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The Manager of cGMP Quality Control supervises internal and external QC resources for testing raw materials, in-process testing, product release, and environmental monitoring in a GMP environment. This role involves maintaining analytical methods, authoring SOPs, improving Quality Control infrastructure, and collaborating with various departments to ensure operational reliability and efficiency.

As a Bioprocess Associate, you will assist in the manufacturing of bulk biological products, including enzymes and master mixes. Your role includes maintaining equipment, following production processes such as liquid blending and chromatography, and adhering to quality system procedures. You'll work as part of a team in a collaborative and inclusive environment at IDT.

The Applications Specialist will provide pre- and post-sales technical support to customers, troubleshoot product use and applications, and document customer interactions in the CRM system. The role involves communication through various channels and collaboration with internal teams to escalate inquiries as needed.

The Sr. Product Manager is responsible for the product lifecycle management of custom oligonucleotides, focusing on market insights, strategic planning, and collaboration with marketing and product development teams. The role includes analyzing trends, optimizing inventory, and driving product performance while aligning with customer needs and business goals.

The Product Marketing Manager NGS will lead cross-functional efforts to address customer needs for IDT’s xGen NGS product portfolio by developing strategic marketing plans, executing marketing campaigns, and collaborating across departments for successful product launches and revenue growth.

The Research Scientist I will perform bench experiments using various molecular biology and laboratory techniques, assist in data analysis, contribute to team objectives, and maintain laboratory equipment.

The Principal Quality Engineer role involves supporting product development phases for regulated medical devices, ensuring compliance with applicable regulations, managing risk processes, and collaborating with cross-functional teams to enhance product development and reduce variability. This includes auditing design processes and coaching colleagues on design control and risk management.