1. Supplier & Product Pipeline：Source, onboard, and manage new suppliers/products to expand portfolio;
2. Go-to-Market Execution：Lead product launches, market research, and promotional campaigns; ensure real-time market intelligence updates;
3. Commercial Strategy：Adapt sales approaches to industry shifts, support key account management, and drive client engagement.    

1. Bachelor's degree or above in pharmaceuticals, biology, or related fields;
2. More than 3 years of experience in the pharmaceutical industry with strong market sensitivity;
3. Proficient in English as a working language; Willing to travel internationally.    

1. Business Development: Identify, onboard, and nurture client relationships to drive long-term partnerships and revenue growth;

2. Strategic Sales Execution: Develop territory-specific sales plans, lead negotiations, and ensure timely project delivery and payment collection;

3. Market Intelligence: Conduct regular client visits to assess needs, monitor competition, and tailor solutions to market demands.

1. 10+ years in B2B sales within pharmaceutical machinery, process equipment, or turnkey engineering solutions；Proficiency in spoken English is a plus；
2. Hunter mentality with proven ability to open new accounts, coupled with strong negotiation and relationship management skills;
3. Agile, data-driven, and resilient—able to thrive in a fast-moving industry with shifting client priorities.    

1. Technical Contract Review – Evaluate and approve technical specifications for new project contracts;
2. Process Design & Optimization – Develop detailed engineering designs for pharmaceutical equipment, systems, or facilities;
3. Technical Leadership – Provide guidance during design handovers,  FAT, SAT and construction phases.    

1. Bachelor’s degree or higher in Pharmaceutical Engineering, Chemical Engineering, Bioengineering, or related field;Proficiency in spoken English is a plus；
2. 5+ years in process design for pharmaceutical equipment/engineering, with strong knowledge of GMP regulations;
3. Collaborative, communicative, and willing to travel occasionally. English fluency is a plus.    

1. Mechanical Design & Documentation：Develop technical drawings and BOMs per project requirements;

2. Standardization Support：Assist in establishing and maintaining mechanical design standards;

3. Technical Documentation：Prepare and organize project files, including design specifications and reports;

4. On-Site Technical Support ：Provide engineering guidance during installation and commissioning.    

1. Bachelor’s degree or higher in Mechanical Engineering or related field;Proficiency in spoken English is a plus；
2. 5+ years in mechanical design, with expertise in national/industry standards (e.g., GB, ASME). Proficiency in 2D/3D CAD tools (e.g., AutoCAD, SolidWorks);
3. Experience in pharmaceutical equipment/system design and R&D is highly valued.    

1. Control System Programming & On-Site Commissioning：Develop automation software and execute field debugging for project execution;
2. Control Documentation：Prepare I/O lists, BOMs, and functional specifications (FS/CLL/SDS) for automation systems;
3. Project Coordination：Ensure timely completion of automation tasks to support overall project delivery and final acceptance.    

1. Associate degree or higher in Automation, Electrical Engineering or related field;Proficiency in spoken English is a plus；
2. Minimum 3 years' experience in automation projects with proficiency in standard programming software and independent programming/debugging capabilities;
3. Pharmaceutical industry automation experience preferred.    

1. Operate validation test equipment and complete testing activities;Organize test data, perform statistical analysis, and prepare validation reports;
2. Execute company project management processes for validation work;Coordinate internal/external resources to manage validation implementation;
3. Track and maintain compliance with GMP regulations (China, EU, FDA, WHO, PDA, ICH, ISO).

1. Bachelor's degree in Pharmaceuticals, Chemical Engineering, Biology or related field;Proficient in English as a working language；
2. 3+ years pharmaceutical experience with 1+ year validation experience. Full validation experience for new equipment/systems,

validation experience under EU/FDA/WHO standards;

3. Team leadership in equipment/system commissioning are preferred.