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Biotechnology Project Manager Jobs in Utah (NOW HIRING)

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

... device and biotech industries. As a vertically integrated company, we specialize in designing ... Support design (NPD) projects with supplier selection and evaluation activities * Provide input on ...

... device and biotech industries. As a vertically integrated company, we specialize in designing ... Support design (NPD) projects with supplier selection and evaluation activities * Provide input on ...

MIA Lab Scientist

American Fork, UT · On-site

$70K - $90K/yr

TCI BioTech USA Legal Address - AMERICAN FORK, UT 84003 Position Type: Full Time Salary Range: $70 ... Partner with the Lab Manager on equipment selection, qualification, and lifecycle management.

Manufacturing Engineer

Logan, UT · On-site

$63K - $81K/yr

Plan and execute engineering projects including equipment upgrades, process improvements ... medical device, pharmaceutical, biotechnology, automotive, or other regulated industrial ...

Showing results 21-40

Biotechnology Project Manager information

See Utah salary details

$19

$42

$69

How much do biotechnology project manager jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for biotechnology project manager in Utah is $42.10, according to ZipRecruiter salary data. Most workers in this role earn between $36.54 and $46.15 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 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 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 popular job titles related to Biotechnology Project Manager jobs in Utah?

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

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

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

Infographic showing various Biotechnology Project Manager job openings in Utah as of August 2026, with employment types broken down into 80% Full Time, 19% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $87,563 per year, or $42.1 per hour.

Process Engineer

Salt Lake City, UT • On-site

Contractor

Posted 7 days ago


Job description

About the Company

Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India. We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success.

Position: Process Engineer

Location: Salt Lake City, UT

Duration: Long Term

Job Overview

We are seeking a Process Engineer to support regulated manufacturing operations. The ideal candidate will have experience in process improvement, root cause analysis, statistical analysis, Lean Six Sigma, process characterization, and validation activities. This role will work closely with Manufacturing, Quality, and Engineering teams to improve process performance, reduce variation, and support continuous improvement.

Key Responsibilities

• Support and sustain manufacturing processes.

• Improve yield, output, quality, and process efficiency.

• Investigate manufacturing issues and identify root causes.

• Apply Lean Six Sigma, DMAIC, and continuous improvement methods.

• Perform process characterization and analyze manufacturing data.

• Use Minitab or similar statistical tools for process analysis.

• Support yield improvement, scrap reduction, and process efficiency projects.

• Support process, equipment, and component changes.

• Support IQ, OQ, and PQ validation activities.

• Support change control and quality system documentation.

• Troubleshoot manufacturing process issues with production teams.

• Collaborate with Manufacturing, Quality, and Engineering teams.

• Provide data-driven technical recommendations.

Required Qualifications

• Bachelor’s degree in Engineering or a related engineering discipline.

• 3–10 years of Process or Manufacturing Engineering experience.

• Experience in a regulated manufacturing environment.

• Experience with Lean Six Sigma and continuous improvement methodologies.

• Strong root cause analysis and problem-solving skills.

• Experience with process characterization and statistical analysis.

• Experience with Minitab or comparable statistical software.

• Experience with process validation, equipment qualification, or related activities.

• Experience with change control and regulated quality systems.

• Experience with DOE, SPC, and process capability analysis is a plus.

• Experience with metal manufacturing processes is a plus.

• Experience with heat treatment, electropolishing, laser cutting, or precision manufacturing is a plus.

• Experience with plastics processing, extrusion, or injection molding is a plus.

• Experience in medical device manufacturing is a plus.

• Lean Six Sigma certification or formal training is a plus.

• Strong communication and cross-functional collaboration skills.

• Ability to work onsite five days per week.

How to Apply

Apply Now: Submit your updated resume to Stark Pharma Solutions Inc. for consideration.

Stark Pharma is an Equal Opportunity Employer and welcomes qualified candidates from diverse backgrounds.