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Internship Downstream Process Development Scientist Jobs in Minnesota

Danaher

Senior Development Scientist

Chaska, MN · On-site

$105K - $115K/yr

The Senior Development Scientist for Beckman Coulter Diagnostics is responsible for completing ... Develop new product designs, processes, new product scale-up, design/product optimization ...

Danaher

Senior Development Scientist

Chaska, MN

$105K - $115K/yr

The Senior Development Scientist for Beckman Coulter Diagnostics is responsible for completing ... Develop new product designs, processes, new product scale-up, design/product optimization ...

Danaher

Development Scientist I

Chaska, MN

$34 - $37/hr

The Development Scientist I is responsible for responsible for participating in development and ... Identify and implement process improvements within the department/field The essential requirements ...

Danaher

Development Scientist I

Chaska, MN · On-site

$34 - $37/hr

The Development Scientist I is responsible for responsible for participating in development and ... Identify and implement process improvements within the department/field The essential requirements ...

Microbiologics

R&D Scientist

Saint Cloud, MN · On-site

Influence how advanced research is translated into scalable, compliant manufacturing processes * Collaborate across R&D, Technology Transfer, Production, QC, Sales, and Marketing to align scientific ...

Microbiologics, Inc.

R&D Scientist

Saint Cloud, MN · On-site

$86K - $107K/yr

Influence how advanced research is translated into scalable, compliant manufacturing processes * Collaborate across R&D, Technology Transfer, Production, QC, Sales, and Marketing to align scientific ...

Nextern

Principal Process Development Engineer

Osseo, MN · On-site

$140K - $160K/yr

As part of a multidisciplinary process development engineering team the Process Development ... Working knowledge of data collection, data analysis, evaluation, and scientific method Benefits ...

Nextern

Director of Process Development

Maple Grove, MN · On-site

$150K - $240K/yr

Director of Process Development to lead the development, optimization, and scale-up of ... Preferred Qualifications • Master's degree in Engineering, Science, or Business • Experience ...

Nextern

Director of Process Development

Maple Grove, MN · On-site

$150K - $240K/yr

Director of Process Development to lead the development, optimization, and scale-up of ... Preferred Qualifications Master's degree in Engineering, Science, or Business Experience supporting ...

Nextern

Director of Process Development

Osseo, MN · On-site

$150K - $240K/yr

Director of Process Development to lead the development, optimization, and scale-up of ... Preferred Qualifications · Master's degree in Engineering, Science, or Business · Experience ...

Abbott

Process Development Engineer II

Plymouth, MN · On-site

$61.30K - $122.70K/yr

... scientists. The Opportunity This position works out of our Plymouth, MN location in the ... Process Development & Implementation: * Lead the design, development, and implementation of new ...

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Internship Downstream Process Development Scientist information

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.

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 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.
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Internship Downstream Process Development Scientist jobs near you
Infographic showing various Internship Downstream Process Development Scientist job openings in Minnesota as of May 2026, with employment types broken down into 2% Internship, 2% As Needed, 19% Full Time, 65% Part Time, 2% Temporary, and 10% Contract. Highlights an 29% Physical, and 71% Remote job distribution.
Clinical Development Scientist

Clinical Development Scientist

ComTec Information Systems

Plymouth, MN • On-site

Contractor

Posted 17 days ago

Job description

Job Title - Clinical Development Scientist;
Hybrid role. 3 days/week in office
Bothell WA/Cambridge MA/ Plymouth MN

12 Months


Ultrasound, Senior Clinical Development Scientist The Senior Clinical Development Scientist for the Ultrasound group will be responsible for developing, generating, and disseminating clinical and economic evidence ensuring innovation, and transformation with best-in-class clinical evidence. Your role: Contribute strategic guidance for clinical and economic evidence related to the end to end (E2E) development process from ideation through post-market for products in the Ultrasound business. Collaborate with key internal and external stakeholders to provide in-depth expertise to develop and lead clinical initiatives through non-clinical and clinical strategies for new product development initiatives and product life cycle management. Drive execution ensuring quality and timeliness of clinical programs and/or trials to support critical regulatory requirements, be agile and responsive during course of design, execution, and interpretation of trial data. Collaborate with investigators, IRBs/ECs, Regulatory Agencies, societies, and associations; and additionally, to support claims, reimbursement, health economic outcomes and/or market access. Ensure appropriate preparation, interpretation and dissemination of all evidence generated, including Clinical Study Reports (CSRs), Clinical Evaluation Reports (CERs), abstracts, peer-reviewed manuscripts, as assigned. Lead or support scientific discussions with regulatory agencies or notified bodies, including proposed clinical investigations; review process of clinical evidence generated for marketing authorization, in line extensions, including during sponsor regulatory inspections.

You are the right fit if:

You have acquired 7+ years of experience in clinical research/development/real world evidence (RWE); scientific study design, strong scientific background and experience with Artificial Intelligence algorithm clinical performance validation. You have deep expertise including innovative clinical trial design, registries, quality improvement initiatives, and creation of data networks and working knowledge of biostatistics. Your skills include a demonstrated working knowledge of GCP, FDA regulations and EU-MDR regulations, and in-depth understanding of product development and associated design controls for medical devices. You have strong writing skills to product quality clinical documents, including final reports. Strong knowledge and experience with study design is also desired. You have an ability to write original scientific documentation such as clinical study reports, regulatory filings, investigator brochures, clinical evaluation reports, internal reports and scientific publications. You have a medical or scientific education (MD or PhD). You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this Clinical position. You are self-directed with a strong work ethic, agile, and have an ability to work in a purposeful environment. You can collaborate effectively and influence decision making with various teams cross-functionally, as well as externally. You can think analytically, present statistical methods and results to a variety of audiences, especially non-statisticians. You can travel up to 15% (domestic and international) according to business needs.,