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Pharmaceutical Project Manager Jobs in Kansas (NOW HIRING)

Principal Project Engineer

Lenexa, KS ยท On-site

$106K - $172K/yr

  • Medical

  • Retirement

  • PTO

This includes technical project management for both capital projects and process improvements. You ... Experience in medical, biotechnology, or Bio-pharmaceutical manufacturing environment is highly ...

Pharmacist PRN

Mcpherson, KS

$52.50 - $63/hr

... management, and during presentations. * High level of accountability, willingness to learn, and ... Ability to assist with meeting the pharmaceutical care needs of neonatal, infant, pediatric ...

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As a Trial Delivery Manager at ICON, you will be responsible for leading and manage projects ... pharmaceutical or biotech industry. * Strong proficiency in project management tools and ...

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... Pharmaceutical Company, you will provide strategic leadership and direction in the design ... project manager for study deployment projects Lead study teams in development of study-specific ...

Pharmacist Technician-CMOP

Leavenworth, KS ยท On-site

$16.75 - $20.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... pharmaceutical dispensing, prescription reconstitution, patient consultation, quality improvement ... Organization - ability to manage projects and activity, and prioritize tasks OTHER REQUIREMENTS:

Showing results 21-40

Pharmaceutical Project Manager information

See Kansas salary details

$40.1K

$93.7K

$151.2K

How much do pharmaceutical project manager jobs pay per year?

As of Aug 19, 2026, the average yearly pay for pharmaceutical project manager in Kansas is $93,667.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,000.00 and $114,600.00 per year, depending on experience, location, and employer.

What is a pharmaceutical project manager?

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 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 are the key skills and qualifications needed to thrive as a pharmaceutical project manager, 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.

How much do pharmaceutical project managers make in the US?

Pharmaceutical project managers in the US typically earn between $90,000 and $130,000 annually, with salaries varying based on experience, location, and company size. Senior roles or those with specialized skills and certifications can earn higher compensation, often exceeding $150,000 per year.

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. Many roles require strong organizational, communication, and leadership skills, often supported by certifications such as PMP (Project Management Professional). Gaining industry-specific knowledge and experience with regulatory requirements can also enhance prospects in this field.

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

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

What cities in Kansas are hiring for Pharmaceutical Project Manager jobs?

Cities in Kansas with the most Pharmaceutical Project Manager job openings:

Infographic showing various Pharmaceutical Project Manager job openings in Kansas as of August 2026, with employment types broken down into 86% Full Time, 12% Part Time, 1% Temporary, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $93,667 per year, or $45 per hour.

Principal Project Engineer

Merck Group

Lenexa, KS โ€ข On-site

$106K - $172K/yr

Full-time

Medical, Retirement, PTO

Posted 19 days ago


Job description

Work Your Magic with us! Start your next chapter and join MilliporeSigma.
Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.
Your Role:
As a Principal Project Engineer at the Lenexa, KS site, you will lead key projects related to the design, qualification, and optimization of the cell culture media manufacturing equipment and facilities to ensure safe, compliant, and scalable production of high-quality media for biopharmaceutical applications.
This includes technical project management for both capital projects and process improvements. You will develop project scope and ensure seamless implementation of the most efficient, viable technical solution in alignment with internal standards. You will collaborate with process engineering, manufacturing, quality, EHS, and maintenance to ensure robust design, commissioning, qualification, and operational readiness.
Additionally, you will drive project timing, budget, and risk management, and prepare and present status reports to leadership and stakeholders. You will ensure adherence to data integrity and change-control practices, owning the engineering change process, and you will mentor engineers and cross-functional teams to foster a culture of safety, quality, and continuous improvement. You will identify and implement cost-saving opportunities, technology upgrades, and energy/water efficiency improvements, and ensure facilities and equipment meet regulatory and MilliporeSigma corporate standards for cell culture media manufacturing operations.
Who You Are
Minimum Qualifications:
  • Education: Bachelor's degree in Chemical, Biochemical, Mechanical, or Biomedical Engineering (or a closely related field); Master's degree preferred
  • 5+ years of professional engineering experience
  • Experience managing projects over $1M

Preferred Qualifications:
  • Technical competencies: Experience with validation strategies (IQ/OQ/PQ) and commissioning/ qualification activities; familiarity with automation concepts, sensors, control systems, data integrity, and change control.
  • Skills: Proven project management and leadership capabilities; ability to influence across functions; excellent problem-solving, risk assessment, and decision-making skills; strong communication and technical writing abilities
  • Experience in medical, biotechnology, or Bio-pharmaceutical manufacturing environment is highly preferred
  • PMP certification preferred

Pay Range for this position: $106,500 - $172,900
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!