Position supports global logistics and distribution of drug substance, drug products and finished goods in cooperation with internal and external partners. The role requires an in depth understanding of GXP, Veeva Quality Management System,...
The Director, Clinical Data Management (CDM) is responsible for oversight, execution, and quality of all data management activities across assigned clinical trials from study start-up through database lock. This role ensures the integrity, ...
The Pre-Pivotal Drug Substance Technologies organization at our client develops, characterizes and supports clinical drug substance manufacturing processes for all early-stage programs in the company portfolio. The Pivotal Drug Substance ...
Achieve territory sales goals by promoting products and services to physicians and other medical personnel within assigned geography. Educate customers on the appropriate use, characteristics, and approved indications of products. Professio...
Deviation Investigator Level I-III is responsible for the investigation and completion of deviations aimed at identification of root cause and implementation of correct actions to prevent recurrence. Level III Investigators are expected t...
Responsibilities: Execute QC second shift activities, working with the day and night shift team leads, including sample receipt, prioritization, and accurate entry into LIMS. Serve as a point of contact for Manufacturing during night shi...
The Site Engineer is responsible for overseeing the maintenance, calibration, operational readiness of equipment, utilities, and facilities supporting cGMP manufacturing and laboratory areas. This role is integral to ensure the efficient, r...