Analytical Scientist (Expert S&T) Full-time

Job Title

Location: Basel, Switzerland #onsite

Role Purpose: We are looking for a motivated Analytical Scientist to join Analytical Research & Development (ARD). ARD sits within the Technical R&D Department of Development and plays an essential role in the characterization and analysis of Drug Substances and Drug Products from the time they leave the discovery lab until they are transferred to commercial production. The role responsibilities include performing and documenting scientific experiments for drug substances (DS) and drug products (DP), small molecules and RLTs portfolio, in collaboration with multifunctional project teams and using state-of-the-art techniques.

Major Accountabilities

• Develop and optimize analytical methods for the characterization and quantification of drug substances and drug products (small molecules and RLTs).
• Plan, execute, document and report scientific experiments (e.g. method development, testing, formulation development analytics etc.) according to the agreed timelines and appropriate quality standards.
• Responsible for good documentation practices (GDP) and good laboratory practices (GLP) during execution of laboratory activities.
• Analyze, interpret and report analytical data to support drug development.
• Troubleshoot analytical methods and instrumentation issues, providing scientific rationale and solutions.
• Implement and maintain lean, efficient and environmentally sustainable practices in the laboratory. Contribute to maintenance of lab instruments / day-to-day operations.
• Timely execute project related activities to support TRD-NCE strategies and goals. Contribute to the continuous improvement of laboratory processes and workflows.

Minimum Requirements

• Technician or Bachelors/Masters in Life Science (e.g., analytical chemistry / chemistry / pharmacy) or equivalent. Minimum experience of 3 years.

Skills

• Experience in analytical separation techniques such as liquid and gas chromatography. Knowledge in Mass Spectrometry is a plus.
• Hands-on experience in the development and troubleshooting of chromatographic methods for pharmaceuticals. Experience with method development / optimization software is a plus.
• Understanding of ICH guidelines, cGMP, and regulatory requirements for analytical testing.
• Strong analytical and problem-solving skills.
• Excellent organizational and time management abilities.
• Ability to work effectively both independently and as part of a team.
• Attention to detail, commitment to quality and accuracy.

Languages

• English

Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.