Salary: 0-0K
Experience requirements:
Educational requirements:
Job Description:
The Head of Comparative Medicine at Shanghai site is a critical leadership role responsible for managing and directing the preclinical research and development activities focused on autoimmune disease and oncology therapeutics. This position requires a deep understanding of comparative medicine and the ability to align local site activities with the broader strategic goals of the company.
Responsibilities
Site Management:
Oversee the day-to-day operations of the comparative medicine site, ensuring alignment with corporate objectives and standards.
Manage a team of scientists and researchers, providing direction, mentorship, and support for their professional development.
Oversee the budget and resource allocation for the team to ensure efficient operations.
Research and Development:
Lead the site’s efforts in developing and implementing preclinical models and assays to evaluate the efficacy and safety of new drug candidates for autoimmune and oncology diseases.
Collaborate with cross-functional teams to translate research findings into clinical development plans.
Collaborate with the Beijing Comparative Medicine team to ensure consistency and integration of research efforts across sites.
Stay abreast of the latest scientific advancements in autoimmune and oncology disease research
Collaboration and Communication:
Maintain regular communication with the Head of Comparative Medicine to align strategies and share updates.
Represent the site at internal meetings, conferences, and events to ensure effective communication and collaboration.
Qualifications:
Education: Ph.D. or equivalent in Comparative Medicine, Immunology, Biology, or a related field. Experience: A minimum of 6 years of experience in industry preclinical research, with a focus on autoimmune or oncology diseases. Expertise: A successful track record of contributing to the advancement of drug candidates from preclinical to clinical stages. Leadership: Proven track record of leading research teams and managing research projects. Communication: Strong communication skills, with the ability to effectively liaise with a central team and present complex scientific information.
BeiGene Global Competence
When we demonstrate the values of 'patient first', 'boundaryless collaboration', 'innovation', and 'pursuit of excellence' through the following twelve global competencies, we can help more patients around the world access more affordable drugs
● Teamwork
Provide and solicit honest and feasible feedback
Self awareness
● Inclusive and inclusive
● Proactive
● Pioneering spirit
● Continuous learning
Embrace change
● Result oriented
Analytical thinking/data analysis
Excellent Finance
● Clear communication
BeiGene Global Competencies
When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity and Driving Excellence, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
●Fosters Teamwork
●Provides and Solicits Honest and Actionable Feedback
●Self-Awareness
●Acts Inclusively
●Demonstrates Initiative
●Entrepreneurial Mindset
●Continuous Learning
●Embraces Change
●Results-Oriented
●Analytical Thinking/Data Analysis
●Financial Excellence
●Communicates with Clarity
Privacy Statement for Job Applicants:
BeiGene is committed to respecting and protecting your personal information rights, and promises to process your personal information (including sensitive personal information) in accordance with the principles of legality, legitimacy, necessity, and integrity
Due to BeiGene's global business operations, we may need to send and/or store your personal information on servers and databases located in countries other than your home country (such as the United States) for reasonable business purposes such as human resource management. For more information, please refer to BeiGene's "Job Seeker Privacy Policy" (BeiGene official website - Privacy Policy - Job Seeker Privacy Policy)
If you voluntarily provide us with your resume information or other personal information, it will be deemed that you have fully understood and confirmed acceptance of BeiGene's "Job Seeker Privacy Policy". If you have any questions about this, please do not submit resume information or other personal information
BeiGene is committed to respect and protect your personal information rights, and will process your personal information, including your sensitive personal information, based on the principles of legality, legitimacy, necessity, and integrity.
Due to the reasonable business need for human resource management as a result of BeiGene’s global operation, your personal information may be transferred and/ or stored in a server/database located in a third country (e.g., the United States) other than your own country. For further details, please refer to BeiGene Job Applicant Privacy Policy (BeiGene official website - Privacy Policy - Job Applicant Privacy Policy).
If you voluntarily provide your resume or other personal information to us, it is deemed as you have thoroughly acknowledged and accepted BeiGene Job Applicant Privacy Policy. If you have any concern, please DO NOT submit your resume or any other personal information.
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.
Search
Job Application
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BeiGene (Beijing) Biotechnology Co., Ltd. - Associate Director, in vivo Pharmacology (MJ017086)
Release time：2024-12-18
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Core Yaohui Technology Co., Ltd. - Serdes System Algorithm Engineer
Release time：2024-12-18
-
Salary: 0-0K
Experience requirements: Unlimited experience
Educational requirements: Job Description:
Job Description
1. Design corresponding DSP algorithms for compensating various channel damages in high-speed SERDES systems, including algorithm research, prototype verification, fixed-point design, and algorithm documentation writing
2. Collaborate with colleagues in the RTL digital design team, participate in algorithm PPA optimization iterations, and cooperate to complete the bitmatch work between algorithm code and RTL circuit
3. Obtain preliminary system performance indicators through tracking protocol standards or discussing with the product department, use or design performance analysis tools to confirm the rationality of the indicators, and participate in relevant development
4. Participate in system simulation modeling work, model common channel damages and circuit components, and output corresponding waveforms for correlation verification with actual system waveforms
Job requirements
1. Master's degree or above in Communication Engineering, Electronic Information, and Applied Mathematics, with a preference for a PhD
2. Familiar with modulation formats such as PAM4/NRZ, including Gray coding, eye diagram analysis, BER calculation, etc; Understand CDR, The principles of DSP algorithms such as FFE, DFE, MLSE, etc., and relevant code has been written for implementation
3. Familiar with various channel impairments (high-frequency impairments, low-frequency impairments, clock jitter, etc.) and able to conduct relevant modeling and analysis, including obtaining channel IPR, spectral response, SNR calculation, etc
4. Have a good programming foundation and be proficient in using MATLAB/Python for relevant simulation modeling
5. Have a certain understanding of FEC encoding, such as RS (544514), and have a certain concept of corrected BER
6. Have a solid foundation in mathematics and physics, and master the relevant knowledge of communication principles and digital signal processing
7. Have rich experience in reading literature or patents, and know how to extract useful information from them to solve problems
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.
-
Guangzhou Zhijing Information Technology Co., Ltd. - Assistant Research and Development Scientist (MJ000152)
Release time：2024-12-18
-
Salary: 0-0K
Experience requirements: Unlimited experience
Educational requirements: Job Description:
[Job Responsibilities]
1. Responsible for drug research and development projects, promoting the progress of gene editing therapy or tumor immunotherapy related projects;
2. Design experimental implementation, solve technical problems, optimize technical routes or participate in methodological innovation, apply molecular/cell biology tools and methods to achieve research objectives;
3. Carry out technical training and guidance, coordinate across technical departments, learn academic achievements and share research and development progress of domestic and foreign peers, study and analyze academic literature and industry information, and support technological route iteration;
4. Assist in drug innovation process development, IND application, and patent work.
[Job Requirements]
1. Outstanding doctoral graduates majoring in biology or medicine;
2. Having solid experience in R&D projects in the fields of biotechnology or pharmaceuticals, have participated in the entire R&D project process, and have the experience and ability to independently solve R&D problems;
3. Interested in the field of genetics and cell drugs, possess pioneering and innovative abilities, and have good teamwork and communication skills;
4. Be able to use the Internet to search academic and technical resources, read and understand English literature, and use English skillfully.
[Company Introduction]
Ruifeng Biotechnology is a leading gene editing drug innovation enterprise in China, driven by gene editing technology and committed to the birth of innovative drugs. Ruifeng Biotechnology is a high-level team in the international early application of gene editing to explore the treatment of genetic diseases, and has continuously accumulated pioneering achievements in the fields of hematology, ophthalmology, and other diseases. It has high-level technological accumulation in areas including gene editing tool innovation, drug strategy discovery, new animal model construction, multi-level efficacy and safety evaluation, and has two innovative drug directions: in vivo and in vitro. The mission of Ruifeng Biotechnology is to provide accessible and curative drugs for patients with severe diseases based on innovative genetic technology. At present, there are pipeline layouts in the fields of genetic diseases, complex diseases, and tumors. Among them, innovative drugs for β - thalassemia have made clinical progress at the global advanced level, and the world's first breakthrough in the cure of α - thalassemia has been achieved. The IND application for global gene edited drugs for Usher syndrome has been approved by regulatory authorities in China and the United States.
Ruifeng currently has nearly 7000 square meters of office, research and development, and GMP facilities and venues. It has two research and development bases in Huangpu Economic Development Zone, Guangzhou, Guangdong Province, and a registered branch in Beijing.
We attach great importance to our employees, offer competitive compensation, and strive to provide a superior and innovative office and technology environment for all staff.
In the rapidly advancing era of life sciences, Ruifeng Biotechnology is committed to the research and development of innovative and curative drugs, enabling patients to overcome the troubles of diseases, bringing hope for treatment to more people, and providing a quality of life similar to that of healthy individuals.
The key to our success is that our talents and technology have sufficient competitiveness. Around our vision, we practice an organizational culture of respect, innovation, and striving, and we look forward to you joining the Ruifeng family if you agree with our philosophy
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.
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BeiGene (Beijing) Biotechnology Co., Ltd. - (Senior) Research Investigator, Upstream Development (MJ016485)
Release time：2024-12-18
-
Salary: 20-30K
Experience requirements: Educational requirements: Job Description:
Responsibilities
- 15% Actively participate in the planning/prioritization of projects, balancing in-house work and outsourced work/activities. Design experiments, prepare protocols, and ensure execution of said experiments. Assemble experimental data and prepare data summaries
- 60% Hands-on execution of experiments on the bench, deliver reliable experimental results for the various development projects; troubleshoot any issues that arise
- 15% Write and/or review technical process development reports and any other relevant process documentation (e.g. SOPs, Process Descriptions, etc.)
- 10% Manage raw material/instrument supplies to ensure efficient and timely upstream operations. Prepare documents/presentations/materials for meetings, conferences and/or publications. Attend internal meetings, participate in training sessions, perform administrative duties
Requirements
- Ph.D. degree with 0~2 years of CHO-based bioprocess development experience in Biotech industry
- Strong skills with mammalian cell culture is a must.
- Hands on experience in upstream process development with CHO-based cell culture in shake flasks, Ambr15/250, rocker-style bioreactors and/or benchtop stirred tank bioreactors is essential
- Experience with development and optimization of cell culture media and/or feeding strategies in bioreactors
- Knowledge of process optimization methods such as Design of Experiments (DoE) and complex problem-solving of science/engineering challenges
- Excellent interpersonal and managing skills with the desire to work collaboratively and effectively in a team environment
- Strong communication skills including verbal, written, and scientific data presentation
- Working knowledge of cGMP environment, ensuring compliant documentation, and transferring the processes to manufacturing sites is a plus
BeiGene Global Competence
When we demonstrate the values of 'patient first', 'boundaryless collaboration', 'innovation', and 'pursuit of excellence' through the following twelve global competencies, we can help more patients around the world access more affordable drugs
● Teamwork
Provide and solicit honest and feasible feedback
Self awareness
● Inclusive and inclusive
● Proactive
● Pioneering spirit
● Continuous learning
Embrace change
● Result oriented
Analytical thinking/data analysis
Excellent Finance
● Clear communication
BeiGene Global Competencies
When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity and Driving Excellence, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
●Fosters Teamwork
●Provides and Solicits Honest and Actionable Feedback
●Self-Awareness
●Acts Inclusively
●Demonstrates Initiative
●Entrepreneurial Mindset
●Continuous Learning
●Embraces Change
●Results-Oriented
●Analytical Thinking/Data Analysis
●Financial Excellence
●Communicates with Clarity
Privacy Statement for Job Applicants:
BeiGene is committed to respecting and protecting your personal information rights, and promises to process your personal information (including sensitive personal information) in accordance with the principles of legality, legitimacy, necessity, and integrity
Due to BeiGene's global business operations, we may need to send and/or store your personal information on servers and databases located in countries other than your home country (such as the United States) for reasonable business purposes such as human resource management. For more information, please refer to BeiGene's "Job Seeker Privacy Policy" (BeiGene official website - Privacy Policy - Job Seeker Privacy Policy)
If you voluntarily provide us with your resume information or other personal information, it will be deemed that you have fully understood and confirmed acceptance of BeiGene's "Job Seeker Privacy Policy". If you have any questions about this, please do not submit resume information or other personal information
BeiGene is committed to respect and protect your personal information rights, and will process your personal information, including your sensitive personal information, based on the principles of legality, legitimacy, necessity, and integrity.
Due to the reasonable business need for human resource management as a result of BeiGene’s global operation, your personal information may be transferred and/ or stored in a server/database located in a third country (e.g., the United States) other than your own country. For further details, please refer to BeiGene Job Applicant Privacy Policy (BeiGene official website - Privacy Policy - Job Applicant Privacy Policy).
If you voluntarily provide your resume or other personal information to us, it is deemed as you have thoroughly acknowledged and accepted BeiGene Job Applicant Privacy Policy. If you have any concern, please DO NOT submit your resume or any other personal information.
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.
-
Tianjin Jiankai Technology Co., Ltd. - Senior Synthesis Director
Release time：2024-12-18
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Salary: 30-45K
Experience requirements: Unlimited experience
Educational requirements: Job Description:
Job Responsibilities:
1. Responsible for overseeing the comprehensive work of the Synthesis Method Development Department and the New Materials and Custom Synthesis Department, organizing and supervising the completion of various tasks within the scope of their respective responsibilities
2. Responsible for the overall plan formulation, research quality and progress control, patent search, key technical problem solving and other R&D process management of the department's synthesis project, and ultimately synthesizing the target compound
3. Track new platforms and technologies discovered and optimized by international innovators, keep abreast of the latest industry trends, enhance the team's R&D and innovation capabilities and efficiency, and provide professional support for topic selection, project approval, and customer cooperation
4. Lead team members to overcome difficult organic synthesis projects, promptly solve problems that arise during experiments, supervise, control, and guide the project process, allocate personnel reasonably, track project progress, and make timely corrections to ensure timely completion of the project
5. Collaborate with the pharmacology team to conduct structure-activity relationship research and explore the drug characteristics and variety advantages of preclinical candidate compounds; Collaborate with production teams to optimize product production processes and other technical improvement projects
6. Timely organize patent applications for innovative processes to ensure effective protection of the company's intellectual property rights
7. Develop a work plan according to company requirements and arrange the work process. Including: planning and scheduling of production tasks; Plan and arrange work environment management; Plan and arrange equipment management work; Plan and arrange safety management work, and provide guidance and supervision for the implementation process
8. Supervise production progress, maintain close communication with the sales department, be able to make corresponding adjustments and arrangements for important or urgent orders based on actual situations, ensure the timely fulfillment of product contracts, and guarantee market supply
9. Responsible for communication and coordination within and outside the department, maintaining close communication with relevant departments such as sales regarding order progress details, production progress, and shipping arrangements; Order delays must be promptly reported to relevant personnel such as the Vice President of Production, Sales, and Shipping to maintain smooth information flow and efficient operation of the system
10. Responsible for the process technology and quality assurance work in the production process, working closely with the quality department, paying attention to product quality, promptly solving and handling problems found, and ensuring that the products shipped meet the company's quality requirements
11. Regularly summarize ongoing projects and work progress, and propose improvement plans; Timely report the progress of production orders, scientific research projects, technical management standards, production processes, new product development, and other work to the leadership, continuously improving the market competitiveness of the company's products
Job requirements:
1. Hold a doctoral degree or above in organic synthesis or pharmaceutical chemistry, with over 10 years of experience in process research and development
2. Have rich experience in process research and synthesis, strong problem-solving ability, proficient in synthetic routes and optimized reaction methods, familiar with compound separation and analysis methods
3. Have team management experience and lead the team to complete the research and data writing of this project 4. Proficient in literature search methods, able to read English literature, and capable of independently conducting research on topics
5. Strong project management skills, able to lead multiple researchers to carry out research projects
6. Strong planning, communication, and organizational management skills, excellent professional and teamwork spirit, able to complete work under high pressure
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.
-
Tianjin Jiankai Technology Co., Ltd. - Manager of Analytical Method Development Department
Release time：2024-12-18
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Salary: 30-50K
Experience requirements: Educational requirements: Job Description:
Job Responsibilities:
1. Together with the analysis method development team, provide technical support for the innovation research institute's analysis projects. Responsible for the development and optimization of analytical methods for company research and development, as well as methodological validation, quality standard confirmation, stability testing plans, and other related work
2. Responsible for reviewing the development of analytical methods led by the department, generating validation reports, stability testing reports, and raw material and finished product testing reports and other related documents
3. Participate in the management and operation of client projects, answer client questions, provide accurate methodology reports, and explain complex data
4. Collaborate with relevant departments such as quality, production, and research and development to participate in the evaluation of the company's new technology and equipment introduction, GMP self inspection, quality problem investigation, and analysis method transfer, in order to improve the quality of the company's products
5. Together with the analysis team, responsible for the daily maintenance and management of all analysis equipment
6. Effective communication and collaboration across departments (production, research and development, quality, sales, etc.) to improve product quality
7. Regularly organize analysis teams to receive SOP training and analysis method training for analytical instruments
8. Complete other tasks assigned by the leader
9. Comply with the company's various rules and regulations
Job requirements:
1. Major in analytical chemistry, pharmaceutical chemistry, drug analysis or related fields, with a doctoral degree from overseas returnees
2. More than 8 years of experience in developing analytical processes, proficient in using HPLC UPLC、Q-TOF、 Mass spectrometry and other related detection instruments
3. Familiar with cGMP and pharmacopoeia testing
4. Possess excellent communication skills, proficient in using both Chinese and English for oral and written expression on behalf of the company in internal and external communication
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.
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Jugang Precision (Guangdong) Co., Ltd. - Senior Engineer
Release time：2024-12-18
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Salary: 30-50K
Experience requirements: Unlimited experience
Educational requirements: Job Description:
Requirements: Doctoral degree, major in mechanical or electrical related fields, experience is not limited, experience in the research and development of precision components for machine tools or electric spindles, motors, etc. is preferred
Responsibilities:
Mechanical major - mainly responsible for the research and development of machine tool structures or precision components Electrical major - mainly responsible for the research and debugging of machine tool electrical
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.
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Sichuan Kelombotai Biopharmaceutical Co., Ltd. - Kelombotai - Innovative Process Synthesis Scientist (J10478)
Release time：2024-12-18
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Salary: 20-25K
Experience requirements: Educational requirements: Job Description:
Job description:
1. Develop an experimental plan based on literature, proficiently complete organic chemical reactions, and summarize and analyze the experimental results under guidance
2. Clearly and completely write experimental records and reports
3. Participate in the daily management of the laboratory
4. Complete other tasks arranged by the company
Job requirements:
1. Doctoral degree or above, major in organic chemistry, pharmaceutical chemistry or other related fields
2. Understand various organic synthesis reactions
3. Good communication skills and collaborative spirit
4. Good teamwork awareness and execution ability, understanding and recognition of company culture and philosophy, dedication to work, honesty and integrity
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.
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Sichuan Kelombotai Biopharmaceutical Co., Ltd. - Kelombotai - Director of Disease Biology (ADC) (J11803)
Release time：2024-12-18
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Salary: 28-55K
Experience requirements: Educational requirements: Job Description:
Job description:
Job Responsibilities:
1. Target recognition and validation
Verify the feasibility of ADC project development by the information approval department through research in disease biology and gene proteomics
Conduct preliminary research on the expression, distribution, metabolism, and drug action mechanism of project targets to provide data for pipeline committee project discussions
Evaluation of ADC treatment strategy and efficacy: evaluation of the relationship between antibody affinity range, activity (activation, blockade), and efficacy
Design and validate the molecular configuration of antibody/ADC drugs: verify the selection of ADC Payload linker, structural simulation and design of dual antibody configurations, antibody FC segment modification, etc
2. Research on the Mechanism of ADC in Tumors and Extratumoral Indications
Research on the biological mechanism of ADC
The impact of different target affinities on the efficacy, stability, drug formation, and toxicity of dual antibody ADCs
Research on the correlation between dual antibody ADC configuration design and target biology and drug development Study on Payload Link Selection, DAR Value, and the Correlation between Drug Efficacy and Toxicity of Non tumor ADCs
Research on ADC drug resistance
Study on the efficacy and mechanism of combination therapy of ADC and IO target drugs or TAA/IO ADC dual antibody
3. Complete other tasks arranged by the company
Job requirements:
Educational requirements: PhD or above
Professional requirements: majors in medicine, molecular biology, cell biology, structural biology, pharmacy, etc
Experience requirement: More than 10 years of relevant work experience; Priority given to those with a background in large overseas pharmaceutical companies
Skills and ability requirements:
Solid knowledge in molecular biology, disease biology, and immunology
2. Familiar with the biopharmaceutical industry and have unique understanding of biopharmaceutical research and development
Proficient in biological analysis techniques, immunological techniques, and research and development of large molecule/ADC drugs
4. Have a good sense of teamwork and execution, understand and identify with the company culture and philosophy, love the job and be dedicated, honest and upright
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.
-
Sichuan Kelombotai Biopharmaceutical Co., Ltd. - Kelombotai - Director of Disease Biology (Immunology) (J11804)
Release time：2024-12-18
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Salary: 28-55K
Experience requirements: Educational requirements: Job Description:
Job description:
Job Responsibilities:
1. Target recognition and validation
Verify the feasibility of the information project approval department's development of self immunity and tumor immunity projects through research in disease biology and gene proteomics
Exploring the interactions and effects between target related proteins and targets, providing judgment and direction for the development of biomarkers related to disease progression and therapeutic efficacy screening Timely track the progress of domestic and international drug research and development, and adjust the research strategy of the project based on relevant information Evaluation of treatment strategies and efficacy: evaluation of the relationship between antibody affinity range, activity (activation, blockade), and efficacy; Bottom level logic and configuration selection strategy for dual antibody design
Verify the significance of biomarkers in evaluating efficacy, toxicity, and biological characteristics; Measure the concentration of soluble targets in serum, etc
2. Development of Bioanalytical Technology:
Develop biological and functional analysis methods and protocol writing according to project needs
Establish drug efficacy, pharmacological research methods, and necessary tools
Communicate with the Translational Medicine and Pharmacology departments to establish in vivo animal models, in vivo pharmacological research methods, and detection indicators
3. Complete other tasks arranged by the company
Job requirements:
Educational requirements: PhD or above
Professional requirements: majors in medicine, immunology, molecular biology, structural biology, pharmacy, etc
Experience requirement: More than 10 years of relevant work experience; Priority given to those with a background in large overseas pharmaceutical companies
Skills and ability requirements:
Solid knowledge in molecular biology, disease biology, and immunology
2. Familiar with the biopharmaceutical industry and have unique understanding of biopharmaceutical research and development
Proficient in biological analysis techniques, immunological techniques, and research and development of large molecule drugs
4. Have a good sense of teamwork and execution, understand and identify with the company culture and philosophy, love the job and be dedicated, honest and upright
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.
-
Sichuan Kelombotai Biopharmaceutical Co., Ltd. - Kelombotai - Director of Disease Biology (Immunometabolism Direction) (J11805)
Release time：2024-12-18
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Salary: 28-55K
Experience requirements: Educational requirements: Job Description:
Job description:
Job Responsibilities:
1. Target recognition and validation
Verify the feasibility of the metabolic disease project development by the information project approval department through research in disease biology and gene proteomics
Conduct preliminary research on the expression, distribution, metabolism, and drug action mechanism of project targets to provide data for pipeline committee project discussions
Exploring the interactions and effects between target related proteins and targets, providing judgment and direction for the development of biomarkers related to disease progression and therapeutic efficacy screening Compare the advantages and disadvantages of antibody and non antibody drugs
Evaluation of treatment strategies and efficacy: evaluation of the relationship between antibody affinity range, activity (activation, blockade), and efficacy
Verify the significance of biomarkers in evaluating efficacy, toxicity, and biological characteristics; Measure the concentration of soluble targets in serum, etc
2. Development of Bioanalytical Technology:
Construction of cell-based disease models, including the construction of expression cell lines and recombinant overexpression cell lines; Target Knockout cell line construction; Construction of cell reporting system, etc
Develop biological and functional analysis methods and protocol writing according to project needs
Establish drug efficacy, pharmacological research methods, and necessary tools
Communicate with the Translational Medicine and Pharmacology departments to establish in vivo animal models, in vivo pharmacological research methods, and detection indicators
3. Complete other tasks arranged by the company
Job requirements:
Educational requirements: PhD or above
Professional requirements: majors in medicine, molecular biology, cell biology, structural biology, pharmacy, etc
Experience requirement: More than 10 years of relevant work experience; Priority given to those with a background in large overseas pharmaceutical companies
Skills and ability requirements:
Solid knowledge in molecular biology, disease biology, and metabolic diseases
2. Familiar with the biopharmaceutical industry and have unique understanding of biopharmaceutical research and development
Proficient in biological analysis techniques and research and development of large molecule drugs
4. Have a good sense of teamwork and execution, understand and identify with the company culture and philosophy, love the job and be dedicated, honest and upright
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.
-
Sichuan Kelombotai Biopharmaceutical Co., Ltd. - Kelombotai - Innovative Process Synthesis Manager (J11917)
Release time：2024-12-18
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Salary: 12-26K
Experience requirements: 3-5 years
Educational requirements: Job Description:
Job description:
1. Small molecule new drug project management
(1) Develop research plans and nodes based on the routes and structural characteristics of small molecules
(2) Participate in project meetings and coordinate with relevant departments such as upstream and downstream during the project progress process (3) Timely organize and coordinate resources to assist in resolving key technical issues
2. Technology transfer and sample production (1) Writing technology transfer materials
(2) Responsible for the smooth transfer of the process from the research department to the base and the completion of sample production
(3) Responsible for providing GLP, pilot, and clinical samples
3. Responsible for daily team management, including but not limited to training, mentoring, and leading the team to achieve KPIs
4. Complete other tasks arranged by the company
Job requirements:
Educational requirements: PhD
Professional requirements: Pharmacy, Organic Chemistry, and related majors
Experience requirements:
PhD with over 4 years of work experience in process research
Experience in drug process development, technology transfer, and application for at least 2-3 projects
Familiar with experience in developing, validating, and establishing quality standards for analytical methods
Skills and ability requirements:
Familiar with professional knowledge related to process research
Understand the development and validation of analytical methods, and possess the ability to organize and analyze experimental data
Capable of designing scientific experimental plans, operating experiments, and writing experimental reports
Having knowledge related to drug research or production
Familiar with the principles and regulations related to drug development
Quality requirements:
Good ability to withstand pressure
Good organizational skills
Good project management skills
Good time management skills
Consistent with the company culture and philosophy, identify with and strictly abide by and implement the company's various rules and regulations
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.
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Sichuan Kelombotai Biopharmaceutical Co., Ltd. - Kelombotai - Deputy Director of Antibody Discovery (J11967)
Release time：2024-12-18
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Salary: 50-80K
Experience requirements: Educational requirements: Job Description:
Job description:
Responsible for the discovery of large molecule drug antibodies and technical guidance for antibody engineering, assisting the VP of large molecule research and development in promoting drug discovery at all stages, platform development, and project management. Serving as the project PL responsible for project initiation, implementation, target validation, MOA research, antibody discovery, efficacy research, and coordinating the promotion of project CMC, non clinical and clinical development, as well as some BD, IP and other related work
1. Participate in the implementation of the company's overall strategic plan, formulate specific implementation plans and risk management
2. Project management. Participate in the research and development of macromolecular antibodies, including project initiation, application, supervision, implementation, and acceptance summary; Responsible for planning, implementing, following up on antibody research and development projects, and communicating with other departments; Establish and continuously optimize the technology platform, solve difficult problems in the company's product development process, coordinate with national government departments for technical research and development, and exchange technology with peers in the industry
3. Cross departmental and external management. Responsible for contacting and coordinating cooperative units, introducing cooperative projects, and tracking project implementation; Responsible for project communication with drug discovery department, process, pharmacology, application, intellectual property and other departments; Responsible for organizing the preparation and review of patent disclosure documents, IND applications, project extrapolation, contracts, and other related materials for new drugs
Job requirements:
Educational requirement: Doctoral degree
Major studied: Biopharmaceuticals, Cell Biology, Molecular Biology, Biochemistry, Immunology, etc
Work experience: Over 5 years of experience in antibody discovery and drug efficacy research
Job knowledge and skill requirements
1. Possess knowledge in immunology, molecular biology, cell biology, and biotechnology drug development, familiar with the process and system of macromolecular drug development
2. Proficient in antibody discovery techniques such as hybridoma, bacteriophage, and single B cell
3. Familiar with antibody humanization and structural modification, drug evaluation CMC、 Non clinical research, intellectual property and other research connotations
4. Familiar with the efficacy, pharmacokinetics, and toxicology of drugs in the body CMC、 Technical and data interpretation in various aspects such as quality testing, non clinical research, IND application, etc., with relevant project management experience
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.
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Hangzhou Taige Pharmaceutical Technology Co., Ltd. - Clinical Research Supervisor/Manager (Overseas Enterprise)
Release time：2024-12-17
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Salary: 15-22K
Experience requirements: Educational requirements: Job Description:
1. Doctoral degree in analytical chemistry (priority), laboratory medicine (mass spectrometry direction) or related majors
2. Candidates with experience in liquid chromatography tandem mass spectrometry are preferred
3. Positive and optimistic, strong sense of responsibility, good teamwork spirit, possessing certain strategies and scientific research thinking
4. Work will involve business trips
5. Will communicate with the hospital director and experts, hoping to have scientific research experience
6. PhD graduates are not considered
7. English listening, speaking, reading, and writing are OK
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.
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BeiGene (Beijing) Biotechnology Co., Ltd. - (Sr.) Director, Business Development, Search&Evaluation (MJ016767)
Release time：2024-12-17
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Salary: 100-150K
Experience requirements: Educational requirements: Job Description:
General Description:?
This position is based in Shanghai, China. The Director or Senior Director of S&E candidate will be a key contributor to the Search & Evaluation strategy to support BGNE’s business vision. The candidate will lead evaluation of preclinical, clinical and commercial stage assets in oncology, immunology and other adjacent therapeutic areas.? The candidate will also be responsible for identifying opportunity for clinical collaboration between partners and BGNE’s pipeline. We are looking for a candidate who is willing to take on new challenges and responsibilities as we grow our business.????
Essential Functions of the job:
Identify areas of innovation and growth opportunities aligned with BeiGene’s strategy in oncology, inflammatory diseases, and/or auto-immune diseases
Lead high profile cross-functional teams and provide strong project management skills to ensure that key risks and opportunities are identified, captured, and presented in an unbiased way to senior management for decision making
Collaborate with other business development colleagues to design partnering structures tailored to the profile of each envisioned collaboration
Proactively monitor the external business environment and maintain a knowledge base of licensing transactions and industry trends
Track opportunities and report progress of projects via database application and BD Dashboard
Has excellent presentation skills and has a track record of public presentations at scientific conferences and publications.
Qualifications:
Has a good understanding of clinical practice of oncology, inflammatory diseases, and/or auto-immune diseases
Has strong drug development expertise in oncology, inflammatory diseases, and/or auto-immune diseases
Ability to make key decisions and prioritize on most interesting partnering opportunities?
Ability to synthesize complex set of facts in order to facilitate decisions by C-level executives?
Hands-on experience in Search and Evaluation, Business Development, or portfolio management would be preferred
For the Director level, we require an MD, PhD or Pharm D with 6 plus years of experience in drug discovery and /or clinical development or clinical practice in oncology, inflammatory diseases, and/or auto-immune diseases
For the Senior Director level, we require an MD, PhD or Pharm D with 10 plus years of experience in drug discovery and/ or clinical development or clinical practice in oncology, inflammatory diseases, and/or auto-immune diseases
Computer Skills:?
Microsoft Words, Excel, Project, financial models
Other Qualifications: ?
Excellent oral and written communication skills, including ability to storyline and prepare executive-level discussion documents
Strong quantitative and qualitative analytic skills
Strong leadership skills with a demonstrated ability to influence different styles
Drug Development knowledge with basic to strong understanding of activities within Research, Preclinical and Clinical Development and Regulatory
Independent, motivated, team member with experience in a matrix environment
Education Required:?
MD, PhD or Pharm D
Travel:?
25% travel: both domestic and international travel
BeiGene Global Competence
When we demonstrate the values of 'patient first', 'boundaryless collaboration', 'innovation', and 'pursuit of excellence' through the following twelve global competencies, we can help more patients around the world access more affordable drugs
● Teamwork
Provide and solicit honest and feasible feedback
Self awareness
● Inclusive and inclusive
● Proactive
● Pioneering spirit
● Continuous learning
Embrace change
● Result oriented
Analytical thinking/data analysis
Excellent Finance
● Clear communication
BeiGene Global Competencies
When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity and Driving Excellence, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
●Fosters Teamwork
●Provides and Solicits Honest and Actionable Feedback
●Self-Awareness
●Acts Inclusively
●Demonstrates Initiative
●Entrepreneurial Mindset
●Continuous Learning
●Embraces Change
●Results-Oriented
●Analytical Thinking/Data Analysis
●Financial Excellence
●Communicates with Clarity
Privacy Statement for Job Applicants:
BeiGene is committed to respecting and protecting your personal information rights, and promises to process your personal information (including sensitive personal information) in accordance with the principles of legality, legitimacy, necessity, and integrity
Due to BeiGene's global business operations, we may need to send and/or store your personal information on servers and databases located in countries other than your home country (such as the United States) for reasonable business purposes such as human resource management. For more information, please refer to BeiGene's "Job Seeker Privacy Policy" (BeiGene official website - Privacy Policy - Job Seeker Privacy Policy)
If you voluntarily provide us with your resume information or other personal information, it will be deemed that you have fully understood and confirmed acceptance of BeiGene's "Job Seeker Privacy Policy". If you have any questions about this, please do not submit resume information or other personal information
BeiGene is committed to respect and protect your personal information rights, and will process your personal information, including your sensitive personal information, based on the principles of legality, legitimacy, necessity, and integrity.
Due to the reasonable business need for human resource management as a result of BeiGene’s global operation, your personal information may be transferred and/ or stored in a server/database located in a third country (e.g., the United States) other than your own country. For further details, please refer to BeiGene Job Applicant Privacy Policy (BeiGene official website - Privacy Policy - Job Applicant Privacy Policy).
If you voluntarily provide your resume or other personal information to us, it is deemed as you have thoroughly acknowledged and accepted BeiGene Job Applicant Privacy Policy. If you have any concern, please DO NOT submit your resume or any other personal information.
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.
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Chengdu Meisherui New Materials Co., Ltd. - Postdoctoral Researcher (Materials Research and Development)
Release time：2024-12-17
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Salary: 20-30K
Experience requirements: Unlimited experience
Educational requirements: Job Description:
Job Responsibilities:
1. Responsible for the development and research of new materials.
2. Provide guidance and support for the research work of the company's R&D team, and enhance the overall research capabilities of the team.
3. Participate in the company's product development major problem solving, closely cooperate with other departments of the company, and promote the transformation and application of scientific research achievements.
4. Participate in the application and management of scientific research projects, complete project execution and summary reports.
5. Write high-quality research papers and actively participate in academic exchanges at home and abroad.
Job requirements:
1. Doctoral degree, background in materials science or related majors. Currently, the company mainly produces powder metallurgy materials and metal ceramics/hard alloy products;
2. Candidates with postdoctoral research experience are preferred, with rich experimental operation experience and the ability to independently carry out scientific research work.
3. Have a deep understanding and unique insights into materials science, and be able to independently conduct high-level scientific research work.
4. Have good English reading and writing skills, able to read and write English research papers.
5. Possess good teamwork spirit and communication skills, able to effectively guide and assist team members.
6. Maintain sensitivity and enthusiasm towards new technologies and methods, possess innovative thinking and problem-solving abilities.
Work location: Chengdu, Sichuan
Working hours: Full time
Salary and benefits: negotiable
We look forward to your joining and working together to promote the development of materials science
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.
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Central Control Technology Co., Ltd. - AI Algorithm Expert
Release time：2024-12-17
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Salary: 40-60K
Experience requirements: Educational requirements: Job Description:
Job Responsibilities:
1. Conduct in-depth research on algorithms such as machine learning, deep learning, transfer learning, and reinforcement learning, and carry out development work on algorithm construction and improvement
2. Participate in or lead the technical feasibility study and algorithm development of key algorithms and models in industrial AI products, and carry out industrial AI product development and application debugging work
3. Conduct problem analysis and scenario research, algorithm development, and application verification based on massive data for industrial scenarios such as prediction and warning, operation optimization, and intelligent control
4. Explore the application verification of the latest cutting-edge technologies such as pre training and large models in the industrial vertical field, supporting the development and implementation verification of industrial large models
Job requirements:
1. Doctoral degree, major in mathematics, computational science, control, chemical engineering, or related fields
2. Proficient in the structure and principles of machine learning, deep learning and other algorithm frameworks, familiar with mainstream frameworks such as PyTorch and TensorFlow
3. Have used programming tools such as MATLAB, Python, C++, conducted data analysis and algorithm design, and have solid programming skills
4. Have good communication and coordination skills, stress resistance, and can adapt to irregular business trips
5. Experience in industrial AI algorithm development and application is preferred
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.
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Guangzhou Zhijing Information Technology Co., Ltd. - Senior Research and Development Scientist (G2026) (MJ000017)
Release time：2024-12-17
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Salary: 0-0K
Experience requirements: Unlimited experience
Educational requirements: Job Description:
[Job Responsibilities]
1. Develop, design, and plan specific drug pipelines for gene editing therapy or tumor immunity, evaluate their scientific and technological feasibility, and conduct technical route competitiveness and risk assessment
2. Lead the team to ensure that R&D progresses as planned, lead technological breakthroughs and innovations, and conduct regular research and evaluation of R&D projects to ensure their sustainability meets the company's needs
3. Guide and enhance the team's technical capabilities, coordinate relevant research and development activities and quality activities, learn about technical achievements in the field and share research and development information from domestic and foreign peers, and maintain the leadership of research and development projects and technologies
4. Support the process development of innovative drugs, assist in IND application, plan and implement patent applications
[Job Requirements]
1. Having a doctoral degree in biology or medicine from a high-level university or research institution at home and abroad, research experience in well-known pharmaceutical/biotechnology companies, or postdoctoral research experience in excellent overseas laboratories
2. Solid research accumulation and profound understanding ability in specific research and development directions, proficient in the latest developments and related resource situations in the field
3. Familiar with molecular biology (such as gene, cell, protein and other related technologies), animal models AAV、 Proficient in one or more aspects of biotechnology such as immunology, proficient in using commonly used research data analysis tools, and preferably with disease-related research experience
4. Having a strong interest in the application of gene editing, genomics, and other fields in the field of biomedicine; Strong understanding, insight, and innovation ability
5. Having excellent communication skills and teamwork spirit, strong learning ability and stress resistance
6. Proficient in both written and spoken Chinese and English, able to quickly grasp academic progress
7. Other experiences that demonstrate research ability can be assisted by the company in obtaining corresponding high-level talent funding
[Company Introduction]
Ruifeng Biotechnology is a leading gene editing drug innovation enterprise in China, driven by gene editing technology and committed to the birth of innovative drugs. Ruifeng Biotechnology is a high-level team in the international early application of gene editing to explore the treatment of genetic diseases, and has continuously accumulated pioneering achievements in the fields of hematology, ophthalmology, and other diseases. It has high-level technological accumulation in areas including gene editing tool innovation, drug strategy discovery, new animal model construction, multi-level efficacy and safety evaluation, and has two innovative drug directions: in vivo and in vitro. The mission of Ruifeng Biotechnology is to provide accessible and curative drugs for patients with severe diseases based on innovative genetic technology. At present, there are pipeline layouts in the fields of genetic diseases, complex diseases, and tumors. Among them, innovative drugs for β - thalassemia have made clinical progress at the global advanced level, and the world's first breakthrough in the cure of α - thalassemia has been achieved. The IND application for global gene edited drugs for Usher syndrome has been approved by regulatory authorities in China and the United States
Ruifeng currently has nearly 7000 square meters of office, research and development, and GMP facilities and venues. It has two research and development bases in Huangpu Economic Development Zone, Guangzhou, Guangdong Province, and a registered branch in Beijing
We attach great importance to our employees, offer competitive compensation, and strive to provide a superior and innovative office and technology environment for all staff
In the rapidly advancing era of life sciences, Ruifeng Biotechnology is committed to the research and development of innovative and curative drugs, enabling patients to overcome the troubles of diseases, bringing hope for treatment to more people, and providing a quality of life similar to that of healthy individuals
The key to our success is that our talents and technology have sufficient competitiveness. Around our vision, we practice an organizational culture of respect, innovation, and striving, and we look forward to you joining the Ruifeng family if you agree with our philosophy
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.
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Wuxi Zhongwei Hi-Tech Electronics Co., Ltd.--Device design engineer
Release time：2024-12-17
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Salary: 0-0K
Experience requirements: Experience is not limited
Educational requirements: Doctor and above
Job Description:
Job Responsibilities:
1. Responsible for the design and optimization of the chip structure of the photodetector and the drawing of the photolithography mask:
2. Be responsible for the process improvement and performance improvement of III-V photodetector chips;
3. Responsible for the test data collation and performance analysis of photodetector chips and components:
4. Cooperate with other departments to carry out technical requirements and problem analysis, and provide solutions;
5. Other work arranged by the leader;
Job requirements:
1. Have relevant knowledge of semiconductor physics, and understand semiconductor process and its principle;
2. Experience in design, fabrication, testing and analysis of semiconductor optoelectronic devices, and background in III-V infrared detectors is preferred;
3. Proficient in using relevant layout design tools and office and analysis software;
4. Good English reading ability, able to complete the collation and analysis of English materials;
5, good at communication, patient and meticulous, rigorous thinking, with a high sense of responsibility and team spirit;
6. Major in microelectronics, materials, electronics, optics, chemistry, physics, etc.
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.
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Beijing Aisi Yipu Biotechnology Co., Ltd. - Director of Pharmacology
Release time：2024-12-17
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Salary: 25-50K
Experience requirements: Unlimited experience
Educational requirements: Job Description:
Job Responsibilities:
1. According to the company's development strategy and the market demand for in vivo pharmacological effects, responsible for the construction of a technical platform for evaluating the efficacy of drugs both inside and outside the body, executing overall project management and tackling new technologies, assisting relevant business departments in technical negotiations and communication with clients
2. Responsible for overall management of the implementation of pharmacological evaluation projects, including experimental design, construction of various disease models, drug efficacy evaluation, mechanism research, data analysis, and issuance of research reports, as well as technical exchanges and communication with clients on project execution, solving various problems during project execution, and ensuring timely and high-quality delivery of the project
3. Responsible for the construction and optimization of the technical system, quality system, document system, and training system within the department
4. Responsible for team development, assessment, and management
Job requirements:
1. Doctoral degree, majoring in pharmacology, veterinary medicine, immunology or biomedical science, with more than 5 years of research and development experience in the biopharmaceutical industry
2. Proficient in relevant animal models, application scenarios, and methods for evaluating the efficacy of anti-tumor/non tumor drugs, with a focus on the cardiovascular field
3. Familiar with experimental techniques in pharmacokinetics and pharmacology research, including in vivo experiments and analysis and processing of experimental data
4. Experience in managing CRO organizations is preferred
5. Strong innovative spirit and scientific and rigorous logical thinking ability, able to independently analyze and solve problems
6. Good English reading and writing skills, able to independently search for literature, write relevant professional reports and application materials
7. The specific job level will be determined based on the candidate's comprehensive qualifications
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: 'Name + Position + Company Name + Location'.