Job Scope
The position reports to the Sr. Scientist, Viral Vector Process Development & MSAT Department. This role is ideally suited for a dynamic bench-focused individual to support translation of research process to GMP-compliant manufacturing. This is a great opportunity to join a fast-paced company, develop, and expand technical expertise while gaining core competency in the biotechnology/life sciences industry.
The individual must currently be an active student in either and undergraduate or graduate programResponsibilities
- Hands-on experimental work in the development and optimization of upstream unit operations (cell culture, transfection, and harvest/clarification) for viral vector manufacturing process.
- Contribute to the planning and execution of cell-culture related experiments to analyze, interpret, and report data summary packages.
- Collaborate with internal/external partnerships to evaluate and implement new bioprocessing technologies and strategies.
- Collaborate with cross functional leads (Manufacturing, Quality Assurance, Quality Control) to support process technology transfer, cGMP risk evaluation, and deviation management.
- Maintain and follow detailed and comprehensive batch records.
- Support scientists in PD viral vector production/purification process
- Learn and perform core bioprocessing techniques such as cell culture, Single Use bioreactor production, Ultrafiltration/Diafiltration and chromatography purification.
- Review and assess production materials purchasing, storing, and monitoring
- Participate in team group discussions as well as the intradepartmental meetings
- Presentation of final project summary in functional subgroup
- Read and understand scientific literature in gene and cell therapy, use the knowledge to generate ideas and contribute to process design and development.
Basic Qualifications
- Must currently be an active student pursuing a Bachelor’s or Master’s degree with 0-1 years of experience in Biology, Biochemistry, Immunology, Chemical Engineering or equivalent in biotech development with particular experience in gene and cell therapy product design. Experience with Oncolytic, Lentivirus, AAV process development for oncology a plus.
- Previous wet lab experience cell culturing, chromatography, and/or PCR is preferred.
- Good understanding of Design of Experiment and statistical analysis.
- Strong interpersonal, time management, and oral/written communication skills.
#PB
#LW
GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.
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What We Do
Founded in 2002 and listed on the Hong Kong Stock Exchange in 2015, GenScript has an established global presence across Greater China, North America, the EU, and Asia Pacific. Today, over 300,000 customers from over 160 countries and regions worldwide have used GenScript’s premier, convenient, and reliable products and services. GenScript currently has over 5,000 employees globally, 33% holding master’s and/or Ph.D. degrees. In addition, GenScript has a number of leading commercial technologies developed in the fields of synthetic biology, immunotherapy, antibody design, chemical synthesis, and bioinformatics, including more than 100 patents and over 270 patent applications. As of June 2022, GenScript's products and services have been cited by 74,700 scientific papers worldwide. GenScript is committed to striving toward its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.
