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Internship Downstream Process Development Jobs in South Carolina

ATI

$75K - $92K/yr

Join us. R&D Engineer - Alloy & Process Innovation Location: Monroe, NC | Full-Time | Exempt ... co-op/internship/postdoc included). * Demonstrated background in one or more of the following:

New

ATI

$67K - $83K/yr

Join us. R&D Engineer - Alloy & Process Innovation Location: Monroe, NC | Full-Time | Exempt ... co-op/internship/postdoc included). * Demonstrated background in one or more of the following:

New

DYNAMIC FLOWFORM CORP.

$75K - $92K/yr

Join us. R&D Engineer - Alloy & Process Innovation Location: Monroe, NC | Full-Time | Exempt ... co-op/internship/postdoc included). * Demonstrated background in one or more of the following:

New

DYNAMIC FLOWFORM CORP.

$67K - $83K/yr

Join us. R&D Engineer - Alloy & Process Innovation Location: Monroe, NC | Full-Time | Exempt ... co-op/internship/postdoc included). * Demonstrated background in one or more of the following:

New

Siemens

$22 - $24/hr

The Finance Leadership Development Program (FLDP) Internship gives you the opportunity to learn ... Process Specialist/Auditor, Business or Plant Controller or Data Analyst for Siemens. What is the ...

Siemens

$22 - $24/hr

The Finance Leadership Development Program (FLDP) Internship gives you the opportunity to learn ... Process Specialist/Auditor, Business or Plant Controller or Data Analyst for Siemens. What is the ...

Siemens

$22 - $24/hr

The Finance Leadership Development Program (FLDP) Internship gives you the opportunity to learn ... Process Specialist/Auditor, Business or Plant Controller or Data Analyst for Siemens. What is the ...

Siemens

$22 - $24/hr

The Finance Leadership Development Program (FLDP) Internship gives you the opportunity to learn ... Process Specialist/Auditor, Business or Plant Controller or Data Analyst for Siemens. What is the ...

Socket.dev

Process Improvement Engineer

Anderson, SC · On-site

$90 - $120/hr

... and downstream production processes. * Monitor and report on ECO backlog, cycle time, and closure ... Demonstrated experience with process mapping, SOP development, and workflow optimization.

Sealed Air Corporation

Process Engineer

Simpsonville, SC · On-site

$81K - $145K/yr

... consistency, and downstream operations. * Drive reductions in scrap, downtime, and process ... Partner with Manufacturing, Quality, Maintenance, and Product Development teams to support product ...

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Internship Downstream Process Development information

What is an internship in downstream process development?

An Internship in Downstream Process Development is a temporary position, typically for students or recent graduates, focused on learning and supporting the processes involved in purifying and formulating biopharmaceutical products after the initial production stage. Interns in this field gain hands-on experience with techniques such as filtration, chromatography, and quality control, and often work within a research and development or manufacturing environment. This internship helps build skills in laboratory methods, data analysis, and process optimization, making it valuable for those interested in careers in biotechnology or pharmaceuticals.

What types of hands-on projects can I expect to work on during an internship in downstream process development?

As an intern in Downstream Process Development, you will typically assist with projects focused on purification and recovery of biological products, such as proteins or antibodies, from complex mixtures. This often includes tasks like preparing chromatography columns, performing filtration techniques, and conducting sample analysis using methods such as SDS-PAGE or HPLC. You’ll also collaborate closely with experienced scientists and engineers, participate in team meetings to review data, and help troubleshoot process challenges. These experiences provide valuable insight into both laboratory workflows and the broader bioprocess development pipeline.

What are the key skills and qualifications needed to thrive as an internship in downstream process development, and why are they important?

To thrive in an Internship Downstream Process Development role, a solid background in biotechnology, chemical engineering, or a related field, along with foundational lab skills, is essential. Familiarity with bioprocessing techniques, analytical instruments, and data analysis software is typically required, and experience with GMP environments can be advantageous. Strong problem-solving abilities, attention to detail, and effective communication are important soft skills for collaborating with team members and documenting results. These competencies ensure interns can contribute to optimizing purification processes and maintaining high standards in biopharmaceutical development.

What is the difference between Internship Downstream Process Development vs Downstream Process Technician?

AspectInternship Downstream Process DevelopmentDownstream Process Technician
CredentialsTypically pursuing or holding a degree in biotech, chemistry, or related fieldsUsually requires technical diploma or associate degree in biotech or related areas
Work EnvironmentLaboratory and development settings, focusing on process optimization and experimental workManufacturing floor, operating equipment, and performing process runs
ResponsibilitiesAssisting in process development, data analysis, and protocol documentationExecuting downstream processing steps, equipment setup, and process monitoring

In summary, Internship Downstream Process Development focuses on learning and supporting process optimization in a lab setting, while Downstream Process Technicians handle the hands-on execution of downstream manufacturing processes in production environments.

What cities in South Carolina are hiring for Internship Downstream Process Development jobs?

Cities in South Carolina with the most Internship Downstream Process Development job openings:

Internship Downstream Process Development jobs near you

Pharma/Biopharma Technology Leader

Ingevity

North Charleston, SC • On-site

Full-time

Re-posted 13 days ago

Ingevity rating

8.0

Company rating: 8.0 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

35th of 100 rated chemical manufacturers

Job description

Job Family Group:
Sales and Business Development
Are you ready to do something remarkable? Ready to collaborate with an incredible team to solve problems that improve people's lives? Meet Ingevity.
At Ingevity, we develop innovations that purify, protect and enhance the world around us. Our products enable oil to flow better, crops to grow fuller, roads to last longer and ensure that the air we all breathe is cleaner.
Our people come from all different backgrounds and help reimagine new possibilities daily. We understand there is no challenge too big and no contribution too small. We seek out new ideas for tackling complex problems and celebrate achieving the improbable. We value each person's unique talents and synergize them to create meaningful impact and sustainable solutions for our customers and our world.
Bold. Energetic. Ingenious. Genuine. If these qualities describe you, we'd love for you to join Ingevity!
Ingevity is seeking an experienced Pharma / Biopharma Technology Leader to help establish and grow our presence in the pharmaceutical and biopharmaceutical purification market.
This is a highly visible, entrepreneurial individual contributor role will be the platform technology leader for our High Putity Liquid Purification platform and will work hand in hand with a commercial leader for the platform to build the book of business. Ingevity is an emerging participant in this market, and this leader will play a critical role in building technical credibility, developing strategic customer relationships, generating application data, and creating new pathways for adoption across pharmaceutical manufacturers, contract development and manufacturing organizations (CDMOs), and purification technology providers.
The successful candidate will combine deep expertise in downstream bioprocessing, pharmaceutical purification, filtration, adsorption, or separation technologies with a proven ability to independently develop customer relationships, support qualification programs, and drive commercialization in highly regulated environments.
This role is ideal for a technically strong "player-coach" who enjoys building new opportunities from the ground up and is energized by operating in a highly autonomous, market-creation environment.
What You'll Do
Technical Leadership & Application Development
  • Lead application development and performance evaluation of activated carbon technologies for pharmaceutical and biopharmaceutical purification processes.
  • Design and execute laboratory studies focused on impurity removal, decolorization, endotoxin reduction, host cell protein (HCP) removal, aggregate reduction, and overall process optimization.
  • Generate technical data packages supporting customer evaluations, qualification efforts, and commercialization activities.
  • Assess adsorption performance, filtration performance, process economics, and scale-up considerations across pharmaceutical applications.
  • Serve as the company's technical subject matter expert for pharmaceutical purification and downstream processing applications.

Customer & Market Development
  • Build and maintain relationships with pharmaceutical manufacturers, biopharma companies, CDMOs, and purification technology providers.
  • Partner with commercial teams to identify and develop new business opportunities, customer trials, and strategic partnerships.
  • Provide technical leadership during customer evaluations, qualification programs, and implementation projects.
  • Translate customer challenges into practical purification solutions and support the development of differentiated offerings.
  • Represent Ingevity at customer meetings, scientific conferences, industry forums, and technical workshops.

Regulatory, Quality & Commercialization Support
  • Drive compliance initiatives related to USP, European Pharmacopoeia, GMP, ICH, and other pharmaceutical quality standards.
  • Support development of pharmaceutical-grade product specifications, technical dossiers, validation documentation, and qualification packages.
  • Collaborate with Quality, Regulatory, Operations, R&D, and Commercial teams to support successful commercialization and scale-up activities.
  • Contribute to strategies involving Drug Master Files (DMFs), extractables and leachables programs, change control requirements, and other qualification activities.

Market Intelligence & Strategic Development
  • Monitor trends in bioprocessing, downstream purification, filtration, chromatography, adsorption science, and emerging pharmaceutical manufacturing technologies.
  • Evaluate competitive technologies and identify opportunities for Ingevity to establish market leadership.
  • Help shape the long-term strategy for pharmaceutical purification solutions and market expansion.

Required Qualifications
  • Ph.D. in Chemical Engineering, Biochemical Engineering, Bioengineering, Pharmaceutical Sciences, Biochemistry, Analytical Chemistry, or a related field preferred. Master's degree with substantial relevant industry experience will be considered.
  • Minimum 5+ years of relevant industry experience with a Ph.D. or 8+ years with a Master's degree.
  • Hands-on experience in pharmaceutical or biopharmaceutical purification, downstream processing, filtration, adsorption, chromatography, or separation technologies.
  • Strong understanding of pharmaceutical qualification and validation requirements within GMP-regulated environments.
  • Experience interfacing directly with pharmaceutical manufacturers, biopharma organizations, CDMOs, or life sciences technology providers.
  • Demonstrated ability to communicate complex technical concepts to both scientific and commercial audiences.
  • Proven success working independently in highly visible technical roles.

Ingevity is a company made up of extraordinary people of every race, religion and background, all worthy of the same dignity. Our differences are one of our great strengths. Join us in building a culture of increasing diversity and respect - a culture where everyone belongs.
Ingevity is an Equal Opportunity Employer, Minorities/Women/Veterans/Disabled.
Recruiting Agencies: Ingevity does not accept unsolicited resumes and therefore, will not be responsible for any fees associated with unsolicited resumes.

What Ingevity employees say

Pay

Benefits

Hours and flexibility

Workplace

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About Ingevity

Sourced by ZipRecruiter

At Ingevity, we develop innovations that purify, protect and enhance the world around us. Our products enable oil to flow better, crops to grow fuller, roads to last longer and ensure that the air we all breathe is cleaner.

Industry

Chemical manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Charleston, SC, US

Year founded

1846

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