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Quality Assurance Associate Jobs in Rio Grande, PR

Mirus Consulting Group

Specialist QA - 35615

Juncos, PR · On-site

$65 - $95/hr

Position Summary The Specialist QA is responsible for ensuring compliance with quality standards, regulatory requirements, and internal procedures throughout validation, commissioning, qualification ...

Danaher

Quality Assurance Specialist II

Fajardo, PR

This position reports to the Sr. Manager QA Engineering and is part of the Quality Assurance Engineering Team located in Fajardo, Puerto Rico and will be an on-site role. What you will do: Provide ...

Danaher

Quality Assurance Specialist II

Fajardo, PR · On-site

This position reports to the Sr. Manager QA Engineering and is part of the Quality Assurance Engineering Team located in Fajardo, Puerto Rico and will be an on-site role. What you will do: Provide ...

Danaher

Quality Assurance Specialist II

Fajardo, PR · On-site

This position reports to the Sr. Manager QA Engineering and is part of the Quality Assurance Engineering Team located in Fajardo, Puerto Rico and will be an on-site role. What you will do: * Provide ...

Danaher

Quality Assurance Specialist II

Fajardo, PR · On-site

This position reports to the Sr. Manager QA Engineering and is part of the Quality Assurance Engineering Team located in Fajardo, Puerto Rico and will be an on-site role. What you will do: * Provide ...

Danaher

Quality Assurance Specialist II

Fajardo, PR

This position reports to the Sr. Manager QA Engineering and is part of the Quality Assurance Engineering Team located in Fajardo, Puerto Rico and will be an on-site role. What you will do: * Provide ...

Danaher

Quality Assurance Specialist II

Fajardo, PR

This position reports to the Sr. Manager QA Engineering and is part of the Quality Assurance Engineering Team located in Fajardo, Puerto Rico and will be an on-site role. What you will do: * Provide ...

Mirus Consulting Group

Specialist QA - 35657

Juncos, PR · On-site

Position Summary The Specialist QA is responsible for supporting Quality and Manufacturing operations through accurate Batch Record Review, documentation compliance, electronic systems management ...

New

Pharma Bioserv

Be Seen First

Sr. Quality Assurance Specialist

San Juan, PR · On-site

$60K - $75K/yr

We are looking candidates with experience within regulated environment for a SR. Quality Assurance Specialist in Hato Rey, Puerto Rico. Requirement: * Bachelor's degree in Engineering in Engineering ...

Veg Group

Specialist QA (5:00 pm - 5:30 am)

Juncos, PR · On-site

$70 - $90/hr

Specialist QA (5:00 pm - 5:30 am) SUMMARY Perform one or more of the following duties and responsibilities in support of Quality Assurance program under minimal supervision. FUNCTIONS * Review and ...

Pinnaql

Specialist QA (5:00 pm - 5:30 am)

Juncos, PR · On-site

Specialist QA (5:00 pm - 5:30 am) SUMMARY Perform one or more of the following duties and responsibilities in support of Quality Assurance program under minimal supervision. FUNCTIONS - Review and ...

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All JobsQuality Assurance Associate JobsQuality Assurance Associate Jobs in Rio Grande, PR

Quality Assurance Associate information

See Rio Grande, PR salary details

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How much do quality assurance associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for quality assurance associate in Rio Grande, PR is $22.56, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $26.49 per hour, depending on experience, location, and employer.

What does a quality assurance associate do?

A Quality Assurance Associate is responsible for monitoring and evaluating the various processes involved in product development and production to ensure they meet established quality standards. Their duties typically include conducting inspections, documenting findings, assisting in process improvements, and ensuring compliance with regulatory requirements. They play a critical role in identifying defects, reducing errors, and maintaining the overall quality of products or services before they reach customers.

What skills and qualifications are needed to be a quality assurance associate?

To excel as a Quality Assurance Associate, you need a solid understanding of quality control principles, attention to detail, and often a degree in a related field like chemistry, biology, or engineering. Familiarity with industry-standard quality management systems (such as ISO 9001), statistical analysis software, and documentation tools is typically required. Strong problem-solving skills, effective communication, and the ability to work collaboratively are highly valued in this role. These skills ensure that products and processes consistently meet standards, reduce errors, and maintain compliance with regulatory requirements.

What are common challenges faced by quality assurance associates in ensuring consistent product quality?

Quality Assurance Associates often encounter challenges such as managing tight production deadlines while maintaining thorough testing standards, addressing unexpected defects, and adapting quickly to new regulatory or product requirements. Effective communication with production, development, and regulatory teams is crucial for resolving issues efficiently. Staying current with evolving quality standards and continuously improving testing processes are also important for success in this role.

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

AspectQuality Assurance AssociateQuality Control Inspector
CertificationsOften requires certifications like ASQ CQIA or related quality assurance trainingMay require certifications such as ISO auditor or specific industry standards
Work EnvironmentInvolves process audits, documentation, and improving quality systemsFocuses on inspecting products or materials for defects
Employer & Industry UsageCommon in manufacturing, pharmaceuticals, and tech industriesPrimarily in manufacturing, food production, and assembly lines

While both roles focus on quality, the Quality Assurance Associate emphasizes developing and maintaining quality systems and processes, whereas the Quality Control Inspector concentrates on inspecting products for defects. Both roles are essential for ensuring product quality but differ in scope and responsibilities.

Is a Quality Assurance Associate an entry-level job?

A Quality Assurance Associate position is often considered entry-level, suitable for candidates with little to no prior experience in quality assurance or related fields. It typically requires basic knowledge of testing procedures, attention to detail, and may involve training on specific tools or software used in quality control processes.

What is the role of a quality assurance associate?

A quality assurance associate is responsible for monitoring and testing products or services to ensure they meet quality standards and specifications. They often develop testing procedures, document issues, and collaborate with teams to improve processes, using tools like checklists and quality management systems. Attention to detail and knowledge of industry regulations are essential for this role.

What cities near Rio Grande, PR are hiring for Quality Assurance Associate jobs?

Cities near Rio Grande, PR with the most Quality Assurance Associate job openings:

Quality Assurance Associate jobs near you
Infographic showing various Quality Assurance Associate job openings in Rio Grande, PR as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 12% Part Time, 4% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $46,931 per year, or $22.6 per hour.

Specialist QA - 35615

Mirus Consulting Group

Juncos, PR • On-site

$65 - $95/hr

Other

Re-posted 6 hours ago

Job description

mîrus Consulting Group is a local company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to pharmaceutical companies and other organizations across the Island and parts of the United States. Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the project management involved.

Position Summary

The Specialist QA is responsible for ensuring compliance with quality standards, regulatory requirements, and internal procedures throughout validation, commissioning, qualification, maintenance, and quality system activities. This role supports manufacturing and laboratory operations by reviewing and approving technical documentation, managing quality records, and ensuring validated systems remain compliant throughout their lifecycle.

Key Responsibilities
  • Support and oversee Commissioning, Qualification, and Validation (CQV) activities for manufacturing equipment, utilities, and laboratory bench equipment.
  • Review and approve Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Functional Testing, and related validation documentation.
  • Perform technical review and approval of validation reports, protocols, technical reports, procedures, forms, and other GMP documentation.
  • Support Process Validation and Cleaning Validation programs through document review, approval, and compliance assessments.
  • Participate in Quality Systems activities, including Deviations, Change Controls, CAPAs, and investigations, ensuring compliance with applicable regulations and company procedures.
  • Review and approve preventive maintenance (PM) documentation, work orders, job plans, and maintenance records.
  • Ensure documentation practices comply with Good Documentation Practices (GDP), cGMP requirements, and internal quality standards.
  • Collaborate with Manufacturing, Engineering, Validation, Laboratory, and Maintenance departments to ensure quality and compliance objectives are met.
  • Provide technical writing support for quality and validation documentation.
  • Identify opportunities for continuous improvement of quality systems, validation processes, and documentation practices.
  • Support internal and external audits, inspections, and regulatory assessments as required.
Minimum Qualifications
  • Doctorate degree; OR
  • Master's degree and 2 years of directly related experience; OR
  • Bachelor's degree and 4 years of directly related experience
Required Experience
  • Experience in Quality Assurance within a regulated manufacturing environment.
  • Hands-on experience with Commissioning, Qualification, and Validation activities for manufacturing and laboratory equipment.
  • Experience with IQ/OQ/PQ execution and Functional Testing.
  • Knowledge of Process Validation and Cleaning Validation requirements.
  • Experience with Quality Systems, including Deviations, Change Control, CAPA, and investigations.
  • Experience reviewing and approving technical and GMP documentation.
  • Knowledge of maintenance systems, including Preventive Maintenance (PM), Work Orders, and Job Plans.
  • Strong technical writing and document management skills.
Preferred Qualifications
  • Experience within the pharmaceutical, biotechnology, medical device, or highly regulated manufacturing industry.
  • Knowledge of cGMP, FDA, EMA, and other applicable regulatory requirements.
  • Strong analytical, problem-solving, and organizational skills.
  • Excellent written and verbal communication skills.Ability to work independently and collaborate within cross-functional teams.

This Company is an equal employment opportunity employer. We adhere to a policy of making employment decisions without regard to race, color, religion, sex, sexual orientation, national origin, citizenship, age or disability. We assure you that your opportunity for employment with this Company depends solely on your qualifications.

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