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Clean Contractor Jobs in Puerto Rico (NOW HIRING)

PACIV

Project Manager

San Juan, PR · On-site

Lead contractor execution from mobilization through mechanical completion and system turnover ... Process and Clean Utilities * Strong problem-solving, planning, and organizational skills with the ...

Techengpr

Process Project Manager

Carolina, PR · On-site

$125 - $150/hr

... clean utilities . * Ensure projects are delivered safely, on schedule, within budget, and in compliance with Lilly standards. * Coordinate multidisciplinary engineering teams, contractors ...

Lemartec

General Superintendent

Juncos, PR

Company Overview Founded in 1979, Lemartec is a national general contractor and construction management firm and is part of the General Building group within MasTec's Clean Energy and Infrastructure ...

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All JobsClean Contractor JobsClean Contractor Jobs in Puerto Rico

Clean Contractor information

What is the difference between Clean Contractor vs Janitorial Worker?

AspectClean ContractorJanitorial Worker
CredentialsMay require contractor licenses, certifications in cleaning techniquesTypically no formal certifications required
Work EnvironmentWorks on multiple client sites, often independentlyWorks primarily in specific buildings like offices or schools
Employer & Industry UsageOperates as independent contractors or cleaning companiesEmployed by a company or facility management
Common Search & ComparisonOften compared for contracting vs employment optionsCompared for job roles within cleaning services

The main difference is that a Clean Contractor operates independently, often managing multiple clients and requiring specific licensing, while a Janitorial Worker is typically employed by a company to perform cleaning tasks within a single facility. Understanding these distinctions helps in choosing the right career path or service provider.

How to be a cleaning contractor?

To become a cleaning contractor, you should gain experience in cleaning services, obtain any necessary business licenses or permits, and consider insurance coverage. Developing strong organizational skills and understanding cleaning equipment and products are also important for managing contracts and ensuring quality work.

What are popular job titles related to Clean Contractor jobs in Puerto Rico?

For Clean Contractor jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Clean Contractor jobs in Puerto Rico look for?

The top searched job categories for Clean Contractor jobs in Puerto Rico are:

What cities in Puerto Rico are hiring for Clean Contractor jobs?

Cities in Puerto Rico with the most Clean Contractor job openings:

Clean Contractor jobs near you

Validation Specialist (Cleaning-In-Place)

Veg Group

Humacao, PR • On-site

$100 - $125/hr

Other

Posted 19 days ago

Key responsibilities

  • 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.

  • Collaborate with Process Engineers, Automation, QA, and Manufacturing to ensure successful integration of CIP/SIP operations with process equipment.

Job description

Validation Specialist (Cleaning-In-Place)

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
  • Bachelor’s degree in Chemical, Mechanical, or Biochemical Engineering (or equivalent).
  • Minimum 7–10 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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