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Internship Downstream Process Development Scientist Jobs in Florence, SC

Tooling or fixture development Process Engineer - Magnet Assembly This role supports assembly ... internships, cooperative education programs, research, or academic projects. * Ability to analyze ...

... Science, or a related technical discipline. * Minimum of 2 years of professional experience in manufacturing, assembly engineering, product development, process engineering, or related technical ...

... downstream decisions remain effective and trustworthy. 60% Research and Algorithm Development ... Implement these methods in a reproducible software framework and connect the information-processing ...

Earn business through our solution generation process, which will lead to the successful execution ... Bachelor's Degree - In Science or equivalent field experience is required. Preferred degrees are in ...

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Internship Downstream Process Development Scientist information

See Florence, SC salary details

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

As of Sep 14, 2026, the average hourly pay for internship downstream process development scientist in Florence, SC is $37.38, according to ZipRecruiter salary data. Most workers in this role earn between $27.40 and $44.62 per hour, depending on experience, location, and employer.

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.

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Infographic showing various Internship Downstream Process Development Scientist job openings in Florence, SC as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 79% Full Time, 16% Part Time, 1% Temporary, and 2% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $77,745 per year, or $37.4 per hour.

Manufacturing Process Manager

Florence, SC • On-site

Thermo Fisher Scientific
Biotechnology Research and Development • 10K+ employees

Full-time

Re-posted 22 days ago


Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 432 frontline employees who took The Breakroom Quiz


Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials
Job Description
Title: Manufacturing Process Manager
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner, and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Division/Site Specific Information
Position will sit onsite at the Florence, SC site and will support the Drug Substance Division (DSD) at Thermo Fisher Scientific. This role, reporting to the Production Planning Manager, ensures the flawless import of materials and goods at our Florence, South Carolina locations.
Discover Impactful Work:
Join us as a Process Manager (Area Manager) in Manufacturing and contribute to excellence in process development and manufacturing optimization of active pharmaceutical ingredients. You'll provide technical leadership in developing, validating, and implementing robust manufacturing processes while collaborating across multiple departments to ensure successful scaling and optimization of new and existing processes. Make meaningful contributions to innovative solutions that help our customers make the world healthier, cleaner, and safer.
A Day in the Life:
  • As a key technical expert, you'll lead complex projects, provide manufacturing support, conduct process improvements, and drive technology transfer initiatives.
  • You'll collaborate with cross-functional teams including R&D, Quality, Engineering, and Production to achieve project goals and maintain high quality standards.
  • Your expertise will be essential in troubleshooting, optimizing processes, and implementing data-driven solutions while ensuring compliance with regulatory requirements.
Keys to Success:
Education
  • BS Degree Required. Preferred Fields of Study: Chemical Engineering, Chemistry, Polymer Chemistry, Process Engineering, or a similar background.
  • Advanced degree preferred.

Experience
  • Advanced Degree plus 6 years of experience, or Bachelor's Degree plus 8 years of experience in process development, scale-up, and manufacturing optimization required.
  • Experience leading cross-functional teams and managing complex technical projects.
  • Experience with quality systems and risk assessment methodologies.
  • Experience developing and supporting team members.
Knowledge, Skills, Abilities
  • Deep technical expertise in process development, scale-up, and manufacturing optimization
  • Strong background in GMP manufacturing and regulatory compliance (FDA, EMA, ISO)
  • Advanced analytical and problem-solving skills with expertise in statistical analysis and DOE
  • Proven ability to troubleshoot complex process issues and implement corrective actions
  • Strong documentation skills including SOPs, batch records, validation protocols and reports
  • Expertise in data analysis, process modeling, and trending
  • Excellence in technical writing and presentation skills
  • Strong interpersonal and communication abilities for collaborating with internal/external stakeholders
  • Ability to work in cleanroom/GMP manufacturing environments
  • Proficiency with statistical software and standard business applications
  • Travel may be required (<20%) to other sites
  • Knowledge of Lean/Six Sigma methodologies preferred

Benefits
We offer competitive remuneration, annual incentive plan bonus scheme, 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.

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