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Internship Downstream Process Development Scientist Jobs in Tooele, UT

BioFire Defense

Scientist 1

Salt Lake City, UT · On-site

$94K - $111K/yr

A Scientist investigates the feasibility of applying a variety of scientific principles and ... Develops processes and procedures to aid in the development and maintenance of product lines.

Hexcel

R&D Data Scientist

Salt Lake City, UT · On-site

$80 - $110/hr

Research and Development Data Scientist** for our **Salt Lake City, UT, USA****The selected ... Develop, validate, and maintain digital twin models of key processes using machine learning and ...

FLSmidth, Inc.

Sr. Process Engineer

Salt Lake City, UT

$100K - $130K/yr

You will be joining the Downstream Gold product line within the FLSmidth group. This team provides ... Lead the development of process engineering deliverables, including P&IDs, PFDs, material and ...

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Internship Downstream Process Development Scientist information

See Tooele, UT salary details

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How much do internship downstream process development scientist jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for internship downstream process development scientist in Tooele, UT is $36.30, according to ZipRecruiter salary data. Most workers in this role earn between $26.63 and $43.32 per hour, depending on experience, location, and employer.

What does an internship downstream process development scientist do?

An Internship Downstream Process Development Scientist works in the biopharmaceutical industry, assisting with the development and optimization of processes that purify biological products such as proteins, antibodies, or vaccines after they are produced by cells. Their role often involves supporting laboratory experiments, analyzing samples, and documenting results to improve the efficiency and scalability of downstream processes like filtration and chromatography. Interns in this position gain hands-on experience with cutting-edge technologies and learn about regulatory requirements and industry standards. This role helps prepare students or recent graduates for a career in process development or biomanufacturing.

What types of projects and responsibilities can an internship downstream process development scientist expect to work on?

As an Internship Downstream Process Development Scientist, you can expect to be involved in hands-on laboratory work focusing on the purification and characterization of biopharmaceutical products. Typical responsibilities include preparing buffer solutions, operating chromatography and filtration systems, analyzing samples using various analytical techniques, and documenting experimental results. Interns often collaborate with experienced scientists and engineers, contributing to process optimization and troubleshooting. The role provides valuable exposure to industry-standard procedures and the opportunity to develop technical skills in a team-oriented environment.

What are the key skills and qualifications needed to thrive as an internship downstream process development scientist, and why are they important?

To thrive as an Internship Downstream Process Development Scientist, you need foundational knowledge in biochemistry, molecular biology, or chemical engineering, often supported by ongoing or recent enrollment in a relevant degree program. Familiarity with laboratory techniques such as chromatography, filtration, and analytical instruments, as well as experience with lab management software, is typically expected. Attention to detail, problem-solving abilities, and effective teamwork are standout soft skills in this role. These skills and qualifications are crucial for conducting reliable experiments, analyzing data, and contributing to the optimization of bioprocesses in a collaborative research environment.

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Internship Downstream Process Development Scientist jobs near you
Infographic showing various Internship Downstream Process Development Scientist job openings in Tooele, UT as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 16% Part Time, and 3% Contract. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $75,502 per year, or $36.3 per hour.

Analytical Scientist

DISCGENICS INC

Salt Lake City, UT • On-site

Full-time

Re-posted 6 days ago

Job description

Welcome to DiscGenics, a pioneering, late-clinical stage biopharmaceutical company dedicated to advancing regenerative cell-based therapies for patients suffering from degenerative diseases of the spine. Privately held and passionately driven, our mission is to enhance lives by alleviating pain and restoring function through innovative treatment.

At DiscGenics, we are committed to improving the quality of life for individuals debilitated by degenerative diseases of the spine. Our focus lies in developing cutting-edge therapies that offer hope and tangible results, fostering a future where patients can regain mobility and comfort.

Our team is characterized by a relentless pursuit of excellence and a nimble approach to addressing challenges. Our core values of Integrity, Innovation, Accuracy, Teamwork, and Stewardship guide everything we do.

Join us at DiscGenics and be part of a transformative journey where your contributions have the potential to impact the lives of millions. Together we innovate with purpose and compassion, striving towards a future where pain and limitations of degenerative spine diseases are a thing of the past.

Discover more about us at discgenics.com and see how you can contribute to revolutionizing patient care through regenerative therapies.

We are looking for a talented and dedicated Analytical Scientist to join our team! The Scientist/Senior Scientist, Analytical Sciences is responsible for the development, optimization, qualification, validation, and execution of analytical methods supporting raw materials, in-process, intermediate, and finished product testing for cell therapy products. This role plays a key part in advancing analytical strategies from early development through commercialization, ensuring compliance with FDA and ICH guidelines.

The position includes leading and supporting cell-based development (e.g., ELISA, flow cytometry, potency assays), evaluating new analytical technologies, and enabling method transfer to Quality Control and external partners. The role also contributes to regulatory filings through authoring and reviewing technical reports and CMC sections.

This role collaborates cross-functionally with Process Development, Manufacturing, and Quality teams, while supporting a culture aligned with company values.

Essential Duties and Responsibilities

Analytical Development & Execution

  • Design, develop, optimize, qualify, validate, and execute analytical methods for product characterization and release.
  • Lead and/or support development of cell-based bioassays, potency assays, immunophenotyping, and multiplexed protein assays.
  • Perform routine testing to support development studies and clinical batch release.
  • Track, trend, and statistically analyze data to evaluate method performance and support specification setting.

Method Lifecycle & Technology Transfer

  • Advance analytical methods from concept through qualification and transfer to Quality Control and external partners.
  • Apply Quality by Design (QbD) and Design of Experiments (DOE) principles to method development. Support scale-up and commercialization of analytical methods.
  • Manage outsourced testing activities when needed.

Collaboration & Leadership

  • Collaborate cross-functionally with Process Development, Manufacturing, and Quality teams.
  • Present scientific data and serve as subject matter expert (SME) for analytical methods.
  • Lead or mentor junior scientists and assist in training on analytical methods.
  • Support and contribute to departmental and organizational initiatives.

Laboratory Operations

  • Maintain, calibrate, and operate laboratory equipment and instrumentation.
  • Ensure proper documentation and organization or experimental data.
  • Participate in equipment qualification and upkeep.

Additional Responsibilities

  • Contribute to risk assessments, comparability studies, and specification justifications.
  • Perform other duties as required.

Education & Experience

  • Bachelor’s degree in biological sciences, biochemistry, chemistry, cell biology, or a related field with 7-10+ years of relevant industry experience, OR Master’s degree in a related field with 5-8+ years of experience, OR PhD in a related field with 2-5+ years of experience.
  • 10+ years of experience preferred, particularly within GMP/CMC or other regulated environments and spanning development through commercialization.
  • Experience supporting clinical and commercial development of pharmaceutical, biological, or cell therapy products, including scale-up to commercialization.
  • Hands-on experience with analytical method development (e.g., immunoassays, multi-parameter flow cytometry, cell-based potency assays) in a QC or regulated setting preferred.

Working Conditions:

Position requires qualified individuals to see, hear and speak (verbally and audibly). Required to ascend and descend stairs; sit, stand, lift, bend, stoop, crawl and kneel. The employee must also use hands to finger, handle or feel. Occasionally reaching with hands and arms, climbing or balancing are required. May be asked to drive or travel by car, air, or other transportation for business purposes.

Must be able to lift and carry up to 20 pounds.

Must be able to function effectively with noise in a lab environment. Natural and regular stressors occur on the job.

Disclaimer:

Please note: DiscGenics reserves the right to change, modify, suspend, interpret, or cancel in whole, or in part, any of the duties outlined above, at any time, and without advance notice to the employee.