Join_Join_Beijing Innovec Pharmaceutical Technology Co., Ltd | TARD

Chief Scientist CSO 2021-09-28 14:08:25

Job Responsibilities 1. Frontier tracking of the company's related technologies; research on industry technology trends; 2. Research pipeline layout and project approval; 3. Supervise all projects and scientific research operations to ensure that they are carried out smoothly on time; 4. Patent layout, paper layout. Qualifications 1. Have the experience of being responsible for the IND on the product; 2. Interested in gene therapy industry; 3. Doctor degree, biological background, neurometabolic diseases related fields. Resume delivery email: HR@innovecbio.com

Pharmaceutical Nanomaterials for Nucleic Acid Delivery 2021-09-28 14:07:00

Job Responsibilities 1. Read the literature extensively to understand the clinical needs of the disease and the characteristics of existing drugs, including defects; 2. According to the needs of the disease and the defects of existing drugs, design a feasible drug delivery system to obtain better absorption, sustained release, targeting, stability, safety, etc.; 3. Preparation, modification and characterization of drug delivery systems (liposomes, hydrogels, etc.); 4. Evaluate the in vitro and in vivo drug delivery capabilities of the nanoformulations, as well as the in vivo pharmacodynamics; 5. Participate in the operation and maintenance of the nano preparation laboratory, the installation and debugging of research equipment and the maintenance of daily instruments; 6. Responsible for the delivery technology of mRNA and sgRNA, the development of new liposome/lipid nanoparticle (LNP)-based mRNA preparation technology, including the design of delivery carrier compounds (such as lipid compounds), formulation design and screening , Process research, preparation process, quality characterization; 7. Responsible for the research and development of nucleic acid drugs, nano, microsphere liposome/lipid nanoparticle (LNP) delivery technology formulations, including formulation development literature research, program design, formulation formulation screening optimization, formulation process research, stability inspection and Pilot scale up and other work; 8. Participate in the development of new nucleic acid drugs, nanometer and microsphere liposome preparation technologies, including related technologies for delivery of carrier compounds (such as lipid compounds). Qualifications 1. Obtain a master's degree or above in the fields of organic chemistry, medicinal chemistry, medicinal polymers, and pharmaceutical preparations; 2. Understand the microenvironment of cells and tissues, and have a certain understanding of disease pathology and cell biology; 3. Have relevant research experience in drug delivery, and be familiar with the advantages and disadvantages of different delivery systems and materials; 4. Be good at thinking, love your job, and have a good team spirit. Resume delivery email: HR@innovecbio.com

Head of Neurology R&D 2021-09-28 14:06:57

Job Responsibilities 1. Lead the neurology gene therapy research and development team to develop gene therapy drugs for neurology; 2. Be able to independently carry out early research and development of neurological gene therapy drugs; 3. Able to lead the team to solve the challenges of neurological gene therapy drug development; 3. Have an in-depth understanding of neurological gene therapy projects, and be able to propose creative problem-solving methods; 4. Familiar with policies, laws and regulations in the field of gene therapy at home and abroad. Qualifications 1. Doctorate degree in neurobiology; 2. Have a comprehensive and in-depth understanding of the design of neurological gene therapy products; 3. Have experience in gene therapy product development; 4. Have innovative thinking and problem-solving skills; 5. Good communication skills, written and oral expression skills; 6. Experience in managing R&D teams and project management. Resume delivery email: HR@innovecbio.com

Head of Ophthalmology R&D 2021-09-28 14:05:57

Job Responsibilities 1. Lead the ophthalmology gene therapy R&D team to develop gene therapy drugs for ophthalmology; 2. Be able to independently carry out early research and development of ophthalmic gene therapy drugs; 3. Able to lead the team to solve the challenges of ophthalmic gene therapy drug development; 4. Have an in-depth understanding of ophthalmic gene therapy projects, and be able to propose creative problem-solving methods; 5. Familiar with policies, laws and regulations in the field of gene therapy at home and abroad. Qualifications 1. Doctorate degree in molecular biology, pharmacy, medicine and other related majors; 2. Have a comprehensive and in-depth understanding of the design of ophthalmic gene therapy products; 4. Have innovative thinking and problem-solving skills; 5. Good communication skills, written and oral expression skills; 6. Have the ability to manage R&D teams and project management experience. Resume delivery email: HR@innovecbio.com

Pre-clinical registration declaration 2021-09-28 14:05:13

Job Responsibilities 1. Support the preparation of registration documents and registration inspection; 2. Support registration, declaration and issuance of supplements; 3. Support the research plan design and clinical institution screening of clinical trial projects; 4. Support researcher communication, seminar organization, and ethical review application in the early stage of the trial; 5. Support the monitoring, quality control, follow-up and visit during the experiment; 6. Support the data transfer and clinical trial report after the trial; 7. Continue to promote the implementation of laws and regulations within the company, and continue to influence company employees to enhance their awareness of laws and regulations; 8. Understand and follow the quality management system, quality manual, quality policy, quality objectives and applicable laws and regulations; 9. Complete the training related to the quality system and regulations on time. Qualifications 1. Bachelor degree or above, major in biology, medicine, chemistry, etc., master degree is preferred; 2. Familiar with laws and regulations in gene therapy; 3. Good communication skills, written and oral presentation skills. Resume delivery email: HR@innovecbio.com

Upstream Process Development Engineer 2021-09-28 14:04:37

Job Responsibilities 1. Development and optimization of upstream processes: including experimental design, operation, data analysis and report writing; 2. Upstream process enlargement, understanding the characteristics of biochemical reactors of different scales, including shake flasks, 2L, 10L, 50L, etc.; 3. Proficiency in using various instruments developed by upstream processes, including different biochemical reactor operations and parameter settings; 4. Skilled operation related characterization experiments, including DLS, SDS-PAGE, TCID50, ddPCR, etc.; 5. Develop relevant upstream processes for different products; 6. Writing experiment reports and standard operating procedures, etc.; 7. Assist in technology transfer and GMP production. Qualifications 1. A doctorate degree in bioengineering, chemical engineering, or pharmaceutical engineering related majors with relevant scientific research background, or a master's degree in related majors and industrial experience in biopharmaceutical process development, or a bachelor degree with years of upstream process development experience; 2. Familiar with the methods of upstream process development; 3. Familiar with DOE and other process optimization methods and data analysis software; 4. Serious and responsible work, self-motivated and teamwork spirit; 5. Good expression and communication skills; 6. Familiar with office software and good writing skills. Resume delivery email: HR@innovecbio.com