Recruitment
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Both moral character and ability
Making the most of people's talents
Job Title
Job Location
Job Nature
Salary and Benefits
Number of Recruitments
Head of Drug Analysis
China Peking
Full-time
Negotiable
Unlimited
Job Responsibilities:
1. Responsible for and participate in new drug clinical research (establishment, validation, and implementation of raw material and preparation analysis methods, sample stability test upgrades, etc.);
2. Responsible for the daily maintenance and upkeep of analytical testing instruments;
3. Responsible for summarizing, analyzing, archiving, and recording original records of experimental data, and writing application materials based on this;
4. Responsible for other related work in drug analysis and quality research.
2. Responsible for the daily maintenance and upkeep of analytical testing instruments;
3. Responsible for summarizing, analyzing, archiving, and recording original records of experimental data, and writing application materials based on this;
4. Responsible for other related work in drug analysis and quality research.
Job Requirements:
1. Bachelor's degree or above in pharmaceutical analysis, analytical chemistry, or related major, with more than 5 years of experience in drug research and development;
2. Able to proficiently read and understand Chinese and English literature;
3. Proficient in using HPLC, GC, dissolution testers, UV-Vis spectrophotometers, and other equipment; able to independently develop and validate analytical methods;
4. Familiar with new drug quality research work;
5. Experience in writing application materials and on-site assessments for 3 or more projects;
6. Strong organizational, management, coordination, analytical, and problem-solving skills;
7. Good sense of responsibility and teamwork spirit;
8. Able to withstand the pressure and workload associated with the position.
2. Able to proficiently read and understand Chinese and English literature;
3. Proficient in using HPLC, GC, dissolution testers, UV-Vis spectrophotometers, and other equipment; able to independently develop and validate analytical methods;
4. Familiar with new drug quality research work;
5. Experience in writing application materials and on-site assessments for 3 or more projects;
6. Strong organizational, management, coordination, analytical, and problem-solving skills;
7. Good sense of responsibility and teamwork spirit;
8. Able to withstand the pressure and workload associated with the position.
Synthesis Researcher
China Peking
Full-time
Negotiable
Unlimited
Job Responsibilities:
1. Design drug research and development plans reasonably according to relevant guidelines;
2. Develop reasonable research and development plans and complete relevant tasks according to the planned timeline;
3. Be able to come up with reasonable solutions to problems encountered and implement them;
4. Summarize the research and development work and write application materials according to CFDA requirements;
5. Provide technical guidance and training to subordinate laboratory technicians.
2. Develop reasonable research and development plans and complete relevant tasks according to the planned timeline;
3. Be able to come up with reasonable solutions to problems encountered and implement them;
4. Summarize the research and development work and write application materials according to CFDA requirements;
5. Provide technical guidance and training to subordinate laboratory technicians.
Job Requirements:
1. Master's degree or above in Organic Synthesis Chemistry or Pharmaceutical Chemistry, with more than 3 years of working experience;
2. Proficient in organic chemistry experimental skills;
3. Familiar with various analytical techniques (HPLC, GC, NMR, MS, etc.);
4. Able to proficiently retrieve and utilize various Chinese and English chemical literature;
5. Possessing good personal qualities, teamwork spirit and communication skills;
6. Able to proficiently read, write and express in English.
2. Proficient in organic chemistry experimental skills;
3. Familiar with various analytical techniques (HPLC, GC, NMR, MS, etc.);
4. Able to proficiently retrieve and utilize various Chinese and English chemical literature;
5. Possessing good personal qualities, teamwork spirit and communication skills;
6. Able to proficiently read, write and express in English.
Pharmacologist
China Peking
Full-time
Negotiable
Unlimited
Job Responsibilities:
Job Responsibilities:
1. Responsible for the preliminary evaluation experiments of relevant molecular biology and in vitro cell-level drugs;
2. Able to work independently under the guidance of the project leader and complete the R&D report independently as required;
3. Summarize the R&D work and write application materials according to CFDA requirements;
4. Complete other tasks assigned by the person in charge.
1. Responsible for the preliminary evaluation experiments of relevant molecular biology and in vitro cell-level drugs;
2. Able to work independently under the guidance of the project leader and complete the R&D report independently as required;
3. Summarize the R&D work and write application materials according to CFDA requirements;
4. Complete other tasks assigned by the person in charge.
Job Requirements:
1. Master's degree or above, major in cell biology, molecular biology or related fields, with more than 2 years of working experience;
2. Possess a solid theoretical foundation in molecular biology and cell biology, and be proficient in basic experimental techniques in molecular biology and/or cell biology, including molecular cloning, cell culture, real-time PCR, ELISA, Western Blot, fluorescence microscopy, etc.;
3. Have strong English reading ability and be able to effectively retrieve and understand relevant English literature;
4. Work diligently and proactively, be ambitious, and be able to cooperate and communicate with colleagues.
2. Possess a solid theoretical foundation in molecular biology and cell biology, and be proficient in basic experimental techniques in molecular biology and/or cell biology, including molecular cloning, cell culture, real-time PCR, ELISA, Western Blot, fluorescence microscopy, etc.;
3. Have strong English reading ability and be able to effectively retrieve and understand relevant English literature;
4. Work diligently and proactively, be ambitious, and be able to cooperate and communicate with colleagues.
R&D QA Manager
China Peking
Full-time
Negotiable
Unlimited
Job Responsibilities:
1. Familiar with NMPA, FDA drug quality management laws, regulations and administrative rules, assist the company's quality management;
2. Assist in establishing a sound laboratory R&D management system and document control system;
3. Responsible for supervising the daily quality management work of the laboratory to ensure compliance with the company's SOP requirements;
4. Responsible for organizing internal staff training on quality system-related work;
2. Assist in establishing a sound laboratory R&D management system and document control system;
3. Responsible for supervising the daily quality management work of the laboratory to ensure compliance with the company's SOP requirements;
4. Responsible for organizing internal staff training on quality system-related work;
Job Requirements:
1. Bachelor's degree or above, pharmaceutical related major, 5 years or more working experience, experience in R&D QA or quality management in foreign companies is preferred;
2. Understand the new drug R&D process and pharmaceutical regulations, have a strong sense of laboratory compliance, and be familiar with relevant national laws and regulations;
3. Familiar with relevant regulations and guidelines of China, FDA, and ICH;
4. Scientific and rigorous, with good communication, coordination and analytical skills.
2. Understand the new drug R&D process and pharmaceutical regulations, have a strong sense of laboratory compliance, and be familiar with relevant national laws and regulations;
3. Familiar with relevant regulations and guidelines of China, FDA, and ICH;
4. Scientific and rigorous, with good communication, coordination and analytical skills.
BD Manager
China Peking
Full-time
Negotiable
Unlimited
Job Responsibilities:
1. In accordance with the company's development needs, seek domestic and foreign partners for the company's products and implement the company's strategic development plan;
2. Promote and coordinate search, evaluation and due diligence;
3. Keep abreast of domestic and foreign trends in new drug R&D, and assist in planning the company's product pipeline and the strategic development of new technologies;
4. Conduct research and evaluation of relevant products, including comprehensive analysis of various aspects such as market, technology, finance and patents;
5. Continuously strengthen industry contacts to ensure that attractive cooperation opportunities are found;
6. Manage existing collaborations.
2. Promote and coordinate search, evaluation and due diligence;
3. Keep abreast of domestic and foreign trends in new drug R&D, and assist in planning the company's product pipeline and the strategic development of new technologies;
4. Conduct research and evaluation of relevant products, including comprehensive analysis of various aspects such as market, technology, finance and patents;
5. Continuously strengthen industry contacts to ensure that attractive cooperation opportunities are found;
6. Manage existing collaborations.
Job Requirements:
1. Master's degree or above from overseas universities, majoring in pharmacy, medicine, business administration, etc., with more than 5 years of experience in the pharmaceutical BD industry;
2. Prior experience working in multinational pharmaceutical companies is preferred;
3. Familiar with the entire process of pharmaceutical BD operations, such as financial modeling and business forecasting expertise, to conduct financial analysis of target assets;
4. Excellent multitasking ability, strong project management skills and excellent communication skills;
5. Ability to adapt flexibly and meet changing business needs;
6. Good written and spoken English and Chinese, and strong interpersonal communication skills. Candidates who can lead cross-functional teams are preferred.
2. Prior experience working in multinational pharmaceutical companies is preferred;
3. Familiar with the entire process of pharmaceutical BD operations, such as financial modeling and business forecasting expertise, to conduct financial analysis of target assets;
4. Excellent multitasking ability, strong project management skills and excellent communication skills;
5. Ability to adapt flexibly and meet changing business needs;
6. Good written and spoken English and Chinese, and strong interpersonal communication skills. Candidates who can lead cross-functional teams are preferred.
Biochemist
China Peking
Full-time
Negotiable
Unlimited
Job Responsibilities:
1. Responsible for data interpretation and communication within and outside the biochemistry group;
2. Collaborate closely with medicinal chemists, cell biologists, and in vivo pharmacologists to accelerate the drug discovery process;
3. Other tasks assigned by the project leader.
2. Collaborate closely with medicinal chemists, cell biologists, and in vivo pharmacologists to accelerate the drug discovery process;
3. Other tasks assigned by the project leader.
Job Requirements:
1. Master's degree or above with a solid theoretical foundation in molecular biology and structural biology, and a certain foundation in bioinformatics;
2. Experience in biochemical research design, assay development/validation and analysis, with experience in lc-ms, HTRF, AlphaLISA/AlphaScreen, FP, SPR and ITC preferred;
3. Experience in protein analysis research skills such as HPLC and mass spectrometry is preferred.
4. High sense of responsibility and dedication; excellent analytical and problem-solving skills, good learning, communication and teamwork skills;
5. Proficient in English listening, reading and writing.
2. Experience in biochemical research design, assay development/validation and analysis, with experience in lc-ms, HTRF, AlphaLISA/AlphaScreen, FP, SPR and ITC preferred;
3. Experience in protein analysis research skills such as HPLC and mass spectrometry is preferred.
4. High sense of responsibility and dedication; excellent analytical and problem-solving skills, good learning, communication and teamwork skills;
5. Proficient in English listening, reading and writing.
Medicinal Chemistry VP
China Peking
Full-time
Negotiable
Unlimited
Job Responsibilities:
1. Lead the team to complete project experiments according to project requirements;
2. Design and improve synthetic routes;
3. Provide a complete experimental design plan and project management plan;
4. Track and manage the project in real time;
5. Improve project completion efficiency;
6. Complete other tasks assigned by the company leaders.
2. Design and improve synthetic routes;
3. Provide a complete experimental design plan and project management plan;
4. Track and manage the project in real time;
5. Improve project completion efficiency;
6. Complete other tasks assigned by the company leaders.
Job Requirements:
1. Organic chemistry, pharmaceutical chemistry related majors, doctoral degree or above, those with overseas background are preferred;
2. Familiar with the entire process of new drug research and development, with no less than 5 years of experience in drug research and development, and no less than 3 years of team management experience;
3. Have a certain understanding of process research, quality research, intellectual property rights, and laws and regulations; have the concept of compound design, can analyze structure-activity relationships and optimize structures according to pharmacological results; can independently lead a team, promote project progress, and solve problems encountered in the project; have strong coordination ability, and can make the best use of personnel's talents within the team.
4. Fluent English listening, speaking, reading and writing skills
2. Familiar with the entire process of new drug research and development, with no less than 5 years of experience in drug research and development, and no less than 3 years of team management experience;
3. Have a certain understanding of process research, quality research, intellectual property rights, and laws and regulations; have the concept of compound design, can analyze structure-activity relationships and optimize structures according to pharmacological results; can independently lead a team, promote project progress, and solve problems encountered in the project; have strong coordination ability, and can make the best use of personnel's talents within the team.
4. Fluent English listening, speaking, reading and writing skills
CMC VP
China Peking
Full-time
Negotiable
Unlimited
Job Responsibilities:
I. CMC Work:
Lead the CMC team to complete IND and NDA work according to the company's development goals;
Lead the team to continuously improve the company's R&D quality assurance system;
Cultivate the core CMC team and reserve personnel.
II. Project Coordination and Management:
Lead the pre-clinical team to complete R&D projects quickly and efficiently;
Supervise and coordinate CRO companies to ensure the timely and high-quality production of clinical drugs.
III. Project Registration and Submission:
Responsible for global registration and submission of company projects. This includes the development of registration strategies, submission of application materials; regular monitoring of registration regulations and competitive product information to provide regulatory support for the company's innovative drug registration;
Review drug registration materials according to FDA and NMPA requirements, control the progress and quality of material preparation in various relevant departments of the company;
Obtain and update drug registration information in a timely manner, and communicate effectively and promptly with the FDA and NMPA to ensure the smooth progress of the project.
Lead the CMC team to complete IND and NDA work according to the company's development goals;
Lead the team to continuously improve the company's R&D quality assurance system;
Cultivate the core CMC team and reserve personnel.
II. Project Coordination and Management:
Lead the pre-clinical team to complete R&D projects quickly and efficiently;
Supervise and coordinate CRO companies to ensure the timely and high-quality production of clinical drugs.
III. Project Registration and Submission:
Responsible for global registration and submission of company projects. This includes the development of registration strategies, submission of application materials; regular monitoring of registration regulations and competitive product information to provide regulatory support for the company's innovative drug registration;
Review drug registration materials according to FDA and NMPA requirements, control the progress and quality of material preparation in various relevant departments of the company;
Obtain and update drug registration information in a timely manner, and communicate effectively and promptly with the FDA and NMPA to ensure the smooth progress of the project.
Job Requirements:
1. Doctorate degree in pharmaceutical chemistry, analytical chemistry, pharmaceutics, or a related field, with more than ten years of relevant experience in multinational pharmaceutical companies or with the FDA;
2. Familiar with FDA, NMPA, ICH, and other drug development regulations and guidelines, and can flexibly apply them to work;
3. Familiar with global drug development and registration processes, those with experience leading a team to complete NDA submissions are preferred.
4. Excellent ability to identify, analyze, and solve problems;
5. High sense of responsibility and dedication, good professional ethics, excellent leadership, ability to efficiently organize and manage teams, and excellent teamwork spirit;
6. Excellent communication and project promotion skills with CRO companies
2. Familiar with FDA, NMPA, ICH, and other drug development regulations and guidelines, and can flexibly apply them to work;
3. Familiar with global drug development and registration processes, those with experience leading a team to complete NDA submissions are preferred.
4. Excellent ability to identify, analyze, and solve problems;
5. High sense of responsibility and dedication, good professional ethics, excellent leadership, ability to efficiently organize and manage teams, and excellent teamwork spirit;
6. Excellent communication and project promotion skills with CRO companies
Medical Manager
China Peking
Full-time
Negotiable
Unlimited
Job Responsibilities:
1. System Development: Responsible for establishing, improving, updating, and maintaining SOPs related to public clinical medicine.
2. Medical Support: Responsible for providing medical professional support and scientific guidance to the Clinical Research Department, improving the quality of clinical trials, and assisting the department in other related work.
3. Documentation: Using professional medical knowledge, scientifically and reasonably designing experimental plans, and communicating with clinical medical experts and review experts on clinical plan design according to the needs of clinical projects to improve medical technical documents.
4. Medical Training: Collect cutting-edge medical information, provide medical training on plans and related treatment areas and other related content, and answer medical questions raised by the clinical team.
2. Medical Support: Responsible for providing medical professional support and scientific guidance to the Clinical Research Department, improving the quality of clinical trials, and assisting the department in other related work.
3. Documentation: Using professional medical knowledge, scientifically and reasonably designing experimental plans, and communicating with clinical medical experts and review experts on clinical plan design according to the needs of clinical projects to improve medical technical documents.
4. Medical Training: Collect cutting-edge medical information, provide medical training on plans and related treatment areas and other related content, and answer medical questions raised by the clinical team.
Job Requirements:
1. Master's degree or above, Ph.D. preferred, oncology background preferred;
2. Clear written and oral expression skills, good communication skills. Solid medical foundation.
3. Possesses industry network resources and maintains good relationships with clinical experts and review experts.
4. Good English reading and writing skills, able to proficiently search and retrieve domestic and foreign medical literature.
5. Good professional ethics, honesty and trustworthiness, respect for laws and regulations
2. Clear written and oral expression skills, good communication skills. Solid medical foundation.
3. Possesses industry network resources and maintains good relationships with clinical experts and review experts.
4. Good English reading and writing skills, able to proficiently search and retrieve domestic and foreign medical literature.
5. Good professional ethics, honesty and trustworthiness, respect for laws and regulations
Purification Supervisor
China Peking
Full-time
Negotiable
Unlimited
Job Responsibilities:
1. Operate and maintain LCMS and preparative HPLC, and keep good usage records;
2. Complete daily purification tasks submitted by the synthesis department, assist them in solving purification problems, mainly the separation and purification work of new drug small molecule compounds;
3. Develop and implement purification methods according to sample properties;
4. Provide professional consultation on preparation to synthesis personnel;
5. Manage preparation data and reports;
6. Establish and implement SOPs for preparation instruments and methods to standardize workflows;
7. Complete other tasks assigned by the company and superiors;
2. Complete daily purification tasks submitted by the synthesis department, assist them in solving purification problems, mainly the separation and purification work of new drug small molecule compounds;
3. Develop and implement purification methods according to sample properties;
4. Provide professional consultation on preparation to synthesis personnel;
5. Manage preparation data and reports;
6. Establish and implement SOPs for preparation instruments and methods to standardize workflows;
7. Complete other tasks assigned by the company and superiors;
Job Requirements:
1. Bachelor's degree or above in analytical chemistry or related disciplines, with more than 2 years of work experience
2. Familiar with chromatographic separation principles, proficient in operating preparative HPLC, and able to independently develop separation methods;
3. Master the basic principles and structure of preparative HPLC and LCMS, be familiar with the daily maintenance of preparative HPLC and LCMS, and be able to handle simple repairs for common faults;
4. Strong sense of responsibility, strong dedication and teamwork spirit, and good communication skills;
2. Familiar with chromatographic separation principles, proficient in operating preparative HPLC, and able to independently develop separation methods;
3. Master the basic principles and structure of preparative HPLC and LCMS, be familiar with the daily maintenance of preparative HPLC and LCMS, and be able to handle simple repairs for common faults;
4. Strong sense of responsibility, strong dedication and teamwork spirit, and good communication skills;
Beijing Danatlas Technology
Address: Building 4A, District 2, Yizhuang International Biomedical Park, No. 7 Liangshuihe 1st Street, Beijing Economic and Technological Development Zone, Beijing
Copyright @ 2019-2022 Beijing Danatlas Pharmaceutical Technology Co., Ltd. All rights reserved. TAG
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