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Internship Downstream Process Development Scientist Jobs in Westminster, MD

Saft America, Inc.

Process Engineer

Cockeysville, MD

$80K - $100K/yr

... internships or co-ops in a manufacturing environment required). * Proficiency in MS Office ... career development and recognition programs. Some of our superior benefits include parental ...

Saft America, Inc.

Process Engineer

Cockeysville, MD

$80K - $100K/yr

... internships or co-ops in a manufacturing environment required). * Proficiency in MS Office ... career development and recognition programs. Some of our superior benefits include parental ...

Saft America, Inc.

Process Engineer

Cockeysville, MD · On-site

$80K - $100K/yr

... internships or co-ops in a manufacturing environment required). * Proficiency in MS Office ... career development and recognition programs. Some of our superior benefits include parental ...

HCI

AI Fall Intern

Ellicott City, MD

$30 - $40/hr

Strong computer science fundamentals , including software design, data structures, algorithms ... development toolkits , coding standards, and implementation patterns within the 90 day internship ...

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Internship Downstream Process Development Scientist information

See Westminster, MD salary details

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

As of Aug 25, 2026, the average hourly pay for internship downstream process development scientist in Westminster, MD is $37.15, according to ZipRecruiter salary data. Most workers in this role earn between $27.26 and $44.38 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

Director, Process & Analytical Development

Walkersville, MD • On-site

Jobtailor
See more jobs at Jobtailorexternal

$180 - $270/hr

Other

Posted 3 days ago

New

Job description

  • Provide overall leadership for analytical development, process development, and project-specific manufacturing activities within the ADS US organization
  • Ensure the ADPD organization delivers services and products safely, compliantly, on time, in full, and within budget
  • Lead, coach, and develop a high-performing ADPD organization
  • Define and execute strategic direction through long-term planning, portfolio management, resource allocation, organizational design, and performance management
  • Establish capabilities, infrastructure, and talent for future manufacturing operations and business growth
  • Contribute to the Sales & Operations Planning (S&OP) process
  • Oversee development and project-specific manufacturing activities against Safety, Quality, Compliance, Delivery, and Cost expectations
  • Own organizational budgets, resource planning, and operational performance
  • Drive Lean maturity, Operational Excellence, and continuous improvement
  • Lead strategic initiatives and transformation programs
  • Partner with R&D, Manufacturing, MSAT, Engineering, Quality, Automation, Supply Chain, and Commercial teams
  • Evaluate, acquire, and implement new technologies
  • Establish governance processes, performance metrics, and decision-making frameworks
  • Support site startup, facility expansion, validation, and capital investment initiatives
Requirements
  • Master’s degree in engineering, Life Sciences, Chemistry, Pharmaceutical Sciences, or a related field required
  • 15+ years of progressive leadership experience within pharmaceutical, biotechnology, CDMO, or related life sciences environments
  • Deep understanding of small molecule and bioconjugate technologies
  • Extensive leadership experience in Process Development, Analytical Development, Technical Operations, Manufacturing, or related GMP-regulated organizations
  • Strong understanding of pharmaceutical manufacturing operations, cGMP requirements, technology transfer, validation, operational readiness, and commercialization activities
  • Experience supporting facility startup, expansion projects, greenfield or brownfield investments, and large-scale capital programs
  • Proven success leading organizations through growth, transformation, and operational scale-up initiatives
  • Strong technical knowledge and experience in small molecule drug substance manufacturing
  • Ability to collaborate across Engineering, Quality, MSAT, Automation, Manufacturing, EHS, HR, Finance, and Commercial functions
  • Ability to translate business requirements into practical, scalable operational solutions
  • Strong executive presence and ability to communicate readiness, risks, performance, and recommendations to senior leadership
  • Experience building organizations, developing talent, and preparing teams for future needs
  • Understanding of Lean Manufacturing, Six Sigma, Operational Excellence, automation, digital systems, and data integrity principles
  • Capability in portfolio management, strategic planning, budget ownership, and resource allocation
  • Ability to navigate ambiguity, manage competing priorities, and lead in a fast-paced environment
  • Strong leadership, communication, problem-solving, and decision-making skills
  • Ability and willingness to transition to an East Coast or Midwest U.S. site location as project needs evolve
  • Willingness and ability to travel to EMEA and NA approximately 25–30% of the time
Core Competencies

Demonstrates extensive leadership in Process Development, Analytical Development, and Technical Operations within GMP-regulated environments, with a strong focus on operational excellence, strategic planning, and budget management. Capable of driving transformation initiatives and collaborating across multiple functions to achieve business growth and compliance.

Highest-signal resume keywords
  • Leadership Experience in Pharmaceutical Manufacturing
  • Process Development and Analytical Development
  • Understanding of cGMP Requirements
  • Lean Manufacturing and Six Sigma Expertise
  • Strategic Planning and Budget Management
ATS Optimization Keywords Hard Skills
  • Process Development
  • Analytical Development
  • Technical Operations
  • Small Molecule Drug Substance Manufacturing
  • Technology Transfer
  • Validation
  • Operational Readiness
  • Commercialization Activities
  • Portfolio Management
  • Resource Allocation
Soft Skills
  • Leadership
  • Communication
  • Problem-Solving
  • Decision-Making
  • Collaboration
Industry Keywords
  • Pharmaceutical
  • Biotechnology
  • CDMO
  • GMP-Regulated Organizations
  • Facility Startup
  • Capital Investment
  • Sales & Operations Planning
  • Operational Excellence
  • Transformation Programs
  • Compliance
Tools & Technologies
  • Lean Manufacturing
  • Six Sigma
  • Digital Systems
  • Data Integrity Principles
  • Automation
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