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Internship Downstream Process Development Jobs in Carrollton, GA

Georgia

Internship - PT

Atlanta, GA

$15/hr

Primary Duties & Responsibilities * Assist with processing participant applications and maintaining ... Provide administrative support to program staff * Assist with development of outreach and ...

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Internship Downstream Process Development information

See Carrollton, GA salary details

$8

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$22

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

As of Aug 19, 2026, the average hourly pay for internship downstream process development in Carrollton, GA is $15.81, according to ZipRecruiter salary data. Most workers in this role earn between $13.37 and $17.84 per hour, depending on experience, location, and employer.

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 near Carrollton, GA are hiring for Internship Downstream Process Development jobs?

Cities near Carrollton, GA with the most Internship Downstream Process Development job openings:

Internship Downstream Process Development jobs near you

Downstream Biomanufacturing Process Expert (US)

UCB

Atlanta, GA • On-site

Full-time

Re-posted 3 days ago

Job description

Make your mark for patients

We are looking for a Downstream Biomanufacturing Process Expert who is collaborative, proactive and innovative to join us in our BioNexUS Internal Manufacturing team, based at our UCB campus in Georgia, United-States.

About the role

This role is part of the BioNexUS project, contributing to the design and delivery of a future-ready biologics manufacturing facility. You will play an important role in a major biopharmaceutical manufacturing project, helping bring end-user knowledge into design and delivery decisions from start to finish. You will represent manufacturing needs, translate operational requirements into practical project inputs, and help ensure the future facility is designed for safe, high-quality and efficient commercial production in a rapidly evolving project environment.

Who you'll work with

You will be working in a team that partners closely with manufacturing colleagues, global cross-functional teams and project stakeholders to shape a new manufacturing facility in Georgia, United States. The team combines operational expertise, technical knowledge and strong collaboration to make sure manufacturing needs are understood, reflected in project decisions and aligned with future business needs working across different time zones.

What you'll do

  • Represent manufacturing in project discussions and ensure operational needs are reflected in facility design, systems and ways of working.
  • Translate technical, process and user requirements into clear project inputs that support practical and future-ready manufacturing solutions.
  • Review technical documents and data to support sound decisions for purification, filtration and buffer preparation processes.
  • Work with manufacturing sites and cross-functional partners to gather best practices, operational insight and lessons learned.
  • Promote strong health, safety, environmental and quality standards in daily project decisions and deliverables.
  • Stay informed on industry developments and help bring new technologies and modern manufacturing approaches into the project.

Interested? For this role we're looking for the following education, experience and skills

Mandatory requirements

  • Degree in a relevant scientific or engineering field, or equivalent experience in biopharmaceutical manufacturing.
  • Minimum of 7 years of experience in biopharmaceutical operations and large-scale drug substance or purification projects within the pharmaceutical industry.
  • Strong knowledge of mammalian biopharmaceutical production, buffer preparation, process operations and supporting digital tools and systems.
  • Ability to communicate clearly, write technical documentation and collaborate effectively across functions and stakeholder groups.
  • Minimum of 5 years of experience working in regulated manufacturing environments, including inspections, audits and compliance-focused decision-making.
  • Willingness to adapt to project variabilities and a rapidly evolving work environment
  • Occasional travel to the Europe may be required.

Strong plus

  • Ability to communicate in French is an advantage.

Internal applicants should be in their current job for at least 12 months, must meet performance standards and are not on formal corrective/disciplinary process (PIP), warning, final warning, or compliance warning letters within the last 12 months. Please inform your Manager or your Talent Partner before applying to any internal job opportunities.

Unlessexplicitlystated in the description, this role is hybrid with 40% of your time spent in the office,regardlessof your current contractual agreement. If your current working arrangements differ, please contact your Talent Partner to discuss before submitting your application.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable federal, state, or local law. UCB invites you to voluntarily self-identify during the application process. Provision of self-identification information is entirely voluntary and a decision to provide or not provide such information will not have any effect on your application for employment, your employment with UCB, or otherwise subject you to any adverse treatment. Any information you provide will be considered confidential and will be kept separate from your application and/or personnel file and will only be used in accordance with applicable laws, orders, and regulations.


Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on US-Reasonable_Accommodation@ucb.com for application to US based roles. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Requisition ID:93233

Recruiter:Megane Libert

Hiring Manager:Nicolas TIECHE

Talent Partner:Hannah Fischer

Job Level:MM II

Please consult HRAnswers for more information on job levels.

Employment Type: OTHER

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