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Pharmaceutical Project Manager Jobs in Indiana (NOW HIRING)

Project Manager (Mechanical Construction) Driven by Vision | Powered by Passion Location: Munster, ... Working for global leaders in the aerospace, chemical, steel, pharmaceutical, oil & gas, power ...

Project Manager (Mechanical Construction) Driven by Vision | Powered by Passion Location: Munster, ... Working for global leaders in the aerospace, chemical, steel, pharmaceutical, oil & gas, power ...

Project Manager (Mechanical Construction) Driven by Vision | Powered by Passion Location: Munster, ... Working for global leaders in the aerospace, chemical, steel, pharmaceutical, oil & gas, power ...

CAPITAL PROJECT MANAGER

Mount Vernon, IN ยท On-site

$100K - $150K/yr

CAPITAL PROJECT MANAGER Salary: $100,000 - $150,000 Pay Grade: 15 ESFM is the corporate facilities ... Possesses broad knowledge of the functional requirements of pharmaceutical facilities and ...

CAPITAL PROJECT MANAGER

Mount Vernon, IN ยท On-site

$100K - $150K/yr

CAPITAL PROJECT MANAGER Salary: $100,000 - $150,000 Pay Grade: 15 ESFM is the corporate facilities ... Possesses broad knowledge of the functional requirements of pharmaceutical facilities and ...

CAPITAL PROJECT MANAGER

Mount Vernon, IN ยท On-site

$100K - $150K/yr

CAPITAL PROJECT MANAGER Salary: $100,000 - $150,000 Pay Grade: 15 ESFM is the corporate facilities ... Possesses broad knowledge of the functional requirements of pharmaceutical facilities and ...

Project Manager- Industrial Construction Driven by Vision | Powered by Passion Location ... Working for global leaders in the aerospace, chemical, steel, pharmaceutical, oil & gas, power ...

Project Manager- Industrial Construction Driven by Vision | Powered by Passion Location ... Working for global leaders in the aerospace, chemical, steel, pharmaceutical, oil & gas, power ...

Lead HVAC project execution activities across pharmaceutical manufacturing, laboratory, utility ... Develop and manage project plans, schedules, budgets, resource strategies, and risk mitigation ...

Lead HVAC project execution activities across pharmaceutical manufacturing, laboratory, and support areas * Develop and manage project plans, schedules, budgets, resource strategies, and risk ...

Lead HVAC project execution activities across pharmaceutical manufacturing, laboratory, utility ... Develop and manage project plans, schedules, budgets, resource strategies, and risk mitigation ...

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Showing results 1-20

Pharmaceutical Project Manager information

See Indiana salary details

$42.8K

$99.9K

$161.3K

How much do pharmaceutical project manager jobs pay per year?

As of Jul 17, 2026, the average yearly pay for pharmaceutical project manager in Indiana is $99,939.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,000.00 and $122,300.00 per year, depending on experience, location, and employer.

What is a Pharmaceutical Project Manager job?

A Pharmaceutical Project Manager oversees drug development projects from initiation to completion, ensuring they meet regulatory, budget, and timeline requirements. They coordinate cross-functional teams, including researchers, regulatory specialists, and manufacturing professionals, to bring pharmaceutical products to market. Their responsibilities include risk management, resource allocation, and stakeholder communication. Strong project management skills, industry knowledge, and attention to compliance are essential for success in this role.

What are the key skills and qualifications needed to thrive in the Pharmaceutical Project Manager position, and why are they important?

A Pharmaceutical Project Manager needs a strong background in life sciences or pharmaceuticals, experience in project management, and often a relevant degree or certification such as PMP. Familiarity with tools like Microsoft Project, regulatory compliance systems (e.g., FDA or EMA guidelines), and document management platforms is crucial. Excellent communication, leadership, problem-solving, and organizational abilities set standout candidates apart. These skills are vital to effectively lead cross-functional teams, ensure regulatory compliance, and successfully deliver projects on time and within budget in a complex industry.

What are the main challenges a Pharmaceutical Project Manager faces during a drug development project?

Pharmaceutical Project Managers often encounter challenges such as navigating complex regulatory requirements, managing tight project timelines, and coordinating across multiple departments like clinical research, regulatory affairs, and manufacturing. Ensuring effective communication among diverse stakeholders and addressing unforeseen obstacles, such as changes in trial protocols or supply chain disruptions, are also common. Strong organizational and leadership skills are essential for adapting to evolving project demands and keeping teams aligned. By anticipating challenges and fostering collaboration, Pharmaceutical Project Managers help ensure successful project outcomes and regulatory approvals.

What cities in Indiana are hiring for Pharmaceutical Project Manager jobs? Cities in Indiana with the most Pharmaceutical Project Manager job openings:
Infographic showing various Pharmaceutical Project Manager job openings in Indiana as of July 2026, with employment types broken down into 82% Full Time, 16% Part Time, 1% Temporary, and 1% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $99,939 per year, or $48 per hour.
Global GxP Quality Project Manager - Pharmaceutical (Hybrid - Indianapolis, IN) Contract

Global GxP Quality Project Manager - Pharmaceutical (Hybrid - Indianapolis, IN) Contract

Pharmavise

Indianapolis, IN โ€ข On-site

Contractor

Re-posted 26 days ago


Job description


Our Fortune 500 global Pharmaceutical client is seeking an experienced Global GxP Quality Project Manager.
Job Summary:
The Global GxP Project Manager will support enterprise-level Global Quality Transformation and Technology initiatives. This role operates within Global Quality leadership and supports strategic transformation efforts across Quality Culture, Quality Maturity Systems, and global QMS modernization. The scope is global and not site-specific. The organization requires a structured, transformation-driven PM who understands regulated environments, Lean deployment, and digital Quality enablement.
Key Responsibilities:
  • Lead global GxP Quality transformation programs across multiple sites and functions

  • Drive QMS harmonization and enterprise process standardization initiatives

  • Support inspection readiness modernization and alignment with FDA expectations

  • Optimize CAPA and Deviation lifecycle processes through structured improvement efforts

  • Deploy Lean methodologies within Quality functions to improve efficiency and reduce waste

  • Support implementation or enhancement of digital Quality systems (Veeva QMS, TrackWise, MasterControl)

  • Lead initiatives involving digital logbooks, eBR, MES integration, and Quality data analytics

  • Enable development of Quality Maturity metrics, dashboards, and executive reporting tools

  • Drive automation and AI-enabled improvements in Quality workflows where applicable

  • Provide structured governance, PMO alignment, and milestone tracking

  • Manage cross-functional stakeholder engagement across Quality, Regulatory, Manufacturing, and Technology

  • Identify and mitigate program risks in a global, regulated environment

  • Prepare executive-level updates and KPI dashboards for senior leadership

Required Qualifications:
  • 8-10+ years of experience in pharmaceutical and/or medical device industries

  • Bachelor's degree in a scientific, life sciences, or health-related field

  • Strong GxP knowledge (GMP, FDA Quality Systems Regulations)

  • Experience leading enterprise-level Quality or QMS transformation initiatives

  • Experience supporting global or multi-site programs

  • Demonstrated Lean deployment or process improvement experience

  • Strong stakeholder management and executive communication skills

  • Ability to work onsite in Indianapolis, IN

Preferred Qualifications:
  • PMP certification

  • Lean certification (Lean Six Sigma Green Belt or Black Belt preferred)

  • Experience with Veeva QMS, TrackWise, or MasterControl

  • Drug and medical device experience

  • Experience supporting inspection readiness or regulatory scrutiny

Other Details:
Schedule: Full Time