Scientist
at Legend Biotech EU
Dublin, County Dublin, Ireland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 10 Oct, 2024 | Not Specified | 10 Jul, 2024 | 2 year(s) or above | Interpersonal Skills,Communication Skills,Flow Cytometry,Engineers,Statistical Software,Data Analysis,Immunology,Organization Skills,Microbiology,Genetics,Oncology,Molecular Biology,Bioengineering,Cell Based Assays,Logical Approach,Biotechnology,Biology | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
COMPANY INFORMATION
Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide.
Legend Biotech entered into a global collaboration agreement with Janssen Biotech, Inc. to develop, manufacture and commercialize ciltacabtagene autoleucel (cilta-cel). Through our strategic partnership, we look to advance the promise of an immunotherapy in the treatment of multiple myeloma.
QUALIFICATION
- Fluent oral communication, reading and writing skill in English
- Cooperation and collaboration spirit
- Trouble shooting and problem solving skill
- Excellent attention to detail and meticulous bench work with a solid understanding of aseptic cell culture techniques (preferably with human primary cells)
EDUCATION:
- At a minimum, a PhD (preferred) or MSc + 2 years of relevant experience in Biology, Immunology, Oncology, Genetics/Microbiology, Biotechnology, Bioengineering, or related fields.
EXPERIENCE:
- Experience of a range of in vitro skills such as in vitro co-cultures, cytotoxicity assays, flow cytometry, molecular biology and PCR.
CAPABILITIES, KNOWLEDGE, AND SKILLS:
- Familiarity with immune and/or tumor cell analytical methods, including cytotoxicity assays, commonly used to characterise cell-therapy-based modalities.
- Prior experience with plate and cell-based assays including techniques such as molecular biology, digital and quantitative PCR desirable.
- Experience with primary immune cell magnetic isolation and culture
- Experienced in independently designing and executing experiments inclusive of data analysis.
- Understanding of statistical analyses and commonly used statistical software (e.g. GraphPad).
- Excellent organization skills: planning and task management including prioritization, creating and keeping deadlines.
- Experience in 3D culture.
- Excellent interpersonal skills and communication skills, both verbal and written.
- A proven ability to be highly productive and successful in a high pace work environment
- Good problem-solving skills and logical approach to solving scientific problems
- Work as part of a multi-disciplinary team with other scientists, engineers and manufacturing personnel.
- Capable of communicating results in concise and clear presentations and reports.
Responsibilities:
Roles/Responsibilities include, but are not limited to, the following:
- Support and/or lead research activities including design, execution, statistical data analysis and interpretation of scientific experiments.
- Collect and analyse data from various assays used to characterize cell-therapy-based modalities.
- Analyse and translate research results into key conclusions linked to experiment deliverables.
- Prepare presentations and present scientific data at internal meetings.
- Author and review SOPs, study protocols, reports and other scientific and quality documents.
- Critically analyse processes for continual improvements.
- Engage in all required departmental meetings and work closely with cross-functional teams.
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Information Technology/IT
Pharma / Biotech / Healthcare / Medical / R&D
Software Engineering
MSc
Biology
Proficient
1
Dublin, County Dublin, Ireland