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

Pinnaql

Project Manager

Humacao, PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Project Manager Position Summary The Project Manager will lead and support a portfolio of capital ...

Pinnaql

Project Manager

Humacao, PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Project Manager Position Summary The Project Manager will lead and support a portfolio of capital ...

Pinnaql

Project Manager

Gurabo, PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Project Manager Position Summary The Project Manager will lead and support a portfolio of capital ...

Pinnaql

Project Manager

Juncos, PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Project Manager Position Summary The Project Manager will lead and support a portfolio of capital ...

Veg Group

Project Manager

Gurabo, PR · On-site

$100 - $125/hr

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier that provides solutions ... Project ManagerPosition Summary The Project Manager will lead and support a portfolio of capital ...

Mirus Consulting Group

Project Manager - 35662

Juncos, PR · On-site

$100 - $125/hr

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 Project ...

Techengpr

Process Project Manager

Carolina, PR · On-site

$125 - $150/hr

... Validation, EHS, and external contractors. Key Responsibilities * Serve as the Owner ... Manage project scope, schedule, budget, risks, and change orders. * Develop project execution plans ...

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Showing results 21-40

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 Sep 7, 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

Project Manager

Pinnaql

Humacao, PR • On-site

Full-time

Re-posted 26 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:
  • Project Manager

Position Summary
The Project Manager will lead and support a portfolio of capital projects and strategic initiatives within regulated pharmaceutical and biotechnology manufacturing environments. This role is responsible for managing projects through all phases of execution while ensuring alignment with business objectives, safety requirements, quality expectations, schedule commitments, and budget targets.
Projects may support manufacturing operations, packaging systems, process improvements, facility upgrades, cleanroom improvements, commissioning and qualification activities, operational excellence initiatives, utilities, and other regulated engineering programs.
The role requires strong leadership, technical coordination, and cross-functional collaboration with Engineering, Operations, Quality, Procurement, EHSS, Construction, external contractors, and equipment vendors.
Key Responsibilities
  • Lead overall project delivery, governance, and execution throughout the project lifecycle.
  • Develop and maintain project plans, schedules, budgets, forecasts, resource strategies, and risk management plans.
  • Coordinate cross-functional teams to ensure projects are delivered safely, on schedule, within budget, and in compliance with applicable GMP and site requirements.
  • Handle project financial performance including cost tracking, forecasting, variance analysis, and reporting.
  • Support procurement coordination, contractor management, vendor management, and technical alignment activities.
  • Lead project meetings and communicate project status, risks, issues, mitigation plans, and key decisions to stakeholders and leadership teams.
  • Coordinate project scope changes, project documentation, and project-related change activities as required.
  • Prepare and maintain project documentation including schedules, status reports, risk logs, budgets, meeting minutes, action trackers, and project closeout packages.
  • Coordinate activities supporting commissioning, qualification, startup, operational readiness, and turnover to operations.
  • Support project execution activities in alignment with applicable EHSS requirements and site procedures.
  • Identify project risks, resource constraints, and execution challenges while driving timely resolution and escalation when needed.
  • Support continuous improvement initiatives related to project execution, compliance, and operational performance.

Qualifications & Experience
  • Bachelor's degree in Engineering required.
  • Minimum of 8 years of experience managing capital projects within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries.
  • Demonstrated experience supporting manufacturing, packaging, facilities, utilities, process equipment, cleanroom environments, and regulated operational systems.
  • Proven experience managing project scope, schedule, budget, risks, stakeholder communications, and cross-functional coordination.
  • Experience supporting projects through design, procurement, construction, commissioning, startup, qualification, and operational handover phases.
  • Experience coordinating with engineering firms, contractors, equipment vendors, and internal technical teams.
  • Strong understanding of GMP environments, regulated project execution, and quality system expectations.
  • Familiarity with project management, scheduling, cost tracking, and reporting tools such as MS Project, SAP, Planisware, Primavera, or similar systems is preferred.
  • PMP certification is preferred.
  • Excellent verbal and written communication skills in both English and Spanish, including technical writing, documentation preparation, meeting facilitation, and communication of project deliverables.
  • Strong leadership, organizational, analytical, and problem-solving skills with the ability to manage multiple priorities and complex project portfolios.

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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