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Contract Pharmaceutical Project Manager Jobs in Puerto Rico

PR · On-site

$101K - $133K/yr

Contract Position Overview We are seeking an experienced Engineering & Design Lead to support ... Experience with Cost Control, Budget Management, and Project Accounting is highly preferred. Main ...

... pharmaceutical manufacturing operations. This role is responsible for managing utility tie-ins, modifications to existing facilities, and other site integration projects while minimizing impacts to ...

PR · On-site

Manage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards

PR · On-site

Manage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards.

PR · On-site

Manage strategic projects for various departments as needed, using project management best ... Knowledge in Pharmaceutical and Medical Devices. * PMP Certification Preferred * Fully Bilingual ...

PR · On-site

For Project Management services in the Capital Projects area. WHAT MAKES YOU A FIT: The Technical ... providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch ...

PR · On-site

Pharmaceutical design, process or project engineer experience * Strong project management skills ... Ability to effectively facilitate conflict to resolution * Ability to influence all levels of the ...

PR · On-site

Pharmaceutical design, process or project engineer experience * Strong project management skills ... Ability to effectively facilitate conflict to resolution * Ability to influence all levels of the ...

For Project Manager services in the Capital Projects area. WHAT MAKES YOU A FIT: The Technical Part ... providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch ...

PR · On-site

Pharmaceutical design, process or project engineer experience * Strong project management skills ... Ability to effectively facilitate conflict to resolution * Ability to influence all levels of the ...

PR · On-site

Pharmaceutical design, process or project engineer experience * Strong project management skills ... Ability to effectively facilitate conflict to resolution * Ability to influence all levels of the ...

PR · On-site

Pharmaceutical design, process or project engineer experience * Strong project management skills ... Ability to effectively facilitate conflict to resolution * Ability to influence all levels of the ...

PR · On-site

Pharmaceutical design, process or project engineer experience * Strong project management skills ... Ability to effectively facilitate conflict to resolution * Ability to influence all levels of the ...

PR · On-site

Pharmaceutical design, process or project engineer experience * Strong project management skills ... Ability to effectively facilitate conflict to resolution * Ability to influence all levels of the ...

PR · On-site

Pharmaceutical design, process or project engineer experience * Strong project management skills ... Ability to effectively facilitate conflict to resolution * Ability to influence all levels of the ...

PR · On-site

Pharmaceutical design, process or project engineer experience * Strong project management skills ... Ability to effectively facilitate conflict to resolution * Ability to influence all levels of the ...

PR · On-site

JOB SUMMARY The Project Manager is responsible for overseeing and managing structural projects from ... contract documents. Submit those records to hotel as part of project closeout. * Deliver close out ...

PR

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Experience coordinating multidisciplinary design work and managing consultant deliverables ... Opportunity to contribute to a high-impact pharmaceutical project in Puerto Rico. * Exposure to ...

Showing results 41-60

Contract Pharmaceutical Project Manager information

What does a contract pharmaceutical project manager do?

A Contract Pharmaceutical Project Manager oversees and coordinates projects within the pharmaceutical industry on a contract basis. Their responsibilities include managing timelines, budgets, and resources for drug development or manufacturing projects, ensuring compliance with regulatory standards, and facilitating communication among cross-functional teams. They often work with external clients or partners, ensuring that project objectives are met efficiently and within agreed-upon parameters. This role requires strong organizational, leadership, and communication skills as well as a solid understanding of pharmaceutical processes and regulations.

How does a contract pharmaceutical project manager typically interact with cross-functional teams during a project lifecycle?

A Contract Pharmaceutical Project Manager plays a central role in coordinating cross-functional teams, including research, regulatory, clinical, manufacturing, and quality assurance. They facilitate regular meetings, track milestones, and ensure that all team members are aligned with project goals and timelines. Effective communication and conflict resolution skills are essential, as the Project Manager often mediates between departments to address challenges and keep the project on track. Collaboration is key, and successful managers foster a culture of transparency and accountability to ensure project deliverables are met.

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

To thrive as a Contract Pharmaceutical Project Manager, you need expertise in project management, pharmaceutical development processes, and regulatory requirements, typically supported by a degree in life sciences or a related field. Familiarity with project management software (like MS Project), quality management systems, and regulatory submission platforms is essential. Exceptional communication, negotiation, and organizational skills help manage cross-functional teams and client relationships effectively. These skills ensure projects are delivered on time, within budget, and in compliance with stringent industry regulations.

What is the difference between Contract Pharmaceutical Project Manager vs Contract Clinical Research Associate?

AspectContract Pharmaceutical Project ManagerContract Clinical Research Associate
Required CredentialsBachelor's in life sciences, PMP certification often preferredDegree in life sciences or related field, clinical research certifications advantageous
Work EnvironmentManages projects across departments, often in office or lab settingsWorks on clinical trial sites, monitoring patient data and compliance
Employer & Industry UsagePharmaceutical companies, biotech firms, contract research organizationsClinical research organizations, pharmaceutical companies, hospitals
Common Search & ComparisonOften compared for project management roles in pharmaCompared for clinical trial monitoring roles

The Contract Pharmaceutical Project Manager focuses on overseeing drug development projects, coordinating teams, and managing timelines. In contrast, the Contract Clinical Research Associate primarily monitors clinical trial sites and ensures compliance with protocols. Both roles require related scientific credentials but differ in daily responsibilities and work environments.

What are popular job titles related to Contract Pharmaceutical Project Manager jobs in Puerto Rico?

For Contract Pharmaceutical Project Manager jobs in Puerto Rico, the most frequently searched job titles are:

Infographic showing various Contract Pharmaceutical Project Manager job openings in Puerto Rico as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

Project Manager / WPO Equipment Manager

PACIV

San Juan, PR • On-site

Contractor

Posted 26 days ago


Job description

PACIV, a global leader in industrial automation solutions servicing the Life Sciences sector, is seeking a PM / WPO Equipment Manager to oversee the planning, delivery, installation, and turnover of major equipment packages for pharmaceutical capital projects. This role combines project management and field execution responsibilities, ensuring equipment is delivered safely, on schedule, within budget, and in compliance with GMP and project quality standards. The position partners with design teams, vendors, contractors, and construction management from equipment design through Commissioning & Qualification (C&Q).
Position Responsibilities / Essential Functions:
  • Manage equipment packages through design, procurement, delivery, installation, testing, and turnover to C&Q.
  • Coordinate scope, budget, schedule, and vendor performance throughout the equipment lifecycle.
  • Support vendor design reviews, hold-point inspections, Factory Acceptance Tests (FAT), and Site Acceptance Tests (SAT).
  • Coordinate equipment integration with design, BIM, logistics, procurement, and construction teams.
  • Oversee equipment delivery, storage, rigging, installation, and protection during construction.
  • Lead field execution of equipment installation activities alongside contractors, vendors, and construction management.
  • Promote and enforce safe work practices through pre-task planning, Job Hazard Analyses (JHAs), and field safety programs.
  • Manage RFIs, field changes, design clarifications, vendor change orders, warranties, and spare parts.
  • Monitor installation progress, productivity, and project performance while providing regular status updates.
  • Ensure compliance with GMP requirements, project quality standards, and applicable industry codes, including ASME BPE and 3-A where applicable.
  • Support successful system turnover to Commissioning & Qualification (C&Q).

Requirements:
  • Bachelor's degree in Mechanical, Chemical, Industrial Engineering, or a related technical discipline.
  • 12+ years of pharmaceutical or biotechnology capital project experience.
  • Minimum of 5 years managing major equipment packages from Factory Acceptance Testing (FAT) through Site Acceptance Testing (SAT).
  • Experience managing equipment installation and field execution activities on large capital projects.
  • Strong knowledge of vendor management, contract administration, and equipment lifecycle management.
  • Working knowledge of GMP regulations, validation practices, and applicable industry standards.
  • OSHA 30 certification or equivalent field safety experience preferred.
  • English required; Spanish preferred.

Desired Skills:
  • Strong project management and organizational skills.
  • Experience serving as an Owner's Representative on pharmaceutical capital projects.
  • Ability to lead cross-functional teams and coordinate multiple stakeholders.
  • Excellent communication, leadership, and problem-solving skills.
  • Experience with one or more of the following equipment disciplines:
    • Automated Storage & Retrieval Systems (ASRS)
    • Sterile Drug Delivery (SDD) or aseptic processing equipment
    • Oral Solid Dosage (OSD) manufacturing equipment
    • Process skids, utility skids, laboratory, warehouse, or other major vendor equipment packages
  • Ability to manage multiple priorities in a fast-paced construction environment while maintaining safety, quality, and schedule objectives.