Job Responsibilities:

1. Objective & Plan Management: Formulate production targets, technical task objectives and detailed implementation plans in accordance with the company’s annual business management goals, and drive the execution and fulfillment of set targets.

2. Production Process Control: Organize and execute production schedules, coordinate and resolve on-site issues arising from production activities in real time.

3. On-time Delivery Assurance: Overall coordinate and supervise adjustments and revisions of production operation plans, establish flexible response mechanisms to ensure on-time order delivery and meet customer requirements.

4. Quality & Safety Supervision: Conduct full-process quality control on purchased semi-finished goods and finished products in strict compliance with production specifications and quality requirements to prevent non-conforming products from flowing into subsequent processes; implement work safety accountability to avoid safety incidents.

5. Process Specification Establishment: Draft and continuously optimize workshop Standard Operating Procedures (SOP) and safety regulations, organize staff training and supervise implementation to consolidate the foundation of production safety.

6. Team Management & Training: Arrange daily workload for workshop production personnel, conduct vocational skill improvement and production safety training, and build an efficient, compliant and safe production team.

Job Requirements:

1. Bachelor’s degree or above, majoring in Materials Science, Chemical Engineering and Technology or related disciplines.

2. Familiar with production process principles, quality standards and safety specifications of pharmaceutical intermediates, APIs or pharmaceutical manufacturing; equipped with systematic expertise in production management, quality management and safety management, and knowledgeable about core industry codes including GMP and work safety standardization regulations.

3. Over 5 years of working experience as production supervisor/manager, among which no less than 3 years in production operation management for pharmaceutical intermediates, APIs or pharmaceutical manufacturers, capable of independently overseeing the entire production workflow.

Implement standardized procedures of the quality system in compliance with GMP requirements.

Job Responsibilities:

1. Document Management and System Establishment: Organize the compilation, revision and implementation of quality management documents, formulate in-house inspection SOPs, and regularly evaluate the effectiveness and applicability of the quality assurance system.

2. Material Quality Control: Ensure accurate procurement and usage of raw, auxiliary and packaging materials, and assess the quality systems of key material suppliers together with relevant departments.

3. In-process Quality Control: Manage intermediate product control items, promote validation activities, and rigorously carry out in-process inspection, testing, review and deviation handling.

4. Product Release and Non-conforming Goods Disposal: Formulate and administer sampling and retention sample protocols, approve the release of raw & auxiliary materials and finished products, and review disposal procedures for non-conforming items.

5. Quality Stability Assessment: Evaluate the quality stability of raw materials and finished products to provide data for defining material shelf life and product expiry period.

6. Post-market Quality Handling & Record Administration: Handle product returns, recalls and customer complaints arising from quality defects; manage quality documents and original test records to guarantee product quality remains intact during storage, shipment and subsequent handling.

Job Requirements:

1. Bachelor’s degree or above in Chemistry, Pharmacy or other related disciplines.

2. Familiar with lab analysis and testing operations in manufacturers engaged in R&D and production of pharmaceutical intermediates and APIs.

3. Minimum 2 years of quality management experience with full understanding of the entire product lifecycle covering production, testing, release, traceability and product recall.

4. Strong capabilities in planning, execution, communication, organization and coordination.

5. Candidates with experience in on-site GMP certification inspection for pharmaceutical manufacturers are preferred.

Job Responsibilities:

1. Take charge of protocol design and experimental implementation for fermentation and enzymatic catalysis projects of the company;

2. Conduct screening and optimization of existing microbial strains;

3. Establish fermentation processes for new products and explore & optimize fermentation process control parameters;

4. Explore practical applications of novel AI-aided enzyme design tools;

5. Assist in troubleshooting technical challenges encountered during R&D and production;

6. Complete other assignments arranged by the department supervisor.

Job Requirements:

1. Master’s degree or above in Synthetic Biology or related majors;

2. Prior R&D experience in industrial microbial fermentation (such as Escherichia coli, yeast) is preferred;

3. Hands-on experience in directed evolution, metabolic engineering, protein engineering and CRISPR technology is preferred;

4. Innovative thinking and proficient problem-solving skills;

5. Familiar with protein structure prediction models including AlphaFold, basic knowledge of Python; experience in model inference, computing resource deployment or bioinformatic analysis is preferred;

6. Strong sense of responsibility, proactive working attitude, good communication skills and teamwork spirit.