Expert Science
vor 2 Monaten
390419BR
**Expert Science & Technology (M/F/d)**:
Switzerland
**About the role**
Location: Basel, Switzerland
Role Purpose:
Analytical Research & Development (ARD) sits within the Global Technical R&D department of Development and plays a crucial role in the characterization and analysis of small molecule drug substances and drug products as well as, e.g., new modalities or oligonucleotides from the time they leave the discovery laboratory until the transfer to commercial production.
We are looking for a highly motivated Expert with expertise in analytics specifically focusing on particle and powder characterization. This role will help ARD to maintain in-house capabilities to deliver on the current and future project portfolio in collaboration with the project teams.
Your responsibilities include but are not limited to:
- Plan, design and perform experiments to characterize pharmaceutical micro
- and nanosuspensions and powders, including illustration, interpretation and reporting of results
- Validate QC methods for particle and powder characterization to analyze drug products, drug substances and excipients
- Actively contribute to analytical method transfer to other development sites, production or contract laboratories
- Provide raw data documentation, evaluation and results interpretation of scientific experiments with high focus on quality, generate lab procedures, reports, instructions and SOPs
- Communicate and address problems, e.g., deviations and unexpected results from experiments, contribute to problems solving
- Contribute to maintenance of infrastructure and equipment, evaluate new equipment
- Meet quality, quantity and timelines in all assigned projects, actively participate in project teams, meetings, networks. Actively contribute to team goals.
- Work according to appropriate SOPs, GMP, Quality Directives, Health and Safety (HSE) regulations and internal Novartis guidelines
**Commitment to Diversity & Inclusion**:
- We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve._
**Role Requirements**
Minimum requirements
- Professional experience (ca. 3-5 years) in GMP environment and analytics (e.g., Quality Control), supporting audits & HA inspections
- Working experience within the pharmaceutical industry and good technical knowledge of Pharmaceutical/Chemical Analytics/Quality Control and equipment qualification
- Educational Background: Minimum: Technician with continuing education (EU) or BS/MS or equivalent
- Desirable: Advanced degree in a scientific or relevant discipline (MS or equivalent)
- Successfully demonstrated several years (minimum of 3 years) of directly related experience as scientist or equivalent
- Adequate understanding of development processes in own function
- Advanced knowledge of laboratory and/or technical tools. Awareness/proven experience for safe handling of chemicals, potentially dangerous materials and equipment
- Fluent in English and German preferable
Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
Accessibility and accommodation
**Division**
Development
**Business Unit**
TECHNICAL R & D GDD
**Work Location**
Basel
**Company/Legal Entity**
Novartis Pharma AG
**Functional Area**
Research & Development
**Job Type**
Full Time
**Employment Type**
Regular
**Shift Work**
No
**Early Talent**
Yes
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