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Internship Downstream Process Development Scientist Jobs in Missouri

Curia, Inc.

Process Chemist II

Springfield, MO · On-site

Review scientific literature to support experimental design, process development, troubleshooting, and technical recommendations. Technical Documentation & cGMP Compliance * Prepare and review ...

AMRI

Process Chemist II

Springfield, MO · On-site

Review scientific literature to support experimental design, process development, troubleshooting, and technical recommendations. Technical Documentation & cGMP Compliance * Prepare and review ...

Eurofins

HPLC Scientist - EMPOWER

Chesterfield, MO · On-site

We are seeking a highly motivated Analytical Scientist to support biotherapeutic process development programs, with a primary focus on large molecule characterization (proteins, polysaccharides ...

Jobtailor

Data Scientist

California, MO · On-site

$90 - $130/hr

Join Amgen's Transformative Digital Capabilities organization within Process Development. * Partner with scientists, engineers, business stakeholders, and technology teams. * Drive data-informed ...

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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 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 most commonly searched types of Downstream Process Development Scientist jobs in Missouri?

The most popular types of Downstream Process Development Scientist jobs in Missouri are:

What are popular job titles related to Internship Downstream Process Development Scientist jobs in Missouri?

For Internship Downstream Process Development Scientist jobs in Missouri, the most frequently searched job titles are:

What job categories do people searching Internship Downstream Process Development Scientist jobs in Missouri look for?

The top searched job categories for Internship Downstream Process Development Scientist jobs in Missouri are:

What cities in Missouri are hiring for Internship Downstream Process Development Scientist jobs?

Cities in Missouri with the most Internship Downstream Process Development Scientist job openings:

Internship Downstream Process Development Scientist jobs near you
Infographic showing various Internship Downstream Process Development Scientist job openings in Missouri as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, and 4% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution.

Process Engineer III, Manufacturing Sciences

Thermo Fisher Scientific

Saint Louis, MO • On-site

Full-time

Posted 9 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 426 frontline employees who took The Breakroom Quiz

199th of 540 rated manufacturers

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
How will you make an impact?
We are searching for a Process Engineer 3 with education and experience in biopharmaceutical processing or a related field. This member of our team provides technological input in the development, validation, and transfer of manufacturing processes. A Process Engineer 3 routinely supports the Process Engineering team as technical owners of customer programs in a manufacturing environment and will be highly involved and act as a subject matter expert in defining and shaping Thermo Fisher Scientific's own technology programs. This role will collaborate internally with supervisors and technicians in the Operations department, Quality Assurance, fellow Engineers, and scientists in Process Development and with the client as a Process Engineer program lead. These activities are conducted in projects and involve teamwork with experts across functional groups to ensure project success.
What will you do?
  • Draft, review and approve Standard Operation Procedures, and Job Aids and consult internally to ensure scientifically sound and robust procedures.
  • Collaborate with the process development to develop standardized methodologies and learn/explore new methodologies for conducting unit operations at the manufacturing scale including cell culture, harvest, and purification.
  • Contribute to Internal and Customer meetings based upon sound evidence guided by minimal supervision.
  • Manages internal projects and tasks and lead client projects and manage timelines with minimal support from supervision.
  • Actively identify error proofing opportunities and initiate and drive engineering initiatives to improve practices and procedures with minimal supervision.
  • Provide scientific expertise for GMP deviations by assessing, reviewing and approving the impact of major deviations on both the product quality and the validation of the process.
  • Lead changes to equipment and process design, proactively and with minimal supervision.
  • Draft, review and approve Manufacturing Batch Records, Performance Qualifications, Process Validation protocols, process flow diagrams, automation methods, and Bill of Materials, ensuring the process is technically accurate and designed for Manufacturing.
  • Draft, review, and approve Process control documents, campaign summary report and process validation reports
  • Reviews, analyzes and trends process data without supervision
  • Provide technical feedback on documents created by other departments, such as Tech Transfer Protocols and SOPs.
  • Troubleshoot technical challenges on the manufacturing floor as needed for a 24/7 manufacturing facility.
  • Support our MSAT team with additional tasks to improve the site, ensure patient safety, and deliver for our customers.
  • Provides development and training for Process Engineers/Scientists.

How will you get here?
Education
  • Bachelor's degree required in a scientific field, preferably an engineering field.
  • 5+ years of experience in GMP regulated Biologics / Pharma Industry, or equivalent experience (or master's degree in a scientific field + 3 years' experience or Ph.D.).

Experience
  • 5+ years of experience in GMP regulated Biologics / Pharma Industry, or equivalent experience (or master's degree in a scientific field + 3 years' experience or Ph.D.).
  • Follow Environmental, Health and Safety policies and procedures and ensure a safe and healthy workplace environment.
  • Ability to self-motivate, prioritize work and time.
  • Demonstrates a foundation in general scientific practices, principles, and concepts.
  • Writes and communicates effectively.
  • Ability to work both independently and as part of a team.
  • Knowledge of current Good Manufacturing Practices and US/EU regulations.
  • Intermediate knowledge of statistical methods used for Pharmaceutical Process Analysis is a plus.
  • Proficient in Microsoft Word and Excel.
  • Ability to stand for prolonged periods of time and gown into manufacturing areas.

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