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Quality Control Associate Jobs in Guayama, PR (NOW HIRING)

QRC Group

QC Incoming Associate

Gurabo, PR · On-site

$55 - $75/hr

Gurabo, Puerto Rico | Posted on 08/06/2026 We are looking for an experienced QC Incoming Associate with experience in regulated industries. Responsibilities: * Managing retain samples of Raw ...

Jj

QC Incoming Coordinator

Gurabo, PR · On-site

$19 - $26.25/hr

Quality Control Job Category: Business Enablement/Support All Job Posting Locations: Gurabo, Puerto ... A minimum of an Associate Degree or BS Natural Sciences (with a major in Biology or Chemistry ...

Johnson & Johnson

QC Incoming Coordinator

Gurabo, PR · On-site

$19 - $26.25/hr

Quality Control Job Category: Business Enablement/Support All Job Posting Locations: Gurabo, Puerto ... A minimum of an Associate Degree or BS Natural Sciences (with a major in Biology or Chemistry ...

Jj

Quality Assurance Technician

San Lorenzo, PR · On-site

Quality Control Job Category: Business Enablement/Support All Job Posting Locations: San Lorenzo ... Support associates on defect awareness and specifications requirements. Qualifications ...

BioPharma Consulting JAD Group

Specialist QA

Juncos, PR · On-site

Associate's + 8 years of directly related experience OR * High School/GED + 10 years of directly ... Experience in Change Control, Documentation Review, Validation, PPQ. * Demonstrated expertise in ...

EssilorLuxottica Group

Sales Associate

Bayamon, PR · On-site

$12.50 - $17/hr

Benefits/Incentive Information At For Eyes, we are an optical retailer that offers high-quality ... Secures & protects company assets in your control. * Informs management of safety opportunities ...

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All JobsQuality Control Associate JobsQuality Control Associate Jobs in Guayama, PR

Quality Control Associate information

See Guayama, PR salary details

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How much do quality control associate jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for quality control associate in Guayama, PR is $24.59, according to ZipRecruiter salary data. Most workers in this role earn between $17.88 and $29.95 per hour, depending on experience, location, and employer.

What does a quality control associate do?

A Quality Control Associate is responsible for ensuring that products meet established standards of quality, including reliability, usability, and performance. They conduct inspections, perform tests, and document their findings to identify defects or deviations from specifications. Quality Control Associates often work closely with production teams to address issues and help maintain compliance with industry regulations. Their role is critical in maintaining customer satisfaction and upholding the reputation of their company. They may work in a variety of industries, including pharmaceuticals, manufacturing, and food production.

What are the key skills and qualifications needed to thrive as a quality control associate?

To thrive as a Quality Control Associate, you need a solid understanding of quality assurance principles, attention to detail, and often a background in science or manufacturing. Familiarity with inspection tools, laboratory equipment, and quality management systems (such as ISO standards) is typically required, and certifications like Six Sigma or ASQ may be advantageous. Strong analytical thinking, problem-solving abilities, and effective communication skills set exceptional candidates apart. These skills ensure that products consistently meet standards, reduce errors, and support overall operational excellence.

What are some common challenges quality control associates face when ensuring product consistency across different production batches?

Quality Control Associates often encounter challenges such as variations in raw material quality, changes in manufacturing processes, and tight production schedules that can lead to inconsistencies between batches. Addressing these issues requires keen attention to detail, effective communication with production teams, and a strong understanding of standard operating procedures. Staying proactive in identifying potential sources of variation and collaborating closely with other departments helps maintain high product standards and minimizes the risk of defects.

What is the difference between Quality Control Associate vs Quality Assurance Technician?

AspectQuality Control AssociateQuality Assurance Technician
CertificationsOften requires GMP, ISO, or industry-specific quality certificationsSimilar certifications, with focus on quality standards and compliance
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or quality compliance environments
Primary FocusInspecting products, testing samples, identifying defectsDeveloping and implementing quality systems, audits, and process improvements
Employer & Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, pharmaceuticals, food industry

While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.

What cities near Guayama, PR are hiring for Quality Control Associate jobs?

Cities near Guayama, PR with the most Quality Control Associate job openings:

Quality Control Associate jobs near you
Infographic showing various Quality Control Associate job openings in Guayama, PR as of September 2026, with employment types broken down into 86% Full Time, and 14% Temporary. Highlights an 100% In-person job distribution, with an average salary of $51,154 per year, or $24.6 per hour.

QC Incoming Associate

Gurabo, PR • On-site

QRC Group
See more jobs at QRC Groupexternal

$55 - $75/hr

Other

This job post has expired 3 days ago. Applications are no longer accepted.

Job description

Gurabo, Puerto Rico | Posted on 08/06/2026

We are looking for an experienced QC Incoming Associatewith experience in regulated industries.

Responsibilities:

  • Managing retain samples of Raw Materials, Finished Goods and Bulk.
  • Storing reserve samples under specified temperature and humidity conditions, preventing loss of integrity.
  • Documenting reserve samples on logbooks and electronic systems, ensuring traceability.
  • Conducting periodic visual inspection of Controlled Substances and reserve samples.
  • Documenting and reporting findings from visual evaluations of customers complaints samples, detailing defect categories to aid corrective actions.
  • Preparing reports regarding inventory and expiration of Controlled Substances and reserve samples.
  • Identifying when reserve samples have met or exceeded their retention period and disposing them utilizing the corresponding documentation and regulatory standards.
  • Contributing to investigations by gathering data and reviewing evidence.
Requirements
  • Bachelor’s degree in a scientific discipline and at least 3 years of experience in pharmaceutical/biotech investigations.
  • Bilingual (Spanish and English).
  • Strong written and verbal communication skills, including facilitation and presentation abilities.
  • Proficient in computer applications and systems.
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