- Deloitte (Los Angeles, CA)
- …Recruiting for this role ends on 1/31/2026 Work you'll do As a Manager you will lead and deliver engagements, or components of large, complex engagements. ... and generating submissions packages + Experience with submissions management, labeling, CMC change control and/or LCM processes + Experience with cloud computing… more
- RTX Corporation (Goleta, CA)
- …world. The Raytheon Industry 4.0 (I4.0) team is seeking an experienced Sr. Manager for the Automation Systems Engineering team in support of the Surveillance ... Consolidated Manufacturing Centers ( CMC ) in Goleta and El Segundo, CA. The ideal candidate will be a strategic thinker with a deep understanding of manufacturing… more
- Eurofins US Network (Lancaster, PA)
- …and products. **Job Description** **Role Overview** The GMP Testing Project Manager is responsible for planning, coordinating, and overseeing Good Manufacturing ... chemistry, or biologics. + Experience in GMP lab operations, especially in CMC testing. + Proven ability to manage complex projects and cross-functional teams.… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …real-world evidence, and creating hope for all facing illness. The Senior Manager , Supply Chain leads, develops, establishes, and manages the supply chain activities ... in preparation, commercialization, and launch of new products in development in North American market (US and Canada) related to planning, procurement, label and packaging development, distribution, importation, export, and vendor management in cooperation… more
- BeOne Medicines (San Mateo, CA)
- **General Description:** The Manager of Clinical Supply Chain manages drug supply activities related to planning, label development, label & pack, and distribution ... service level to internal stakeholders (eg Clinical Operations, Regulatory, Quality, CMC ). + Work with Clinical Operations to understand clinical demand requirements… more
- Takeda Pharmaceuticals (Lexington, MA)
- …the best of my knowledge. **Job Description** **About the role** The Principal Manager , R&D GMP Pharmaceutical Sciences Quality EU & US provides Quality oversight ... + Contribute technical quality content to regulatory filings and collaborate with CMC submission teams. + Participate as SME in external audits, support PAI… more
- ThermoFisher Scientific (Highland Heights, KY)
- …a globally diverse organization and business units spanning bioanalytical, vaccines, CMC /GMP (small and large molecule), and central laboratory clinical enablement ... functions. Enables harmonization across site-based organizations while respecting each site's unique business needs. Tactically, oversees coordination and management of projects by monitoring status, timelines, and outcomes; strategically identifies new… more
- Takeda Pharmaceuticals (Lexington, MA)
- …5+ years of experience + Must have exceptional working knowledge of CMC operations relating to research and development and investigational drug manufacturing. Must ... have direct management experience with external contract manufacturing organizations. + Demonstrated excellence in project management and effectively managing multiple projects/priorities. + Act as the key contributor in authoring Statements of Work in and… more
- RTX Corporation (Carlsbad, CA)
- …Slurry and Melt Infiltration processes used to manufacture ceramic matrix composite ( CMC ) turbine components. CMCs are an enabling material that increases the ... temperature capability of jet engine components. Through successful development and application of these materials, P&W will deliver engines that are more fuel efficient, lighter weight and durable for commercial and military applications. **What You Will… more
- Otsuka America Pharmaceutical Inc. (Richmond, VA)
- …with members of the global regulatory team (GRL, regional leads, CMC -RA, labeling, medical writing, regulatory operations, etc.) to develop global regulatory ... plans, address global regulatory issues, health authority queries, and regulatory obligations. - Authors, coordinates, reviews, and executes submissions and responses to regulatory authorities related to INDs, amendments, supplements, aggregate reports, NDAs… more
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