1

Pharma Project Manager Jobs in Charleston, SC (NOW HIRING)

Manage complex testing workflows and analytical methods * Simplify compliance and support ... is used in labs across pharma & biotech, life sciences, food & beverage, manufacturing ...

Pharma Project Manager information

See Charleston, SC salary details

$20

$43

$71

How much do pharma project manager jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for pharma project manager in Charleston, SC is $43.27, according to ZipRecruiter salary data. Most workers in this role earn between $37.55 and $47.45 per hour, depending on experience, location, and employer.

What does a Pharma Project Manager do?

A Pharma Project Manager oversees and coordinates pharmaceutical projects, ensuring they are completed on time, within scope, and on budget. This role involves managing cross-functional teams, planning project timelines, handling risks, and ensuring compliance with regulatory standards. Pharma Project Managers often work closely with research and development, clinical, regulatory, and manufacturing teams to bring new drugs or treatments to market efficiently and safely. Their responsibilities also include stakeholder communication and resource management throughout the project lifecycle.

How does a Pharma Project Manager typically collaborate with cross-functional teams throughout a drug development project?

A Pharma Project Manager plays a central role in coordinating cross-functional teams, including research, clinical, regulatory, and manufacturing departments. They facilitate regular meetings, ensure clear communication of project goals, and address any obstacles that arise. Effective Pharma Project Managers build strong relationships with team members, align timelines, and manage resources to keep projects on track. This collaborative approach is essential for navigating the complexities of drug development and meeting regulatory and company milestones.

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

To thrive as a Pharma Project Manager, you need strong project management expertise, knowledge of pharmaceutical regulations, and a background in life sciences or a related field. Familiarity with project management tools (such as Microsoft Project or Smartsheet), regulatory compliance systems, and certifications like PMP or PRINCE2 are commonly required. Exceptional organizational skills, problem-solving ability, and effective communication help you excel when coordinating cross-functional teams and managing complex timelines. These skills are crucial for ensuring projects are delivered on time, on budget, and in compliance with industry standards.

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

AspectPharma Project ManagerClinical Research Associate
CredentialsBachelor's or higher in life sciences, PMP certification often preferredBachelor's in life sciences, relevant clinical research certifications
Work EnvironmentCoordinates multiple projects across departments in pharmaceutical companiesMonitors clinical trial sites, ensuring protocol compliance
Employer & Industry UsagePharmaceutical companies, biotech firmsContract research organizations, clinical trial sites

While both roles are essential in the pharmaceutical industry, a Pharma Project Manager oversees multiple projects and teams, focusing on planning and execution, whereas a Clinical Research Associate primarily monitors clinical trial sites to ensure compliance and data integrity.

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.

What job categories do people searching Pharma Project Manager jobs in Charleston, SC look for?

The top searched job categories for Pharma Project Manager jobs in Charleston, SC are:

What cities near Charleston, SC are hiring for Pharma Project Manager jobs?

Cities near Charleston, SC with the most Pharma Project Manager job openings:

Infographic showing various Pharma Project Manager job openings in Charleston, SC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $90,011 per year, or $43.3 per hour.

Pharma/Biopharma Technology Leader

North Charleston, SC


Ingevity
Chemical Manufacturing • 1 - 5K employees

8.0

Company rating: 8.0 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

37th of 101 rated chemical manufacturers

Great coworkers

People enjoy working here

Good employer


Full-time

Re-posted 19 days ago


Job description

Job Family Group:

Sales and Business Development

Are you ready to do something remarkable? Ready to collaborate with an incredible team to solve problems that improve people's lives? Meet Ingevity.

At Ingevity, we develop innovations that purify, protect and enhance the world around us. Our products enable oil to flow better, crops to grow fuller, roads to last longer and ensure that the air we all breathe is cleaner.

Our people come from all different backgrounds and help reimagine new possibilities daily. We understand there is no challenge too big and no contribution too small. We seek out new ideas for tackling complex problems and celebrate achieving the improbable. We value each person's unique talents and synergize them to create meaningful impact and sustainable solutions for our customers and our world.

Bold. Energetic. Ingenious. Genuine. If these qualities describe you, we'd love for you to join Ingevity!

Ingevity is seeking an experienced Pharma / Biopharma Technology Leader to help establish and grow our presence in the pharmaceutical and biopharmaceutical purification market.

This is a highly visible, entrepreneurial individual contributor role will be the platform technology leader for our High Putity Liquid Purification platform and will work hand in hand with a commercial leader for the platform to build the book of business. Ingevity is an emerging participant in this market, and this leader will play a critical role in building technical credibility, developing strategic customer relationships, generating application data, and creating new pathways for adoption across pharmaceutical manufacturers, contract development and manufacturing organizations (CDMOs), and purification technology providers.

The successful candidate will combine deep expertise in downstream bioprocessing, pharmaceutical purification, filtration, adsorption, or separation technologies with a proven ability to independently develop customer relationships, support qualification programs, and drive commercialization in highly regulated environments.

This role is ideal for a technically strong "player-coach" who enjoys building new opportunities from the ground up and is energized by operating in a highly autonomous, market-creation environment.

What You'll Do

Technical Leadership & Application Development

  • Lead application development and performance evaluation of activated carbon technologies for pharmaceutical and biopharmaceutical purification processes.
  • Design and execute laboratory studies focused on impurity removal, decolorization, endotoxin reduction, host cell protein (HCP) removal, aggregate reduction, and overall process optimization.
  • Generate technical data packages supporting customer evaluations, qualification efforts, and commercialization activities.
  • Assess adsorption performance, filtration performance, process economics, and scale-up considerations across pharmaceutical applications.
  • Serve as the company's technical subject matter expert for pharmaceutical purification and downstream processing applications.

Customer & Market Development

  • Build and maintain relationships with pharmaceutical manufacturers, biopharma companies, CDMOs, and purification technology providers.
  • Partner with commercial teams to identify and develop new business opportunities, customer trials, and strategic partnerships.
  • Provide technical leadership during customer evaluations, qualification programs, and implementation projects.
  • Translate customer challenges into practical purification solutions and support the development of differentiated offerings.
  • Represent Ingevity at customer meetings, scientific conferences, industry forums, and technical workshops.

Regulatory, Quality & Commercialization Support

  • Drive compliance initiatives related to USP, European Pharmacopoeia, GMP, ICH, and other pharmaceutical quality standards.
  • Support development of pharmaceutical-grade product specifications, technical dossiers, validation documentation, and qualification packages.
  • Collaborate with Quality, Regulatory, Operations, R&D, and Commercial teams to support successful commercialization and scale-up activities.
  • Contribute to strategies involving Drug Master Files (DMFs), extractables and leachables programs, change control requirements, and other qualification activities.

Market Intelligence & Strategic Development

  • Monitor trends in bioprocessing, downstream purification, filtration, chromatography, adsorption science, and emerging pharmaceutical manufacturing technologies.
  • Evaluate competitive technologies and identify opportunities for Ingevity to establish market leadership.
  • Help shape the long-term strategy for pharmaceutical purification solutions and market expansion.

Required Qualifications

  • Ph.D. in Chemical Engineering, Biochemical Engineering, Bioengineering, Pharmaceutical Sciences, Biochemistry, Analytical Chemistry, or a related field preferred. Master's degree with substantial relevant industry experience will be considered.
  • Minimum 5+ years of relevant industry experience with a Ph.D. or 8+ years with a Master's degree.
  • Hands-on experience in pharmaceutical or biopharmaceutical purification, downstream processing, filtration, adsorption, chromatography, or separation technologies.
  • Strong understanding of pharmaceutical qualification and validation requirements within GMP-regulated environments.
  • Experience interfacing directly with pharmaceutical manufacturers, biopharma organizations, CDMOs, or life sciences technology providers.
  • Demonstrated ability to communicate complex technical concepts to both scientific and commercial audiences.
  • Proven success working independently in highly visible technical roles.

Ingevity is a company made up of extraordinary people of every race, religion and background, all worthy of the same dignity. Our differences are one of our great strengths. Join us in building a culture of increasing diversity and respect - a culture where everyone belongs.

Ingevity is an Equal Opportunity Employer, Minorities/Women/Veterans/Disabled.

Recruiting Agencies: Ingevity does not accept unsolicited resumes and therefore, will not be responsible for any fees associated with unsolicited resumes.


Ingevity logo

About Ingevity

Sourced by ZipRecruiter

At Ingevity, we develop innovations that purify, protect and enhance the world around us. Our products enable oil to flow better, crops to grow fuller, roads to last longer and ensure that the air we all breathe is cleaner.

Industry

Chemical manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Charleston, SC, US

Year founded

1846

Social media


What Ingevity employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom