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Change Control Coordinator Jobs in Puerto Rico (NOW HIRING)

Veg Group

Work Package Owner (WPO)

Carolina, PR · On-site

... coordinates interfaces, and ensures timely decision-making necessary to support successful ... Practical experience with schedule management, cost tracking, and change-control processes.

JLL

Senior Project Manager

Gurabo, PR

... change control, reporting, and closeout. * Strong written and verbal communication skills in both ... Experience coordinating multidisciplinary teams, including contractors, vendors, consultants ...

PRPDG

Sr Project Mgr

Juncos, PR · On-site

Oversees, manages and coordinates all operational aspects of ongoing department level projects ... Previous experience in change control management, project controls and capital projects.

New

FITS LLC

Engineer

Juncos, PR · On-site

GDP, change control, and risk assessment knowledge. * Cross-functional coordination with Engineering, Operations, Quality & Validation. The Personality Part: * Our Next Piece is someone who treats ...

Quality Consulting Group, LLC

JT630 - SR ENGINEER

Juncos, PR · On-site

$102K - $140K/yr

Risk Management & Change Control * Lead and document risk assessments related to system ... Cross-functional Coordination * Collaborate with Engineering, Validation, Quality Assurance (QA), ...

Quality Consulting Group

JT630 - SR ENGINEER

Juncos, PR · On-site

$102K - $140K/yr

Risk Management & Change Control * Lead and document risk assessments related to system ... Cross-functional Coordination * Collaborate with Engineering, Validation, Quality Assurance (QA), ...

Pinnaql

Validation Specialist

Aibonito, PR · On-site

Knowledge of change control, deviations, CAPA, calibration, maintenance, and equipment ... Strong technical writing, documentation, organizational, and project coordination skills. * Ability ...

Veg Group

Validation Specialist

Aibonito, PR · On-site

Knowledge of change control, deviations, CAPA, calibration, maintenance, and equipment ... Strong technical writing, documentation, organizational, and project coordination skills. * Ability ...

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Change Control Coordinator information

What is a change control coordinator?

Change Control Coordinators are professionals responsible for managing and overseeing changes to processes, systems, or products within an organization. They ensure that all modifications are properly documented, evaluated for risks, and approved before implementation. Their role is crucial in maintaining compliance, minimizing disruptions, and ensuring that changes align with company policies and regulatory requirements. Change Control Coordinators often work in industries like pharmaceuticals, manufacturing, or IT, where strict control over changes is essential for quality and safety.

What are the key skills and qualifications needed to thrive as a change control coordinator?

To thrive as a Change Control Coordinator, you need a solid understanding of change management processes, document control, and quality assurance, often supported by a bachelor's degree in a relevant field. Familiarity with change control software, electronic document management systems (EDMS), and regulatory compliance frameworks (such as FDA or ISO standards) is typically required. Strong organizational skills, attention to detail, and effective communication help you efficiently coordinate changes and collaborate with cross-functional teams. These skills ensure that changes are implemented smoothly, risks are minimized, and regulatory requirements are consistently met.

What are some common challenges a change control coordinator faces when managing multiple change requests simultaneously?

A Change Control Coordinator often juggles several change requests at once, which can present challenges in prioritization and communication. Balancing urgent changes with routine updates requires strong organizational skills and attention to detail. Coordinators must ensure all stakeholders are informed and that changes comply with regulatory and company standards, which can be complex when requests overlap. Effective time management, clear documentation, and proactive follow-up are essential to avoid bottlenecks and ensure smooth implementation.

What is the difference between Change Control Coordinator vs Document Control Specialist?

AspectChange Control CoordinatorDocument Control Specialist
Primary RoleManages and oversees change processes in projects or manufacturingMaintains and organizes project or quality documentation
CertificationsOften requires quality or project management certificationsTypically requires document management or quality certifications
Work EnvironmentManufacturing, engineering, or pharmaceutical settingsQuality assurance, engineering, or regulatory departments
Key FocusChange implementation, approval, and trackingDocument accuracy, version control, and accessibility

The Change Control Coordinator focuses on managing change processes within projects or manufacturing environments, ensuring proper approval and documentation. In contrast, the Document Control Specialist primarily handles maintaining accurate and organized documentation. Both roles require attention to detail and quality certifications, but their core responsibilities differ significantly.

What are popular job titles related to Change Control Coordinator jobs in Puerto Rico?

For Change Control Coordinator jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Change Control Coordinator jobs in Puerto Rico look for?

The top searched job categories for Change Control Coordinator jobs in Puerto Rico are:

Change Control Coordinator jobs near you
Infographic showing various Change Control Coordinator job openings in Puerto Rico as of July 2026, with employment types broken down into 1% As Needed, 72% Full Time, 23% Part Time, and 4% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Microbiological Cleaning Validation Specialist

Dorado, PR • On-site

FITS LLC
See more jobs at FITS LLCexternal

Contractor

Posted 15 days ago

Job description

For Microbiological Cleaning Validation Specialist services in the Microbiological area
WHAT MAKES YOU A FIT:
The Technical Part:
  • Bachelor's degree in Microbiology, Biology, Biotechnology, Biomedical Sciences, or a related scientific discipline
  • Five or more years of relevant experience in microbiology, contamination control, environmental monitoring, cleaning validation, or related quality functions within a regulated industry.
  • Bilingual: English & Spanish.
  • Shift: Administrative and according to business needs.
  • Experience in:
    • Medical device, pharmaceutical, biotechnology, biologics, or combination-product manufacturing.
    • Cleaning-validation lifecycle management, recovery studies, hold-time assessments, environmental monitoring trending, or disinfectant effectiveness studies.
    • Supporting remediation programs, manufacturing transfers, regulatory inspections, or external audits.
    • Coordinating work performed by contract laboratories or other external service providers.

The Personality Part:
  • If you have a commitment to serving customers with high-quality research and products, to embracing a diverse work culture, and even to the environment, you might just be what we're looking for!

AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job)
  • Support the development, revision, execution, and closure of cleaning validation and cleaning verification protocols, reports, and supporting records.
  • Provide microbiological input to sampling plans, sampling locations, sample collection methods, recovery studies, and acceptance criteria.
  • Evaluate equipment configuration, product-contact surfaces, cleaning methods, storage conditions, and hold times for potential microbiological risk.
  • Coordinate study execution with Operations, Engineering, Quality, and internal or external laboratories.
  • Review study data for completeness, accuracy, traceability, and conformance with approved protocol requirements.
  • Support periodic review, continued monitoring, requalification, and change-impact assessments for validated cleaning processes.
  • Assess microbiological risks associated with equipment, manufacturing areas, cleaning practices, materials, utilities, and product-contact surfaces.
  • Support development or improvement of contamination-control strategies and preventive controls.
  • Evaluate whether routine cleaning, equipment drying, storage, and sanitization practices adequately control microbial proliferation.
  • Support microbiological evaluation of cleaning agents, sanitizers, and disinfectants proposed for controlled manufacturing environments or equipment surfaces.
  • Review available supplier information, efficacy data, intended use, concentration, contact time, application method, and material-surface considerations.
  • Support investigations involving cleaning failures, microbiological contamination, environmental excursions, atypical laboratory results, or validation deviations.
  • Contribute microbiological expertise to root-cause analysis, product-impact assessment, risk assessment, nonconformance, CAPA, and change-control activities.
  • Author or revise protocols, reports, procedures, work instructions, technical assessments, risk assessments, data summaries, and scientific rationales.
  • Ensure deliverables follow approved templates, Good Documentation Practices, data-integrity expectations, and applicable document-control requirements.

WHO WE ARE:
We are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS!
Are you the Next Piece?

Apply