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Internship Downstream Process Development Jobs in Missouri

kindeva

Manufacturing Engineer

Maryland Heights, MO

$70K - $90K/yr

Collaborate with cross-functional teams (Process Development, Quality Assurance, and Production) to ... Internship or co-op experience in pharmaceutical manufacturing or packaging operations. * Knowledge ...

Oakes Kia

Sales Internship Program

Kansas City, MO · On-site

$18/hr

... development. Pay & Benefits * Competitive pay based on experience * Health, dental, and vision ... Learn dealership CRM systems and customer follow-up processes * Support inventory merchandising ...

Oakes GMC

Sales Internship Program

Kansas City, MO · On-site

$18/hr

... development. Pay & Benefits * Competitive pay based on experience * Health, dental, and vision ... Learn dealership CRM systems and customer follow-up processes * Support inventory merchandising ...

Ameren Services

Supply Chain Internship

Saint Louis, MO · Hybrid

$21 - $30/hr

... development and analysis, gathering data for demand planning and process improvements or assisting in inventory/material processes. * Measurable Objectives: Interns will be measured against ...

Ameren Services

Supply Chain Internship

Saint Louis, MO · On-site

$21 - $30/hr

... development and analysis, gathering data for demand planning and process improvements or assisting in inventory/material processes. * Measurable Objectives: Interns will be measured against ...

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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.

Internship Downstream Process Development jobs near you

Manufacturing Engineer

kindeva

Maryland Heights, MO

$70K - $90K/yr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 2 days ago

Kindeva rating

6.7

Company rating: 6.7 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

Job description

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make

We are seeking a motivated and detail-oriented Manufacturing Engineer to support technical operations in our Inspection, Assembly & Packaging plant. 

Key Responsibilities

  • Support achievement of safety, quality, delivery, and cost objectives for operations.
  • Support the monitoring and optimization of assembly, visual inspection, labeling, and packaging processes for vials, syringes, cartridges, and other pharmaceutical products.
  • Assist in developing and updating process documentation, including SOPs, batch records, and process flow diagrams.
  • Collect and analyze production data to identify opportunities for improving yield, throughput, and Overall Equipment Effectiveness (OEE).
  • Participate in troubleshooting manufacturing issues related to automated packaging lines, vision systems, and serialization equipment.
  • Assist in the execution of validation protocols (IQ/OQ/PQ, process validation) for inspection, assembly and packaging equipment.
  • Support deviation investigations, CAPA implementation, and change control processes.
  • Help maintain equipment and processes in a validated state in accordance with cGMP, FDA, and EMA regulations.
  • Participate in internal audits and prepare documentation for regulatory inspections.
  • Collaborate with cross-functional teams (Process Development, Quality Assurance, and Production) to ensure smooth scale-up and successful product launches.
  • Track actions, timelines, and deliverables to support project execution and site priorities.
  • Support equipment qualification, preventive maintenance, and calibration activities.
  • Work with senior engineers and maintenance teams to improve equipment reliability and uptime.
  • Learn and support the operation of high-speed automated inspection systems, assembly and packaging lines.
  • Participate in Lean and continuous improvement initiatives (Kaizen events, 5S, etc.).
  • Prepare technical reports and presentations as required.
  • Support daily production floor activities and provide engineering support during manufacturing campaigns.

Qualifications & Requirements

  • Bachelor’s degree in Mechanical Engineering, Chemical Engineering, Industrial Engineering, Biomedical Engineering, or a related technical discipline.
  • 3+ years of experience in pharmaceutical, biotechnology, or regulated manufacturing environment (internships or co-op experience in manufacturing is highly valued).
  • Exposure to Assembly, Inspection, or Packaging processes is preferred but not required.
  • Basic understanding of cGMP principles and pharmaceutical regulatory requirements.
  • Strong analytical and problem-solving skills.
  • Familiarity with statistical tools, root cause analysis, and Microsoft Office (Excel, Word, PowerPoint).
  • Ability to read and interpret technical drawings and equipment manuals is a plus.

Preferred Qualifications

  • Internship or co-op experience in pharmaceutical manufacturing or packaging operations.
  • Knowledge of Lean Manufacturing or Six Sigma principles.
  • Familiarity with automated inspection systems, serialization, or high-speed packaging equipment.
  • Experience working in a cleanroom or GMP environment

What We Offer

  • Competitive base salary + performance bonus
  • Comprehensive benefits package (health, dental, vision, 401k, etc.)
  • Structured mentorship and professional development programs
  • Exposure to cutting-edge pharmaceutical manufacturing technologies
  • Clear career progression path toward Senior Manufacturing Engineer roles
  • Collaborative and supportive work culture

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