloads in a highly dynamic production environment.
  • Solid working background utilizing quality management methods and tools (CAPA, Root Cause Analysis, FMEA, Control Plans, Statistical Techniques, MSA, etc.)
  • Demonstrated experience using trending and analysis reporting to drive organizational improvements.
  • Ability to develop and deliver clear communications (written and verbal), ensuring timely and relevant communication.
  • Some travel, domestic or international, may be required (up to 25%).

 

Preferred

  • ASQ Certified Quality Manager or Certified Quality Engineer
  • ISO 13485 Lead Auditor
  • Lean Six Sigma Green Belt or Black Belt
  • Working knowledge of IEC 60601 and IEC 62366
  • Experience with sterile product assembly and packaging
  • Experience with electronics assembly

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