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Internship Downstream Process Development Scientist Jobs in Greensburg, PA

Actalent

R&d Scientist

Pittsburgh, PA

$100K - $130K/yr

Job Title: R&D Scientist We are seeking a hands-on R&D Scientist to lead the development and ... Ensure robust transfer from lab to production, including process parameters and quality controls.

Actalent

R&d Scientist

Pittsburgh, PA · On-site

$100K - $130K/yr

Job Title: R&D Scientist We are seeking a hands-on R&D Scientist to lead the development and ... Ensure robust transfer from lab to production, including process parameters and quality controls.

Covestro AG

Senior R&D Scientist I

Pittsburgh, PA · On-site

$88.80K - $121.40K/yr

... development. This may include the direction of others, and mentorship of team members. * Possess ... Design tests, processes and develop new technical approaches. Create formulations that pass small ...

Covestro

Senior R&D Scientist I

Pittsburgh, PA

$88.80K - $121.40K/yr

... development.This may include the direction of others, and mentorship of team members. * Possess ... Design tests, processes and develop new technical approaches.Create formulations that pass small ...

ATI

Process Engineer

Vandergrift, PA · On-site

In this position you will be responsible for process development and improvement, and quality cost ... Bachelor's degree in Material Science, Metallurgical Engineering, Chemical Engineering, or related ...

Danaher

R&D Internships

Pittsburgh, PA

By submitting your interest, you'll be among the first to know when internship opportunities open ... You'll work in a collaborative environment alongside experienced scientists and contribute to real ...

Waabi

Research Scientist, World Models

Pittsburgh, PA · On-site +1

$155K - $269K/yr

... for downstream planning, testing, and training. You will... - Conduct fundamental and applied ... Mentor junior scientists and interns; foster a culture of scientific rigor and rapid ...

Waabi

Research Scientist, World Models

Pittsburgh, PA · On-site +1

$155K - $269K/yr

... for downstream planning, testing, and training. You will... - Conduct fundamental and applied ... Mentor junior scientists and interns; foster a culture of scientific rigor and rapid ...

Epistemix

Data Scientist

Pittsburgh, PA · Remote

... downstream effects that cannot be safely tested before action is taken. Traditional analytical ... Support recommendation development and action plans * Participate in reviews with customers to ...

POWEREX INC

Process Engineer

Youngwood, PA · On-site

$60K - $95K/yr

... the development, improvement, and standardization of production processes * Assist in the ... May supervise interns or co-op students. QUALIFICATIONS: * BS in relevant engineering field ...

POWEREX, INC.

Process Engineer

Youngwood, PA

... the development, improvement, and standardization of production processes * Assist in the ... May supervise interns or co-op students. QUALIFICATIONS: * BS in relevant engineering field ...

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

As of May 28, 2026, the average hourly pay for internship downstream process development scientist in Greensburg, PA is $35.58, according to ZipRecruiter salary data. Most workers in this role earn between $26.11 and $42.45 per hour, depending on experience, location, and employer.

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 Greensburg, PA as of May 2026, with employment types broken down into 1% Locum Tenens, 2% Internship, 2% As Needed, 7% Full Time, 79% Part Time, and 9% Contract. Highlights an 29% Physical, and 71% Remote job distribution, with an average salary of $73,997 per year, or $35.6 per hour.
Process Validation Associate / Engineer

Process Validation Associate / Engineer

Krystal Biotech

Pittsburgh, PA • On-site

Full-time

Posted 9 days ago

Job description

About Krystal Bio:
At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases with high unmet medical needs.
Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented gene therapy platform, innovative manufacturing supported by our commercial scale facilities, and a unique commercialization model that focuses on the patient's end-to-end experience.
Krystal received U.S. FDA approval for the first and only redosable gene therapy treatment, VYJUVEK®, for the treatment of Dystrophic Epidermolysis Bullosa (DEB). Krystal continues to leverage our proprietary platform to rapidly advance a robust pipeline of investigational genetic medicines in respiratory, oncology, dermatology, and ophthalmology.
Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP manufacturing facilities with teams around the world and satellite offices in Switzerland, Germany, and Japan. We are a company built and run by people who care, are fearless in the face of a challenge, love the work they do, and practice the highest level of scientific integrity. As we grow, we are seeking team members that embody these values.
Job Description Summary:
Krystal Biotech is seeking a highly motivated Process Validation Associate (1+ years' experience) or Engineer (3+ years' experience) to support process validation planning, design, and execution. This person will be responsible for risk assessments, process improvements, investigations, and other projects. They will also play a pivotal role in technology transfer and ensuring processes transition properly from site to site.
Primary Responsibilities:
  • Partner with Process Development and Manufacturing to ensure upstream and downstream processes are well controlled.
  • Apply QbD and traditional process validation principles to existing and new gene therapy products.
  • Perform and document risk assessments to capture existing process knowledge and to identify gaps.
  • Perform experiments (bench scale and manufacturing scale) to close gaps in process understanding and to support process development.
  • Troubleshoot process and equipment issues to help ensure efficiencies in processes.
  • Help implement a continuous improvement mindset to processes and departments.
  • Produce high-quality documentation that meets applicable standards and is appropriate for its intended use.
  • Work on development of new manufacturing facility to ensure proper transfer of technology and processes.
  • Work with CMC counterparts to draft materials intended for the agency review.

Minimum Qualifications & Desired Competencies:
  • Bachelors' Degree in Chemical Engineering, Biomedical Engineering, or related
  • Relevant validation and/or engineering experience in the Biotech or Pharmaceutical industry (1+ yr for Associate, 3+ yr for Engineer level)
  • Background that includes knowledge/experience in GMP, GLP, and statistics
  • Strong knowledge of GMP and ICH requirements and QbD
  • Prior experience in the gene therapy field is desired
  • Must be a self-starter and capable of working with minimal oversight
  • Must be able to handle multiple roles and work in a fast paced and changing environment and know how to prioritize activities appropriately
  • Excellent oral and written communication skills

Krystal Biotech, Inc. is an Equal Employment Opportunity and Affirmative Action Employers. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. Headhunters and recruitment agencies may not submit resumes/CVs through this Web site or directly to managers. Krystal Biotech, Inc. does not accept unsolicited headhunter and agency resumes. Krystal Biotech, Inc. will not pay fees to any third-party agency or company that does not have a signed agreement with Krystal Biotech, Inc.

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