This is a temporary contractor opportunity at Novartis
Novartis touches the lives of a tenth of the world’s population. Every role here, regardless of contract type, makes an impact on human life!
Novartis partners with external managed service provider Magnit Global to offer engaging temporary contractor opportunities like this, to those who are looking for flexibility in their career while looking to gain new skills and experiences providing services to an inclusive global medicines company. Click here to learn more about Magnit.
Ready to work with/through Magnit at Novartis? Please read on…
Job Purpose:
The line function Analytical Research and Development (ARD) is within the Global Technical R&D department of Global Drug Development (GDD) and plays an essential role in the characterization and analysis of small molecules and synthetic large molecules Drug Substances and Drug Products from the time they leave the discovery laboratory until they are transferred to Commercial Production. We are looking for a highly motivated Analytical Expert in the field of small molecules.
Your main responsibilities:
• Planning, interpreting and reporting results of scientific experiments for timely supply of drug substances (DS) and drug products (DP).
• Performing raw data checks for externalized activities
• Writing & reviewing analytical documents (e.g Analytical methods, Specifications, Validation reports, Stability reports, Batch records for stability and release testing) and aligning the corresponding activities within a global project team.
• Managing interactions with internal and external stakeholders, including outsourced activities to CROs by providing scientific and technical guidance whenever necessary.
• Proactively identifying scientific, technological and GMP challenges, propose creative solutions and communicate key issues to the Analytical Project Leader or respective technical project team.
• Working according to appropriate SOPs, GMP, Quality Directives, Health and Safety & internal Novartis guidelines.
Requirements:
• PhD or minimum Master in analytical chemistry or equivalent
• At least 5 years’ experience in the pharmaceutical industry with a track record in GMP activities for development or marketed products.
• Profound expertise in analytical raw data documentation, documentation writing (Stability Report, Validation etc)
• Broad scientific knowledge in chemistry, pharmaceutical or analytical sciences, ability to perform in a highly dynamic environment.
• Advanced knowledge of laboratory and/or technical tools (e.g. HPLC, LC-MS, Quality management systems, statistical evaluation tools ...)
• Background/experience with inhaled dosage forms is a must have
• Good knowledge of commonly used software and computer tools.
• Good scientific/technical writing skills.
• Fluent in English (oral and writing),
• Experience is Inhaled dosage form is highly desirable
Workload: 100% (40 hours per week)
Role type: Onsite
Required start date: September 2025
Why Novartis:
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?
EEO Statement:
The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.
Accommodation:
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to Magnit at directsourceproteam@prounlimited.com.
