【Job Responsibilities】: 1. Establish and expand domestic and international client relationships, maintain communication with potential partners, follow important industry trends, and stay sharp and sensitive to market changes.
2. Participate in business cooperation-related engagements, including pre-cooperation and during cooperation research and analysis, negotiation of cooperation details, terms negotiation, agreement signing, payment processes, as well as post-agreement tracking and implementation management.
3. Assist in the analysis, research, and feasibility assessment of target projects or potential cooperation opportunities, organize internal project initiation materials, evaluation reports, and review proposals.
4. Follow and track domestic and international industry news, organize industry information for internal learning and reference, explore cooperation opportunities and partners, negotiate and design cooperation models, and maintain close contact and communication.
5. Based on the company's development direction and needs, assist in tracking and collecting key dynamic information from domestic and international industries, regularly compile and organize it into a presentable form for management reference.
6. According to the company's and department's strategic planning, assist in acquiring external cooperation opportunities and coordinate internal resources to actively promote project progress.

【Requirements】: 1. Master's degree or above in Nuclear Medicine, Pharmacy, Clinical Medicine, Biology, or related biomedical fields.
2. 5-10 years of work experience in the pharmaceutical industry, strong communication skills, some negotiation experience, proficient in English listening, speaking, reading, and writing, experience in license in/out, alliance management experience.
3. Strong information search and literature retrieval ability, good at summarizing, with certain problem analysis and solving ability.
4. Ability to adapt to short-term business trips, proficient in using office software.
5. Capable of working in English, proficient in English reading, writing, and communication.
6. Gender is not limited, honest and upright, dedicated and diligent, strong execution ability, and self-learning awareness.

【Job Responsibilities】: 1. Responsible for radiochemical labeling, formulation process research, process validation, and related registration data review in drug development.
2. Develop project plans, reasonably arrange subordinates to carry out work, provide business guidance, and ensure project progress and quality.
3. Organize subordinates to accept registration research on-site inspections, assist with registration production site inspections, and respond to supplementary opinions related to processes during drug registration.
4. Responsible for team building, department management, personnel development, with a focus on training and enhancing technical personnel.

【Requirements】: 1. Ph.D. with at least 5 years, Master's with at least 8 years, or Bachelor's with at least 10 years of drug development experience, with preference for experience in radiopharmaceutical development.
2. Educational or professional background in chemistry, radiochemistry, radiopharmaceutical chemistry, radioactive isotopes, nuclear medicine, or nuclear physics.
3. Independently handled at least 5 drug development projects, capable of independently completing radiochemical labeling, formulation process research, process validation, familiar with related technical requirements of active pharmaceutical ingredients and injectables.
4. Familiar with drug development, registration processes, and requirements, able to complete related registration application materials as required.
5. Strong problem analysis and solving ability, capable of leading a team to solve project difficulties.
6. Strong communication and coordination skills, rich department management experience.
7. Proficient in English reading and writing, able to independently review and translate related literature.
8. Exceptional candidates may be granted equity incentives.

【Job Responsibilities】: 1. Responsible for quality research, stability studies, and related registration data review in drug development.
2. Based on project plans, reasonably arrange subordinates to carry out work, provide business guidance, ensure project progress and quality.
3. Organize subordinates to accept registration inspections, assist with registration production site inspections, and respond to supplementary opinions related to analysis during drug registration.
4. Responsible for team building, department management, personnel development, with a focus on training and enhancing technical personnel.

【Requirements】: 1. Bachelor's degree or above in Pharmacy or related fields, with 10+ years of experience in drug development analysis and 6+ years of management experience, with preference for experience in radiopharmaceutical development.
2. Independently handled more than 6 drug development projects, capable of independently completing quality research work, familiar with related technical requirements of active pharmaceutical ingredients and injectables, familiar with main analytical instruments.
3. Familiar with drug development, registration processes, and requirements, able to complete related registration application materials as required.
4. Ability to build R&D systems and strong problem analysis and solving ability, capable of leading a team to solve technical barriers in projects.
5. Strong communication and coordination skills, rich department management experience.
6. Proficient in English reading and writing, able to independently review and translate related standard literature.
7. Exceptional candidates may be granted equity incentives.

【Job Responsibilities】: 1. Assist the General Manager in handling daily affairs of the production center and coordinating resources among the divisions of the production center.
2. Assist the General Manager in formulating the annual strategic plan of the production center, assisting in the implementation of work goals for various divisions and stages, tracking progress, and conducting assessments.
3. Responsible for establishing a production technology training improvement plan for the production center, coordinating the organization of professional ability training and evaluation for each division of the production center.
4. Participate in solving technical and quality issues during the production process, optimizing production processes, coordinating the configuration, organization, management, and work arrangements of workshop personnel to ensure normal production operations.
5. Assist in the construction of production quality systems for each division to meet FDA/GMP and customer audit requirements.
6. Complete other related tasks assigned by superiors.

【Requirements】: 1. Master’s degree or above in Nuclear Medicine, Pharmacy, Chemistry, or related fields.
2. More than 5 years of relevant work experience in radiopharmaceutical research and production.
3. Familiar with relevant laws, regulations, standards, and guidelines in the pharmaceutical industry; understanding of radiopharmaceutical process development or production processes; certain experience in radiopharmaceutical production and quality management.
4. Strong communication, coordination, learning, and adaptability skills, with problem-solving abilities and the capacity to handle pressure.
5. Under 40 years old.

【Job Responsibilities】: 1. Responsible for the procurement of consumables, reagents, low-value items, equipment, and services according to the tasks assigned by the purchasing supervisor.
2. Liaise with various departments on relevant business and procurement process training, and coordinate between divisions.
3. Strictly follow procurement procedures, conduct inquiries/comparisons, sign procurement contracts, and communicate contract terms to save company costs and control procurement costs.
4. Conduct market research, develop new suppliers, and develop alternative products to find cost-effective suppliers and products.
5. Perform other work tasks assigned by leadership.

【Requirements】: 1. Bachelor's degree or above, 1-3 years of relevant procurement experience in the pharmaceutical industry, preferably with CDMO experience.
2. Excellent verbal communication and business negotiation skills, clear and principled in work.
3. Good cost control ability, serious and responsible, fair and honest.
4. Proficient in computer and office software operations.

【Job Responsibilities】: 1. Responsible for the overall accounting processing of the company.
2. Review financial documents: expense reimbursements, fund reviews, etc.
3. Regularly review general and detailed accounts, ensuring consistency.
4. Regularly reconcile with business departments, ensuring consistency between accounts and actual situations.
5. Handle daily issuance of various invoices and tax declarations.
6. Liaise with tax, banking, industrial, and commercial departments.
7. Assist in completing regular audit-related work.
8. Complete other tasks assigned by superiors.

【Requirements】: 1. Bachelor’s degree or above in Accounting or related fields.
2. 3-5 years of work experience, with at least 2 years in general ledger accounting.
3. Experience in overall accounting processing, preferably in manufacturing or R&D enterprises.
4. Proficient in financial-related office software.
5. Good communication and coordination skills, able to handle significant pressure.

【Job Responsibilities】: Implement HR and administrative services according to headquarters policies, systems, and processes, including but not limited to:
1. Local employee relationship management, policy-based welfare maintenance, and employee master data management.
2. Salary budget, calculation, and analysis.
3. Local employee recruitment and talent development to ensure the quantity and quality of employees match business development needs.
4. Employee communication, culture building to enhance team cohesion and positivity.
5. Administrative external relations, customer reception, continuously maintaining and enhancing the company's brand image.
6. Management of administrative resources such as cafeteria, dormitory, cleaning to provide warm services for employees.
7. Horizontal support, participation in headquarters project-based work.
8. Other tasks assigned by leadership.

【Job Responsibilities】: 1. Assist in conducting feasibility assessments and external business quotations based on company resource information.
2. Assist R&D project leaders in forming project teams, developing project plans, setting major milestones, and breaking down project tasks.
3. Supervise project execution according to plan, pre-empt deviations from the actual execution plan, carry out necessary changes, and predict and control project risks.
4. Supervise internal project deliveries, organize project phase summaries, and review meetings, establish and manage R&D project archives.
5. Coordinate internal and external cooperation, communication, and liaison, tracking the progress of project cooperation units to ensure smooth project progress.
6. Determine income and payment milestones, initiate accounts receivable processes in time, and organize project closure work promptly.
7. Complete other tasks assigned by superiors.

【Requirements】: 1. Bachelor’s degree or above in Pharmacy or related fields, with at least 1 year of R&D or project management experience for Master's holders, or at least 3 years for Bachelor's holders.
2. Positive work attitude, good service awareness, and excellent team coordination skills.
3. Proficient in using computers and project management software.
4. Good English reading, writing, and speaking skills.

【Job Responsibilities】: 1. Ensure that testing processes, execution, and laboratory environments comply with EHS and cGMP requirements.
2. Arrange, coordinate, and track work within the physics and chemistry group based on project and operational needs.
3. Manage the entire lifecycle of QC-related products, including sampling, receiving, testing, reporting, and sample disposal, ensuring data integrity.
4. Confirm, calibrate, validate, maintain, and repair laboratory instruments and equipment.
5. Investigate OOS (Out of Specification), OOT (Out of Trend), and abnormal phenomena in the laboratory testing process.
6. Draft plans and reports for CV (Chemical Validation), PV (Process Validation), MV (Method Validation), MT (Method Transfer), and draft STP (Standard Test Procedures) and SOP (Standard Operating Procedures).
7. Train and mentor new and existing QC staff.
8. Manage stability investigations for relevant materials.
9. Support production process validation, cleaning validation, and environmental monitoring.
10. Support quality-related customer audits and complaint investigations.
11. Perform other tasks assigned by supervisors.

【Job Responsibilities】: 1. Responsible for GMP system document management, able to establish, maintain, and improve quality system documents and review various documents. Responsible for the preparation and improvement of quality management system-related documents and processes.
2. Collect various pharmaceutical management and related laws, regulations, and technical requirements. Able to propose modification requirements for relevant documents according to regulatory requirements and regularly participate in system document reviews.
3. Responsible for change control, deviation investigation, OOS investigation, and CAPA tracking and confirmation.
4. Receive quality complaint information, report it in a timely manner, and cooperate in complaint investigation work.
5. Organize and implement relevant training according to regulatory and system requirements.
6. Conduct various quality supervision and inspection work.
7. Organize and implement material audit management work.
8. Participate in quality system self-inspections and GMP compliance inspections.

【Requirements】: 1. Graduated in Pharmacy or related fields, with at least 6 years for an associate degree, 5 years for a bachelor's degree, or 3 years for a master's degree.
2. Familiar with GMP and relevant laws, regulations, and guidelines related to radiopharmaceuticals.
3. At least 3 years of pharmaceutical production quality management experience, with no less than 1 year of experience in managing sterile/injectable radiopharmaceuticals.
4. Good communication and coordination skills.
5. Proficient in using office software and relevant management software.

【Job Responsibilities】: 1. Responsible for establishing and maintaining the pharmaceutical quality management system, drafting and revising internal quality documents.
2. Organize and promote the implementation and continuous improvement of the quality management system.
3. Familiar with quality control in product development processes, able to guide related activities in the input, output, analysis, and improvement stages of R&D.
4. Responsible for project review and checking the integrity and standardization of original records.
5. Ensure production site monitoring management according to GMP requirements, coordinate technical transfer from R&D to production, participate in laboratory audits, and manage audit records.
6. Conduct quality management-related training, establish personnel quality awareness, and ensure personnel work according to requirements.
7. Draft or revise documents for deviations, CAPA, changes, self-inspection management, number and track events according to document requirements, submit solutions, and supervise execution.
8. Responsible for verification management, auditing verification plans, and verification reports.
9. Arrange calibration work for laboratory instruments and equipment.
10. Conduct laboratory site inspections and corrections.

【Requirements】: 1. Bachelor's degree or above in Pharmacy, Biology, Pharmaceutical Preparations, Pharmaceutical Engineering, Biochemistry, or related fields.
2. Familiar with pharmaceutical GMP quality control, related regulations, and guidelines.
3. Over 3 years of experience in pharmaceutical quality management, familiar with clean environment and facility equipment confirmation and validation processes, experience in sterile pharmaceutical GMP certification preferred.
4. Knowledge of microbiology, understanding laboratory workflows, capable of coordinating pharmaceutical R&D management, production management, and inspection work.
5. Strong sense of responsibility, good problem-solving and communication skills, meticulous work style, and good team cooperation spirit.

【Job Responsibilities】: 1. Responsible for inspecting raw materials, intermediates, finished products, and retained samples, determining results, recording, and reporting; maintaining and controlling quality-related documents and records.
2. Draft, revise, and execute operating procedures related to the position, products, and facility equipment; daily inspection, basic maintenance, and periodic calibration of laboratory instruments.
3. Responsible for receiving, distributing, inspecting, and retaining samples; handling post-inspection samples and equipment cleaning; daily management of retained samples and procurement of laboratory consumables.
4. Compile laboratory management documents; participate in instrument calibration or validation, method validation, clean environment, and facility equipment confirmation or validation.
5. Inspect clean environments and purified water, record data accurately and completely.
6. Participate in investigating abnormal data during inspections, investigate and monitor quality incidents, and review product quality analysis.

【Requirements】: 1. Bachelor's degree or above in Chemistry, Analytical Chemistry, Pharmacy, Pharmaceutical Preparations, Pharmaceutical Engineering, Biochemistry, or related fields.
2. Familiar with pharmaceutical GMP quality control and inspection knowledge; understanding laboratory workflows, related regulations, and guidelines, able to conduct excipient and physicochemical testing.
3. Skilled in operating HPLC, GC, IR, ICP-MS, titrator, and other physicochemical testing equipment preferred.
4. Capable of coordinating pharmaceutical inspection and laboratory management work, with certain learning and organizational skills.
5. Strong sense of responsibility, good problem-solving and communication skills, meticulous work style, and good team cooperation spirit.

【Job Responsibilities】: 1. Inspect raw materials, intermediates, finished products, and retained samples, determine results, record, and report; maintain and control quality-related documents and records.
2. Draft, revise, and execute operating procedures related to the position, products, and facility equipment; daily inspection, basic maintenance, and periodic calibration of laboratory instruments.
3. Responsible for receiving, distributing, inspecting, and retaining samples; handling post-inspection samples and equipment cleaning; daily management of retained samples and procurement of laboratory consumables.
4. Compile laboratory management documents; participate in instrument calibration or validation, method validation, clean environment, and facility equipment confirmation or validation.
5. Inspect clean environments and purified water, record data accurately and completely.
6. Participate in investigating abnormal data during inspections, investigate and monitor quality incidents, and review product quality analysis.

【Requirements】: 1. Associate degree or above in Biological Sciences, Biological Engineering, Biotechnology, Biochemistry, Microbiology, Food Science, or related fields.
2. Familiar with pharmaceutical GMP quality control and inspection knowledge; understanding laboratory workflows, related regulations, and guidelines, able to conduct microbiological testing and bacterial endotoxin detection.
3. Skilled in operating microbiological limit instruments, aseptic equipment, wet heat/dry heat sterilizers, biosafety cabinets, and other inspection equipment preferred.
4. Capable of coordinating pharmaceutical inspection and laboratory management work, with certain learning and organizational skills.
5. Strong sense of responsibility, good problem-solving and communication skills, meticulous work style, and good team cooperation spirit.

【Job Responsibilities】: 1. Responsible for research and analysis of key production technologies and equipment, providing decision support for procurement. Supervise and coordinate equipment delivery,installation, acceptance, use, and maintenance. Assist in safety and quality construction work.
2. Supervise and coordinate equipment delivery, installation, acceptance, use, and maintenance.
3. Responsible for production line work.
4. Investigate, analyze, assess risks, and handle deviations in the production process.
5. Manage daily operations of the production operation department.
6. Responsible for product transportation and allocation.
7. Participate in process equipment installation and commissioning.
8. Draft relevant departmental regulations.
9. Establish and optimize internal work processes.
10. Assist in safety and quality construction work.
11. Participate in obtaining drug production licenses and GMP compliance inspections.
12. Build and manage the production team, establish radiopharmaceutical production processes, systems, and operating standards, reasonably allocate resources, and establish a rapid and efficient production operation system.
13. Assist the quality department in validation work.

【Requirements】: 1. Relevant professional background in Radiochemistry, Pharmacy, Bioengineering, Pharmaceutical Engineering, Nuclear Physics, and Nuclear Engineering.
2. Over 5 years of work experience, preferably with experience in radiopharmaceutical manufacturing.
3. Familiar with related regulations and GMP requirements.
4. Familiar with production processes related to radiopharmaceuticals.
5. Proficient in cyclotron and radiolabeling professional knowledge and skills.
6. Strong communication and coordination skills, strong sense of responsibility, good team cooperation spirit.