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Las Piedras Jobs (NOW HIRING)

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Gurabo / Juncos / Las Piedras, Puerto Rico (On-Site) Job Overview We are seeking an experienced Cleaning Validation Specialist to support regulated pharmaceutical manufacturing operations in Puerto ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Las Piedras / Gurabo / Juncos We are seeking a Commissioning & Qualification Specialist to support a pharmaceutical manufacturing facilities in Juncos/Gurabo area. The specialist will be responsible ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

On Site - Pharmaceutical Manufacturing Site, Puerto Rico (Juncos/ Gurabo/ Las Piedras) We are seeking a Project Scheduler to support capital and facility improvement projects at a pharmaceutical ...

New

PROVIDER NETWORK SOLUTIONS OF PUERTO RICO LLC

PR · On-site

Ceiba, Fajardo, Luquillo, Naguabo, Humacao, Yabucoa, San Lorenzo y Las Piedras. ???? Lunes a viernes | 8:00 a.m. - 5:00 p.m. No requiere turnos rotativos como parte de la jornada regular. Nuestra ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Gurabo / Juncos / Las Piedras, Puerto Rico (On-Site) Job Overview We are seeking an experienced Cleaning Validation Specialist to support regulated pharmaceutical manufacturing operations in Puerto ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

On Site - Pharmaceutical Manufacturing Site, Puerto Rico (Juncos/ Gurabo/ Las Piedras) We are seeking a Project Scheduler to support capital and facility improvement projects at a pharmaceutical ...

New

Compass Group

SHIFT SUPERVISOR

Las Piedras, PR · On-site

$12/hr

JLL - ROAD 183 KM 19.8, Las Piedras, PR 00771 Note: online applications accepted only. * Schedule : Full time schedule. Monday - Friday, hours may vary. More details upon interview. * Requirement

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

On Site - Pharmaceutical Manufacturing Site, Puerto Rico (Juncos/ Gurabo/ Las Piedras) We are seeking a Project Scheduler to support capital and facility improvement projects at a pharmaceutical ...

New

Eurest

PR · On-site

$12/hr

JLL - ROAD 183 KM 19.8, Las Piedras, PR 00771 Note: online applications accepted only. * Schedule : Full time schedule. Monday - Friday, hours may vary. More details upon interview. * Requirement

Kelly Services

PR

$15 - $18.50/hr

Las Piedras Salario y diferencial si aplica:12.50 p/h + dif de turno Únase como Operador Mecánico y apoye los procesos de manufactura industrial, involucrándose en la mejora de procesos ...

Eurest

PR · On-site

$11/hr

JLL - ROAD 183 KM 19.8., Las Piedras, PR 00771 Note: online applications accepted only. * Schedule : Full time schedule. Monday - Friday, 5:00 am - 1:30 pm. More details upon interview. * Requirement

Kenvue

Manufacturing Supervisor

Las Piedras, PR · On-site

$60K - $82K/yr

North America, United States, Puerto Rico, Las Piedras Work Location: Fully Onsite What you will do The Manufacturing Supervisor coordinates the activities necessary for the completion of all ...

Compass Group

DISHWASHER

Las Piedras, PR · On-site

$11/hr

JLL - ROAD 183 KM 19.8., Las Piedras, PR 00771 Note: online applications accepted only. * Schedule : Full time schedule. Monday - Friday, 5:00 am - 1:30 pm. More details upon interview. * Requirement

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How much do las piedras jobs pay per week?

As of Aug 7, 2026, the average weekly pay for las piedras in the United States is $1,366.40, according to ZipRecruiter salary data. Most workers in this role earn between $1,346.15 and $1,423.08 per week, depending on experience, location, and employer.

What is Las Piedras?

Las Piedras is not a job title but rather a term that refers to various locations, most notably cities or towns in Spanish-speaking countries such as Uruguay and Puerto Rico. If you are referring to a specific occupation or job title associated with 'Las Piedras,' please provide additional context. Otherwise, 'Las Piedras' generally means 'The Stones' in Spanish and is commonly used as a place name.

What is the difference between Las Piedras vs Warehouse Associate?

AspectLas PiedrasWarehouse Associate
Required CredentialsHigh school diploma or equivalent, forklift certification often preferredHigh school diploma or equivalent, forklift certification optional
Work EnvironmentDistribution centers, warehouses, logistics facilitiesWarehouses, distribution centers, manufacturing plants
Employer & Industry UsageLogistics companies, retail distribution, manufacturingRetail, manufacturing, logistics companies

Las Piedras and Warehouse Associate roles both operate within warehouse and logistics environments, often requiring similar certifications like a high school diploma and forklift training. While Las Piedras may refer to a specific location or company, Warehouse Associate is a common job title across various industries. Both roles involve handling inventory, operating equipment, and maintaining safety standards, making them comparable in work environment and employer usage.

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    Las Piedras jobs near you
    Infographic showing various Las Piedras job openings in the United States as of August 2026, with employment types broken down into 91% Full Time, 7% Part Time, and 2% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $71,053 per year, or $34.2 per hour.

    Cleaning Validation Specialist

    LEGAL PROJECT MANAGEMENT PARTNERS LLC

    PR • On-site

    Contractor

    Posted 15 days ago

    Job description

    Location: Gurabo / Juncos / Las Piedras, Puerto Rico (On-Site)

    Job Overview

    We are seeking an experienced Cleaning Validation Specialist to support regulated pharmaceutical manufacturing operations in Puerto Rico. This role is fully on-site and will focus on the execution, documentation, and lifecycle management of cleaning validation activities for manufacturing equipment, utilities, and laboratory environments.

    The ideal candidate will have strong experience in cleaning validation, including disinfectant and sanitization validation for Microbiology QC Laboratories and manufacturing areas, ensuring compliance with FDA and international regulatory requirements. This position requires expertise in developing validation strategies, performing risk assessments, and maintaining validated cleaning processes.


    Main Responsibilities

    • Develop, execute, and approve Cleaning Validation protocols, reports, and supporting documentation.
    • Lead cleaning validation activities for manufacturing equipment, production areas, and process support equipment.
    • Perform disinfectant and sanitization validation for Microbiology QC Laboratories and manufacturing environments.
    • Validate cleaning agents, disinfectants, sanitization procedures, and environmental cleaning processes.
    • Develop and maintain the Cleaning Validation Master Plan.
    • Establish scientifically justified acceptance criteria, sampling plans, and worst-case product/equipment selection.
    • Perform risk assessments to support cleaning validation strategies.
    • Collaborate with Quality, Manufacturing, Engineering, Validation, and Microbiology teams.
    • Analyze validation data, investigate deviations, and recommend corrective actions when necessary.
    • Maintain compliance with cGMP, FDA, EMA, ICH, and company quality standards.
    • Support internal audits and regulatory inspections as the Subject Matter Expert (SME) for Cleaning Validation.

    General Requirements

    • Fluency in English and Spanish (written and spoken).
    • Strong technical writing and documentation skills.
    • Excellent analytical and problem-solving abilities.
    • Proficiency with Microsoft Office 365 (Excel, Word, PowerPoint).
    • Strong communication and cross-functional collaboration skills.
    • Ability to manage multiple validation projects simultaneously.
    • Strong attention to detail and organizational skills.

    Education Requirements

    • Bachelor's Degree in Engineering, Chemistry, Biology, Microbiology, Pharmaceutical Sciences, Life Sciences, or related discipline.
    • Equivalent combination of education and relevant pharmaceutical experience may be considered.

    Experience Requirements

    • Minimum 2 years of pharmaceutical industry experience.
    • Minimum 2 years of Cleaning Validation experience in FDA-regulated pharmaceutical, biotechnology, or medical device manufacturing.
    • Hands-on experience developing and executing Cleaning Validation protocols and reports.
    • Experience performing disinfectant validation and sanitization validation.
    • Experience supporting Microbiology QC Laboratories (QC Micro) and manufacturing operations.
    • Knowledge of cleaning process lifecycle and contamination control strategies.
    • Experience performing risk assessments for cleaning validation.
    • Strong understanding of cGMP regulations and FDA expectations.

    Preferred Experience

    • Experience with environmental monitoring programs.
    • Experience validating cleaning procedures for aseptic or sterile manufacturing.
    • Experience with CIP (Clean-In-Place) and COP (Clean-Out-of-Place) systems.
    • Familiarity with TOC, conductivity, swab sampling, rinse sampling, and recovery studies.
    • Experience supporting regulatory inspections.

    Physical Requirements

    • Ability to sit for extended periods.
    • Occasional standing and walking throughout manufacturing and laboratory areas.
    • Ability to wear required Personal Protective Equipment (PPE).
    • Ability to access manufacturing, laboratory, and controlled environments.
    • Ability to perform work in regulated industrial environments.