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Internship Downstream Process Development Scientist Jobs in Boca Raton, FL

Open Scientific

Sr Engineer, Process Development

Sunrise, FL

$99.20K - $128.30K/yr

Company Description Open Scientific provides contract staffing and direct hire recruitment services ... Lead and manage key process items to bring new products through the design phase into efficient ...

Open Scientific

Sr. Engineer of Process Development

Sunrise, FL · On-site

$99.20K - $128.30K/yr

... and Life Sciences worldwide. This is a great step for someone who is looking to take a seat in a ... Design, evaluate, implement and monitor processes and operating systems for the manufacture aortic ...

Danaher

R&D Internships

Lake Worth, FL

By submitting your interest, you'll be among the first to know when internship opportunities open ... You'll work in a collaborative environment alongside experienced scientists and contribute to real ...

Danaher

R&D Internships

Boca Raton, FL

By submitting your interest, you'll be among the first to know when internship opportunities open ... You'll work in a collaborative environment alongside experienced scientists and contribute to real ...

OneHope, Inc

Cultivate Internship

Pompano Beach, FL · On-site

$14 - $18.75/hr

... Science & Analytics, Digital Media, Graphic Design, Human Resources, International Relations, Journalism, Marketing, Psychology/Sociology, Software Development. * What are the internship dates?

OneHope, Inc

Cultivate Internship

Pompano Beach, FL · On-site

$14 - $18.75/hr

... Science & Analytics, Digital Media, Graphic Design, Human Resources, International Relations, Journalism, Marketing, Psychology/Sociology, Software Development. * What are the internship dates?

D1 Training

Sports Marketing Internship

Margate, FL · On-site

$13.50 - $18.25/hr

Training & development Sports Marketing Internship - Community Engagement & Digital Media (College ... With all who participate in the D1 training process moving aggressively towards their goals.

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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 Boca Raton, FL is $36.69, according to ZipRecruiter salary data. Most workers in this role earn between $26.92 and $43.80 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

Process Engineer II, Process Development

ADMA BIOMANUFACTURING LLC

Boca Raton, FL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 22 days ago

Job description

Job Description Header:
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Process Engineer II, Process Development in Boca Raton, FL!
Job Title: Process Engineer II, Process Development
Job Description:
Position Summary
The Process Engineer II provides process development and transfer expertise for IgG Immunotherapy Production. Provide updates to Process Development (PD) Management team on a regular basis to ensure compliance issues are being met. Responsible for maintaining compliance in PD laboratory and executing process development/evaluation studies as well as process validations using a scale down model. As a key member of the PD group, provide support for Manufacturing, Quality Control/Quality Assurance, and Regulatory departments.
Essential Functions (ES) and Responsibilities
The standard schedule for this position is 8:00 AM to 5:00 PM, but employees may occasionally be required to work 12-hour rotating shifts during operational campaigns and manufacturing model runs.
  • Provide support for technical issues related to the manufacturing process and product quality.
  • Develop new processes as required for production of plasma derived therapies.
  • Be familiar with regulatory guidelines to process development/validation as well as implementing manufacturing process changes.
  • Optimize and maintain compliance in PD laboratory by ensuring all equipment calibration/IQ/OQ/PM status are current.
  • Design and plan scientific experiments to achieve corporate goals for existing projects. Write protocols and reports in support of PD studies.
  • Review and/or approve cGMP documentation generated by other PD group members as necessary.
  • Lead execution of process development/evaluation studies as well as process validations using a qualified scale down model.
  • Be responsible for transferring process changes and/or new processes from PD to Manufacturing.
  • Act as a liaison between PD and Manufacturing for supporting deviations and investigations as well as when transferring new and/or optimized processes.
  • Maintain and review process development Batch Records for scale down process models.
  • Perform other activities as assigned by the PD Managers.
  • Support Manufacturing, Engineering, and Quality Management departments with the development and implementation of new process/technology.
  • Assist manufacturing personnel in the execution of process development and process validation studies in cGMP production environment as necessary.

Job Responsibilities or Job Requirements
Competencies
Ability to follow the cGMP's and procedures with great attention to detail
Able to work in high-pressure, deadline-driven environment
Demonstrated ability to achieve goals, overcome obstacles, and meet deadlines
Possess time management skills and be able to balance multiple job assignments at once
Possesses excellent oral and written communication skills with close attention to detail and accuracy to collaborate effectively with cross-functional teams and communicate findings and recommendations
Experience Requirements
Education Requirements:
  • Bachelor's degree in Science or Engineering required.

Experience Requirements:
  • A minimum of five (5) years of experience in a cGMP, Pharmaceutical/Biological manufacturing environment is required.
  • Familiarity with many aspects of process development is expected.
  • Knowledge of FDA cGMP requirements is required.

Preferred Experience
Compliance Requirements (ES)
The minimum compliance expectation for this role entails strict adherence to FDA regulations and company policies governing sales and marketing activities. This includes completion of required compliance training, accurate documentation of sales interactions, and adherence to data privacy regulations. Additionally, the role requires proactive participation in compliance reviews, prompt reporting of any potential issues, and ongoing education to stay updated on relevant FDA regulations.
Job Description Footer:
In addition to competitive compensation, we offer a comprehensive benefits package including:
  • 401K plan with employer match and immediate vesting
  • Medical, Vision, Life and Dental Insurance
  • Pet Insurance
  • Company paid STD and LTD
  • Company Paid Holidays
  • 3 Weeks' Paid Time Off (within the first year)
  • Tuition Assistance (after the first year)
  • Easily accessible to Tri-Rail
  • Free shuttle to the Boca Tri-Rail station

ADMA Biologics uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit www.dhs.gov/E-Verify.
ADMA Biologics is an Equal Opportunity Employer.

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