Lean Specialist

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, 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. Key Responsibilities Diagnose on-site pain points and work with the production team on implementing and sustaining improvements Responsible for ensuring that continuous improvement opportunities are identified, and that any barriers and issues are raised, communicated and removed in a timely fashion Develop monthly work plans and implement them based on established change control procedures Ensure that process and product documentation are updated and maintained to reflect the current approved process and settings Improve the production capacity of the connected business lines and reduce costs Undertake the information collection and data feedback tasks within their reporting department Actively participate in the planning and implementation of company-wide lean activities including gathering training materials and initiating regular communication to disseminate content. Actively cooperate with the work related to internal cooperation of the team, and deliver the required work results in a timely manner Comply with company and laboratory safety-related rules and regulations and confidentiality systems, and complete other job-related tasks as arranged by superior(s). Qualifications and Preferred Skills Bachelor with 1 year of relevant industry experience or MS degree, in Industrial, Biological or Chemical Engineering or a related field Proven track record of in production process analysis and improvement Proficiency in process analysis methodologies such as Lean Six Sigma (Certified Green Belts would be preferred)Proficient in operating Office, Visio, CAD, JMP and other software, with the ability to analyse, problem-solve and present findings in a clear logical manner. Ability to adapt in a fast-paced, changing environment with good work ethic, strong communication, analytical, creative problem-solving and stakeholder management skills, and emotional intelligence 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. #J-18808-Ljbffr