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Internship Downstream Process Development Scientist Jobs in Tucson, AZ

Raytheon

Low Observable Materials Engineer

Tucson, AZ · On-site

Fabrication process development * Composites operations support * Material testing and ... Typically requires a degree in Science, Technology, Engineering or Mathematics (STEM) and a minimum ...

Department of the Air Force

DATA SCIENTIST

Tucson, AZ · On-site

Job Duties Help 1. Performs developmental assignments in support of projects assigned to higher ... Performs special research tasks designed to utilize and enhance knowledge of work processes and ...

Sedgwick

Principal Data Scientist

Tucson, AZ · On-site +1

Lead the design and development of advanced statistical and machine learning models that improve ... Familiarity with distributed data processing tools and modern data platforms preferred.

Arrowhead Talent Solutions

Quality Manager

Tucson, AZ · On-site

Support new product introductions, process development, inspection methods, and testing procedures ... Bachelor's degree in Engineering, Chemistry, Materials Science, Ceramics, or related technical ...

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$19

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

As of May 28, 2026, the average hourly pay for internship downstream process development scientist in Tucson, AZ is $36.56, according to ZipRecruiter salary data. Most workers in this role earn between $26.83 and $43.65 per hour, depending on experience, location, and employer.

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.

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 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.
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Internship Downstream Process Development Scientist jobs near you
Technical Transfer Specialist

Technical Transfer Specialist

Dawar Consulting, Inc.

Tucson, AZ

$32 - $39.70/hr

Full-time

Medical, Dental, Vision, Retirement

Posted 28 days ago

Job description

Our client, a world leader in diagnostics and life sciences, is looking for a "Technical Transfer Specialist” based out of Tucson, AZ.


Job Duration: Long term Contract (Possibility Of Further Extension)

Pay Rate: $32/hr on W2 DOE


Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K

We are seeking a Technical Transfer Specialist to support the transfer of new assays, reagents, and diagnostic products from R&D into manufacturing. This role ensures smooth product integration with a focus on manufacturability, quality, compliance, and scalability. The ideal candidate will have experience in GMP environments, strong coordination skills, and a foundation in process improvement and technical documentation

Key Responsibilities:
Technical Transfer
  • Support product and process transfer from development to manufacturing.
  • Coordinate cross-functional activities with R&D, Operations, Quality, and Regulatory teams.
  • Track project milestones and ensure timely execution of transfer activities.
  • Document manufacturing processes, scalability considerations, and best practices.
  • Assist with process validation readiness and troubleshooting during transfers.
Quality & Compliance
  • Ensure adherence to cGMP, SOPs, and regulatory standards.
  • Support audit readiness and documentation for compliance activities.
  • Assist in investigations, deviations, and corrective actions (CAPA/NCR).
Continuous Improvement
  • Apply Lean principles and problem-solving tools (e.g., 5 Whys, Fishbone).
  • Analyze process data using tools like Minitab to improve efficiency and reduce risk.
  • Develop and maintain standardized procedures and documentation
Required Qualifications:
  • Bachelor’s or Master’s degree in Life Sciences (Biology, Chemistry, Biochemistry, etc.) or Engineering(Biomedical/Chemical).
  • 1+ year of relevant experience in biotech, pharma, or medical device industry.
  • Experience working in a GMP/regulated environment.
  • Strong understanding of SOPs, documentation, and quality compliance.
  • Excellent communication, teamwork, and project coordination skills
Preferred Qualifications:
  • Exposure to technical transfer, manufacturing, or process development.
  • Knowledge of Lean / Six Sigma methodologies.
  • Familiarity with assay, reagent, or diagnostic product manufacturing.


If interested, please send us your updated resume at

hr@dawarconsulting.com/kavitha@dawarconsulting.com