Scientist, Investigative and Immunosafety, pRED Pharmaceutical Sciences
View: 167
Update day: 25-04-2024
Location: Basel Basel-Stadt BS
Category: R & D Science Labor High Technology Mechanical / Technical Electrical / Electronics
Industry: Medical Equipment Manufacturing Biotechnology Research Pharmaceutical Manufacturing
Position: Associate
Job type: Full-time
Job content
The PositionIn Roche’s Pharmaceutical Research and Early Development organisation pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs. At pRED, we are united by our mission to transform science into medicines. Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.Pharmaceutical Sciences (PS) is a global function which covers several research areas including Immunosafety and Investigative Safety (I2S). In I2S, we help bring the best medicine to patients using innovative safety science. We are inspired to provide a transparent roadmap of preclinical safety assessment, balancing our safety findings against efficacy considerations. We use advanced, science-based models, back-translating from the clinic to generate forward-translatable, human-relevant safety strategies.Job MissionAs an experienced in vitro model scientist in the Department of Pharmaceutical Sciences, you will focus on the qualification of in vitro models with an emphasis on teratogenicity and reproductive toxicology assessment.As part of the Investigative Safety and Immunosafety group, you will work in close collaboration with scientists from different departments within PS/pRED including Nonclinical Safety and the Institute of Human Biology (IHB) to generate and integrate molecular, cellular, tissue and functional data with the goal of delivering unique and holistic insights into drug safety and enable informed decisions to bring the best drugs to patients.Your ImpactIn this position:- You will be responsible for set-up, applying and validating in vitro models for safety assessment specifically in the area of developmental and reproductive toxicology.
- You will perform and guide related wet lab activities.
- In addition, you will contribute and, based on experience gained, be ultimately responsible for our in-house in vitro DART strategy in close collaboration with your stakeholders in pharmaceutical sciences.
- Background on in vitro model development and application and strong skills in the wet lab.
- Expertise in vitro models evaluation and qualification, as well as solid experience in applying this knowledge to answer complex biological questions
- Knowledge of developmental and reproductive toxicology is an asset
- Excellent interpersonal and communication skills and strong attitude to teamwork
- Excellent strategic thinking, self-initiative and a strong sense of accountability
- Ability and willingness to challenge, be challenged and learn
- Proficient in spoken and written English
Deadline: 09-06-2024
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