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Change Control Coordinator Jobs in Puerto Rico (NOW HIRING)

PR · On-site

GMP: Strong understanding of GMP requirements, change control, and compliance expectations for ... Capital project design coordination (conceptual, basic, and detailed phases). * A/E firm management ...

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

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 ...

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

PR · On-site

Coordination & Stakeholder Interface * Facilitate schedule review meetings with Project Managers ... Expertise with project management concepts and tools (scope, schedule, cost, risk, change control)

PR · On-site

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

PR · On-site

Coordination & Stakeholder Interface * Facilitate schedule review meetings with Project Managers ... Expertise with project management concepts and tools (scope, schedule, cost, risk, change control)

Validation Specialist

Aibonito, PR · On-site

$85 - $120/hr

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

New

PR · On-site

Coordination & Stakeholder Interface * Facilitate schedule review meetings with Project Managers ... Expertise with project management concepts and tools (scope, schedule, cost, risk, change control)

Quality - Quality Engineer I

Vega Baja, PR · On-site

$60K - $78K/yr

... coordination, and follow-up of manufacturing methods and procedures. Supports the delivery of high ... Company tools: ERP, Data collection, document change control.

Quality - Quality Engineer I

Vega Baja, PR · On-site

$60K - $78K/yr

... coordination, and follow-up of manufacturing methods and procedures. Supports the delivery of high ... Company tools: ERP, Data collection, document change control.

Showing results 41-60

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:

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.

JT678 - QUALITY APPLICATIONS SPECIALISTS

Quality Consulting Group, LLC

Villalba, PR • On-site

$120 - $160/hr

Other

Posted 25 days ago


Job description

QUALITY CONSULTING GROUP, a leader inthe 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 enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities
  • Conducts a compliant validation process for quality information technology systems which requires formal validation documentation (including standard operating procedures) under appropriate federal regulations.
  • Coordinates activities with clients, programmers/developers and operating personnel, domestic and, as appropriate, global.
  • Identifies current and anticipated requirements for compliant computerized operations and suggests methods for the identification, implementation and maintenance of the procedures, actions and documentation necessary to assure compliance according to the appropriate federal and international regulations which govern the user’s applications.
  • Reports on the status of validation activities to fulfill regulatory requirements.
  • Keeps abreast of changing federal and international regulatory requirements, government audit policies, and the availability of current techniques.
Qualifications
  • Bachelor’s degree in Engineer or Science
  • 10+ years of experience in the medical device industry, with a strong background in field corrective actions, CAPA, or product quality management. Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, EU MDR, and other relevant medical device regulations.
  • Proven experience leading FCA and CAPA processes, ideally within a medical device or regulated industry.
  • Outstanding communication and interpersonal skills, capable of effectively working with cross-functional teams and external stakeholders.
  • Proficiency in Microsoft Office Suite and quality management systems (QMS). Strong technical writing capability
  • Experience in equipment IQ
  • Experience in OQ (Operational Qualification) and PQ (Performance Qualification) and/or process validation
  • Process Validation Lifecylce ( from process characterization, operational qualification to performance qualification)
  • Preferred experience in DOE (with minitab)
  • Computer and software validation CSV
  • SOP Development
  • Change control of Medical Devices
  • 1st shift

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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