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Jobs
- Director of Pharmacology and Pharmacodynamics
If you are interested in one or more job opportunities, please email your resume to: HR1@szbr.cn
Responsibilities：
- Provide technical support in the early stage of new drug development process, including target research, project setup, target validation, etc.
- Lead pharmacology team to develop and optimize relevant in vivo and in vitro experimental models
- Efficient and high-quality completion of the pharmacological part of the new drug registration, such as data collecting, review, coordination of on-site verification and registration review, etc.
- Responsible for recruitment training, team division of labor, and SOP development and implementation to ensure high quality and efficient completion of projects
Qualifications：
- PhD degree or above in biology, medicine, pharmacy or a related discipline
- Familiar with in vitro pharmacology and in vivo pharmacodynamic animal modeling
- Good management ,coordination, and communication skills
- Decent English skills
- Relevant experience in new drug development is preferred
- QA/QC Director/Manager
If you are interested in one or more job opportunities, please email your resume to: HR1@szbr.cn
Responsibilities：
- Fully organize all the work of the R&D QA/QC department to establish a compliant laboratory that meets the requirements. Ensure that the management of the R&D QA/QC department meets the quality control requirements of China, EU and FDA for non-clinical studies
- Establish and improve the R&D QA/QC related management system and operating procedures, and organize and implement them in strict accordance with the approved documents
- Responsible for organizing skill training and business guidance for departmental staff. Do a good job of training and reserving talents.
Qualifications：
- Master (MS) degree or above in biology, chemistry, and other related majors
- CET-6, decent English skills (listening, speaking, reading, and writing), able to write operational documents and reports in English
- At least 3 years of experience in R&D laboratory QA/QC management and mastering the corresponding pharmaceutical regulations. Overseas working experience is preferred.
- Proficiency in the use and maintenance of various analytical instruments, familiar with physical, chemical, activity, micro-assay and other methods of biological drug analysis and detection, such as: enzyme-linked immunoassay, liquid chromatography, gas chromatography, ultraviolet, infrared, cell activity, etc.
- Bioanalytical Director/Researcher
If you are interested in one or more job opportunities, please email your resume to: HR1@szbr.cn
Responsibilities：
- Design, develop and validate experimental methods for LC/MS/MS bioanalysis of various biological samples under GLP regulations, including but not limited to tissue homogenates, plasma, serum, urine, etc.
- Write and review bioanalytical data and study reports, including test development, validation, and sample analysis reports. Communicate with clients on project progress in a timely manner, resolve technical issues in experiments, full flow control of samples and reagents and data delivery
- Compliance with regulatory regulations and principles (GLP/GCLP) and familiarity with key Chinese and global regulatory provisions and reporting requirements (CDE, FDA, EMA, HGRAO)
- Develop contingency plans and take corrective action for unforeseen events that occur during the project
Qualifications：
- Master (MS) degree or above in pharmacy, chemistry, biology, immunology, or related fields
- Proficient in immunology laboratory analytical methods such as ELISA, ECLIA, cellular immunoassay, etc.; or familiar with GLP laboratory knowledge of LC-MS/MS bioanalytical methods
- Experience in managing GLP laboratories and research projects or relevant work experience in CRO companies is preferred
- Team management experience and fluent English speaking, reading and writing skills, with overseas education background preferred
- Director/Researcher of Drug Metabolism
If you are interested in one or more job opportunities, please email your resume to: HR1@szbr.cn
Responsibilities：
- Responsible for directing the program design, execution, analysis and interpretation of data and information for PK studies
- Responsible for providing preclinical and translational medicine DMPK results to support lead compound optimization, candidate selection, and IND-enabling studies
- Ensure close working relationship with relevant departments and BD, PM to provide technical advice, solve technical and operational problems and promote business development
- Responsible for communicating and collaborating with Party A on all aspects involved in the DMPK study
- Responsible for the daily operation and management of DMPK business segment, responsible for the echelon building and training of DMPK team, and responsible for the corporate culture promotion of DMPK team.
Qualifications：
- PhD in DMPK or Master (MS) degree or above in a drug science related field with at least 3 years of DMPK related work experience
- Hands-on experience with in vitro and in vivo PK studies
- Familiar with PBPK, PKPD modeling is preferred
- Candidate should possess good teamwork spirit and values, excellent professionalism and innovation ability, and decent English skills
- Mass Spectrometry Scientist
If you are interested in one or more job opportunities, please email your resume to: HR1@szbr.cn
Responsibilities：
- Responsible for the development of application methods for high performance liquid chromatography (HPLC), liquid chromatography mass spectrometry (LCMS), high resolution mass spectrometry Q-TOF, inductively coupled plasma mass spectrometer
- Responsible for the preparation of experimental sample, analysis and resolution of problems arising in the process of analytical method development
- Participate in the daily management of the laboratory, including the calibration of instruments and equipment, maintenance and necessary documentation management, etc.
- Assist with other tasks as assigned by the company and the lab
Qualifications：
- Bachelor (B.S.) degree or above in medical testing, drug analysis, biotechnology, analytical chemistry or basic medicine related majors
- Responsible for liquid chromatography method development and analytical testing, familiar with biological sample enrichment and pretreatment process, data processing and related analytical software
- Able to independently complete experimental analysis, records, reports, etc.
- Director of International Business
If you are interested in one or more job opportunities, please email your resume to: HR1@szbr.cn
Responsibilities：
- Develop customers through multiple channels, collect and integrate potential customer information, contact and maintain existing customers, and develop new customers
- Collect and analyze customer needs, formulate and review project plans and quotations, and be responsible for project bidding and business negotiation
- Responsible for drafting cooperation agreement, reviewing contract terms and negotiating contract. Responsible for customer business negotiation and signing business agreement
- Expand project sources, collect new products (especially hepatoenteropathy, and related cancer indications) and new technologies in biomedical field at home and abroad, screen projects, comprehensively evaluate and draft project report materials
- Coordinate relevant departments to cooperate with the commercial implementation of the project
Qualifications：
- Master degree or above in medicine, pharmacy or biochemistry
- Have good management, communication, expression, business negotiation and ability to work under pressure
- Understand domestic and foreign pharmaceutical enterprises, pharmaceutical products, market status and development trend
- Understand the drug management regulations and the whole process of drug R & D process, and it is better to have certain technical control ability
- Fluent in Chinese and English, good PPT presentation skills and presentation experience
- Have a strong sense of responsibility and execution, and identify with corporate culture and values
- More than 5 years of experience in new drug research and development (ideal for hepatoenteropathy, and related cancer indications), with the motivation and ability of continuous learning; relevant working experience in overseas pharmaceutical companies is preferred
