Qualifications

(1) More than 5 years experience in CxO business, sales or BD position;

(2) Experience in clinical supply chain related field is preferred;

(3) Bachelor degree or above, pharmacy, clinical, biological, marketing, business management, supply chain and other related majors;

(4) English listening, speaking, reading and writing fluently;

(5) under 40 years of age priority;

Job responsibilities

(1) Responsible for the introduction of projects in the company's clinical supply chain business and achieving the company's annual turnover and profit targets;

(2) Find and develop target customers, establish and maintain relationships with key customers, understand customer needs, provide solutions, and seek long-term cooperation opportunities;

(3) Responsible for project bidding, quotation, commercial negotiations and other pre-sales affairs, with customers on the project contract tracking and negotiation;

(4) Plan and execute marketing activities for products or services to improve the company's visibility and competitiveness in the target market;

(5) Manage the business development team, including recruiting, training, mentoring and evaluating the performance of team members;

(6) Communicate with relevant departments within the company, integrate resources, and promote the rapid development and smooth operation of the company's business;

(7) Regularly report to senior management on the progress and results of business development and provide data-supported decision-making recommendations;

Qualifications

(1) Familiar with domestic and foreign GSP\GMP\GCP and other pharmaceutical related laws and regulations;

(2) Able to work in English working environment;

(3) Able to skillfully use office software (Excel, word, PowerPoint, etc.) and ERP system;

(4) Graduated from pharmacy, clinical, biological, management, supply chain related majors;

(5) Two years or above clinical trial supply chain or clinical research related working experience is preferred;

Job responsibilities

(1) Able to communicate and cooperate with sponsors, CROs, and customers of new drug development institutions to develop supply chain solutions that meet regulatory requirements and ensure timely delivery of drugs for clinical trials;

(2) Draft project description, drug management manual, participate in the preparation and revision of clinical supply chain SOP, and constantly improve the existing process;

(3) Provide supervision for the storage and cold chain transportation of drugs for clinical trials, including but not limited to the review of process specifications, deviation control, batch records, distribution instructions and procedures and documents related to order processing and delivery;

(4) Be familiar with the blind management requirements, packaging design, packaging standards and processes of clinical trial drugs, and be able to provide process supervision and guidance for the secondary packaging and labeling of experimental drugs;

(5) responsible for daily project management, customer communication and relationship maintenance, problem follow-up;

(6) Responsible for monthly bill review, invoicing and collection management;

(7) Responsible for supplier management;

(8) Management of customer agreements, contracts, order documents and other documents;

(9) Cooperate with quality to complete customer audits;

(10) Complete other business tasks arranged by superior leaders;

Qualifications

(1) Bachelor degree or above in pharmacy major or medicine, biology or chemistry related major, or intermediate professional technical title or licensed pharmacist qualification;

(2) Familiar with drug research and development, GMP, GSP, GCP and other relevant laws and regulations, familiar with medicine-related laws and policies, with certain management knowledge and logistics knowledge;

(3) Good English reading and writing ability;

(4) More than 2 years of practical experience in drug research and development or drug production quality management, clinical supply chain related quality management experience is preferred; familiar with the quality management process methods;

(5) have good communication and expression skills, with a sense of teamwork.

Job responsibilities

(1) to assist the company quality system establishment, internal self-inspection, external quality audit, verification and audit release and other quality management activities;

(2) Participate in the formulation and implementation of annual and medium-term development plans for the company's quality management;

(3) Review or review the process of receiving, accepting, warehousing, warehousing and storage of drugs or materials;

(4) Manage the production plan and process of secondary packaging and labeling of drugs for clinical trials, and conduct on-site quality supervision;

(5) Learn about the latest regulations and quality requirements related to the supply of drugs for clinical trials, and train relevant personnel;

(6) Manage the change, deviation and CAPA process to ensure that all major deviations and inspection results have been investigated and dealt with in a timely manner;

(7) Prepare verification plans and reports to ensure the completion of all necessary confirmation or verification work;

(8) Receive customers and official audits and inspections, organize relevant personnel of the company to assist in the inspection, and ensure that defective items are effectively rectified; approve the company-level self-inspection plan and report to ensure the completion of self-inspection.

(9) Organize the evaluation, approval and audit of suppliers.

(10) Maintain good communication with government regulatory agencies such as the Market Supervision Administration and the Food and Drug Administration to maintain the company's quality image;

Qualifications

(1) Junior College degree or above, major in medicine, pharmacy, biology, logistics, supply chain, etc.

(2) Have a comprehensive understanding of warehousing, logistics and supply chain knowledge;

(3) Knowledge of pharmaceutical production, especially pharmaceutical packaging;

(4) Proficient in operating various ERP systems;

(5) Understand the requirements of drug research and development, GMP, GSP, GCP and other relevant laws and regulations;

Job responsibilities

(1) Warehousing: record the arrival information of drugs or materials, check the completeness and accuracy of the arrival documents, check the integrity of the outer package, and download the temperature with the goods; Perform the acceptance of drugs or materials, check specific information, and record abnormalities such as deviation/damage; Complete system filling and storage on shelves as required;

(2) Outgoing: sorting drugs or materials according to the outbound order to ensure no deviation and damage; Review the outbound drugs or materials to ensure that the drugs are consistent with the order and picking list; Organize delivery to ensure that the products are packaged in good condition, complete documents, accurate thermometer settings and accurate outbound;

(3) Packaging production: Participate in pre-packaging training, perform primary packaging or secondary packaging and labeling work in accordance with the project operation guide, and ensure packaging quality and progress;

(4) Inventory counting: Perform inventory counting to ensure that the system inventory is consistent with the actual inventory, and provide timely feedback until the problem is solved;

(5) Warehouse management: to ensure that the warehouse is clean and orderly, and to carry out safety inspection, temperature and humidity inspection and record according to regulations;

(6) Facilities and equipment management: daily management, maintenance and repair of facilities and equipment to ensure the safety and working status of equipment in any emergency state.

(7) document management: related documents sorting, review, filing;

(8) Other related work assigned by leaders;