The Sr. Distribution Center Process Development Manager is responsible for the development, implementation, and management of Rivian's standardized warehouse processes. This role is a critical contributor to the strategic and day to day operations of the distribution operations and business teams and will require initiative, independent judgement, and cross team collabora

Lead and manage multiple commissioning / qualification / validation activities performed at facility with minimal supervision. Equipment Qualification / Re Qualification (IQ, OQ, PQ) for process equipment, QC equipment, packaging equipment, clean utilities. Cleaning Verification / Validation studies for transferred products. Media Fills / process simulations protocols. En

The Thought Leader Liaison (TLL) is responsible for developing, managing, and engaging with Key Opinion Leaders throughout their assigned geography reporting to the Thought Leader Liaison Lead, reporting through Specialty Brands Marketing. He/she works closely with commercial colleagues and other staff to help build advocacy of Mallinckrodt's products with KOLs. TheThough

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.

The Thought Leader Liaison (TLL) is responsible for developing, managing, and engaging with Key Opinion Leaders throughout their assigned geography reporting to the Thought Leader Liaison Lead, reporting through Specialty Brands Marketing. He/she works closely with commercial colleagues and other staff to help build advocacy of Mallinckrodt's products with KOLs. TheThough

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. The Senior Medical Director will lead the development and execution of the medical strategy for Rett Syndrome. This will be accomplished by working in close collaboration with colleagues in Commercial, Regulatory, Market

Responsible for managing all pharmaceutical activities including the purchase, inventory, control, and record keeping of all Drug Enforcement Administration (DEA) controlled substances stored in the pharmacy. Responsible for securing and maintaining a current facility DEA Registration Number and maintaining necessary legal records on controlled substance items. Provides t

The Senior Director, Medical Affairs, Parenteral Nutrition (PN) is a critical role as this individual serves as the lead for the US PN Medical Affairs team and is responsible for developing and executing the US Medical Affairs strategy. This individual also collaborates closely with the Global business unit (BU) and the regional marketing organization to identify US nutri

Manage Regulatory Affairs, Advertising & Promotion and Compliance Group Manage the US RA Ad Promo, submission operations, labeling and compliance group staff, including objective setting and career development activities and motivate line reports to achieve shared and individual goals. Regulatory Leadership of Advertising and Promotional Materials Serve as subject matter

The Senior Director, Clinical Development Medical Affairs (CDMA) drives strategy and accountability for the hepatology drug program execution, ensuring alignment with brand team objectives, incorporation of relevant internal and external insights and the generation of an R&D plan that delivers for unmet patient need, generates competitive differentiation, and prepares for

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

Create and approve regulatory content documents that drive artwork and labeling language Review and approve final artwork Manage preparation of regulatory documents for new product launches and maintenance of current products in the market with the correct alignment and compliance to regulations Maintain required regulatory compliance databases, systems and processes Supp

Job Title Associate Scientist II Job Id 24 01899 Location East Hanover, NJ Duration 05 Months On W2 Contract The role is to provide technical lab support to project managers. Familiarity with sample prep, bench based chemistry and measurement techniques, data collection and data management. Experience working in a lab environment is a must. We are looking for a candidate

We exist to help people thrive. Advancing health and nutrition is what we do best and care about.

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. This position will serve as a technology partner in the Research and Development (R&D) and Technology Development & Operations (TD&O) domains, providing technology leadership, operational support and project management fo