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Cleaning Validation Engineer Jobs in Puerto Rico

FITS LLC

Sr. Quality Engineer

Juncos, PR · On-site

$86K - $117K/yr

For engineering services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part ... validation, cleaning validation, and cleanroom qualification activities in GMP-regulated ...

FITS LLC

Sr. Manufacturing Engineer

Juncos, PR · On-site

$80 - $100/hr

For Engineering services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part ... Strong experience with equipment qualification (IQ/CSV/OQ/PQ), process validation, cleaning ...

FITS LLC

Sr. Manufacturing Engineer

Juncos, PR · On-site

$89K - $121K/yr

For Engineering services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part ... Strong experience with equipment qualification (IQ/CSV/OQ/PQ), process validation, cleaning ...

Mirus Consulting Group

Specialist QA - 35615

Juncos, PR · On-site

$65 - $95/hr

Support Process Validation and Cleaning Validation programs through document review, approval, and ... Collaborate with Manufacturing, Engineering, Validation, Laboratory, and Maintenance departments to ...

Veg Group

C&Q Specialist

Juncos, PR · On-site

$60 - $80/hr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... systems, clean utilities, facilities, cleanroom environments, process improvements, utilities ...

Pinnaql

C&Q Specialist

Punta Santiago, PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... systems, clean utilities, facilities, cleanroom environments, process improvements, utilities ...

Pinnaql

Specialist Tech Engineering

Juncos, PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... cleaning issues, validation issues, electrical issues and process maintenance issues. * Provide ...

Pinnaql

C&Q Specialist

Humacao, PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... systems, clean utilities, facilities, cleanroom environments, process improvements, utilities ...

Pinnaql

C&Q Specialist

Gurabo, PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... systems, clean utilities, facilities, cleanroom environments, process improvements, utilities ...

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Cleaning Validation Engineer information

What is a cleaning validation engineer?

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 the key skills and qualifications needed to thrive as a cleaning validation engineer, 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 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 August 2026, with employment types broken down into 83% Full Time, 6% Part Time, and 11% Contract. Highlights an 94% In-person, and 6% Hybrid job distribution.

C&Q Specialist

Validation & Engineering Group, Inc.

Gurabo, PR • On-site

Full-time

Re-posted 6 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:
  • C&Q Specialist

Position Summary
The C&Q Specialist will support commissioning and qualification activities associated with capital projects and technical initiatives within regulated pharmaceutical and biotechnology manufacturing environments.
This role is responsible for supporting protocol development, field execution activities, equipment startup support, commissioning and qualification documentation, and coordination activities associated with regulated systems and operational readiness initiatives.
Projects may support one or more of the following areas: manufacturing systems, process equipment, packaging systems, clean utilities, facilities, cleanroom environments, process improvements, utilities infrastructure, automation-related systems, or other regulated operational systems.
The role requires strong technical documentation skills, field coordination capabilities, and collaboration with Engineering, Operations, Quality, contractors, vendors, and project teams to support compliant project execution activities.
Key Responsibilities
  • Support assigned commissioning and qualification.
  • Generate, review, and execute commissioning and qualification protocols and related technical documentation.
  • Support field execution activities including commissioning support, verification activities, and operational readiness coordination.
  • Participate in FAT & SAT activities, equipment inspections, field walkthroughs, and startup support activities as required.
  • Support collection, review, and organization of commissioning and qualification documentation and test records.
  • Document test results and execution activities in accordance with applicable GMP and data integrity expectations.
  • Support identification, documentation, and follow-up of deviations, punch-list items, corrective actions, and technical observations during execution activities.
  • Coordinate with Engineering, Operations, Quality, contractors, vendors, and project teams to support project execution and turnover activities.
  • Support scheduling and coordination of field execution activities, testing activities, and resource needs.
  • Participate in project meetings and support communication of execution status, technical issues, risks, and action items.
  • Support continuous improvement initiatives related to commissioning, qualification, documentation, and operational readiness activities.
  • Ensure commissioning and qualification activities are performed in alignment with applicable site procedures, GMP requirements, safety rules, policies and project expectations.

Qualifications & Experience
  • Bachelor's degree in Engineering, Science, Business Administration, or related technical field preferred.
  • Minimum of 2 years of relevant C&Q, validation, startup, or field execution experience required for candidates with Engineering or Science degrees.
  • Candidates with Business Administration or other non-technical degrees should have a minimum of 3 years of relevant experience.
  • Experience supporting one or more of the following areas is preferred: manufacturing systems, process equipment, packaging systems, clean utilities, facilities, cleanrooms, automation systems, or regulated operational infrastructure.
  • Familiarity with commissioning and qualification documentation, protocol execution, technical field support, and GMP documentation practices.
  • Familiarity with GMP regulations, data integrity principles (ALCOA), and regulated documentation practices.
  • Familiarity with systems such as Kneat, Bluebeam, TrackWise, CMMS platforms, or similar technical and quality systems is preferred.
  • Excellent verbal and written communication skills in both English and Spanish, including technical writing, protocol documentation, and communication of technical deliverables.
  • Strong organizational, troubleshooting, analytical, and problem-solving skills with the ability to support multiple priorities and field activities simultaneously.

Additional Requirements
  • Ability to work on-site in the eastern region of Puerto Rico.
  • Must be eligible to complete client-required onboarding, training, and site access requirements.
  • Ability to work effectively within fast-paced and highly regulated environments.

The above statements describe the general nature and level of work performed and do not represent an exhaustive list of responsibilities.
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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