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Internship Downstream Process Development Scientist Jobs in Anderson, SC

jadex

Alltrista - Engineer, Process

Greenville, SC · On-site

Performs mold process development using scientific approach, aiming at optimum process, also meeting quality and productivity specifications. * Develop, implement and document procedures designed to ...

Jadex

Alltrista - Engineer, Process

Greenville, SC · On-site

Performs mold process development using scientific approach, aiming at optimum process, also meeting quality and productivity specifications. * Develop, implement and document procedures designed to ...

CYNET SYSTEMS

Mechanical Engineer II

Greenville, SC · On-site

$44 - $49/hr

Bachelor's degree in Engineering (Mechanical, Materials, Electrical, Computer Science, or related ... Academic or hands-on experience in process development areas such as fixture development, machining ...

CYNET SYSTEMS

Mechanical Engineer II

Greenville, SC · On-site

$44 - $49/hr

Bachelor's degree in Engineering (Mechanical, Materials, Electrical, Computer Science, or related ... Academic or hands-on experience in process development areas such as fixture development, machining ...

Rising Sun Technologies LLC

Be Seen First

Mechanical Engineer II - 3072

Greenville, SC · On-site

$48/hr

Coursework, internships, or practical experience related to gas turbine design, repair ... Academic or hands-on experience with process development, including: * * Fixture development

Michelin

Quality Process Engineer

Greenville, SC · On-site

Foster the development of operators through the teaching of quality related competencies (mentoring ... For Entry Level, this can include internship, Co-op, apprentices, military service, or similar ...

Michelin

Quality Process Engineer

Greenville, SC · On-site

Foster the development of operators through the teaching of quality related competencies (mentoring ... For Entry Level, this can include internship, Co-op, apprentices,military service,or similar ...

Michelin

Quality Process Engineer

Anderson, SC · On-site

For Entry Level, this can include internship, Co-op, apprentices, military service, or similar ... S. Degree in Mechanical, Chemical, Material Science Engineering or other technical degree is ...

Michelin

Quality Process Engineer

Anderson, SC · On-site

For Entry Level, this can include internship, Co-op, apprentices,military service,or similar ... S. Degree in Mechanical, Chemical, Material Science Engineering or other technical degree ...

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

As of Aug 31, 2026, the average hourly pay for internship downstream process development scientist in Anderson, SC is $35.39, according to ZipRecruiter salary data. Most workers in this role earn between $25.96 and $42.26 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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Internship Downstream Process Development Scientist jobs near you

Technical Services Scientist

Kelly Services

Greenville, SC

$100K - $120K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 25 days ago

Job description

Lead Technical Services Scientist/Supervisor
Location: Greenville SC
Shift: Monday-Friday First shift with flexibility to work overtime as needed
Salary: $100,000-$120,000/year + 10% annual bonus potential
Position Summary

The Lead Technical Services Scientist/Supervisor provides technical leadership and direct people management for pharmaceutical process development, technology transfer, and manufacturing support activities related to new liquid pharmaceutical products. This role is responsible for ensuring safe, compliant, efficient, and scalable manufacturing processes through process ownership, technical troubleshooting, deviation investigations, exhibit batch oversight, and cross-functional collaboration.

This position serves as the primary technical escalation point for manufacturing operations and has direct supervisory responsibility for Technical Services Scientists and supporting staff.

Key Responsibilities
  • Lead and direct Technical Services Scientists supporting process development and technology transfer activities
  • Serve as the technical lead for development products, ensuring process understanding, control strategy development, and successful exhibit batch execution
  • Support process scale-up activities and identify/mitigate technical risks for commercial manufacturing readiness
  • Provide technical support for packaging studies, investigations, protocols, and reports related to development products
  • Generate, review, and approve technical documentation including:
    • batch records
    • protocols
    • reports
    • change controls
    • regulatory submission support documents
  • Evaluate manufacturing readiness and process capability for exhibit batch manufacturing
  • Assess manufacturing equipment and facility capabilities to support new process development and scale-up activities
  • Collaborate with Engineering on equipment requirements and User Requirement Specifications (URS)
  • Support equipment qualification and validation activities through protocol review and technical input
  • Lead or support manufacturing investigations and process troubleshooting activities
  • Partner cross-functionally with Operations, QA, Engineering, Validation, Maintenance, Regulatory, and R&D teams
  • Monitor project timelines, communicate risks, and manage resources to support project execution
  • Train, coach, mentor, and develop Technical Services staff
  • Participate in hiring, onboarding, performance management, and professional development activities
Qualifications
  • Bachelor’s degree in Engineering, Pharmaceutical Sciences, Chemistry, Biology, or related scientific field
  • Minimum 8+ years of pharmaceutical manufacturing experience or equivalent combination of education and industry experience
  • Prior leadership, supervisory, mentoring, or team lead experience preferred
  • Strong knowledge of:
    • pharmaceutical manufacturing processes
    • process development
    • technology transfer
    • cGMP regulations
    • FDA/DEA/OSHA requirements
  • Oral liquid pharmaceutical experience preferred
  • Excellent technical writing, analytical, communication, and presentation skills
  • Ability to manage multiple priorities and work effectively in cross-functional environments
  • Strong troubleshooting, problem-solving, and project management capabilities

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.