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Quality Coordinator Jobs in Puerto Rico (NOW HIRING)

medplast

Quality - Quality Engineer I

Vega Baja, PR

$60K - $78K/yr

Applies basic to intermediate knowledge in Process and Quality Engineering to support the implementation, coordination, and follow-up of manufacturing methods and procedures. Supports the delivery of ...

medplast

Quality - Quality Engineer I

Vega Baja, PR · On-site

$60K - $78K/yr

Applies basic to intermediate knowledge in Process and Quality Engineering to support the implementation, coordination, and follow-up of manufacturing methods and procedures. Supports the delivery of ...

medplast

Quality - Quality Engineer I

Vega Baja, PR · On-site

$60K - $78K/yr

Applies basic to intermediate knowledge in Process and Quality Engineering to support the implementation, coordination, and follow-up of manufacturing methods and procedures. Supports the delivery of ...

Ultimate Solutions

Quality Engineer

San Juan, PR

$70K - $91K/yr

Position Summary The Quality Engineer will support quality and compliance activities within a ... cross-functional coordination. * Create, review, and maintain pFMEA documentation to identify ...

trane technologies

Quality Engineer

Arecibo, PR · On-site

$62K - $80K/yr

  • Medical

  • Retirement

  • PTO

Develops and coordinates programs to recognize groups or individuals for quality / continuous improvement actions. * Participate actively in MDI, SQDIP and other meetings as required. * Coordinate ...

Trane Technologies plc

Quality Engineer

Arecibo, PR · On-site

$62K - $80K/yr

  • Medical

  • Retirement

  • PTO

Develops and coordinates programs to recognize groups or individuals for quality / continuous improvement actions. * Participate actively in MDI, SQDIP and other meetings as required. * Coordinate ...

Trane Technologies plc

Quality Engineer

Arecibo, PR · On-site

$62K - $80K/yr

  • Medical

  • Retirement

  • PTO

Develops and coordinates programs to recognize groups or individuals for quality / continuous improvement actions. * Participate actively in MDI, SQDIP and other meetings as required. * Coordinate ...

JC Automation Corp

PR · On-site

$40/hr

It's mission is to add value by delivering quality services & solutions on time all the time by transforming processes & technology into business advantages. ABOUT THE ROLE The Project Coordinator ...

Eaton

Quality Senior Engineer

Arecibo, PR · On-site

$76K - $103K/yr

Define, coordinates, lead and execute projects to improve Quality and plant indicators, such as scrap, DPPMs, warranty claims, CONC, LPA, capacity increase and safety improvements. Use A3 documents ...

MENTOR TECHNICAL GROUP CORP

PR · On-site

The Facilities Coordinator work is managed under a Site Lead or a Facilities Manager to maintain ... Including Quality Calendar, Quality Plans, EHS Plan, Self-Inspections actions, BMP, C-Seguro ...

JC Automation Corp

PR · On-site

Its mission is to add value by delivering quality services & solutions on time all the time by ... Serve as coordinator as required by Client, leading the drawing revision and approval process.

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Quality Coordinator information

What is a quality coordinator?

Quality coordinators ensure that employees follow quality assurance standards and procedures established by the company. As a quality coordinator, you analyze data, review policies, and suggest process improvements. You create reports and train employees on expectations of quality goals. Depending on the industry, your job may involve product testing, customer service audits, or reviewing operations data. Qualifications to become a quality coordinator include several years of production experience in the industry in which you wish to work.

What does a quality coordinator do?

A Quality Coordinator is responsible for ensuring that an organization’s products or services meet established standards of quality, including reliability, usability, and performance. They develop and implement quality assurance processes, conduct audits, and monitor compliance with industry regulations. Quality Coordinators also collaborate with other departments to address quality issues, provide training on quality standards, and help drive continuous improvement initiatives. Their goal is to maintain high standards and minimize defects or errors in products and services.

What are the key skills and qualifications needed to thrive as a quality coordinator, and why are they important?

To thrive as a Quality Coordinator, you need a solid understanding of quality management principles, process improvement methodologies, and relevant industry standards, often supported by a degree in quality assurance or a related field. Familiarity with quality management systems (QMS), ISO standards, and data analysis tools like Six Sigma or Lean certifications is typically required. Strong attention to detail, effective communication, and problem-solving abilities are vital soft skills that set top-performing Quality Coordinators apart. These competencies are crucial for ensuring compliance, driving continuous improvement, and maintaining high standards within an organization.

What are some common challenges faced by quality coordinators, and how can they be effectively managed?

Quality Coordinators often encounter challenges such as ensuring compliance with evolving industry standards, managing documentation accuracy, and fostering consistent communication across departments. To effectively manage these issues, it's important to stay updated on regulatory changes, implement robust document control systems, and build strong relationships with both production and management teams. Proactive problem-solving and ongoing training are also key to maintaining a high standard of quality across all processes.

What is the difference between Quality Coordinator vs Quality Inspector?

AspectQuality CoordinatorQuality Inspector
CertificationsISO 9001, Six Sigma, quality management certificationsISO 9001, industry-specific inspection certifications
Work EnvironmentOffice-based, coordinating quality processes across departmentsManufacturing or production floor, inspecting products
Primary ResponsibilitiesDeveloping quality procedures, coordinating audits, ensuring complianceInspecting products, identifying defects, recording inspection results

While both roles focus on quality, the Quality Coordinator manages quality systems and processes, whereas the Quality Inspector performs hands-on product inspections. The Coordinator ensures overall compliance and process improvement, while the Inspector verifies product quality at specific stages.

What skills do you need to be a quality coordinator?

A quality coordinator needs strong attention to detail, excellent communication skills, and knowledge of quality management systems and standards. They should be proficient in data analysis, problem-solving, and often use tools like spreadsheets or quality software. Certifications such as Six Sigma or ISO auditor training can also enhance their qualifications.
More about Quality Coordinator jobs

What are the most commonly searched types of Quality jobs in Puerto Rico?

The most popular types of Quality jobs in Puerto Rico are:

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For Quality Coordinator jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Quality Coordinator jobs in Puerto Rico look for?

The top searched job categories for Quality Coordinator jobs in Puerto Rico are:

What cities in Puerto Rico are hiring for Quality Coordinator jobs?

Cities in Puerto Rico with the most Quality Coordinator job openings:

Quality Coordinator jobs near you

JT678 - QUALITY APPLICATIONS SPECIALISTS

Quality Consulting Group

Villalba, PR • On-site

Temporary

Posted 27 days ago

Job description

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.
Responsibilities:
  • Conducts a compliant validation process for quality information technology systems which requires formal validation documentation (including standard operating procedures) under appropriate federal regulations.
  • Coordinates activities with clients, programmers/developers and operating personnel, domestic and, as appropriate, global.
  • Identifies current and anticipated requirements for compliant computerized operations and suggests methods for the identification, implementation and maintenance of the procedures, actions and documentation necessary to assure compliance according to the appropriate federal and international regulations which govern the user's applications.
  • Reports on the status of validation activities to fulfill regulatory requirements.
  • Keeps abreast of changing federal and international regulatory requirements, government audit policies, and the availability of current techniques.

Qualifications:
  • Bachelor's degree in Engineer or Science
  • 10+ years of experience in the medical device industry, with a strong background in field corrective actions, CAPA, or product quality management. Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, EU MDR, and other relevant medical device regulations.
  • Proven experience leading FCA and CAPA processes, ideally within a medical device or regulated industry.
  • Outstanding communication and interpersonal skills, capable of effectively working with cross-functional teams and external stakeholders.
  • Proficiency in Microsoft Office Suite and quality management systems (QMS). Strong technical writing capability
  • Experience in equipment IQ
  • Experience in OQ (Operational Qualification) and PQ (Performance Qualification) and/or process validation
  • Process Validation Lifecylce ( from process characterization, operational qualification to performance qualification)
  • Preferred experience in DOE (with minitab)
  • Computer and software validation CSV
  • SOP Development
  • Change control of Medical Devices
  • 1st shift

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

Apply