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Internship Downstream Process Development Scientist Jobs in Kentucky

You'll work alongside experienced scientists and cross-functional teams in a fast-paced, highly ... and process development. * Develop, optimize, and validate analytical test methods for components ...

You'll work alongside experienced scientists and cross-functional teams in a fast-paced, highly ... and process development. * Develop, optimize, and validate analytical test methods for components ...

You'll work alongside experienced scientists and cross-functional teams in a fast-paced, highly ... and process development. * Develop, optimize, and validate analytical test methods for components ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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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 Kentucky? The most popular types of Downstream Process Development Scientist jobs in Kentucky are:
What job categories do people searching Internship Downstream Process Development Scientist jobs in Kentucky look for? The top searched job categories for Internship Downstream Process Development Scientist jobs in Kentucky are:
What cities in Kentucky are hiring for Internship Downstream Process Development Scientist jobs? Cities in Kentucky with the most Internship Downstream Process Development Scientist job openings:
Infographic showing various Internship Downstream Process Development Scientist job openings in Kentucky as of July 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, and 4% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution.

Scientist II, Analytical Chemistry

Kindeva Drug Delivery

Lexington, KY โ€ข On-site

Full-time

Posted 17 days ago


Job description

Our Work Matters
At Kindeva, we make products that save lives, ensuring better health and well-being for patients around the world.
Why Kindeva?
At Kindeva, we're more than a pharmaceutical manufacturer-we partner with leading pharmaceutical companies to develop and manufacture life-changing therapies that improve the lives of patients around the world.
Joining Kindeva means becoming part of a collaborative team where your work directly supports the successful delivery of therapies from development through commercialization. You'll work alongside experienced scientists and cross-functional teams in a fast-paced, highly regulated environment where scientific excellence, innovation, and collaboration make a meaningful impact every day.
The Impact You Will Make
Advance Science. Deliver Quality. Improve Lives.
Reporting to the Manager, Analytical Chemistry, the Analytical Chemistry Scientist II supports the development, validation, and transfer of analytical methods for components, excipients, drug substances, and drug products across multiple stages of pharmaceutical development. In this role, you'll apply your analytical expertise to generate high-quality scientific data that supports formulation development, regulatory submissions, technology transfers, and commercialization activities.
You'll collaborate with scientists, formulation development teams, quality, manufacturing, and external partners to develop robust analytical methods, troubleshoot technical challenges, and ensure laboratory activities are performed in compliance with cGMP, GLP, and regulatory requirements. Your scientific contributions will help ensure the safety, quality, and successful delivery of innovative therapies to patients around the world.
In this role, you will:
  • Develop, optimize, validate, and transfer analytical methods supporting pharmaceutical development and commercialization.
  • Generate, interpret, and communicate analytical data to support formulation development, regulatory submissions, and technical decision-making.
  • Collaborate with cross-functional teams to solve complex analytical challenges and support technology transfer activities.
  • Maintain compliance with cGMP, GLP, and company quality standards while producing accurate scientific documentation.
  • Drive continuous improvement initiatives that enhance laboratory efficiency, analytical capabilities, and overall project success.

Responsibilities
Analytical Testing & Method Development
  • Perform routine and non-routine testing of raw materials, in-process samples, drug substances, and finished drug products to support formulation and process development.
  • Develop, optimize, and validate analytical test methods for components, drug substances, excipients, and drug products.
  • Interpret and report analytical data with a high degree of accuracy and scientific integrity.
  • Troubleshoot analytical methods and instrumentation, proposing and implementing effective solutions.
  • Support qualification of new analytical laboratory equipment.

Documentation & Compliance
  • Prepare technical documents including analytical method protocols, validation reports, technical reports, and SOPs.
  • Prepare and maintain accurate and timely laboratory records in accordance with company policies and regulatory requirements.
  • Ensure all laboratory work complies with cGMP, GLP, and company quality standards.
  • Participate in cross-functional project teams and contribute to CMC documentation for regulatory submissions (IND, NDA, ANDA).

Collaboration & Continuous Improvement
  • Support method transfer and qualification activities to internal and external laboratories (e.g., CROs, CDMOs).
  • Prioritize personal workload to ensure that key objectives are met on time and to budget.
  • Implement continuous improvement projects that improve laboratory effectiveness and organization.
  • Support qualification of new analytical laboratory equipment.
  • Utilize creative thinking to generate solutions to complex technical problems.
  • Cross-functional training and execution of activities within the R&D Product Development & Design Team as needed.
  • Stay up to date with industry trends, technologies, and regulatory changes relevant to analytical sciences.
  • Perform other duties as assigned.

Qualifications
Required Qualifications
  • Degree in a scientific field:
    • PhD or MS with 0+ years of experience; or
    • BS with 3+ years of experience; or
    • 7+ years of experience without a Bachelor's degree.
  • Strong attention to detail and scientific rigor.
  • Ability to work both independently and collaboratively in a fast-paced environment.
  • Proficiency in analytical instrumentation and techniques including HPLC, GC, UV-Vis, FTIR, Karl Fischer, spray testing, and related analytical techniques.
  • Familiarity with cGMP, ICH, and FDA guidelines.
  • Competency in analytical data interpretation, documentation, and scientific reasoning.
  • Strong organizational, written, and verbal communication skills.
  • Ability to work independently and manage time efficiently.

Preferred Qualifications
  • Experience in an FDA-regulated environment.
  • Experience with nasal spray drug products and devices.

Physical Requirements
  • Regularly use hands to handle laboratory materials and supplies.
  • Use a computer for extended periods throughout the workday.
  • Communicate effectively by telephone, electronic communication, and in person.
  • Regularly stand and walk for extended periods of time.
  • Occasionally lift and/or move up to 25 pounds.
  • Utilize proper lifting techniques and remain aware of laboratory and workplace hazards.

Join Our One Team Mission
At Kindeva, we're driven by one mission: improving patients' lives through innovation, scientific excellence, and collaboration. As part of our One Team culture, you'll work alongside talented colleagues who are passionate about solving complex scientific challenges and advancing pharmaceutical development. If you're ready to make a meaningful impact while growing your career in analytical chemistry, we encourage you to apply and join our team.
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California residents should review our Notice for California Employees and Applicants before applying.
Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees-regardless of format-without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.
Equal Opportunity Employer:
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.
Do you see yourself as part of the Kindeva mission? Click Apply Now Today!