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Pharmaceutical Project Management Jobs (NOW HIRING)

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Pharmaceutical Manufacturing Position Overview We are seeking an experienced and results-driven ... This individual will play a key role in driving project governance, risk management, and successful ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Pharmaceutical Manufacturing Position Overview We are seeking an experienced and results-driven ... This individual will play a key role in driving project governance, risk management, and successful ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Pharmaceutical Manufacturing Position Overview We are seeking an experienced and results-driven ... This individual will play a key role in driving project governance, risk management, and successful ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Pharmaceutical Manufacturing Position Overview We are seeking an experienced and results-driven ... This individual will play a key role in driving project governance, risk management, and successful ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Pharmaceutical Manufacturing Position Overview We are seeking an experienced and results-driven ... This individual will play a key role in driving project governance, risk management, and successful ...

Catalent, Inc.

Project Manager

Greenville, NC · On-site

Bachelor's degree with 3+ years of pharmaceutical project management experience OR Associate degree with 4+ years of pharmaceutical project management experience OR High school diploma/GED with 6+ ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Lead and manage pharmaceutical C&Q projects from planning through completion. * Develop project schedules, timelines, budgets, and resource plans. * Coordinate cross-functional teams including ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Lead and manage pharmaceutical C&Q projects from planning through completion. * Develop project schedules, timelines, budgets, and resource plans. * Coordinate cross-functional teams including ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Lead and manage pharmaceutical C&Q projects from planning through completion. * Develop project schedules, timelines, budgets, and resource plans. * Coordinate cross-functional teams including ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Lead and manage pharmaceutical C&Q projects from planning through completion. * Develop project schedules, timelines, budgets, and resource plans. * Coordinate cross-functional teams including ...

MMR Consulting

PR · On-site

Previous Pharmaceutical/Biotech experience is mandatory for this role (Commissioning, Qualification ... Its services include Engineering, Project Management, and Validation. MMRConsulting ...

MMR Consulting

PR · On-site

Previous Pharmaceutical/Biotech experience is mandatory for this role (Commissioning, Qualification ... Its services include Engineering, Project Management, and Validation. MMR Consulting has offices in ...

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Pharmaceutical Project Management information

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How much do pharmaceutical project management jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for pharmaceutical project management in the United States is $51.41, according to ZipRecruiter salary data. Most workers in this role earn between $40.62 and $60.34 per hour, depending on experience, location, and employer.

What is pharmaceutical project management?

Pharmaceutical project management involves overseeing and coordinating all aspects of drug development projects, from research and clinical trials to regulatory approval and product launch. Project managers in this field ensure that timelines, budgets, and quality standards are met while collaborating with cross-functional teams such as scientists, regulatory specialists, and marketing professionals. Their role is critical in navigating the complex, highly regulated environment of the pharmaceutical industry to bring new medications to market efficiently and safely.

What is the difference between Pharmaceutical Project Management vs Pharmaceutical Clinical Research Coordinator?

AspectPharmaceutical Project ManagementPharmaceutical Clinical Research Coordinator
CredentialsProject management certifications, life sciences degreeClinical research certifications, healthcare or life sciences degree
Work EnvironmentCross-functional teams, corporate offices, labsClinical sites, hospitals, research facilities
Employer & Industry UsagePharmaceutical companies, biotech firmsResearch institutions, clinical trial sites
Primary FocusManaging drug development projects, timelines, budgetsOverseeing clinical trial activities, patient coordination

Pharmaceutical Project Management involves overseeing drug development projects, coordinating teams, and managing budgets within pharmaceutical companies. In contrast, Pharmaceutical Clinical Research Coordinators focus on managing clinical trial activities, ensuring protocol compliance, and coordinating patient participation. Both roles require knowledge of the industry, but project managers have a broader scope overseeing entire projects, while coordinators focus on clinical trial execution.

What is the role of project management in pharmaceutical project management?

In pharmaceutical project management, the project manager oversees planning, execution, and completion of drug development projects, ensuring they meet regulatory standards, timelines, and budgets. They coordinate cross-functional teams, manage risks, and utilize tools like Gantt charts and project management software to track progress. Effective project management is essential for bringing new medicines to market efficiently and compliantly.

What are the key skills and qualifications needed to thrive as a pharmaceutical project manager?

To succeed as a Pharmaceutical Project Manager, you need a strong background in life sciences or pharmacy, project management expertise, and often a relevant degree or PMP certification. Familiarity with industry-specific tools like Microsoft Project, regulatory compliance systems, and drug development software is critical. Exceptional organizational, leadership, and communication skills help you coordinate cross-functional teams and manage complex timelines. These skills ensure projects are delivered efficiently, compliantly, and on schedule in a highly regulated environment.

What are some common challenges faced by professionals in pharmaceutical project management, and how can they be addressed?

Pharmaceutical project managers often navigate complex regulatory requirements, shifting timelines due to clinical trial results, and cross-functional team coordination. Managing communication between diverse stakeholders—such as research, regulatory, manufacturing, and marketing teams—can be particularly challenging. To address these issues, successful project managers employ robust project tracking tools, maintain transparent communication, and proactively identify risks to keep projects on schedule and compliant with industry standards.

What does a pharmaceutical project management do?

A pharmaceutical project management professional oversees the planning, execution, and completion of drug development projects, ensuring they meet regulatory standards, budgets, and deadlines. They coordinate cross-functional teams, manage risks, and utilize project management tools to deliver successful outcomes in a highly regulated industry.

How to become a pharmaceutical project manager?

To become a pharmaceutical project manager, candidates typically need a bachelor's degree in pharmacy, life sciences, or a related field, along with experience in pharmaceutical development or project coordination. Certifications such as PMP (Project Management Professional) can enhance prospects, and strong organizational, communication, and leadership skills are essential for managing cross-functional teams and projects in the industry.
More about Pharmaceutical Project Management jobs
What cities are hiring for Pharmaceutical Project Management jobs? Cities with the most Pharmaceutical Project Management job openings:
What states have the most Pharmaceutical Project Management jobs? States with the most job openings for Pharmaceutical Project Management jobs include:
Pharmaceutical Project Management jobs near you
Infographic showing various Pharmaceutical Project Management job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $106,926 per year, or $51.4 per hour.

Project Manager | Pharmaceutical Manufacturing

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR • On-site

Contractor

Re-posted 14 hours ago

Job description

Location: Gurabo, Puerto Rico (On Site)
Industry: Pharmaceutical Manufacturing

Position Overview

We are seeking an experienced and results-driven Project Manager to lead and support capital and operational projects within a GMP-regulated pharmaceutical manufacturing environment. This role will oversee project execution from initiation through completion, ensuring alignment with business objectives, timelines, compliance standards, and stakeholder expectations.

The ideal candidate will bring strong experience managing pharmaceutical projects involving manufacturing processes, packaging operations, equipment implementation, facility improvements, and cross-functional coordination. This individual will play a key role in driving project governance, risk management, and successful project delivery.

Main Responsibilities:

  • Lead overall project delivery and project governance activities.
  • Develop, maintain, and monitor project plans, schedules, timelines, budgets, risk registers, and stakeholder communications.
  • Manage pharmaceutical capital and operational projects related to manufacturing processes, equipment, packaging operations, facility improvements, and operational initiatives.
  • Coordinate cross-functional teams including Manufacturing, Engineering, Quality, Validation, Facilities, and Operations.
  • Chair project meetings and communicate project status, risks, milestones, and updates to stakeholders.
  • Monitor project deliverables and ensure timely execution of activities.
  • Manage scope changes and support approval of project-level deliverables according to delegated authority.
  • Identify project risks, issues, and potential roadblocks while driving mitigation strategies.
  • Escalate unresolved issues and support decision-making processes to maintain project momentum.
  • Support documentation activities including change controls, project records, technical reviews, and compliance-related documentation.
  • Collaborate with external vendors, design firms, contractors, and internal stakeholders throughout project execution.
  • Ensure projects are executed in compliance with GMP requirements, company procedures, and safety standards.
  • Support process improvements and site initiatives aligned with manufacturing priorities and business goals.

General Requirements:

  • Fluent in English (spoken and written).
  • Proficiency in Microsoft Office 365 (Teams, Outlook, SharePoint, Excel, Word, PowerPoint) and project management tools.
  • PMP certification preferred.
  • Excellent communication, leadership, and stakeholder management skills.
  • Strong organizational and problem-solving abilities.
  • Strong understanding of pharmaceutical manufacturing and GMP environments.
  • Experience managing multiple stakeholders and project priorities simultaneously.
  • Knowledge of solid dosage manufacturing processes preferred.

Education Requirements:

  • Bachelor’s Degree in Engineering required.
  • Master's Degree in Project Management, Engineering, Business, or related field is a plus.

Experience Requirements:

  • Minimum of 8 years of Project Management experience within the pharmaceutical industry.
  • Proven experience managing capital projects within GMP-regulated pharmaceutical environments.
  • Experience with RFP processes and management of design firms and external contractors.
  • Experience supporting pharmaceutical manufacturing and packaging processes and equipment.
  • Experience with clean room design, facility improvements, and infrastructure-related projects preferred.
  • Proven track record delivering projects in pharmaceutical manufacturing environments.
  • 5+ years of process improvement experience preferred.
  • Experience supporting solid dosage manufacturing environments is highly preferred.

Physical Requirements:

  • Ability to sit for extended periods.
  • Light physical activity may occasionally be required.
  • Must be able to visit manufacturing and field locations as needed.
  • Must be able to wear required Personal Protective Equipment (PPE).
  • Ability to perform in a variety of industrial and manufacturing environments.