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Bio Pharmaceutical Project Manager Jobs (NOW HIRING)

... pharmaceutical company, with pharmaceutical project management experience. 6. Experience in digitalization and automation. 7. Project management Professional (PMP) certification. 8. Experience ...

Project Manager / HSE Lead - Pharmaceutical Construction Location: Charlotte NC Initially working on a project in Lebanon, Indiana until Feb 27 (10 days onsite, 4 from home, 2 week work pattern ...

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Bio Pharmaceutical Project Manager information

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$38.5K

$102.7K

$162K

How much do bio pharmaceutical project manager jobs pay per year?

As of Sep 11, 2026, the average yearly pay for bio pharmaceutical project manager in the United States is $102,682.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,500.00 and $123,000.00 per year, depending on experience, location, and employer.

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

AspectBio Pharmaceutical Project ManagerClinical Research Associate
Required credentialsBachelor's degree in life sciences, project management certification often preferredBachelor's degree in life sciences or related field, clinical research certification optional
Work environmentOversees multiple projects, manages teams, coordinates with departmentsMonitors clinical trial sites, ensures protocol compliance, reports progress
Employer and industry usagePharmaceutical companies, biotech firms, contract research organizationsClinical trial sites, pharmaceutical companies, CROs

The main difference is that Bio Pharmaceutical Project Managers oversee entire projects and coordinate teams, while Clinical Research Associates focus on monitoring clinical trials at specific sites. Both roles require a background in life sciences, but project managers have broader responsibilities in planning and management.

What cities are hiring for Bio Pharmaceutical Project Manager jobs?

Cities with the most Bio Pharmaceutical Project Manager job openings:

What states have the most Bio Pharmaceutical Project Manager jobs?

States with the most job openings for Bio Pharmaceutical Project Manager jobs include:

What are popular job titles related to Bio Pharmaceutical Project Manager jobs?

For Bio Pharmaceutical Project Manager jobs, the most frequently searched job titles are:

Infographic showing various Bio Pharmaceutical Project Manager job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $102,682 per year, or $49.4 per hour.

Project Manager | Pharmaceutical Manufacturing

Juncos, PR โ€ข On-site

Other

Posted 7 days ago


Job description

Project Manager | Pharmaceutical Manufacturing

Contract Professional BAYAMON, PR, PR

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:

  • Bachelorโ€™s Degree in Engineering required.
  • Master's Degree in Project Management, Engineering, Business, or related field is a plus.

Experience Requirements:

  • Minimum of 5 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.
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