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

Ferrovial

Quality Control Inspector

San Juan, PR

The Quality Inspector will support the Construction Quality Control (CQC) plan by monitoring field ... Associate or Bachelor's degree in Civil Engineering, Construction Management, or related field.

BioPharma Consulting JAD Group

Specialist QA

Juncos, PR · On-site

... contamination control posture. FUNCTIONS * Review and approve product MPs. * Approve process ... Associate's + 8 years directly related experience OR * High School/GED + 10 years directly related ...

Inteldot

Specialist QA 35615

Juncos, PR · On-site

Quality Systems (Deviations, Change Control) and Maintenance (PM, Work Orders, Job Plans review and ... Associates + 8 years of directly related experience OR High school/GED + 10 years of directly ...

Baxter

Training Leader QA Compliance

Aibonito, PR · On-site

Maintain file control of each employee manual certification records and assure employees are ... Associate Degree in Administration, Education, Information System, Office Administration and ...

Quality Consulting Group

JT409 - SR. ENGINEER

Juncos, PR · On-site

$102K - $140K/yr

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and ... Supervise, coordinate and review work of a small staff of engineers, associates and/or technicians ...

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Quality Control Associate information

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How much do quality control associate jobs pay per hour?

As of Aug 19, 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 August 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.

Sr Associate Quality Control - Microbiology

Amgen, Inc.

Juncos, PR • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 10 days ago

Job description

Career Category
Quality
Job Description
Join Amgen's Mission of Serving Patients
At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Sr. Associate Quality Control- Microbiology
What you will do
Let's do this. Let's change the world. In this vital role you will perform critical testing and analysis to ensure the quality, safety, and consistency of our products before they reach patients.
Specific responsibilities include but are not limited to:
  • Perform routine and sophisticated analytical testing with precision and accuracy, ensuring compliance with SOPs and regulatory standards.
  • Maintain meticulous documentation in systems such as LIMS, CIMS, and LMES, following Good Documentation Practices.
  • Serve as a subject matter expert on cGMPs and SOPs, mentoring peers and modeling adherence to safety and quality protocols.
  • Troubleshoot testing issues independently and bring up complex problems to management or technical leads as needed.
  • Review laboratory results for accuracy and compliance, contributing to data integrity and product quality.
  • Participate in method validation and verification activities to support the lab's analytical capabilities.
  • Manage samples efficiently, ensuring proper handling, tracking, and documentation throughout the testing process.
  • Support continuous improvement initiatives by identifying inefficiencies and contributing to SOP revisions.
  • Communicate test results and task updates clearly and concisely to team members and stakeholders.
  • Demonstrate strong time management by prioritizing tasks, meeting deadlines, and supporting team workload balance.

What we expect of you
We are all different! Yet, we all use our unique contributions to serve patients. The Sr. Associate Quality Control professional we seek is an individual contributor with these qualifications.
Basic Qualifications:
Master's Degree
Or
Bachelor's Degree + 6 months of Quality and/or Laboratory work experience
Or
Associate's Degree + 2 years of Quality and/or Laboratory work experience
Or
High school/GED + 4 years of Quality and/or Laboratory work experience
Preferred Qualifications:
  • Educational background in Microbiology, Biotechnology or Medical Technologies.
  • Laboratory experience in a GMP environment within the Pharmaceutical and/or Biotech industry
  • Good communications and presentation skills in English and Spanish
  • Project management skills
  • Strong organizational skills, including ability to follow assignments through to completion
  • Enhanced skills in leading, influencing and negotiating
  • Knowledge of and experience with processes involved in manufacturing and distribution, QA, QAL, validation and process development
  • Basic Knowledge and skills of word processing, presentations, and spreadsheet applications
  • Available to support non-standard shift (including 1st, 2nd, 3rd and weekend shifts)
  • Ability to understand, apply, and evaluate basic chemistry, biology, physical principles and mathematics
  • Ability to adhere to regulatory requirements, written procedures and safety guidelines
  • Evaluate documentation/data according to company and regulatory guidelines
  • to organize work, handle multiple priorities and meet deadlines
  • Written and oral communication skills
  • Technical writing capabilities

What you can expect of us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:
  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental & vision coverage, and life & disability insurance
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans
  • Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

Apply now and make a lasting impact with the Amgen team.
careers.amgen.com
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
Sponsorship
Sponsorship for this role is not guaranteed.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
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