Senior Expert Science & Technology

Novartis seeks a Senior Expert Science & Technology in Basel, CH, to lead analytical research for oligonucleotides within the ARD team. The role requires a PhD with 3+ years’ experience or a Master’s with 10+ years in pharmaceutical analytics, focusing on mass spectrometry and regulatory-compliant methods.

This position is part of the Analytical Research & Development (ARD) team within Technical R&D, tasked with characterizing and analyzing drug substances and products from early discovery through to commercial production.

Responsibilities

• Plan, carry out, and report on scientific experiments aligned with the ARD Oligonucleotides Analytics project.
• Independently design, execute, interpret, and document analytical work for oligonucleotides (drug substance and drug product) using advanced analytical methods.
• Develop and implement mass spectrometry techniques tailored for oligonucleotide analysis.
• Promote best practices and share technical knowledge within the project team and broader organization.
• Prepare analytical documentation in line with global project strategies and support strategic planning and execution.
• Contribute to laboratory experiment planning, including scheduling, monitoring, and data evaluation.
• Act as primary point of contact for scientific and technical matters with internal stakeholders.
• Provide scientific guidance and mentorship to lab associates.
• Manage technical analytical deviations and propose corrective and preventive actions (CAPAs).
• Support audits and health authority inspections to ensure no major findings in assigned areas.
• Adhere to SOPs, GMP, GLP, QM, HSE, ISRM, and Novartis guidelines.
• Collaborate effectively and encourage knowledge sharing across teams.

Requirements

• PhD in analytical chemistry with at least 3 years of experience, or a Master’s degree with 10+ years in the pharmaceutical industry.
• Strong skills in hyphenated analytical separation and detection methods, including mass spectrometry.
• Solid understanding of laboratory management and techniques such as HPLC, UV-spectrometry, and titration.
• Experience with quality principles in drug development, including GMP, and awareness of regulatory and quality expectations.
• Ability to thrive in a fast-paced, dynamic environment.
• Excellent coordination, communication, teamwork, self-motivation, and quick learning capabilities.

About the company

Novartis is dedicated to fostering an inclusive workplace and building diverse teams that reflect the patients and communities they serve. The company supports reasonable accommodations for all individuals.

• Commitment to an inclusive and diverse work environment.
• Support for reasonable accommodations for all employees.