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Internship Downstream Process Development Scientist Jobs in Florida

AIS Inc

Data Scientist

Miami, FL · On-site +1

... downstream analytical and AI/ML applications * Maintain familiarity with diverse data types and ... data processing efficiency * Support annotation of datasets and development of machine learning ...

AIS, Inc.

Data Scientist

Miami, FL · On-site

... downstream analytical and AI/ML applications * Maintain familiarity with diverse data types and ... data processing efficiency * Support annotation of datasets and development of machine learning ...

PODS

Data Scientist III- Operations

Clearwater, FL · On-site

... processes. * Contribute to shared tooling, frameworks, and standards so that solutions are ... Maintain data models in Snowflake that other analysts and downstream tools rely on. * Create ...

New

Radiance Technologies

Radiance is seeking a highly qualified and motivated scientist to support Geospatial Intelligence ... Perform algorithm development for complex data exploitation processes Required Skills and ...

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Internship Downstream Process Development Scientist information

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 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.
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Internship Downstream Process Development Scientist jobs near you

Principal Scientist, QC Analytical

Goodwin Biotechnology Inc

Fort Lauderdale, FL • On-site

Full-time

Re-posted 21 days ago

Job description

Description:

The Principal Scientist, QC Analytical serves as a senior scientific expert within the Quality Control organization, providing advanced technical leadership, method development oversight, and subject-matter expertise for analytical activities supporting raw materials, intermediates, drug substances, and final products. This role drives the development, qualification, and validation of complex analytical methods, supports technology transfer activities, and ensures analytical programs meet regulatory, corporate, and scientific standards. The Principal Scientist leads high-level investigations, provides technical mentorship across departments, and contributes to strategic initiatives supporting continuous improvement of QC Analytical operations.

Requirements:
  • Provide expert leadership in analytical testing for biologics, vaccines, cell/gene therapies, or APIs, including techniques such as HPLC/UPLC, GC, CE, ELISA, compendial methods, spectroscopy, and bioassays.
  • Provide expert guidance for method lifecycle management, including phase-appropriate validation strategies and regulatory expectations.
  • Lead technical transfer of analytical methods from Process Development, Protein Characterization, and external partners into QC, ensuring successful integration into routine testing operations.
  • Act as primary scientific reviewer of QC analytical data, reports, protocols, and investigations to ensure accuracy, compliance, and scientific integrity.
  • Support the design, review, and execution of stability studies; develop stability-indicating methods and oversee evaluation of long-term and accelerated data.
  • Serve as the QC Analytical SME during audits, regulatory inspections, client meetings, and cross-functional technical discussions.
  • Provide advanced technical support for atypical results, including OOS, OOT, and ABT investigations; lead root cause analysis and propose scientifically sound corrective and preventive actions.
  • Contribute to continuous improvement initiatives, including new technologies, workflow optimization, data integrity enhancements, and analytical efficiency improvements.
  • Collaborate with QA, Manufacturing, Process Development, and Protein Characterization groups to resolve complex analytical issues and ensure alignment across teams.
  • Prepare and review scientific documentation including method development reports, validation protocols, stability reports, and analytical risk assessments.
  • Mentor and guide QC Analysts and Scientists, providing training in new methods, instrumentation, regulatory expectations, and scientific best practices.
  • Maintain deep knowledge of compendial, ICH, and FDA guidance and ensure analytical strategies align with current regulatory expectations.

This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice.


Education and Skills Required:

  • Ph.D. in biological sciences, biochemical sciences, analytical chemistry, or related field preferred or Master’s degree with extensive relevant experience may be considered.
  • Minimum of 8–10 years of experience in a GMP, FDA-regulated environment with a strong focus on analytical development, validation, and QC laboratory operations
  • Proven track record of leading analytical teams and complex technical projects
  • Expert-level knowledge of analytical methodologies such as HPLC/UPLC, CE, MS, ELISA, qPCR, and other characterization techniques.
  • Strong organizational, documentation, and time-management capabilities with high attention to detail.