Dfind Science & Engineering is now searching for a Consultant who will be working within Upstream process development at Sobi in Solna. The assignment will start asap and for 1 year.About SOBI
Sobi is an international pharmaceutical company focusing on finding new orphan drugs. Sobi’s main therapeutic areas are inflammation, hemophilia and genetically diseases. Sobi R&D’s mission is to develop and deliver innovative therapies that improve the lives of patients and their families.
Expression and Upstream Development is a section within Biopharmaceuticals R&D responsible for the development of robust and efficient cell cultivation processes in reactor scale. The section work with both mammalian and microbial cells. The team is highly experienced and the environment is very collaborative.Employer:
Dfind Science & EngineeringCity:
Consultant position (permanent after 6 months of probation).Deadline for application:
2019-04-29. Selection is continuous.For information:
Patricia Torregrosa, email@example.com
As a consultant you will take leadership of activities for the development, refinement and execution of laboratory methods in Upstream development within reactor scale mammalian cell culture.Key Responsibilities:
Knowledge and experiences
- Sub project lead and responsible for study design, data evaluation and compilation of study results.
- Performance and documentation of bioreactor experiements (Ambr or glass bioreactor)
- Supervise coworkers as required
- Impact upon decisions taken in cross-functional CMC project team(s).
- Can provide timelines and resource estimates for project activities to director or project leader
- Contributes to new knowledge within cell culture process development, scale-up, and tech transfers.
- Responsible for relevant preclinical / CMC reports and / or regulatory documentation
- Collaborates with experts (both internal and external) to solve complex technical or scientific problems
Organization and Business description:
- MSc/PhD in relevant discipline Experience
- Minimum 5 years in pharmaceutical/biotechnology industry with experience from upstream process development projects
- Established expertise and extensive theoretical / practical experience within upstream CMC process development.
- Experience in report writing and regulatory documentation.
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