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Internship Downstream Process Development Scientist Jobs in Covington, KY

Actalent

Analytical Development Scientist

Cincinnati, OH · On-site

$27/hr

Urgently hiring Analytical Scientist to start in June! Description What will you do? · Prepare ... We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing ...

Mattr

Process Engineer I

Fairfield, OH

The Process Engineer will support continuous improvement projects and product process development ... Solid understanding of engineering, material science, and scientific principles.Technical aptitude ...

Mattr

Process Engineer I

Fairfield, OH · On-site

The Process Engineer will support continuous improvement projects and product process development ... Solid understanding of engineering, material science, and scientific principles.Technical aptitude ...

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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 Covington, KY is $37.53, according to ZipRecruiter salary data. Most workers in this role earn between $27.55 and $44.81 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
Scientist III-Process Development

Scientist III-Process Development

Thermo Fisher Scientific

Florence, KY

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 21 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 384 frontline employees who took The Breakroom Quiz

185th of 511 rated manufacturers

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Laboratory Setting

Job Description

Division/Site Specific Information

Our Florence (West) site specializes in process development and chemical production of intermediates and Active Pharmaceutical Ingredients (APIs) supporting toxicology, pre-clinical, and clinical supply. Operations are conducted under both non-cGMP and cGMP conditions. This site is recognized for its specialized capabilities in delivering high-quality chemical solutions across the drug development lifecycle.

Discover Impactful Work:

As part of our Florence (West) team, you will contribute to the development and production of critical pharmaceutical intermediates and APIs that support early-stage and clinical programs. Your work will directly impact the advancement of life-saving therapies by ensuring robust, scalable, and compliant chemical processes. You will collaborate across multidisciplinary teams to solve complex challenges and drive innovation in chemical development and manufacturing.

Day in the Life:

  • Support process development activities for intermediates and APIs

  • Execute chemical synthesis and scale-up activities in lab and/or manufacturing environments

  • Ensure compliance with cGMP and non-cGMP requirements as applicable

  • Collaborate with cross-functional teams including Quality, Manufacturing, and Analytical

  • Document experimental work, batch records, and technical reports accurately

  • Troubleshoot process issues and identify opportunities for optimization

  • Maintain a safe working environment and follow all safety protocols

Education:

  • PhD in Chemistry or commensurate experience required – Organic Chemistry PhD preferred

Experience:

  • 2-5 years of scientific experience in a related field. Experience working in Pharmaceutical Industry preferred.

  • Project management experience strongly preferred.

  • Process Validation experience preferred.

  • Ability to handle multiple projects simultaneously

  • Ability to mentor and manage junior chemists

Competencies:

Good knowledge and understanding of chemistry and analytical instrumental technologies. Good knowledge of qualitative and quantitative chemical or microbiological analysis. Good knowledge of quality and regulatory requirements in the pharmaceutical industry, including pharmaceutical GMPs and descriptive organic chemistry. Good problem solving skills and logical approach to solving scientific problems. Proficiency with HPLC, GC, LC/MS and Dissolution techniques. Good interpersonal and communication skills (both oral and written). Good presentation skills to present information to customers, clients, and other employees. Ability to read, analyze, and interpret technical procedures and governmental regulations. Ability to write standard operating procedures, simple protocols, and reports. Ability to respond to common inquiries or complaints from customers or regulatory agencies. Ability to apply mathematical operations, to such tasks as determination of test reliability, analysis of variance and correlation techniques.

Physical Requirements / Work Environment

  • Ability to work in laboratory and manufacturing environments

  • May require standing for extended periods and handling chemicals with appropriate PPE

Benefits

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Excellent Benefits

  • Medical, Dental, & Vision benefits effective Day 1

  • Paid Time Off & Designated Paid Holidays

  • Retirement Savings Plan

  • Tuition Reimbursement

What Thermo Fisher Scientific employees say

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