Analytical Expert

This is a temporary contractor opportunity at NovartisNovartis touches the lives of a tenth of the world’s population. Every role here, regardless of contract type, makes an impact on human lifeNovartis 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.Ready to work with/through Magnit at Novartis? Please read on…We are looking for an Analytical Expert to support Analytical Research & Development (ARD). ARD sits within the Global Technical R&D department of Global Drug Development and plays an essential role in the characterization and analysis of Small Molecule 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, experienced Analytical Expert with a strong background and experience in parenteral development to join our team. Expertise in RLT, peptide analytics and parenteral dosage form is required.Your main responsibilities:Plan, interpret and report results of scientific experiments for timely supply of drug substances (DS) and drug products (DP).Write & review analytical documents (e.g Analytical methods, Specifications, Validation reports, Stability reports, Batch records for stability and release testing) and align the corresponding activities within a global project team.Drive method development for peptide drug substances and RLT Drug product.Manage interactions with internal and external stakeholders, including outsourced activities to CROs by providing scientific and technical guidance whenever necessary.Proactively identify scientific, technological and GMP challenges, propose creative solutions and communicate key issues to the Analytical Project Leader or respective technical project team.Work according to appropriate SOPs, GMP, Quality Directives, Health and Safety & internal Novartis guidelines.Provide valuable input to the analytical CMC documents and support regulatory submissions.Drive, lead, and manage analytical activities including impurity profiling related to the analytical development of RLTs compounds (e. g. method development, validation, stability, and release testing).Provide scientific guidance to the cross-functional and global project teams and thereby scientifically driving our exciting RLT portfolio.Display a collaborative and inspired attitude within project teams and our stakeholders and partners is key.Good understanding and awareness of regulatory guidelines for analytical developmentWhat you’ll bring to the role:PhD in analytical chemistry or equivalentAt least 5 years experience in the pharmaceutical industry with a track record in GMP activities for development or marketed products.Profound expertise in documentation writing (Stability Report, Validation, IND IMPD modules 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 ...)Good knowledge of commonly used software and computer tools.Excellent scientific/technical writing skills.Eager to develop new methods and assess new analytical techniques.Proven leadership in guiding and mentoring colleaguesStrong coordination skills, collaborative spirit, self-driven attitude, high level of learning agility.Strong quality focusExcellent communication and role model skillsFluent in English (oral and writing)Work details:Workload: 100% (40 hours per week)Role type: OnsiteRequired start date: 1st December 2025Contract: 12 monthsWhy 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. #J-18808-Ljbffr