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Innovent Hiring
作者:Hazel43
发表时间:2021-05-21
更新时间:2021-05-21
浏览:116次
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地址:45.
::: 栏目 :::

1 Title: Scientist in functional biology
Report Line: Senior manager in functional biology
Location: Suzhou
Job responsibilities
 Execute studies for drug candidates screening; investigate the mechanism of action of drugs based on molecular and cellular biology experiment.
 Design, establish and accomplish in vitro assays independently. Interpret scientific data and author technical documentation including protocols and reports.
 Communicate with collages within/outside of team. Take responsibility for technology training and public issues. Solve scientific problems.
Qualifications
 PhD in biology, immunology or pharmacology;
 Hands-on experience in molecular and cellular biology skills (cell culture, FASC, ELISA, immunofluorescence, molecular coloning etc.)
 Strong communication skills and ability to learn.
 Open-minded, hard-working. Ability to identify problems and find solutions to scientific challenges. Passionate about science and new drug discovery.
 Ability to Work independently in a collaborative setting.




Please send your CV to Joyena Wang(Recruiter)
[email protected]





2 Title:Cell Therapy QC Principal Scientist
Location: Suzhou
Responsible for the day to day oversight of the QC team, responsible for environmental monitoring program, water and utility testing and final product testing.
Job responsibilities:
 Sustain environmental monitoring program and on-time release of product lots to patients for INNOVENT CT
 Support the optimization of the Aseptic gowning training and qualification program
 Support internal and external audits
 Maintain and support of QC analyst training
 Subject Matter Expert on EMs, Cell biological, Molecular biological, and microbiological testing
 Responsible for the stability program of product and key starting materials
 Support the lifecycle management of analytical method and specification, including analytical technical transfer, method verification/validation, periodic review.
 Assemble reports on findings from environmental monitoring of INNOVENT’s CT GMP facility. Frequently update management on environmental trends. Implement corrective action plans when necessary
 Complete routine record review of test data and related documents for in-process and routine environmental monitoring testing, drug product release
 Generation of COAs for product release
 Develop, revise and review SOPs, qualification/validation protocols and reports
 Conduct investigations regarding out of specifications (OOS) results and address and manage deviations related to micro procedures
 Monitor the GMP systems currently in place to ensure compliance with documented policies
 Review proposed changes to systems, procedures, methods, and submissions to regulatory agencies, as appropriate
 Gather metric information for use in continuous improvement of areas of responsibility
 Supervision of all QC Micro laboratory testing
 Provide updates at daily and weekly meetings
 Conduct performance management of reports and have regular development discussions
 Represent the group in interdepartmental and global meetings
 Other duties as assigned
Job Qualifications:
 Bachelor/MD/PhD
 The ideal candidate is well versed in various microbiological and molecular biology techniques including PCR, ELISA, FACS, Cell culture, rapid release methods, and qualifying environmental monitoring processes with reference to cell/gene therapy product
 Experience in the application of microbiological techniques such as air monitoring, water testing, surface monitoring, genus and species identification of various microbes, endotoxin testing and sterility testing of final product
 The incumbent will need to have the ability to gown for entry into Aseptic core and supporting areas, on an as-needed basis
 Working knowledge of quality systems and regulatory requirements (Ch.P, USP, EP, 21 CRF Part 11/210/211, ATMP, ICH Qs)
 Quality Control, GMPs, molecular cell biology, microbiological method development and validation
 Knowledge of regulatory requirements for data integrity and practices.
 Identifying, writing evaluating and closing OOS’s and investigations
 Strong knowledge of aseptic manufacturing and EM processes
 Knowledge of equipment and utility systems maintenance and IQ/OQ/PQ/PV
 PhD/Master’s Degree and 3+ years’ experience with Industry Quality Control expertise in Aseptic processing and facility and cell/gene therapy products quality controls
 Bachelor’s Degree and 5+ years’ experience in Industry Quality Control expertise in Aseptic processing and facility and cell/gene therapy products quality controls
 5+ experience working in the Environmental Monitoring and Molecular Cell biology laboratories in an aseptic sterile manufacturing facility is preferred.
 3+ years’ experience supervising/managing Cell biology and environmental monitoring labs within the biotechnology or pharmaceutical industry
 Proficient in MS Word, Excel, Power Point and other applications
 Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment, proficient in Chinese and English
 Comfortable in a fast-paced environment with minimal direction and able to adjust workload and flexibility based upon changing priorities
 Demonstrated leadership and management skills, including establishing direction and goals, and building good work ethics for the team










3 Title: International BD Director
Location: London
INNOVENT BIOLOGICS (EUROPE)
Inspired by the spirit of "Start with Integrity, Succeed through Action,” Innovent’s mission is to develop and commercialize high-quality biopharmaceutical products that are affordable to ordinary people. Established in 2011, Innovent is committed to developing, manufacturing and commercializing high-quality innovative medicines for the treatment of cancer, metabolic, autoimmune and other major diseases. On October 31, 2018, Innovent was listed on the Main Board of the Stock Exchange of Hong Kong Limited with the stock code: 01801.HK.
Innovent Biologics (Europe) was established in London in July 2020. The European Office is a key component of the company’s globalization strategy, together with the US International Office located in San Francisco. The company is now looking for an experienced BD Director or Senior BD Director to join the London based team, reporting directly to the COO and Head of Europe. The Director/Senior Director Business Development will be responsible for independently or with support as needed identifying, evaluating, negotiating and closing regional or global deals in Innovent core strategic areas, with a focus on identifying and progressing partnership related to European companies seeking global or regional incl. China deals. Whilst based in London and a member of the International BD team, the Director International Business Development will be an integrated member of the global BD community and work closely also with the Global VP Business Development, based at global HQ.
Key duties
• Key member of Innovent Global Business Development community
• Leads or supports in material way all elements of BD transactions with companies in Europe, regardless of area (oncology, immunology or other core Innovent area), type of deal (license, joint venture, M&A, other) and regardless of whether the deal relate to global or regional (China, European or other) rights. This involves being responsible for initial scouting as well as leading or supporting the business case, building of terms, due diligence, negotiation of terms and definitive agreement and closing of deal.
• Supports the COO and Head of Europe in providing high level direction and recommendations to Innovent’s senior management team on matters of strategic importance related to Europe as a source of in-licensing, out-licensing, strategic partnerships, joint ventures, M&A transactions with European partners.
• Represents Innovent externally at key industry conferences
• Identifies and build relationships with key European biopharmaceutical industry potential partners
• Understand and know how to navigate the European, China and Global biopharmaceutical market, including companies, products, and company strategies in order to enable Innovent to be able to effectively attract key partners.
• Effectively collaborate with internal departments (Marketing, Medical, R&D, Development) throughout the process of establishing and executing key partnerships.
• Possess a strong understanding of Innovent’s biopharmaceutical products, key competitors, and positioning to win.
• Track and communicate ongoing industry developments to internal team members and more broadly where appropriate to stay up-to-date on the competitive environment.
Required Job Qualifications
• At least 5 years experience in biotech or pharma industry business development, venture capital, investment banking or life sciences technology transfer
• Significant track record of negotiating and successfully closing a broad range of different deal types including in-licensing, out-licensing and commercial agreements.
• Bachelor degree or more in a science and/or technology related area
• Team player
• Strong analytical and quantitative skills
• Strong negotiation, communication and presentation skills
• Strong understanding of Intellectual Property matters
• International experience
• Fluent English speaking, reading and writing skills.
• Excellent organizational skills, with emphasis on prioritization and goal setting.
• Understanding of biological sciences and biopharmaceutical product development
Additional helpful Job Qualifications
• MBA or JD
• Intermediate or above mandarin
• Education or past work experience in China












4 Principal Scientist, Medicinal/Organic Chemistry (Suzhou / Maryland)
Research and Development
Job responsibilities:
• The chemistry group seeks medicinal or organic chemists with experience in organic synthesis. You will design synthetic routes and execute the synthetic steps for bioactive compounds, including warheads and linkers of antibody-drug conjugates.
• You are expected to draw conclusions from data analysis, and scout literature for reaction design and propose new ideas.
• You will work with the internal chemists and external CROs to do technical transfer for the timely progress of projects.

Job Qualifications:
• Ph.D. (more than 4 years’ experience) in Medicinal or Organic Chemistry.
• Extensive knowledge of medicinal or organic chemistry, good analytical skills, including the characterization of compounds using NMR, LC-MS.
• Good knowledge of lab safety, maintain lab safety with colleagues.
• Keep clear and complete records of experiments and data.
• Excellent interpersonal, communication, and presentation skills.
• Team player with a strong desire to achieve broad team goals.


 
5 Principal Scientist, Analytical Chemistry (Maryland)
Research and Development
Position Summary
We are seeking a highly skilled and motivated Principal Scientist to join Innovent Biologics. You will lead the analytical program both on small molecules and biologics, including metabolites and antibody-drug conjugates. You will also take on the internal QC responsibility for the development of small molecule compounds, drug-linkers, and antibody-drug conjugates. You will work closely with synthetic chemists, conjugation chemists, and biologists to push the platform and pipeline projects forward, and act as a liaison between discovery and development groups. You may engage with external CROs for bioanalytical tasks.

Job responsibilities:
• Maintain a significant level of productivity in the laboratory setting.
• Stay up to date with the bioanalytical technology, especially technologies related to antibody-drug conjugates.
• Facilitate the publication and patent protection of research work.

Job Qualifications:
• Ph.D. in Analytical Chemistry, or related scientific disciplines.
• 5+years of post-doctoral work experience in bioanalysis that required advanced mass spectrometry assay development, preferably in the pharma/biotech industry.
• In-depth knowledge of small molecule, biologics analysis using various analytical tools, especially LC-MS.
• Good understanding of the principles of biology, DMPK.
• Experience to execute analysis plans for pharmacokinetics, pharmacodynamics data.
• Experience with immunoassay methods.
• Prior experience with targeted delivery platforms (antibody-drug conjugates or small-molecule drug conjugates) is desirable.
• Leadership skills, including project management, technical issue identification and resolution, and a good knowledge of lab safety.
• Excellent interpersonal, communication, and presentation skills.
• Team player with a strong desire to achieve broad team goals




6 Principle Scientist , Immunology (Suzhou)
Research and Development
Job responsibilities:
• Lead discovery efforts from target nomination, validation through pipeline development. Independently conceive, execute experiments and analyze data for proof of concept and mechanism of action studies.
• Recruit and manage a research team to understand the mechanisms of immune disorders including, but not limited to, asthma, COPD, atopic dermatitis, rheumatoid arthritis, inflammatory bowel disease, systemic lupus erythematosus, type 1 diabetes, psoriasis and multiple sclerosis.
• Establish and sustain cross-functional collaborations internally and externally with industrial and academic partners.
• Actively contribute to the research community through publications and conference presentations. Supervise staff members and foster a rigorous and dynamic research environment within team.

Job Qualifications:
• Ph.D. in immunology/biochemistry, with at lest 4 years of post-doctoral experience or work experience.
• Experience in in vivo oncology is a plus.
• Solid experience in one or more of the following:
• T/DC/B cell biology;
• Antibody/protein discovery;
• Oncology;
• In vitro and in vivo efficacy evaluation.
• Good verbal and written skills in English;excellent presentation skills is a preferred plus.


 
7 Senior Scientist , Immunology (Suzhou)
Research and Development
Job responsibilities:
• Lead projects in early target discovery, target validation;
• Prepare the data for IND application,draft the scientific papers and patents;
• Support new molecule design;
• Develop and execute/support assays for in vitro and in vivo MOA and efficacy experiments;
• Assist the daily management of the laboratory.

Job Qualifications:
• Doctor degree in immunology/biochemistry,work experience in in vivo oncology is a plus.
• Solid experience in one or more of the following:
• T/DC/B cell biology;
• Antibody/protein discovery;
• Oncology;
• In vitro and in vivo efficacy evaluation.
• Good verbal and written skills in English;excellent presentation skills is a preferred plus.




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