ZipRecruiter

Log In

1

Quality Assurance Associate Jobs in Puerto Rico (NOW HIRING)

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 ...

AbbVie

PR · On-site

The primary purpose of this position is to ensure the quality of product manufactured and also make ... Associate Degree in Science with zero (0) years of experience. * Knowledge of good manufacturing ...

FITS LLC

Quality Specialist- 02

Juncos, PR · On-site

$85 - $115/hr

For QA Services in the Drug Substance area. WHAT MAKES YOU A FIT: The Technical Part: * Bachelor'sDegree with four(4)years of experiencewithin the pharmaceutical or regulated industry. * Bilingual ...

Kelly Services

Quality Analyst

Barceloneta, PR

Serve as backup for the QA Manager leading the team and providing support to quality initiatives ... Associate Rotating shift - 4 days at 10hours 2 months rotation on each shift 1st, 2nd, 3rd shift ...

Pinnaql

Associate Quality Analyst II

Barceloneta, PR · On-site

Associate Quality Analyst II Description: Responsible for implementing and maintaining the ... Manage QA lists, spreadsheets, and databases required to support business operations. * Participate ...

previous page

Showing results 41-60

All JobsQuality Assurance Associate JobsQuality Assurance Associate Jobs in Puerto Rico

Quality Assurance Associate information

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

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

What job categories do people searching Quality Assurance Associate jobs in Puerto Rico look for?

The top searched job categories for Quality Assurance Associate jobs in Puerto Rico are:

What cities in Puerto Rico are hiring for Quality Assurance Associate jobs?

Cities in Puerto Rico with the most Quality Assurance Associate job openings:

Quality Assurance Associate jobs near you
Infographic showing various Quality Assurance Associate job openings in Puerto Rico as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 14% Part Time, 2% Temporary, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution.

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

Veg Group

Juncos, PR • On-site

$70 - $90/hr

Other

Posted 4 days ago

Key responsibilities

  • Review and approve product manufacturing protocols, validation reports, environmental characterization reports, work orders, and change controls.

  • Lead investigations, site audits, and support quality programs, including risk assessments, automation activities, and environmental programs.

  • Provide quality oversight for manufacturing, testing, and disposition of drug substances, ensuring compliance with cGMP, cGLP, and other regulations.

Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

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 approve product MPs.
  • Approve process validation protocols and reports for manufacturing processes.
  • Request Quality on incident triage team.
  • Approve Environmental Characterization reports.
  • Release of sanitary utility systems.
  • Approve planned incidents.
  • Represent QA on NPI team.
  • Lead investigations.
  • Lead site audits.
  • Own site quality program procedures.
  • Designee for QA manager on local CCRB.
  • Review Risk Assessments.
  • Support Automation activities.
  • Support facilities and environmental programs.
  • Review and approve Work Orders.
  • Review and approve EMS/BMS alarms.
  • Approve NC investigations and CAPA records.
  • Approve change controls.
  • Provide lot disposition and authorize lots for shipment.
EDUCATION
  • Doctorate OR
  • Masters + 2 years of directly related experience OR
  • Bachelors + 4 years of directly related experience OR
RESPONSIBILITIES
  • Execute Quality disposition (approval or rejection) of bulk drug substances.
  • Provide Quality oversight to ensure that operations for clinical and licensed pharmaceutical Drug Substance (API) are manufactured, tested, stored, and managed according to current Good Manufacturing Practices (cGMP), Good Laboratory Practices (cGLP), and other applicable regulations.
  • Ensure that deviations from established procedures are identified, reported, and documented per procedures.
  • Ensure that changes that could potentially impact drug substance quality are assessed according to procedures.
  • Ensure that production records and testing results are complete, accurate, and documented according to written procedures and cGMP requirements.
  • Ensure that facilities, equipment, materials, organization, processes, and procedures align with cGMP practices and other applicable regulations.
  • Champion continuous improvement initiatives, programs, and projects, including developing efficiency projects and supervising progress.
  • Ensure completion of required training and maintain assigned training adherence to support successful task execution.
  • Collaborate and partner cross functionally to ensure the Quality Management System (QMS) processes are completed in accordance with established procedures.
  • Support internal and external audits and inspections as part of the audit/inspection management team, including acting as Quality Unit representative as needed.
  • Alert senior management of quality, compliance, supply, and safety risks.
  • Provide support and oversight for New Product Introduction (NPI).
ATTRIBUTES
  • Experience with key electronic systems, such as documentation platforms (e.g., CDOCS), Maximo, TrackWise, LIMS, MES/electronic batch record systems, and SAP.
  • Experience in computer systems validation (CSV) or computer systems quality assurance, including consulting level technical proficiency.
  • Experience with validation of GxP applications, including Validation Master Plans, GxP risk assessments, IQ/OQ/PQ protocols, test scripts, and summary/approval reports.
  • Robust knowledge of manufacturing and distribution processes, including QA, QC, and Process Development operations.
  • Validated experience serving as Quality Contact for complex projects involving packaging, inspection, commissioning, qualification, and new drug substances/products.
  • Strong organizational skills, with the ability to drive assignments through successful completion.
  • Demonstrated leadership, influencing, and negotiation skills, including interactions with regulatory agencies and evaluation of compliance issues.
  • Strong communication skills (written and oral), facilitation abilities, and full bilingual proficiency in English and Spanish, with the ability to work independently and effectively across all organizational levels.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

#J-18808-Ljbffr

Apply