What are the responsibilities and job description for the Product Inspection Platform Supervisor position at GenScript?
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 Title: Product Inspection Platform Supervisor
Location: Piscataway, NJ
Responsibilities
Operations Management: Responsible for the daily operations of the order and quality management team, coordinating internal and external resources, analyzing internal production data, adjusting work plans in a timely manner to achieve objectives, optimizing, training, implementing, and supervising job SOPs to enhance operational efficiency, and ensuring the smooth functioning of the team.
Team Management: Assist the department in continuously enhancing platform technology and building a talent echelon, formulate and assess team members' PBC (Personal Business Commitments) and job KPIs (Key Performance Indicators).
Quality Management: Optimization of plasmid detection and release-related system processes, assessment of job risk points, process streamlining, to ensure product quality and timeliness meet customer requirements.
Platform Management: Improve the order distribution system and the system for entering shipping information.
Other Duties: Cooperate and assist with the completion of related job functions within and outside the department; complete temporary critical tasks assigned by senior management.
Qualifications
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.
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 Title: Product Inspection Platform Supervisor
Location: Piscataway, NJ
Responsibilities
Operations Management: Responsible for the daily operations of the order and quality management team, coordinating internal and external resources, analyzing internal production data, adjusting work plans in a timely manner to achieve objectives, optimizing, training, implementing, and supervising job SOPs to enhance operational efficiency, and ensuring the smooth functioning of the team.
Team Management: Assist the department in continuously enhancing platform technology and building a talent echelon, formulate and assess team members' PBC (Personal Business Commitments) and job KPIs (Key Performance Indicators).
Quality Management: Optimization of plasmid detection and release-related system processes, assessment of job risk points, process streamlining, to ensure product quality and timeliness meet customer requirements.
Platform Management: Improve the order distribution system and the system for entering shipping information.
Other Duties: Cooperate and assist with the completion of related job functions within and outside the department; complete temporary critical tasks assigned by senior management.
Qualifications
- Bachelor's degree or higher is preferred
- 2~3 years of biological and quality related experience
- Be well-organized, hard-working, proactive, and have good learning ability
- Outstanding interpersonal and communication skills with a proven ability to influence and build consensus across diverse teams
- Proactive, self-motivated, and results-oriented with excellent time management
- Proven leadership experience managing teams or projects
- Excellent language skills in English and Chinese
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.
