- Merck & Co. (Rahway, NJ)
- …and robust scientific methodology, we partner to deliver the next medical breakthrough. Biologics Process Research & Development (BPR&D) within our company's ... providing a diverse and inclusive environment for all. Beyond process development for pipeline biologics , we innovate...interest in contributing to upstream and/or downstream bioprocessing.As an Associate Scientist in BPR&D you will work… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders.Summary The Associate Director, RACMC Portfolio Products, will be responsible for regulatory CMC ... assigned projects. The individual will also contribute to regulatory process optimizations on relevant topics.Responsibilities- Supports CMC regulatory compliance… more
- Merck & Co. (Rahway, NJ)
- …Description Role and Responsibilities: We are seeking an experienced talented scientist to join the Quantitative Pharmacology and Pharmacometrics - Immune/Oncology ... (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global...understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …agencies. Supervise designated personnel. Relationships Report to the Director/ Associate Director/Lead Regulatory Scientist /Sr. Manager Regulatory Affairs. ... Position Manage and oversee all assigned projects/products/processes. Assist the Director/ Associate Director in assuring Novo Nordisk compliance with internal SOPs… more
- Merck (Rahway, NJ)
- **Job Description** ** Biologics Process R&D Associate Scientist ** Our Research Scientists are our Inventors. Using innovative thinking, state-of-the-art ... methodology, we partner to deliver the next medical breakthrough. Biologics Process Research & Development (BPR&D) within...in contributing to upstream and/or downstream bioprocessing. As an Associate Scientist in BPR&D you will work… more
- Merck (Kenilworth, NJ)
- …individual to join our Biologics Process Development Department as Associate Principal Scientist . In this role, the successful candidate will work ... Manufacturing while providing a diverse and inclusive environment for all. Beyond process development for pipeline biologics , we innovate and build next… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …areas centered around rare diseases and immune disorders. **Summary** The Associate Director, RACMC Portfolio Products, will be responsible for regulatory CMC ... the assigned projects. The individual will also contribute to regulatory process optimizations on relevant topics. **Responsibilities** - Supports CMC regulatory… more
- Merck (Trenton, NJ)
- …preclinical assay method development, validation, and sample testing in support of biologics and small-molecule programs. This group is seeking a dynamic and ... objectives in line with strategy. + As a senior scientist in the group, mentor junior scientists on solving...inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here… more
- Sanofi Group (Bridgewater, NJ)
- **Consumer Experience Strategy Lead** **/ Associate Director** **US / Cambridge (US) /** **Bridgewater (US)** **Purpose & Context** + Sanofi is a leading pharma ... digital transformation, Sanofi Digital launched major strategic initiative in 2023: Biologics x AI Moonshot ("BioAIM"), in collaboration with Large Molecule… more
- Merck (Trenton, NJ)
- …**Role and Responsibilities:** We are seeking an experienced talented scientist to join the **Quantitative Pharmacology and Pharmacometrics -** **Immune/Oncology** ... **(QP2-IO)** team in the role of Associate Director QP2-IO team is part of the Global...understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs,… more
- Novo Nordisk (Plainsboro, NJ)
- …agencies. Supervise designated personnel. Relationships Report to the Director/ Associate Director/Lead Regulatory Scientist /Sr. Manager Regulatory Affairs. ... Position Manage and oversee all assigned projects/products/processes. Assist the Director/ Associate Director in assuring Novo Nordisk compliance with internal SOPs… more
