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Project Manager Pharmaceutical Internship Jobs (NOW HIRING)

PR · On-site

Pharmaceutical Manufacturing - Solid Dosage Position Overview We are seeking an experienced and results-driven Project Manager to lead and support capital and operational projects within a GMP ...

PR · On-site

Pharmaceutical Manufacturing - Solid Dosage Position Overview We are seeking an experienced and results-driven Project Manager to lead and support capital and operational projects within a GMP ...

This dedicated project manager will be responsible for the administrative management of projects for a specific client from inception to close for our pharmaceutical business. Key functions include ...

PR · On-site

Pharmaceutical Manufacturing Position Overview We are seeking an experienced and results-driven Project Portfolio Manager to lead and oversee a portfolio of capital and operational projects within a ...

PR · On-site

Pharmaceutical Manufacturing Position Overview We are seeking an experienced and results-driven Project Portfolio Manager to lead and oversee a portfolio of capital and operational projects within a ...

This dedicated project manager will be responsible for the administrative management of projects for a specific client from inception to close for our pharmaceutical business. Key functions include ...

Account Manager (Pharmaceutical) Hawkins Pharmaceutical is a leading manufacturer, repackager, and ... Manage projects with internal departments and customers. * Build strong relationships with internal ...

New

Sr Project Manager

Cambridge, MA

$143K - $143K/yr

... Pharmaceutical or Bio-Technology industry experience Experience working in a GxP validation environment Experience managing IT projects in Biotech/Pharma involving processes and systems is required!

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Project Manager Pharmaceutical Internship information

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$20K

$34.4K

$46.5K

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

As of Jun 9, 2026, the average yearly pay for project manager pharmaceutical internship in the United States is $34,391.00, according to ZipRecruiter salary data. Most workers in this role earn between $30,000.00 and $35,000.00 per year, depending on experience, location, and employer.

What types of projects and responsibilities can I expect as a Project Manager Pharmaceutical Intern?

As a Project Manager Pharmaceutical Intern, you can expect to support cross-functional teams working on drug development, regulatory submissions, or process improvement projects. Your responsibilities may include assisting with project scheduling, tracking milestones, preparing status reports, and helping to coordinate meetings with stakeholders across departments such as R&D, quality assurance, and regulatory affairs. You'll gain exposure to industry-standard project management tools and methodologies, while also learning how to manage timelines and communicate effectively within a highly regulated environment. This role provides valuable insights into pharmaceutical project workflows and offers opportunities to build foundational project management skills.

What does a Project Manager Pharmaceutical Intern do?

A Project Manager Pharmaceutical Intern supports project managers in planning, coordinating, and monitoring pharmaceutical projects. Their tasks often include tracking project timelines, assisting with documentation, preparing reports, and helping to ensure that regulatory requirements are met. Interns may also participate in meetings, collaborate with cross-functional teams, and contribute to process improvements. This internship provides hands-on experience in managing drug development or clinical trial projects within the pharmaceutical industry.

What are the key skills and qualifications needed to thrive as a Project Manager Pharmaceutical Intern, and why are they important?

To thrive as a Project Manager Pharmaceutical Intern, you need a background in life sciences or pharmacy, strong organizational skills, and foundational knowledge of project management principles. Familiarity with Microsoft Project, Excel, and regulatory compliance systems, as well as any coursework or certification in project management (such as CAPM), is highly beneficial. Outstanding communication, attention to detail, and adaptability will set you apart when coordinating cross-functional teams and timelines. These skills ensure you can effectively manage project deliverables, support compliance, and contribute to the successful development of pharmaceutical products.
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Project Manager | Pharmaceutical Manufacturing

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR • On-site

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.


Job description

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

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.