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Strictly execute RCV projects in accordance with standard testing operating procedures, including but not limited to RCL testing, rcAAV testing, RCA testing, and RCR testing.

Familiar with relevant biosafety knowledge, with strong self-protection awareness; prior experience in P3 laboratories is preferred.

Good awareness of GMP and GDP requirements.

Responsible for documenting experimental raw data, archiving original records, and issuing individual test reports.

Prepare reagents for testing experiments, manage material requisitions, and conduct regular cleaning and maintenance of the laboratory.

Operate equipment correctly and in full compliance with standard operating procedures, and maintain corresponding operation records.

Responsible for inventory updates and procurement applications for testing‑related materials and reagents.

Senior/Intermediate Testing Engineers are also required to draft validation protocols for new testing methods, execute validation experiments, and summarize validation reports.

Key Skills:​

Proficient in experimental techniques such as cell culture.

Familiar with TCID50 and virus inoculation procedures; prior experience is preferred.

Independent and innovative thinking, strong logical reasoning, attention to detail, adept at analysis and problem‑solving, and highly execution‑oriented.

Responsibilities:​

Assist in advancing the validation of qPCR testing methods.

Master experimental skills such as qPCR.

Conduct project qPCR testing tasks according to work plans and ensure on‑time completion.

Complete experimental raw data records, organize project raw data, and generate result reports.

Manage inventory updates and procurement applications for experimental reagents and materials.

Operate, maintain, and clean related instruments and equipment, and document activities accordingly.

Familiar with regulatory requirements such as pharmacopoeia and GMP.

Perform other tasks as assigned by supervisor.

Qualifications:​

Bachelor's degree or above in a biology‑related field.

1–2 years of laboratory experience; fresh graduates are also welcome.

Understanding of molecular biology experimental techniques and qPCR theoretical knowledge.

Complete tasks with quality and on schedule, without delays or negative work attitude, provide timely feedback, and meet expected outcomes.

Willing to work overtime as assigned by supervisor.

Responsibilities:​

Conduct market research in the assigned region, identify potential customer clusters, analyze competitive landscapes, and formulate market expansion strategies.

Based on the company's overall business objectives, develop a business plan for the assigned area, including sales targets, key client lists, and activity planning.

Systematically collect, analyze, and report customer needs, technical challenges, competitor activities, and market trends, providing key inputs for company and product strategy adjustments.

Proactively identify and validate sales leads and explore business opportunities through industry conferences, literature review, interpersonal networks, and independent visits, among other channels.

Engage deeply with customer groups to uncover potential market demands.

Lead the quotation process, contract negotiations, bidding activities, and follow through to sales closure and payment collection.

Perform other tasks as assigned by supervisors.

Qualifications:​

Bachelor's degree or above in a biology-related field.

Outgoing personality, excellent communication skills, and the ability to communicate in daily English is preferred.

Strong sense of responsibility, diligence, logical reasoning ability, and a well-organized work style.

At least 2 years of work experience.

Collaborate with partner hospitals to interpret the core requirements of Decree 818, assist in organizing clinical translation filing materials, and ensure full compliance with regulatory standards throughout the cooperation process.

Fulfill industrial client needs: Interface with industrial clients regarding technology translation requirements, deliver customized solutions, track project implementation progress, and coordinate to resolve execution challenges.

Professional enablement for the sales team: Provide training on Decree 818 compliance and technology translation knowledge to the sales team, and address professional inquiries during client interactions.

Technical support collaboration and management: Establish a sales‑technical support coordination mechanism, define response timelines for client issues, and oversee issue resolution to closure.

Holistic project coordination and advancement: Lead the alignment of internal technical platforms, develop milestone plans covering the entire translation process, and ensure project delivery.

Coordination in tackling technical bottlenecks: Organize cross‑departmental workshops to formulate and implement solutions for technical challenges encountered during translation.

Quality and compliance control in translation: Work with the Quality Assurance Center to conduct quality reviews of the translation process in accordance with Decree 818, ensuring compliance and output quality.

Implementation of compliance systems: Develop compliance management procedures for translation activities, organize internal compliance training, and maintain end‑to‑end regulatory adherence.

Pipeline target management and assessment: Set annual/quarterly pipeline targets, allocate responsibilities to relevant teams, implement performance evaluation, and review operational outcomes.

Fulfill other duties assigned by supervisors: Support the overall company development strategy and carry out other related tasks as assigned by senior management.