Top 73 Quality assurance Jobs in Barceloneta Pr

Commissioning & Qualification (C&Q) Support
JC Automation Corp —Manatí, PR
- $25 - $45 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Engineering
Quick Apply
Lead Investigator
Weil Group, Inc —Manatí, PR
- Temporary
- Bilingual
- Background check
- Bachelor's degree
Quick Apply
Quality Assurance Technician
Nova Atlas Manufactura, Inc. —Barceloneta, PR
- $14 an hour
- Full-time
- Health insurance
Quick Apply
14d
Regulatory QA Specialist
HR Works —Barceloneta, PR
- $30 - $45 an hour
- Contract
- Senior level
Quick Apply
14d
Quality Engineer
Abbott Laboratories —Barceloneta, PR
- $54,300 - $109,000 a year
- Full-time
- Spanish
- Engineering
- English
- Disability insurance
- Health insurance
20h
Quality - Quality Assurance Inspector I
Viant Medical —Vega Baja, PR
- Full-time
- ERP systems
- Windows
- Mechanical knowledge
Quick Apply
8d
Inspector de Calidad
Eaton —Arecibo, PR
Quality Manager
Elements Solutions Inc —Manatí, PR
- $92,402 - $138,604 a year
- Spanish
- 5 years
- English
- Health insurance
- 401(k) matching
Quality Technician
Industrial C&S of P.R. LLC —Arecibo, PR
- Full-time
- Spanish
- Engineering
- English
Quick Apply
7d
Quality Auditor - 2nd Shift
Hubbell Incorporated —Vega Baja, PR
- Commercial
Quality Assurance Technical Reviewer
Mentor Technical Group —Vega Baja, PR
- Full-time
- Spanish
- English
- Mid-level
Computer System Validation
Validation & Engineering Group —Manatí Municipio, PR
- Mid-level
- Data entry
Quick Apply
QA Specialist I
Artech LLC —Barceloneta, PR
- $60 - $64 an hour
- Contract
- Bachelor of Science
- Microsoft Office
- 3 years
Quick Apply
C&Q Specialist | Pharmaceutical
LPMP | Legal Project Management Partners —Barceloneta, PR
- Contract
- Spanish
- Microsoft Excel
- Microsoft Outlook
Quick Apply
Computer System Validation (CSV) Specialist (EBR System)
Validation & Engineering Group, Inc —Barceloneta, PR
- Full-time
- 5 years
- Senior level
Quick Apply
2d
Quality Engineer
Trane Technologies —Arecibo, PR
- $72,000 a year
- Full-time
- Spanish
- Management
- Customer service
- Paid holidays
- Health insurance
Cleaning Validation Specialist
Validation & Engineering Group —Barceloneta, PR
- Spanish
- OSHA
- 5 years
Quick Apply
Senior Parenteral Inspection Technology
ProQualityNetwork —Manatí, PR
- Contract
- In-person
- Senior level
CAPA Investigator
Baxter —Jayuya, PR
- Extended hours
- 3 years
- Master's degree
- Bachelor's degree
- Paid parental leave
- Employee stock purchase plan
Validation Quality Engineer
Professional Pharma Solutions —Dorado, PR
- $35 - $45 an hour
- Full-time
- Engineering
- Mid-level
- In-person
Quick Apply

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Commissioning & Qualification (C&Q) Support

JC Automation Corp -
Manatí, PR

Quick Apply

Job Details

Full-time
$25 - $45 an hour

Qualifications

Project team coordination
Microsoft Excel
Microsoft Outlook
Technical documentation
Mechanical system commissioning projects
Piping and instrumentation diagrams (P&IDs)
Manufacturing facility experience
Bachelor's degree in engineering
Pharmaceutical company experience
Microsoft Teams
Regulatory/legal compliance standards in production
Commissioning phase involvement
Cross-functional collaboration
Field commissioning
Field engineering
Cross-functional communication
Pharmaceutical manufacturing facility experience

Full Job Description

About Company:

JC Automation Corp. (JCA) was founded in 1997 with the mission of filling a gap between technology and regulatory requirements in the life science manufacturing industry. The company offers highly capable resources at an affordable cost to build solutions and execute projects in: Automation, Control Systems Integration, Information Technology, System Integration and Regulatory Compliance.

JCA is a HUBZone Certified Small Business Firm, NMSDC Certified Minority Business Enterprise, and Certified Critical Industry Supplier. It’s mission is to add value by delivering quality services & solutions on time all the time by transforming processes & technology into business advantages.

ABOUT THE ROLE

We are looking for a hands-on and detail-driven Commissioning & Qualification (C&Q) Support professional to join our team in a dynamic, fast-paced pharmaceutical manufacturing environment. In this role, you will play a key part in ensuring that equipment and systems are properly installed, tested, and qualified before being released to production operations.

You will work closely with engineering, automation, quality, and vendor teams throughout the execution of commissioning and qualification activities, contributing directly to the successful startup of critical manufacturing systems. This is a field-intensive, documentation-focused role that requires strong attention to detail, a collaborative mindset, and a solid understanding of GMP principles and validation lifecycle requirements.

RESPONSIBILITIES

Support Commissioning & Qualification (C&Q) activities for equipment and systems installed within GMP-regulated pharmaceutical facilities.
Assist in the execution of commissioning and qualification protocols (IQ, OQ, PQ) in coordination with validation and engineering teams.
Support preparation and review of C&Q documentation, including protocols, test scripts, and summary reports.
Coordinate field activities related to equipment startup, testing, and system verification.
Interface with engineering, automation, vendors, and quality/validation teams during all execution phases.
Ensure all C&Q activities are performed in full compliance with GMP requirements, company SOPs, and applicable regulatory expectations.
Support identification, documentation, and resolution of deviations and discrepancies encountered during testing and qualification.
Assist with punch list tracking and closure activities prior to system release.
Support system readiness for hand-off to operations, ensuring all acceptance criteria have been met.
Maintain accurate, organized, and audit-ready C&Q documentation throughout the project lifecycle.

REQUIREMENTS & QUALIFICATIONS

Education

Bachelor's degree in Engineering (Mechanical, Chemical, Electrical, or a related technical discipline).

Experience

Experience supporting Commissioning & Qualification (C&Q), validation, or startup activities in pharmaceutical or regulated manufacturing environments.
Hands-on experience executing or supporting IQ/OQ/PQ protocols for manufacturing equipment or utility systems.
Direct experience working in GMP-regulated facilities.
Experience coordinating with cross-functional teams including Engineering, Automation, and Quality/Validation.
Exposure to equipment installation, startup, or system turnover activities.

Preferred

Familiarity with commissioning and qualification documentation practices in a pharmaceutical or biotech setting.
Experience supporting deviation management and CAPA processes during qualification phases.
Knowledge of regulatory frameworks such as FDA 21 CFR Part 11, GAMP 5, or EU GMP Annex 11.

SKILLS

Technical Skills

Working knowledge of GMP, validation lifecycle, and pharmaceutical regulatory expectations
Hands-on execution of IQ, OQ, and PQ protocols for manufacturing and utility systems
C&Q documentation development, review, and audit readiness
Deviation identification, documentation, and resolution support
Punch list management and system turnover coordination
Familiarity with engineering drawings, P&IDs, and equipment manuals
Microsoft Office 365 (Word, Excel, Outlook, Teams)

Soft Skills

Strong attention to detail and commitment to documentation accuracy
Clear and proactive communication across multidisciplinary teams
Ability to work independently in a structured field environment
Organized, methodical, and adaptable under project timelines
Team-oriented with a collaborative approach to problem solving
Willingness to work on-site during testing, startup, and qualification phases

Quick Apply

Refine Your Search

quality assurance jobs in barceloneta pr

Commissioning & Qualification (C&Q) Support

Lead Investigator

Quality Assurance Technician

Regulatory QA Specialist

Quality Engineer

Quality - Quality Assurance Inspector I

Inspector de Calidad

Quality Manager

Quality Technician

Quality Auditor - 2nd Shift

Quality Assurance Technical Reviewer

Computer System Validation

QA Specialist I

C&Q Specialist | Pharmaceutical

Computer System Validation (CSV) Specialist (EBR System)

Quality Engineer

Cleaning Validation Specialist

Senior Parenteral Inspection Technology

CAPA Investigator

Validation Quality Engineer

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