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Contract Pharmaceutical Project Manager Jobs in Puerto Rico

Project Manager

Humacao, PR · On-site

$85 - $110/hr

... Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following ... Project Manager Description We are looking for a dedicated Project Manager with a strong background ...

... Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following ... Project Manager Description: We are looking for a dedicated Project Manager with a strong ...

Project Manager

Barceloneta, PR · On-site

$90 - $140/hr

... Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following ... Project Manager Description We are looking for a dedicated Project Manager with a strong background ...

Technical & Engineering Consulting LLC is seeking an experienced Enabling Works Project Manager to support a major pharmaceutical capital expansion program in Puerto Rico. This position is ...

Oversee assigned project contract work. Review and approve project contractor bids, request for ... providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch ...

Bachelor of Science in Engineering and at least seven (8) years of previous exposure managing capital projects in the pharmaceutical industry; experienced with RFP process, design firms' management ...

PR · On-site

For Project Management services supporting Capital Projects within pharmaceutical manufacturing operations. WHAT MAKES YOU A FIT: The Technical Part: * Bachelor of Science in Mechanical, Chemical ...

Manage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all ... Deliver projects by managing project scope, schedule and budget while identifying and mitigating ...

Bachelor of Science in Engineering and at least seven (8) years of previous exposure managing capital projects in the pharmaceutical industry; experienced with RFP process, design firms' management ...

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.

Full-time

Re-posted 13 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

Description:
We are looking for a dedicated Project Manager with a strong background in the manufacturing industry, particularly in sectors like pharma, biotech, or medical devices. The successful candidate will have a minimum of 5 years of experience overseeing diverse projects including Commissioning & Qualification, capital projects, construction projects, NPI, and expansion projects. As a pivotal member of our team, the Project Manager will need to demonstrate exceptional leadership skills and a proactive approach to project management.
Qualifications:
  • Bachelor's degree in Engineering, Business, Project Management, or a related field.
  • Minimum of 5 years of experience in project management within the manufacturing industry.
  • Proven track record of managing projects in areas such as Commissioning & Qualification, capital projects, construction projects, NPI, and expansion projects.
  • Proficiency in project management methodologies and tools.
  • Excellent communication and interpersonal abilities.
  • PMP certification is a plus.

Responsibilities:
  • Develop, implement, and oversee project plans to achieve project goals within budget and schedule.
  • Lead project teams effectively, providing guidance and direction to team members.
  • Coordinate project activities, resources, and deliverables to ensure successful project completion.
  • Monitor project progress, identify risks, and take corrective actions as necessary.
  • Communicate with stakeholders to provide updates on project status and address concerns.
  • Resolve project-related issues promptly to keep projects on track.
  • Ensure compliance with industry regulations and company standards throughout the project lifecycle.

  • Available to work extended hours, possibility of weekends and holidays.

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.