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Quality Assurance Assistant Jobs in Puerto Rico (NOW HIRING)

MENTOR TECHNICAL GROUP CORP

PR · On-site

... quality assurance or regulatory affairs within a regulated industry (e.g., pharmaceuticals ... 8. Assist in the creation, review, and training for Validation Qualifications and Protocols. 9. ...

SOLX HOLDINGS LLC

PR · On-site

... quality assurance. · Collect and analyze production data to identify trends, anomalies, and opportunities for improvement. · Assist in implementing and documenting engineering change orders (ECOs ...

Bayer

Greenhouse Worker

Juana Diaz, PR · On-site

$20K - $25K/mo

Adhere to Bayer's Health, Safety & Environmental (HSE) and quality assurance/quality control (QA/QC ... Assist in other projects and duties as required or assigned; WHO YOU ARE Bayer seeks an incumbent ...

New

Marriott

Recreation Experience Expert (PT)

San Juan, PR · On-site

$15.50 - $18.50/hr

... Assist when hosting private functions within the recreation facilities with group activities and ... Comply with quality assurance expectations and standards. Read and visually verify information in a ...

FITS LLC

Project Manager

Manati, PR · On-site

Oversee and assist Engineers with their assigned projects. * Support the execution activities of ... quality assurance, and/or validation departments. * Work under the direct supervision of project ...

aspensurgical

Mechanic

Las Piedras, PR · On-site

Mentor other team technicians assist with the design, installation, and improvement of new and ... sound quality assurance principles. * Execute Set - up operator role if is required. * Other ...

Fresenius Medical Care

Charge Nurse

Bayamon, PR · On-site

... * Assist with the interviewing of potential direct patient care staff * Promote efficient use of medical supplies. * Attend and participate in monthly Quality Assurance meetings. Additional ...

Tetra Tech

Project Manager

Guaynabo, PR · On-site

Monitor program performance and assist in identifying operational risks, developing mitigation ... Support quality assurance, schedule management, cost control, resource planning, and risk ...

Tetra Tech, Inc.

Project Manager

Guaynabo, PR · On-site

Monitor program performance and assist in identifying operational risks, developing mitigation ... Support quality assurance, schedule management, cost control, resource planning, and risk ...

ProQualityNetwork

Senior Engineer 35449

Juncos, PR · On-site

$101K - $139K/yr

... vendors. * Assist in the development and management of project budgets. Cross-Functional ... Facilities * Quality Assurance * Validation to support equipment installations, facility ...

ProQualityNetwork

Engineer-35631

Juncos, PR

... Quality Assurance, and Validation teams to develop requirements and recommendations for system ... system performance. * Assist with engineering activities associated with manufacturing and ...

New

Boston Scientific

Financial P&A - P5

Dorado, PR

Prepare journal entries and assist in month end close as needed to ensure proper accounting at the ... QA, Engineering, Operations, etc.). * Significant experience with SAP Business Systems

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All JobsQuality Assurance JobsQuality Assurance Assistant JobsQuality Assurance Assistant Jobs in Puerto Rico

Quality Assurance Assistant information

How much do entry-level quality assurance assistants jobs pay?

Entry-level quality assurance assistant positions typically pay between $30,000 and $45,000 annually, depending on the industry and location. These roles often require basic knowledge of testing procedures, attention to detail, and familiarity with quality standards or tools like Excel or testing software.

What are the key skills and qualifications needed to thrive as a quality assurance assistant, and why are they important?

To thrive as a Quality Assurance Assistant, you need a strong attention to detail, knowledge of quality control processes, and at least a high school diploma or relevant associate degree. Familiarity with quality management systems (QMS), inspection tools, and software like Microsoft Excel or SAP is typically required. Strong organizational skills, effective communication, and a proactive approach to problem-solving make you stand out in this role. These skills ensure the consistent delivery of high-quality products and help maintain compliance with industry standards.

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

AspectQuality Assurance AssistantQuality Control Technician
CertificationsTypically requires certifications in quality management or related fieldsOften requires certifications in inspection or testing methods
Work EnvironmentSupports quality assurance processes, documentation, and auditsPerforms product inspections and testing on production lines
Industry UsageUsed across manufacturing, healthcare, and service industriesCommonly found in manufacturing and production settings

While both roles focus on quality, the Quality Assurance Assistant primarily supports the development and maintenance of quality systems, whereas the Quality Control Technician conducts physical inspections and tests to ensure product standards are met.

What are some common challenges faced by quality assurance assistants, and how can they be effectively managed?

Quality Assurance Assistants often encounter challenges such as handling tight deadlines, maintaining attention to detail during repetitive tasks, and keeping up with changing quality standards. To manage these, it's important to develop strong organizational skills, actively communicate with team members, and stay updated on best practices and regulatory requirements. Building a habit of double-checking work and seeking feedback can also help ensure high-quality outcomes and support continuous improvement within the team.

What is a quality assurance assistant?

Quality assurance assistants work in the quality assurance (QA) department of a company. They are found in a variety of industries and help QA analysts and other team members ensure that a product meets industry standards, design specifications, and customer satisfaction measurements. As a quality assurance assistant, your duties and responsibilities vary, depending on the company and the industry. For example, in manufacturing, you may assist in overseeing the entire production process to ensure quality control at every stage. Software development quality assurance assistants collaborate with testers and quality control (QC) staff once the development stage is complete. Qualifications for the job depend on the field, but many employers prefer candidates with an associate degree and who have strong attention to detail and analytical problem-solving skills.

Is a quality assurance assistant a good entry-level job?

A quality assurance assistant is often considered a suitable entry-level position, as it typically requires basic knowledge of quality standards and attention to detail. It provides opportunities to develop skills in inspection, documentation, and understanding quality processes, which can serve as a foundation for advancement in quality management roles.
More about Quality Assurance Assistant jobs
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 are popular job titles related to Quality Assurance Assistant jobs in Puerto Rico? For Quality Assurance Assistant jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Quality Assurance Assistant jobs in Puerto Rico look for? The top searched job categories for Quality Assurance Assistant jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Quality Assurance Assistant jobs? Cities in Puerto Rico with the most Quality Assurance Assistant job openings:
Quality Assurance Assistant jobs near you
Infographic showing various Quality Assurance Assistant 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.

Validation Specialist (Cleaning-In-Place)

Validation & Engineering Group Inc.

Juana Diaz, PR • On-site

Full-time

Re-posted 25 days ago

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:

  • Validation Specialist - CIP

Summary:
The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and Sterilization-In-Place (SIP) systems within a biotech manufacturing environment. This role ensures that cleaning and sterilization systems are installed, tested, and qualified in compliance with GMP, FDA, EMA, and ASTM E2500 standards, supporting readiness for process validation and commercial manufacturing.

Key Responsibilities:
Commissioning & Qualification Execution:

  • Review and approve vendor FAT/SAT protocols for CIP/SIP equipment.
  • Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam sterilization cycle qualification, and temperature mapping.
  • Oversee the qualification of utilities supporting CIP/SIP systems (Clean Steam, WFI, Process Air).
  • Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity.


Documentation & Compliance:

  • Generate and review URS, FAT/SAT, IOQ, and PQ documentation in compliance with ASTM E2500 and GAMP 5.
  • Ensure traceability from design specifications through executed testing.
  • Assist in managing deviations, non-conformances, and change controls related to CIP/SIP systems.
  • Prepare summary reports for Quality Assurance approval.


Cross-functional Collaboration:

  • Collaborate with Process Engineers, Automation, QA, and Manufacturing to ensure successful integration of CIP/SIP operations with process equipment.
  • Support operations during process validation batches and cleaning validation campaigns.
  • Provide training and technical guidance to CQV engineers and contractors executing test protocols.


Qualifications:

  • Bachelors degree in Chemical, Mechanical, or Biochemical Engineering (or equivalent).
  • Minimum 710 years of experience in CQV within biotech or pharmaceutical manufacturing environments.
  • Experience in generating and executing documentation for CQV activities.
  • Strong knowledge of cleaning validation, sterilization principles, and automation integration.
  • Familiarity with DeltaV, SCADA, or PLC systems for CIP/SIP recipe management.
  • Expertise in ASTM E2500, ISPE Baseline Guides, GAMP 5, and FDA/EMA guidelines.
  • Proficiency in reviewing P&IDs, piping isometrics, and functional design specifications.
  • Experience executing or overseeing FAT/SAT, IOQ, PQ activities.
  • Knowledge of data integrity, 21 CFR Part 11, and electronic validation systems (e.g., Kneat, ValGenesis).
  • Must be fully bilingual (English / Spanish) with excellent oral skills.
  • Available to work extended hours, possibility of weekends and holidays.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
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.

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