Scientists in Pharmaceutical Development PTD Europe Biologics
Pharma Technical Development Europe Biologics (PTDE) brings game-changing therapies from clinical phase I into the market to serve every patient, every day. Our core business is to develop safe, innovative and effective drugs using cutting edge technologies for manufacturing processes (Drug Substance and Drug Product), clinical supply, formulation, device, packaging, and analytical development. Our daily work also includes compiling of regulatory documents and the transfer of development projects to commercial manufacturing.
We are striving for a caring and sensing network organization which lives a culture of trust and collaboration. Our smart people drive innovation through their expertise, passion and "getting it done" mentality. The benefit for the patient is in the center of our thoughts and efforts. To achieve this goal we have embraced new ways of working and thinking.
As a Scientist in Formulation and Process Development, you are part of the Department “Pharmaceutical Development” in Pharma Technical Development (PTD) Biologics Europe in Basel, Switzerland. The department Pharmaceutical Development is responsible for the development of parenteral drug products from Phase 0 up to Launch. Activities encompass formulation and manufacturing process development for parenteral drug products for all clinical stages and the market, the transfer of product and process to commercial manufacturing sites, commercial product support and line extension development.
Your major responsibilities in this position are the following:
Pharmaceutical development of biologics, peptides and small molecules, cell and gene therapy parenteral formulations for clinical development and market (including line extensions).
Planning and execution of formulation screening, knowledge building and, formulation robustness studies, as well as clinical enabling studies (e.g. in use stability and compatibility studies)
Representation of Pharmaceutical Development as pharmaceutical project leader in global CMC teams, functional representative in cross-functional teams and international committees within Roche.
Providing input to global regulatory submissions for Phase 1-3 and the market (BLA/MAA/NDA)
Evaluation and implementation of new methods and technologies, scientific contributions (e.g. publications and conference talks), supervision of research projects and initiation of new research activities.
Contribution to the organizational development of Pharmaceutical Development PTD Biologics Europe.
Your Qualification:
As the successful candidate you hold a Ph.D. or master degree in pharmaceutical sciences, chemistry, chemical/process engineering, biochemistry, biotechnology, or related fields and bring a minimum of 1-3 years of professional experience (industry) in formulation development of parenteral dosage forms for biologics, peptides and small molecules parenterals.
Experience in relevant technologies and processes (e.g. parenteral formulation development, aseptic manufacturing, biochemical and biophysical analytical techniques, lyophilization)
Experience in aseptic process development for parenterals
Experience in ocular formulation and product development, as well as understanding their challenges is desired for the one position
Experience in analytical instrument connection and/or establishing digital workflows in general is desired for another position
Excellent communication skills and collaborative behaviors, with end-to-end and global thinking, proven organizational and planning abilities as well as excellent stakeholder management skills
In depth knowledge or experience in digital tools, ELN, data analytics is a plus
Excellent command of English.
Excellent IT knowledge. Ability to use data analysis and visualization software systems such as JMP, Matlab, LabView.
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