Senior Scientist Manufacturing Statistics
Role details
Job location
Tech stack
Job description
The successful candidate will provide statistical support to manufacturing programs across therapeutic modalities, including synthetics, proteins, and advanced therapies. They will support data-driven manufacturing decisions by applying analytical reasoning, performing thorough analyses, advising on experimental design, and clearly communicating evidence. The role includes developing and applying Bayesian predictive models, collaborating with cross-functional teams, and coordinating with external contractors., * Work closely with researchers on experimental design, data analysis, interpretation, and clear communication of evidence to support research, development, and product commercialization.
- Ensure the appropriate application of high-quality statistical methodologies tailored to each research need.
- Serve as a co-author on scientific publications and present research findings at external venues.
- Build and maintain trusted relationships with colleagues and stakeholders through clear, reliable statistical guidance.
- Support internal statistical trainings and contribute to the development and dissemination of best practices and reproducible workflows.
Requirements
Do you have experience in SAS?, Do you have a Master's degree?, * Ph.D. in Statistics or related field, or Master's in Statistics or related field with commensurate years of relevant experience, * Knowledge of (non)-linear mixed effects models and multivariate analysis is required
- Knowledge of Bayesian statistics is desirable
- Expertise in experimental design (Optimal DoE, Definitive Screening designs, Bayesian Optimization and Active learning) is a plus
- Proficient in R programming
- Eager to expand expertise, strong intellectual curiosity
- Ability to work autonomously and within a team environment
- Highly effective written and verbal communication and presentation skills
- Fluency in English, both written and spoken, Advanced Analytics, Biostatistics, Clinical Trials, Collaborating, Consulting, Critical Thinking, Data Privacy Standards, Data Quality, Data Savvy, Digital Fluency, Good Clinical Practice (GCP), Quality Assurance (QA), Report Writing, Standard Operating Procedure (SOP), Statistical Analysis Systems (SAS) Programming, Statistics, Systems Development, Technologically Savvy
Benefits & conditions
We offer you a place in our wonderful diverse and supportive team dedicated to service and wellbeing. You will be rewarded through a competitive renumeration package along with continuous training, support, and career development programs. You will also receive other benefits such as on-site sport accommodations, health care services and meal vouchers.