Develops qualification protocols, and associated reports while adhering to a change management process. Supports the execution of equipment qualifications and validation protocols. Supervises vendors for qualification functions. Develops written procedures for calibration and preventive maintenance of equipment. Supports equipment qualification and validation activities.

As an active team member of the Computational Biology (CompBio) research group at Boehringer Ingelheim, US research facility in Ridgefield, CT. The successful candidate will contribute to drug discovery efforts through analysis of multiple disease relevant data sets, as well as development of core informatics pipelines and data organization. This position will be able to

Develops qualification protocols, and associated reports while adhering to a change management process. Supports the execution of equipment qualifications and validation protocols. Supervises vendors for qualification functions. Develops written procedures for calibration and preventive maintenance of equipment. Supports equipment qualification and validation activities.

Lexicon is a biopharmaceutical company with a mission of pioneering medicines that transform patients' lives. Through our Genome5000 program, Lexicon scientists studied the role and function of nearly 5,000 genes and identified more than 100 protein targets with significant therapeutic potential in a range of diseases. Through the precise targeting of these proteins, Lexi

About Strategic Project Management, Conferences Strategy & Development As a part of the Conferences Strategy & Development team, the Strategic Project Management (SPM) Center of Excellence (COE) focuses on high impact projects, ensuring a centralized approach to fully leverage our capabilities across the conferences business. This highly collaborative team helps drive for

About Strategic Project Management, Conferences Strategy & Development As a part of the Conferences Strategy & Development team, the Strategic Project Management (SPM) Center of Excellence (COE) focuses on high impact projects, ensuring a centralized approach to fully leverage our capabilities across the Conferences business. This highly collaborative team helps drive for

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Contribute to lab scale process development to implement upstream discovery of flavor and modulation ingredients through microbial fermentation and biocatalysis Design and conduct microbial strain screening. Conduct instrumental analysis (GC MS & HPLC) of flavor components in samples to establish an in depth knowledge of flavor chemistry, pathways and molecular mechanisms

Advance innovative technologies that transform sustainable raw materials to high value ingredients that modulate tastes and enhance authentic flavors through microbial fermentation and biocatalysts. Design and conduct lab scale process development to implement upstream discovery into pipeline. Conduct instrumental analysis (GC MS & HPLC) of flavor components in samples to

Design and conduct innovative research to develop proprietary, global, natural, sustainable modulation and taste ingredients as part of IFF's flavor portfolio. Coordinate and conduct analytical research as related to natural products isolation, identification, and quantification. Analyze natural product profiles and functions using advance analytical tools including HPLC

Manager, Regulatory Affairs North America (Hybrid) It's an exciting time to be part of IFF's Global Regulatory Affairs. This hybrid role requires presence in the office minimum of 1 day/week in the Holmdel, NJ location. As the Manager of Regulatory Affairs, you will be responsible for the regulatory compliance and conformity to customer requirements for fragrance products