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Biotechnology Project Manager Jobs in Iowa (NOW HIRING)

Formulation Scientist I

Iowa City, IA · On-site

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

Our vision is to be the premier partner for biotech, government, and research institutions. We are ... Administrative and Project Management * Collaborate and interact with collegiate faculty ...

Commercial Product Manager - Custom Oligos

Coralville, IA · On-site +1

$110K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biotechnology? At Integrated DNA Technologies (IDT), one of Danaher's 15+ operating companies, our ... Formal project management (PMP or similar not required). * Influencing all levels of an ...

Commercial Product Manager - Custom Oligos

Coralville, IA · On-site

$110K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biotechnology? At Integrated DNA Technologies (IDT), one of Danaher's 15+ operating companies, our ... Formal project management (PMP or similar not required). * Influencing all levels of an ...

Health & Safety Program Manager

Coralville, IA · On-site

$91K - $100K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biotechnology? At Integrated DNA Technologies (IDT), one of Danaher's 15+ operating companies, our ... Strong analytical and project management skills. * Strong leadership and excellent in communication ...

Health & Safety Program Manager

Coralville, IA

$91K - $100K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biotechnology? At Integrated DNA Technologies (IDT), one of Danaher's 15+ operating companies, our ... Strong analytical and project management skills. * Strong leadership and excellent in communication ...

Bachelor's degree in Reproductive Biology, Animal Science, Biological Sciences, Biotechnology ... Ability to work independently, manage multiple priorities, and organize work around project ...

Operations Manager

Davenport, IA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... scope projects with site and regional impact - Build and execute productivity plans through ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

Operations Manager

Davenport, IA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... scope projects with site and regional impact - Build and execute productivity plans through ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

Operations Manager

Bondurant, IA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... scope projects with site and regional impact - Build and execute productivity plans through ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

Showing results 21-40

Biotechnology Project Manager information

See Iowa salary details

$20

$43

$71

How much do biotechnology project manager jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for biotechnology project manager in Iowa is $43.43, according to ZipRecruiter salary data. Most workers in this role earn between $37.69 and $47.64 per hour, depending on experience, location, and employer.

What does a biotechnology project manager do?

A Biotechnology Project Manager oversees and coordinates projects within the biotechnology industry, ensuring that research and development initiatives, product launches, or clinical trials are completed on time and within budget. They work with cross-functional teams, including scientists, engineers, and regulatory experts, to set project goals, manage resources, and monitor progress. Their responsibilities also include risk management, stakeholder communication, and ensuring compliance with industry regulations. This role is vital for driving innovation and bringing new biotech products or solutions to market efficiently.

What is the difference between Biotechnology Project Manager vs Research Scientist?

AspectBiotechnology Project ManagerResearch Scientist
Required CredentialsBachelor's or Master's in Biotechnology, Project Management certification often preferredMaster's or PhD in Biotechnology or related field
Work EnvironmentProject teams, corporate labs, industry settingsResearch labs, academic institutions, industry research divisions
Employer & Industry UsageBiotech companies, pharmaceutical firms, biotech startupsUniversities, research institutes, biotech companies

The main difference is that a Biotechnology Project Manager oversees project planning, coordination, and execution within biotech companies, focusing on timelines and budgets. In contrast, a Research Scientist conducts experiments and develops new biotech products or knowledge. Both roles require strong biotech credentials, but their daily tasks and focus areas differ significantly.

What are the key skills and qualifications needed to thrive as a biotechnology project manager, and why are they important?

To thrive as a Biotechnology Project Manager, you need a solid background in biological sciences or engineering, project management expertise, and often an advanced degree such as an MSc or PhD. Familiarity with tools like Microsoft Project, Gantt charts, regulatory compliance systems, and certifications such as PMP are commonly required. Strong leadership, communication, and problem-solving skills set exceptional candidates apart in managing cross-functional teams and complex timelines. These skills and qualities are essential to effectively coordinate scientific projects, ensure regulatory compliance, and deliver successful outcomes in a dynamic biotech environment.

What are some common challenges faced by biotechnology project managers in cross-functional team environments?

Biotechnology Project Managers often work with multidisciplinary teams composed of scientists, regulatory specialists, manufacturing experts, and business development professionals. One common challenge is ensuring clear communication and alignment across these diverse groups, especially when technical jargon or differing priorities create misunderstandings. Additionally, managing project timelines in a highly regulated environment, where unexpected trial results or compliance issues may cause delays, requires strong adaptive planning. Successful Biotechnology Project Managers foster collaboration by setting clear goals, conducting regular check-ins, and proactively addressing potential roadblocks.

What are popular job titles related to Biotechnology Project Manager jobs in Iowa?

For Biotechnology Project Manager jobs in Iowa, the most frequently searched job titles are:

What job categories do people searching Biotechnology Project Manager jobs in Iowa look for?

The top searched job categories for Biotechnology Project Manager jobs in Iowa are:

What cities in Iowa are hiring for Biotechnology Project Manager jobs?

Cities in Iowa with the most Biotechnology Project Manager job openings:

Infographic showing various Biotechnology Project Manager job openings in Iowa as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $90,342 per year, or $43.4 per hour.

Formulation Scientist I

The University Of Iowa

Iowa City, IA • On-site

Full-time

Medical, Dental, Life, Retirement, PTO

Posted 22 days ago


University Of Iowa rating

6.9

Company rating: 6.9 out of 10

Based on 85 frontline employees who took The Breakroom Quiz

458th of 618 rated colleges and universities


Job description

The Formulation Scientist I will report to the Director of Preformulation and Formulation Development and provide support by conducting experiments, investigations, or evaluations. The incumbent will participate in the formulation and process development for small molecule and biotherapeutic agents. This is a laboratory-based position performing formulation and process development activities specifically for therapeutic products from pre-clinical and Ph I clinical trials through late stage, license application and commercialization. This position performs all assigned formulation and analytical chemistry techniques with minimal supervision after the training period. This position will demonstrate a strong desire and ability to learn scientific principles and their cause and effect on scientific outcomes. This position will review other scientist's protocols, reports, specifications and test methods and will be responsible to efficiently learn to present interpretations. This position will be responsible for preparing data summary presentations, compiling data, and authoring technical reports and regulatory filings associated with their work. Effective communication skills are desirable for interactions with laboratory scientists, project managers and colleagues performing various functions, serving on multi-disciplinary project teams within UI Pharmaceuticals.

About the University of Iowa Pharmaceuticals

UI Pharmaceuticals is a Contract Development and Manufacturing Organization (CDMO) within the College of Pharmacy at the University of Iowa. Our mission is to improve quality of life by applying our pharmaceutical expertise to advance innovative products into clinical trials. Our vision is to be the premier partner for biotech, government, and research institutions.  

We are located on the main campus in Iowa City, which offers a great place to live, top rated schools, a vibrant night life, and world class health care facilities. As a University of Iowa employee, you will have access to an excellent benefits package.

Key Areas of Responsibility

Research, Experiments, Investigations and Evaluations

  • Coordinate and implement multiple research projects/programs under the direction of departmental Director.
  • Perform basic and complex techniques as outlined in research plans, assure fidelity to scientific protocols, assist in design of research plans/protocols.
  • Experience in lab scale process of drug product formulation and scale-up of formulations through pilot scale.

Collect, Analyze and Summarize Data

  • Collaborate and interact with scientists, chemists, and manufacturing personnel, and plan and execute the generation, characterization, and analysis of pharmaceutical materials.
  • Collect and interpret experimental data to guide subsequent experiments aimed at pharmaceutical product and process development.
  • Develop formulations and processes suitable for manufacturing clinical trial supplies, in co- operation with internal manufacturing and analytical research groups.

Compliance

  • Assure safety and compliance with required organization and regulatory policies for laboratory activities, respond to compliance and safety violations.
  • Responsible for the appearance, function, maintenance, and compliance of the group's equipment and physical space.
  • Ensure compliance with UI policies and procedures.

Administrative and Project Management

  • Collaborate and interact with collegiate faculty, particularly in the division of Pharmaceutics and Translational Therapeutics (PTT) to advance research and development projects within University of Iowa Development Consortium (UIPDC).
  • Coordinate and manage equipment at facility.
  • Produce written materials in business- and industry-specific technical language related to development of a variety of pharmaceutical products.

Human Resources

  • Assist with Human Resource functions, including interviewing, selection, training, performance review, may provide input in annual staff performance reviews.
  • Design, evaluate, and coordinate training of employees on basic and new laboratory techniques and procedures needed to execute development projects.

To obtain the full job description including key areas of responsibility, technical competencies, and desirable qualifications, please contact Libby Kleppe at libby-kleppe@uiowa.edu.


 

Required Qualifications

Education

  • MS in Pharmaceutics, Chemistry, or Chemical Engineering; or equivalent combination of relevant education and experience.

Experience

  • Minimum 2 years Industry experience in preformulation/formulation development functions preferred or equivalent postgraduate experience to include:
    • Demonstrated ability to apply scientific principles to preformulation/formulation development of pharmaceutical dosage forms.
    • Hands on experience with basic analytical techniques such as HPLC, UV-Vis, and other routine lab instruments.
    • Demonstrated ability to work independently and collaboratively.
    • Excellent written and oral communication skills.
    • Demonstrated ability to apply good documentation and record practices.
    • Candidate should be knowledgeable with scientific investigation and thinking, proactively identify issues, and develop solutions.

Desirable Qualifications

  • Expertise in the development of freeze-dried formulations for small molecules and biologicals.
  • Expertise in addressing solubility and bioavailability issues in the development for oral or parenteral pharmaceutical products.
  • Expertise in characterization of pharmaceutical materials and an understanding of material properties and their influence on product quality.
  • Working knowledge of cGMPs, including CMC regulatory information required for INDs/NDAs/ANDAs with respect to API, preformulation, formulation, analytical methods, and dosage form manufacturing processes.
  • Working knowledge of statistics relevant to pharmaceutical product development.
  • Knowledge of requirements to safely work with Safebridge 3 compounds.
  • Skillful at authoring and reviewing technical documents including, standard operating procedures, product development reports, batch records etc.

Application and Position Details

  • In order to be considered for an interview, applicants must upload the following documents and mark them as a "Relevant File" to the submission:
    • Resume
    • Cover Letter
  • Job openings are posted for a minimum of 14 calendar days. This job may be removed from posting and filled any time after the minimum posting period has ended. Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential/education verification. 5 professional references will be requested at a later step in the recruitment process. For additional questions, please contact Libby Kleppe at libby-kleppe@uiowa.edu.
     

Benefits Highlights

  • Regular salaried position. Pay level 4A. Located in Iowa City, Iowa.
  • Fringe benefit package including paid vacation; sick leave; health, dental, life and disability insurance options; and generous employer contributions into retirement plans.
  • For more information about Why Iowa? Click here.

Joining the University of Iowa means becoming a vital part of the Hawkeye community, where your work directly impacts education, research, and student success.

Enjoy exceptional health coverage, university-paid life insurance, robust retirement plans, and generous leave policies. Benefit from 24/7 support services, well-being resources, and access to UI Health Care specialists. Grow professionally with advanced training, leadership development, and tuition assistance.

Iowa City offers a great quality of life with world-class performances at Hancher Auditorium, Big Ten athletics, top-ranked public schools, and outdoor recreation.

Join us in making a difference at a leading Big Ten university and premier public research institution. 


 

Additional Information
  • Classification Title: Research Associate
  • Appointment Type: Professional and Scientific
  • Schedule: Full-time
  • Work Modality Options: On Campus
Compensation
  • Pay Level: 4A
Contact Information
  • Organization: College of Pharmacy
  • Contact Name: Libby Kleppe
  • Contact Email: libby-kleppe@uiowa.edu

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