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发帖数: 1 | 1 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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