Job Description

Key responsibilities of this role include:

• Key point of contact / interface with CDMOs / CROs, managing projects, spanning development and clinical manufacture in close collaboration with Yisheng Biopharma\xe2\x80\x99s technical and functional leads (Drug Substance, Drug product, Analytical, Quality, Supply Chain, and others)
• Ability to work under minimal guidance to manage multiple assignments and/or business processes.
• Build and maintain positive relationships with all Process Development and Operations functions to increase overall efficiency and success of programs.
• Supplier evaluation and outsourcing management including site selection activities.
• Develop scopes of work in close partnership with technical leads and cross functional leads
• Ensure projects and/or programs meet results, compliance, speed, quality, and cost.
• Budget management, including purchase orders, financial forecasting, and associated finance cycles for externalization, adhering to financial targets and systems.
• Establish and maintain external collaborations and monitor supplier performance to continuously improve efficiency and effectiveness of suppliers
• Identify project optimization opportunities (e.g., timeline, budget, technical completion)
• Present analyses and recommendations to Senior Management
• Occasional domestic and international travel to support project results
• Opportunity to lead external projects in areas beyond synthetic small molecule Drug Substance, including hybrid modalities, based on portfolio needs

Basic Qualifications:

• Master\xe2\x80\x99s degree and 8 years of relevant industry experience, within a cGMP manufacturing environment Or
• Bachelor\xe2\x80\x99s degree and 10 years of relevant industry experience, within a cGMP manufacturing environment

Preferred Qualifications:

• Advanced degree in Biological Science or chemical engineering
• Demonstrated understanding of drug development and commercialization for biologicals product, including raw material and starting material sourcing, drug substance manufacture, process development, process engineering, and process characterization
• 2+ years of experience working with domestic and international CDMOs/CROs
• 2+ years of cGMP, Regulatory/CMC, legal, quality requirements, and import/export policies
• Self-starter with a high-level of comfort with ambiguity and complexity and the ability to multi-task while consistently delivering quality results.
• Experienced team member of cross-functional and matrixed teams including effective writing, presentation, and interpersonal skills to address a broad scope of audiences.
• An eye for business, high-level critical thinking, and strong problem-solving skills with the ability to structure, pragmatically scope, and solve problems.
• Demonstrated quantitative skills including experience in business process development, continuous improvement, operational excellence, and performance management.
• Strong knowledge in the use of project management methodologies and tools, resource management practices and change management techniques

Office Address: High Street South Corporate Tower 1, 19th Floor, Unit LZ 12 and 15, 9th Avenue, Corner 16th Street, Bonifacio Global City, Taguig, Philippines Interested applicants are required to email your updated resume/CV to Gabriel Email: gabriel.tan@yishengbio.com WeChat: chenyouren003 Viber: +65 8821-3425 Corporate Website: http://www.liaoningyishengbio.com/

Applicants who possess relevant experience for the above responsibilities are most welcome to apply. If you do not possess the above experience, your application will still be considered on individual merits, and you may be contacted for other opportunities. By submitting your personal data and/or resume, you give consent to collection, use and disclosure of your personal data and/or resume by the company for the purpose of the processing and administration by the company relating to this job application.