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Internship Downstream Process Development Jobs in Maryland

Biologist (50849)

Gaithersburg, MD · On-site

$92K - $102K/yr

Develop downstream (purification) processes, under the supervision of a project lead scientist, for ... Coordinate with project management to ensure development milestones and study deliverables are met ...

Develop downstream (purification) processes, under the supervision of a project lead scientist, for ... Coordinate with project management to ensure development milestones and study deliverables are met ...

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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.

Senior Scientist, Process Development

Gaithersburg, MD • On-site

Scorpion Therapeutics
51 - 200 employees

$125 - $150/hr

Other

Posted 10 days ago


Job description

Your Contribution
  • Develop and qualify scale-down models for downstream purification processes to support monoclonal antibody manufacturing
  • Execute studies and FMEA assessments to establish critical process parameters and proven acceptable ranges for process characterization
  • Lead development, optimization, and characterization of downstream processes, including scale-up, virus/impurity clearance, and resin/membrane lifetime
  • Conduct downstream process unit operations such as depth filtration, chromatography, viral inactivation, viral filtration, tangential flow filtration, and formulation
  • Collaborate with cross-functional teams to design experiments, analyze results, support technology transfers, and meet project timelines
  • Contribute to CMC documentation by drafting process descriptions, characterization reports, QbD risk assessments, and other technical reports
  • Drive the creation of best practices and workflows for process development in a fast-paced environment
A Good Match
  • PhD in Biomedical Engineering, Chemical Engineering, Biochemistry or related discipline with 6+ years of relevant experience (including post-doctoral training), or MS with 8+ years of industry experience
  • 6 years' experience in global pharma PD or MS&T for monoclonal antibodies or related biologics
  • Expertise in downstream process development including scale-up and technology transfer
  • Proven ability to design and execute process characterization studies using scale-down models that inform PPQ strategy
  • Strong understanding of biologics CMC processes including PPQ/BLA readiness; antibody or ADC development preferred
  • Demonstrated technical leadership within cross-functional teams and programs
  • Willingness to travel domestically and internationally as required
Benefits
  • Expected Pay Range: $113,600/year to $181,600/year + benefits, annual bonus & equity
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