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Associate Quality Analyst Jobs in Cidra, PR (NOW HIRING)

QC Incoming Coordinator

Gurabo, PR

$19 - $26.25/hr

Audits the Certificate of Analysis and Certificate of Compliance Receiving Report of Raw Materials ... A minimum of an Associate Degree or BS Natural Sciences (with a major in Biology or Chemistry ...

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Associate Quality Analyst information

See Cidra, PR salary details

$16

$31

$48

How much do associate quality analyst jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for associate quality analyst in Cidra, PR is $31.00, according to ZipRecruiter salary data. Most workers in this role earn between $23.22 and $35.38 per hour, depending on experience, location, and employer.

What does an associate quality analyst do?

An Associate Quality Analyst is responsible for assisting in the testing and evaluation of products or software to ensure they meet established quality standards. Their duties typically include executing test cases, documenting defects, and collaborating with developers to resolve issues. They also help maintain quality documentation and participate in continuous improvement initiatives. This entry-level role is essential for supporting the quality assurance team and ensuring the final product is reliable and meets customer expectations.

What are the key skills and qualifications needed to thrive as an associate quality analyst?

To thrive as an Associate Quality Analyst, you need a solid understanding of quality assurance processes, basic knowledge of software testing methodologies, and often a bachelor's degree in a related field. Familiarity with tools like Jira, Selenium, or other test management systems and certifications such as ISTQB can be advantageous. Strong attention to detail, analytical thinking, and effective communication skills help you collaborate with teams and identify issues efficiently. These skills and qualities are crucial to ensuring product quality, reducing defects, and supporting seamless software development cycles.

What are some common challenges faced by an associate quality analyst during software testing cycles?

Associate Quality Analysts often encounter challenges such as managing tight testing deadlines, quickly adapting to evolving project requirements, and effectively communicating defects to development teams. They may also need to balance multiple testing tasks while ensuring thoroughness and accuracy. Collaborating with cross-functional teams and learning new testing tools or methodologies can require adaptability, but overcoming these challenges helps build strong analytical and communication skills for future career growth.

What is the difference between Associate Quality Analyst vs Quality Control Inspector?

AspectAssociate Quality AnalystQuality Control Inspector
CertificationsBasic quality assurance certifications, such as Six Sigma Green BeltOften requires industry-specific certifications or training
Work EnvironmentCollaborative, involves data analysis, testing, and process improvementHands-on inspection, physical testing, and product evaluation
Employer & Industry UsageUsed across manufacturing, software, and service industries for process improvementPrimarily in manufacturing and production for product quality checks

The Associate Quality Analyst focuses on analyzing data, improving processes, and supporting quality assurance initiatives, often working closely with teams to implement standards. In contrast, a Quality Control Inspector primarily conducts physical inspections and tests products to ensure they meet quality specifications. Both roles are essential in maintaining quality but differ in scope and daily tasks.

Is an Associate Quality Analyst a good entry-level job?

An Associate Quality Analyst is typically considered an entry-level position in quality assurance and testing roles. It provides foundational skills in process evaluation, testing methodologies, and tools like Excel or testing software, making it suitable for those starting a career in quality assurance or software testing.

What cities near Cidra, PR are hiring for Associate Quality Analyst jobs?

Cities near Cidra, PR with the most Associate Quality Analyst job openings:

Infographic showing various Associate Quality Analyst job openings in Cidra, PR as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $64,486 per year, or $31 per hour.

Sr Associate Quality Control - Microbiology

Amgen

Juncos, PR โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 16 days ago


Job description

Career CategoryQualityJob DescriptionJoin 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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