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Validation Project Manager Jobs in Caguas, PR (NOW HIRING)

Cencora

Sr PM

Juncos, PR · On-site

Applying project management principles to lead cross functional teams to develop project scopes ... validation to implement facilities and equipment upgrades, changes and installations. Provide ...

Inteldot

Capital Projects Director

Gurabo, PR · On-site

$120 - $150/hr

Experience supporting PMO governance structures in capital project environments. * Familiarity with pharmaceutical facility design, construction, and validation activities. * Experience managing ...

Mirus Consulting Group

CSV Specialist

Gurabo, PR · On-site

Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the project management involved. Position Summary: The CSV ...

Mirus Consulting Group

CSV Specialist

Gurabo, PR · On-site

Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the project management involved. Position Summary: The CSV ...

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All JobsValidation Project JobsValidation Project Manager JobsValidation Project Manager Jobs in Caguas, PR

Validation Project Manager information

See Caguas, PR salary details

$46.3K

$102.8K

$156.5K

How much do validation project manager jobs pay per year?

As of Aug 17, 2026, the average yearly pay for validation project manager in Caguas, PR is $102,793.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,600.00 and $128,700.00 per year, depending on experience, location, and employer.

What is a validation project manager?

A Validation Project Manager is a professional responsible for overseeing and coordinating validation activities in industries such as pharmaceuticals, biotechnology, or manufacturing. Their main duties include ensuring that systems, equipment, and processes meet regulatory standards and operate as intended. They manage project timelines, resources, and communication among cross-functional teams to ensure successful validation outcomes. Additionally, they maintain documentation and ensure compliance with industry regulations such as FDA or GMP. This role is crucial for maintaining product quality, safety, and regulatory compliance.

How does a validation project manager typically collaborate with cross-functional teams during a project?

A Validation Project Manager regularly collaborates with cross-functional teams such as quality assurance, regulatory affairs, engineering, and production to ensure that all validation activities meet regulatory standards and project timelines. This collaboration often involves coordinating meetings, aligning on project milestones, and facilitating clear communication to address any technical or compliance issues. Building strong working relationships across departments is crucial for anticipating challenges and ensuring a smooth validation process. Effective coordination helps to minimize delays and ensures that all documentation and testing requirements are thoroughly met.

What are the key skills and qualifications needed to thrive as a validation project manager, and why are they important?

To thrive as a Validation Project Manager, you need expertise in regulatory compliance, project management, and validation protocols, often supported by a degree in engineering, life sciences, or a related field. Familiarity with validation software, quality management systems (QMS), and certifications like PMP or Six Sigma are commonly required. Exceptional organizational, leadership, and communication skills help coordinate cross-functional teams and manage complex timelines. These skills are crucial to ensure validated processes comply with industry standards, mitigate risks, and deliver successful project outcomes.

What is the difference between Validation Project Manager vs Quality Assurance Specialist?

AspectValidation Project ManagerQuality Assurance Specialist
CertificationsGMP, ISO, PMPISO, Six Sigma, GMP
Work EnvironmentRegulated industries like pharma, biotechManufacturing, software, healthcare
Primary FocusEnsuring validation processes and protocolsMaintaining quality standards and procedures
Employer UsagePharmaceutical, biotech, medical device companiesManufacturers, software firms, healthcare providers

The Validation Project Manager primarily oversees validation activities, ensuring compliance with industry standards, while the Quality Assurance Specialist focuses on maintaining overall quality standards across processes. Both roles require similar certifications and are common in regulated industries, but their core responsibilities differ in scope and focus.

What are popular job titles related to Validation Project Manager jobs in Caguas, PR?

For Validation Project Manager jobs in Caguas, PR, the most frequently searched job titles are:

Validation Project Manager jobs near you

Packaging Project Manager

Mirus Consulting Group

Gurabo, PR • On-site

Full-time

Re-posted 20 days ago

Job description

mîrus Consulting Group is a Puerto Rico based technical services firm headquartered in Humacao. The company specializes in Computer System Validation (CSV) and Information Technology consulting for the pharmaceutical and life sciences industries across Puerto Rico and parts of the United States. Its services include the assessment and validation of automation systems, network infrastructures, and business processes, as well as comprehensive project management support to ensure compliance, efficiency, and operational excellence.Key Responsibilities

  • Lead end-to-end execution of packaging-related projects, including planning, scheduling, budgeting, coordination, and implementation.

  • Coordinate activities across Packaging Operations, Engineering, Validation (CSV/CQV), Automation, Manufacturing, and Facilities to ensure successful project execution.

  • Manage packaging equipment installation, upgrades, modifications, integration, and startup activities.

  • Develop and maintain detailed project plans, schedules, resource plans, and risk mitigation strategies for packaging initiatives.

  • Ensure compliance with cGMP regulations, safety requirements, internal procedures, and quality standards throughout all project phases.

  • Oversee commissioning, qualification, and validation activities (IQ/OQ/PQ) associated with packaging equipment and systems.

  • Coordinate change control activities, impact assessments, technical documentation, and implementation plans.

  • Support packaging process improvements, operational readiness activities, and efficiency initiatives.

  • Serve as the primary point of contact between clients, vendors, contractors, and cross-functional internal teams.

  • Monitor project performance, budgets, deliverables, and KPIs while providing regular project status updates to leadership.

  • Identify and resolve project risks, operational challenges, scheduling conflicts, and resource constraints.

  • Support audits, inspections, and maintain projects in a state of compliance and inspection readiness.

Minimum Qualifications

  • Bachelor’s Degree in Engineering (Mechanical, Electrical, Chemical, Industrial, or related discipline required).

  • Minimum of 5+ years of project management experience within pharmaceutical, biotechnology, or medical device industries.

  • Proven experience supporting packaging operations, packaging equipment, serialization, labeling systems, inspection systems, or manufacturing support projects.

  • Strong knowledge of cGMP regulations and pharmaceutical packaging operations.

  • Hands-on experience with Commissioning, Qualification, and Validation (CQV) activities related to packaging systems and equipment.

  • Experience managing Change Control systems within regulated manufacturing environments.

  • Experience coordinating vendors, contractors, packaging equipment manufacturers, and cross-functional project teams.

  • Strong leadership, organizational, communication, and problem-solving skills.

  • Bilingual communication skills (English and Spanish preferred).

  • Proficiency in MS Office applications including Word, Excel, PowerPoint, and Microsoft Project.

This Company is an equal employment opportunity employer. We adhere to a policy of making employment decisions without regard to race, color, religion, sex, sexual orientation, national origin, citizenship, age or disability. We assure you that your opportunity for employment with this Company depends solely on your qualifications.