M.E. in Biopharmaceutical Processing

Claremont, California

 

INTAKE: August

Program Overview

The M.E. in Biopharmaceutical Processing is an intensive two-year, 60-credit graduate program. It is designed for students with undergraduate degrees in biology, biochemistry, biotechnology, chemical engineering, biomedical engineering, or related fields. The curriculum provides a comprehensive understanding of bioprocess engineering, from upstream cell culture and fermentation to downstream purification and finished product formulation. A cornerstone of the program is the industry-sponsored Team Master's Project (TMP) or Team Design Project (TDP), a capstone experience where students work in interdisciplinary teams on real-world problems for biopharma/biotech companies. Students also undertake a mandatory 400-hour paid industry internship, further solidifying their practical experience and professional network.

STEM-designated: Yes, the Master of Engineering in Biopharmaceutical Processing program at Keck Graduate Institute is STEM-designated. This is a significant advantage for students, particularly international students on an F-1 visa, as it makes them eligible for a 24-month extension of their Optional Practical Training (OPT) after their initial 12-month OPT period. This allows for a total of up to three years of valuable post-graduation work experience in the U.S., greatly enhancing their career opportunities in the highly technical and in-demand biopharmaceutical sector.

Curriculum: The 60-credit curriculum is meticulously structured to cover the entire biopharmaceutical processing pipeline. Core coursework includes in-depth studies in bioprocess engineering principles, upstream processing (e.g., cell culture, bioreactor design), downstream processing (e.g., protein purification, bioseparations), quality systems and regulation for biologics (CMC, regulatory compliance), and bioprocess economics. The program integrates substantial laboratory components, including a Biopharmaceutical Processing LAB, and offers electives in areas such as data analytics, machine learning in life sciences, and advanced bioprocessing for emerging therapeutics. The capstone Team Master's Project provides a comprehensive, hands-on application of learned concepts to an industry-sponsored challenge.

Research Focus: KGI's research focus within the M.E. in Biopharmaceutical Processing program is inherently applied and industry-driven. While it's a professional master's degree, the program strongly emphasizes research and development relevant to real-world biomanufacturing challenges. The Amgen Bioprocessing Center at KGI serves as a hub for innovation, with faculty and students engaged in projects that address critical areas like process development and optimization, new technology evaluation, quality control, and scale-up for commercial production. The mandatory Team Master's Project (TMP) or Team Design Project (TDP) is a direct manifestation of this research focus, allowing students to contribute to industry-sponsored studies on topics such as cell culture, protein purification, facility design, and regulatory aspects. This applied research experience is crucial for developing problem-solving skills highly valued in the biopharma industry.

Industry Engagement: Industry engagement is a cornerstone of the M.E. in Biopharmaceutical Processing program at KGI. The institute boasts robust connections with leading biopharma and biotech companies, evident through its Industry Advisory Boards and the Amgen Bioprocessing Center Advisory Board (ABCAB). Faculty members often have extensive industry experience, bringing real-world case studies and current trends into the classroom. The program mandates a paid, 400-hour industry internship, providing invaluable hands-on experience and networking opportunities. Furthermore, the capstone Team Master's Project is consistently sponsored by major biopharma companies such as Amgen, Boehringer Ingelheim, Catalent, Gilead, Pfizer, and ThermoFisher Scientific, offering students direct exposure to industry-level problem-solving and potential employment pathways. This deep integration ensures graduates possess the practical skills and professional network vital for immediate career success.

Global Perspective: Keck Graduate Institute fosters a global perspective within its M.E. in Biopharmaceutical Processing program, recognizing the inherently international nature of the biopharmaceutical industry. The diverse student body, drawing from various international backgrounds, enriches classroom discussions and team collaborations with a broad range of viewpoints and experiences. The curriculum addresses global regulatory standards (e.g., cGMP, ICH guidelines) and quality systems that are universally applicable in biomanufacturing. KGI also has international partnerships, such as its collaboration with Biocon Academy in India, which facilitates global understanding and pathways into the bioprocessing field. This global outlook prepares graduates to work effectively in multinational corporations, contribute to international drug development initiatives, and navigate the complexities of a globally interconnected biopharma supply chain.

Pollster Education

Location

Claremont, California

Pollster Education

Score

IELTS 6.5

Pollster Education

Tuition Fee

USD 37000

Postgraduate Entry Requirements

Academic Qualifications: Applicants for postgraduate programs typically require a minimum academic achievement of 70% or above in their bachelor's degree.

English Language Proficiency:

  • IELTS: Overall band score of  6.5 or 7.0 with a minimum of 6.0 in each component.
  • TOEFL: Overall score of 75 or higher.

Keck Graduate Institute (KGI) is dedicated to supporting talented international students pursuing advanced education in the fields of applied life sciences, biotechnology, healthcare, and pharmaceutical sciences. To make its programs more accessible, KGI offers a variety of scholarship opportunities specifically for international applicants, helping to reduce the financial burden and recognize academic excellence.

Merit-Based Scholarships: KGI awards merit-based scholarships automatically during the admission process to international students who demonstrate outstanding academic achievements, leadership qualities, and innovation in their field. These scholarships can cover a significant portion of tuition fees and are highly competitive.

Global Impact Scholarship: This prestigious scholarship targets international students with a vision to make a meaningful difference in global health, science, and technology. Candidates are evaluated on academic performance, research potential, and dedication to solving worldwide challenges through science and healthcare.

Dean’s and Presidential Scholarships: Exceptional international candidates may be considered for Dean’s or Presidential Scholarships, which provide substantial tuition assistance. These awards recognize exemplary scholarship, professional experience, and contributions to their academic community.

Program-Specific Scholarships: Certain programs at KGI, such as the Master of Science in Applied Life Sciences, Master of Business and Science, and Doctor of Pharmacy, offer dedicated scholarships. These awards help attract students with strong backgrounds and align their talents with KGI’s mission.

A Master of Engineering (M.E.) in Biopharmaceutical Processing from Keck Graduate Institute (KGI), located in Claremont, California, is a highly specialized and STEM-designated program designed to address the critical talent needs of the rapidly expanding biopharmaceutical industry.

Process Development Scientist/Engineer: This is a core role, involving the design, optimization, and scaling up of manufacturing processes for biopharmaceutical products, ensuring efficiency, reproducibility, and compliance with regulatory standards.

Manufacturing Science and Technology (MS&T) Specialist: Acts as a bridge between process development and commercial manufacturing, providing technical support, troubleshooting production issues, and implementing process improvements for existing biopharmaceutical products.

Upstream Processing Scientist/Engineer: Specializes in the initial stages of biopharmaceutical production, including cell line development, cell culture, fermentation, and bioreactor optimization for producing therapeutic proteins or other biologics.

Downstream Processing Scientist/Engineer: Focuses on the purification and isolation of biopharmaceutical products from cell cultures, utilizing techniques like chromatography, filtration, and ultrafiltration to achieve high purity and yield.

Quality Assurance (QA) / Quality Control (QC) Scientist: Ensures that biopharmaceutical products and processes meet strict regulatory standards and quality specifications throughout development and manufacturing, performing testing, audits, and documentation.

Regulatory Affairs Specialist: Navigates the complex landscape of global biopharmaceutical regulations (e.g., FDA, EMA), preparing and submitting documentation for drug approvals, ensuring compliance, and interacting with regulatory agencies.

Validation Specialist/Engineer: Conducts and documents validation studies for equipment, processes, and cleaning procedures in biopharmaceutical manufacturing to ensure they consistently meet quality and regulatory requirements.

Bioprocess Automation Engineer: Designs, implements, and maintains automation systems (e.g., PLCs, DCS) used in biopharmaceutical manufacturing facilities to control and monitor bioprocesses efficiently and reliably.

Field Application Scientist (Bioprocessing): Provides technical support and expertise to customers using bioprocessing equipment, reagents, or services, often involving troubleshooting, training, and demonstrating new technologies.

Project Manager (Biopharmaceutical Development/Manufacturing): Manages complex projects within biopharmaceutical companies, overseeing timelines, budgets, and resources for drug development, facility construction, or process improvement initiatives.


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