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Cleaning Validation Engineer Jobs in Puerto Rico

CIS International LLC

PR

Participate in the coordination of TECHSUPPORT on engineering, regulatory, compliance, calibration, quality, microbial/environmental, technical cleaning, validation, electrical and process automation ...

FITS LLC

Associate Tech Engineering

Juncos, PR · On-site

Calibration, quality, microbial/environmental, technical cleaning, validation, electrical, and process automation issues. * Assist in the evaluation and implementation of engineering improvements ...

InfoTree

Be Seen First

Principal Engineer (Clean Utilities)

Juncos, PR · On-site

$55 - $59/hr

FUNCTIONS 1. Establish engineering policies for a major segment of the company. 2. Interpret ... validation departments in developing requirements and recommendations for large and/or highly ...

New

Kelly Services

Principal Scientist

Carolina, PR

... cleaning validation programs. Responsibilities: * Technical leadership - Provide DPO expertise for ... PhD in Chemical Engineering, Chemistry or scientific related field. Minimum of five (5) years ...

MMR Consulting

PR · On-site

Its services include Engineering, Project Management, and Validation. MMR Consulting has offices in ... Clean utilities * HVAC systems * Automation and control systems * Manufacturing and packaging lines

ProQualityNetwork

Principal Engineer 35424

Juncos, PR

$43 - $47/hr

Clean Utilities * GMP Compliance * Deviation Investigations * Root Cause Analysis * Validation ... engineering professional to lead high-impact projects, influence operational strategy, and ...

Kelly Services

PR · On-site

... cleaning validation programs. Responsibilities: * Technical leadership - Provide DPO expertise for ... PhD in Chemical Engineering, Chemistry or scientific related field. Minimum of five (5) years ...

MMR Consulting

PR

Its services include Engineering, Project Management, and Validation. MMRConsulting ... Clean utilities * HVAC systems * Automation and control systems * Manufacturing and packaging lines

MMR Consulting

PR · On-site

Its services include Engineering, Project Management, and Validation. MMRConsulting ... Clean utilities * HVAC systems * Automation and control systems * Manufacturing and packaging lines

ProQualityNetwork

Principal Engineer 35423

Juncos, PR

$43 - $47/hr

... Validation, and Research organizations to drive strategic projects and ensure compliance with ... Experience supporting Clean Utilities systems within pharmaceutical, biotechnology, or highly ...

Inteldot

Principal Engineer 35424

Juncos, PR · On-site +1

Experience working on Clean Gases (Process Air, GMP gases supply like Oxygen, Nitrogen ... with validation processes and documentation in a highly regulated environment. 3. Establish ...

Inteldot

Principal Engineer 35423

Juncos, PR · On-site +1

Experience working on Clean Gases [Process Air, GMP gases supply like Oxygen, Nitrogen ... with validation processes and documentation in a highly regulated environment. 3. Establish ...

FITS LLC

Principal Engineer

Juncos, PR · On-site

For Clean Utilities & Deviation services in the Engineering area. WHAT MAKES YOU A FIT: The ... and validation departments in developing requirements. * Established a corporate Engineering ...

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Cleaning Validation Engineer information

What is the hourly rate for product validation expert?

The hourly rate for a product validation expert, such as a Cleaning Validation Engineer, typically ranges from $30 to $70 depending on experience, location, and industry. Senior professionals with specialized certifications may earn higher rates, especially in regulated environments like pharmaceuticals or biotech.

Are validation engineers in demand?

Validation engineers, including those specializing in cleaning validation, are in demand across industries such as pharmaceuticals and biotechnology due to strict regulatory requirements. They are valued for their expertise in ensuring compliance, quality, and safety, often requiring knowledge of GMP standards and validation tools. The demand is expected to grow with increased focus on quality assurance and regulatory compliance in manufacturing environments.

What does a cleaning validation engineer do?

A cleaning validation engineer is responsible for developing, executing, and documenting cleaning procedures to ensure pharmaceutical or manufacturing equipment is free of contaminants. They verify that cleaning processes meet regulatory standards, often using analytical tools and validation protocols, to prevent cross-contamination and ensure product safety. This role requires knowledge of GMP regulations, validation techniques, and attention to detail.

What are the key skills and qualifications needed to thrive in the Cleaning Validation Engineer position, and why are they important?

To thrive as a Cleaning Validation Engineer, you need a strong background in chemical engineering, microbiology, or a related field, often complemented by experience in GMP-regulated industries. Familiarity with validation protocols, analytical testing methods, and documentation tools (such as LIMS or QMS software) is essential, and certifications like Six Sigma or ASQ may be advantageous. Strong attention to detail, analytical thinking, and effective communication are key soft skills for success in the role. These capabilities are crucial to ensure regulatory compliance, product safety, and effective cross-functional collaboration in pharmaceutical or biotech manufacturing environments.

What does a validation engineer do?

A validation engineer is responsible for developing, executing, and documenting validation protocols to ensure that manufacturing processes, equipment, and systems meet regulatory standards and quality requirements. In the context of cleaning validation, they verify that cleaning procedures effectively remove contaminants, often using analytical tools and following strict industry guidelines. Their work helps ensure product safety and compliance in regulated industries such as pharmaceuticals and biotechnology.

What is a Cleaning Validation Engineer job?

A Cleaning Validation Engineer ensures that manufacturing equipment and processes meet regulatory standards for cleanliness in industries like pharmaceuticals, biotech, and medical devices. They develop validation protocols, conduct tests, analyze data, and document results to confirm that cleaning procedures effectively remove contaminants. This role involves collaborating with quality assurance, production, and regulatory teams to maintain compliance with FDA, GMP, and other industry regulations.

What are the main challenges faced by Cleaning Validation Engineers in the pharmaceutical industry?

Cleaning Validation Engineers in the pharmaceutical industry often face challenges such as staying up-to-date with evolving regulatory requirements, troubleshooting complex cleaning failures, and thoroughly documenting all validation activities. Balancing the needs for robust contamination control with operational efficiency requires analytical thinking and strong problem-solving abilities. Collaboration with manufacturing, quality assurance, and laboratory teams is frequent, as cleaning validation projects require input and support from multiple departments. Successfully managing these challenges ensures product safety, regulatory compliance, and continuous process improvement within manufacturing operations.

What are popular job titles related to Cleaning Validation Engineer jobs in Puerto Rico? For Cleaning Validation Engineer jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Cleaning Validation Engineer jobs in Puerto Rico look for? The top searched job categories for Cleaning Validation Engineer jobs in Puerto Rico are:
Cleaning Validation Engineer jobs near you
Infographic showing various Cleaning Validation Engineer job openings in Puerto Rico as of June 2026, with employment types broken down into 62% Full Time, 36% Part Time, 1% Temporary, and 1% Contract. Highlights an 88% Physical, 5% Hybrid, and 7% Remote job distribution.

JT805 - ASSOCIATE TECH ENGINEERING

Quality Consulting Group

Juncos, PR • On-site

Contractor

Posted 8 days ago

Job description

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you'll work with a highly dynamic, contributing in a world-class manufacturing industry in Puerto Rico & USA.
Responsibilities:
  • Provide automation support on all system/equipment optimization strategies, upgrades, replacements, and modifications and ensure that supported areas and activities are maintained in compliance with respect to current corporate policies, industry standards, regulatory standards and FDA standards.
  • Evaluate and determine if utility systems, process maintenance, instrumentation/calibration/electrical systems and technical cleaning systems are maintained in compliance with all applicable industry standards, regulatory standards and FDA standards.
  • Participate in the coordination of TECHSUPPORT on engineering, regulatory, compliance, calibration, quality, microbial/environmental, technical cleaning, validation, electrical and process automation issues.
  • Assist during FDA and other regulatory agency inspections.
  • Provide TECHSUPPORT in response to the FDA and other regulatory agencies.
  • Assist in the evaluation and implementation of engineering improvements, policy changes, compliance Improvements and optimization programs.
  • Monitor inspection and packaging equipment, with ability to investigate and troubleshoot advance issues or problems including mechanical, electrical, or automation.
  • Assist the team with maintaining an up-to-date working spare parts inventory system.
  • Develop, revise, and review SOPs or job plans/work plans for work related areas.
  • Evaluate the current maintenance procedures and assist in the changes to optimize the maintenance program.
  • Provides customer service to internal and external clients including ongoing support with detailed technical information and solving technical situations.
Qualifications:
  • Bachelor's degree or Associate's degree in related area
  • 2 to 4 years of directly related experience
  • Experience with pneumatics, automatic control and vision inspection systems required.
  • All work must be guided by team requirements or department objectives and completed in accordance with CFRs, cGMPs, SOPs, job plans and client's policies.
  • Non-Standard 12-hour shifts

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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