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 Clinical Research Technician position is based within our Clinical Photobiology department, and works with departmental management and the Principal Investigator in the implementation of Photobiology trials. Job Type Full Time. Base Hours 9 00AM 6 00PM OR 10 30AM – 7 30PM Monday through Friday MINIMUM QUALIFICATION REQUIREMENTS To perform this job, an individual

Postdoctoral Fellowships on basic science and translational medicine of hematologic cancers Dr. Lingbo Zhang's Laboratory at Cold Spring Harbor Laboratory (CSHL) is part of a $75 million Center for Therapeutics Research at CSHL. There are multiple fully funded postdoctoral fellowships available in the Zhang Laboratory to investigate roles of nervous system activities and

Act as a System Administrator that manages all aspects of this system including user access and periodic reviews for the Document Management System (DMS), the LMS, and CAPA. Perform document management activities in the electronic document management system for controlled documents throughout its lifecycle (e.g. SOPs, Policies, Work Instructions, Forms). Design and develo

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

In line with our mission, Bayer: Science for A Better Life we aim to improve quality of life.

The Associate Director, Regulatory Affairs CMC will be responsible for leading global regulatory CMC strategy for product development and registration, and for preparation of CMC dossier for primarily small molecule regulatory submissions (INDs and NDAs) according to global regulatory expectations and requirements. This position works cross functionally with Regulatory Af

One of the nation’s largest independent testing facilities seeks an Analytical Chemist with a minimum 2 years experience testing products for the pharmaceutical, nutritional cosmetic, personal care, medical device or allied industries. The position requires a working knowledge of testing products in a GMP regulated facility. Responsible for performing physical, chem

Conde Nast is a global media company producing the highest quality content with a footprint of more than 1 billion consumers in 32 territories through print, digital, video and social platforms. The company's portfolio includes many of the world's most respected and influential media properties including Vogue, Vanity Fair, Glamour, Self, GQ, The New Yorker, Conde Nast Tra

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

A postdoctoral fellow position is available in the laboratory of Dr. Linda Van Aelst, Professor at Cold Spring Harbor Laboratory. The main focus of research will be to study the roles of genes associated with human diseases in the development and function of neural circuits, using molecular, genetic and viral engineering, optogenetics, imaging, electrophysiology, and beha

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

Under supervision, performs laboratory analyses of raw materials, in process (IP), finished products (FP) and stability (ST) samples for pilot and submission batches, according to SOPs and cGMP procedures. Prepares method validation protocols/reports, and carries out method validation activities, including interim method validation, to meet project timelines. Supports lab

Position Title Senior Clinical Scientist I, Skin Clinical & Physics (Instrumental) Sciences, Evaluation Intelligence Location Clark, New Jersey (Hybrid) Department Research & Innovation Evaluation Intelligence For more than one hundred years, L'Oreal believes that beauty needs Science. In a world now transformed by digital technology and the emergence of new scientific do

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