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Quality Coordinator Jobs in Puerto Rico (NOW HIRING)

QC Incoming Coordinator

Gurabo, PR · On-site

$19 - $26.25/hr

The Coordinator must ensure compliance with all quality control policies, procedures, and systems to facilitate the timely release of high-quality products to support the supply chain process.

PR · On-site

Coordinates with the Project Manager to ensure timely submission of daily reports. * Writes clear ... Ensures the quality management systems are properly integrated to provide the most efficient and ...

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 ...

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 ...

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 ...

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 ...

Quality Engineer

Arecibo, PR · On-site

$62K - $80K/yr

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 ...

Quality Engineer

Arecibo, PR · On-site

$62K - $80K/yr

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 ...

Quality Engineer

Arecibo, PR · On-site

$62K - $80K/yr

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 ...

Training Coordinator

Carolina, PR · On-site

$60 - $80/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 Training Coordinator ...

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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.

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

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

What are popular job titles related to Quality Coordinator jobs in Puerto Rico?

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:

QC Incoming Coordinator

Gurabo, PR • On-site

$19 - $26.25/hr

Full-time

This job post has expired today. Applications are no longer accepted.


Key responsibilities

  • Coordinates and executes sampling, inspection, testing, and approval activities of Packaging Components in accordance with internal and external regulations, policies, and supply chain cycle time goals.

  • Ensures that the sampling and testing of Raw Materials is performed in compliance with internal and external regulations, policies, and supply chain cycle time goals.

  • Coordinates and executes the inspection of labeling, quantity, and material or product to be shipped.


Johnson & Johnson rating

8.3

Company rating: 8.3 out of 10

Based on 113 frontline employees who took The Breakroom Quiz

25th of 86 rated pharmaceutical


Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Quality

Job Sub Function:

Quality Control

Job Category:

Business Enablement/Support

All Job Posting Locations:

Gurabo, Puerto Rico, United States of America

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

We are searching for the best talent for QC Incoming Coordinator located in Gurabo, PR.

The QC Incoming Coordinator is responsible for sampling, inspecting, and approving Packaging Components. Also responsible for testing Packaging Components and some Raw Materials.

The Coordinator must ensure compliance with all quality control policies, procedures, and systems to facilitate the timely release of high-quality products to support the supply chain process. Failure to effectively perform their functions may lead to product recall, production delays, and/or back-order status.

Key Responsibilities:

  • Coordinates and executes (when necessary) sampling, inspection, testing, and approval activities of Packaging Components in accordance with internal and external regulations, policies, and supply chain cycle time goals.

  • Ensures that the sampling and testing of Raw Materials is performed in compliance with internal and external regulations, policies, and supply chain cycle time goals.

  • Coordinates and executes (when necessary) the inspection of labeling, quantity, and material or product to be shipped.

  • Maintains a well-organized Retention Room.

  • Audits the Certificate of Analysis and Certificate of Compliance Receiving Report of Raw Materials and Packaging Components in accordance with internal and external regulations, policies, and supply chain cycle time goals.

  • Keeps accurate and organized records of all work performed.

  • Collaborates with the Technical Development group during the validation activities and transfer of new products.

  • Assigns appropriate disposition to materials/products through the Computer System within established cycle time and schedules.

  • Verifies data/results generated by another Incoming Inspector as a Peer Reviewer.

  • Maintains and controls documents in safe files, ensuring that active records are protected.

  • Comply with the goals of the quality team and overall business and process goals.

  • Follows Safety and Environmental procedures in all areas.

  • Adheres to the principles of conduct expressed in the Company Credo and policies.

  • Coordinates and performs other duties as necessary to support the supply chain process.

  • Support Internal and External Audit process as applicable.

  • As an Environmental Trainer Auditor, the following responsibilities apply:

  • Acts as a member of the OMP ISO 14001 Team, providing support to the Environmental Management System Coordinator in implementing, training, and improving the EMS in their operational area and other required activities.

  • Conducts monthly environmental audits in their operational area.

  • Delivers environmental talks to their operational area on a bi-monthly basis.

  • Conducts weekly inspections of chemical cabinets in their operational area.

  • Assists in conducting semi-annual Environmental Management System audits at the Gurabo site.

Qualifications:

  • A minimum of an Associate Degree or BS Natural Sciences (with a major in Biology or Chemistry preferably) is required.

  • A minimum of 6 years of experience in pharmaceutical GMP Environment is required, preferable in the Incoming Area.

  • Availability to provide support by working in external locations as per business needs is required.

  • Knowledge of SAP, eLIMS applications is preferred

  • Forklift certification is desired.

  • Availability to work overtime, various work schedules, which may include 1st, 2nd, 3rd shifts and/or other work shifts, including weekends and holidays.

  • This position may require up to a 10% of domestic and/or international travel.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers , internal employees contact AskGS to be directed to your accommodation resource.

Required Skills:

Preferred Skills:

Communication, Compliance Management, Execution Focus, ISO 9001, Problem Solving, Quality Control (QC), Quality Control Testing, Quality Standards, Quality Systems Documentation, Quality Validation, Report Writing, Standard Operating Procedure (SOP), Teamwork, Technologically Savvy

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