SUMMARY

In this individual contributor role, the Quality Control Scientist will support patient throughput and compliance activities within the Quality department.

EXPERIENCE:

• Experience in Analytical Quality Control, method development, or a technical support function.
• At least 3 years of experience.
• Demonstrated knowledge and skills in multiple analytical techniques
• Understanding of ICH and FDA/EMEA GMP requirements
• Ability to prioritize and execute multiple tasks simultaneously under tight deadlines
• Strong verbal and written technical communication skills
• Strong interpersonal skill
• Proficiency using MS Word, Excel, and MS project
• Knowledge of cGMP, USP and FDA guidelines.
• Knowledge of LIMS systems.
• Knowledge of Quality Management Systems, such as Trackwise and 1QEM
• Ability to communicate clearly with a variety of individuals in various aspects of Novartis operations.
• Detail-oriented with ability towards problem solving and solid decision-making abilities.
• Strong written and verbal communication skills are essential.