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Senior QC Specialist

genscript · 30+ days ago
Negotiable
Full-time
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About GenScript

GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.

GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology

About ProBio

ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy (CGT), vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio’s total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. In terms of plasmid service, ProBio supports the most clinical approvals for CGT drugs including mRNA vaccines, CAR-T in China. It is also the first GMP manufacturing platform to provide in vitro transcription (IVT) template linearized plasmids for mRNA vaccines and has supported several mRNA vaccine global enterprises to obtain clinical approvals. In terms of viral vector service, \ProBio has a stable and high-yield viral vector platform.

Job Scope:

  • Responsible for coordinating QC and QA work in the team
  • Responsible for the completion of key orders and trouble shooting
  • Responsible for statistics and analysis of production data, and assist the supervisor to optimize and improve the production process or technology
  • Participate in or be responsible for the management of multiple promotion projects and promote the achievement of project objectives
  • Responsible for the formulation and update of SOP, summarize and solidify work experience and train up junior employees
  • Assist the supervisor to complete quality monitoring and safety inspection, and timely complete problem rectification
  • Complete other tasks assigned by the supervisor

Key Requirements: 

  • Bachelor’s degree or above in cell biology, molecular biology, biomedicine and other related majors
  • Familiar with the experimental operation of SDS-PAGE, Western blot, LC-MS, HPLC and other protein detection, with more than 3 years of laboratory experience
  • Good trouble shooting and project management skills
  • Good communication skills (verbal and written)
  • Good team working skills

 

#GS

#LI-LF1

 

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.

Last updated on Aug 15, 2024

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