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Internship Downstream Process Development Scientist Jobs in Indiana

Seymour, IN This position is viewed as a technical resource in process development and/or daily commercial support. A Technical Services Pr. Scientist applies a thorough understanding and a wide ...

Seymour, IN This position is viewed as a technical resource in process development and/or daily commercial support. A Technical Services Pr. Scientist applies a thorough understanding and a wide ...

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Internship Downstream Process Development Scientist information

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.

What are the most commonly searched types of Downstream Process Development Scientist jobs in Indiana?

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

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

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

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

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

R&D Manufacturing Process Engineer

The Resource Co

Bloomington, IN • On-site

$64K - $85K/yr

Other

Posted 7 days ago


Job description

R&D / Manufacturing Process Engineer – Medical Device Manufacturing


The Resource is hiring for a R&D/Manufacturing Process Engineer for our client, a leading medical device manufacturer in Bloomington, IN.


This is an excellent opportunity for an engineer who wants to build on their experience in manufacturing, process development, and process validation within a medical device environment.


While this position is titled R&D Engineer, the client is specifically seeking someone with hands-on manufacturing/process engineering experience—someone who has worked directly with production or assembly processes and understands how to develop, optimize, and validate manufacturing processes.


Position Details

  • Location: Bloomington, IN
  • Schedule: 1st Shift, Monday–Friday, 8:00 AM–5:00 PM
  • Work Environment: 100% onsite
  • Hours: 40 hours/week; no overtime
  • Industry: Medical Device Manufacturing


What You’ll Do

  • Support the development and implementation of manufacturing and assembly processes for new and/or modified medical products.
  • Assist with setting up and improving production or assembly lines.
  • Develop, establish, and optimize manufacturing process parameters.
  • Design and execute process Design of Experiments (DOEs) to evaluate and improve processes.
  • Support the transition of processes from development into process validation.
  • Participate in process validation activities and help ensure manufacturing processes consistently meet established requirements.
  • Initiate and support pre-production runs of new products.
  • Work closely with Production personnel to identify opportunities for process improvements and implement product or process changes.
  • Build, test, and evaluate prototypes or production-related components as needed.
  • Assist with technical documentation related to product and process development.
  • Support documentation required for FDA and regulatory submissions.
  • Maintain appropriate engineering and design documentation throughout product development.
  • Work collaboratively with Production, Engineering, Quality, vendors, and other cross-functional teams.
  • Evaluate raw materials and manufacturing considerations with suppliers and vendors.
  • Apply strong analytical and problem-solving skills to troubleshoot manufacturing and process issues.


What We’re Looking For

Candidates will have hands-on manufacturing or process engineering experience, particularly experience working directly with production or assembly operations.


Required/Preferred Experience:

  • Bachelor's degree or higher in Biomedical, Mechanical, Chemical Engineering, Engineering Technology, or a related discipline.
  • Hands-on experience in manufacturing, production, process engineering, or assembly operations.
  • Experience developing, establishing, or optimizing manufacturing processes and process parameters.
  • Experience with process Design of Experiments (DOE).
  • Experience progressing from process development into process validation.
  • Understanding of engineering validation principles and documentation.
  • Strong problem-solving and analytical abilities.
  • Excellent written and verbal communication skills.
  • Ability to work independently while also collaborating effectively with cross-functional teams.
  • Ability to work onsite in a fast-paced manufacturing environment.


Medical device experience is not required if you have the right manufacturing/process engineering background.


Candidates with pharmaceutical manufacturing or process engineering experience are encouraged to apply. The client is open to engineers from different industries whose experience transfers well to medical device manufacturing—particularly candidates with experience in:

Manufacturing Lines | Assembly Processes | Process Development | Process Optimization | DOE | Process Parameters | Process Validation | Production Engineering


Important Candidate Requirement

Candidates must have relevant hands-on, on-the-job engineering experience, which may include:

  • Full-time professional experience
  • Internship experience
  • Fellowship experience
  • Co-op experience


Experience should be directly related to manufacturing, process engineering, production, validation, or medical device/pharmaceutical manufacturing.