The CPL is a permanent member of the cross functional R&D global Core Team (CT) who plays a key role in defining the target disease profile (TDP), target product profile (TPP), and the development and life cycle strategies of a given project. The CPL leads the Clinical Development Plan (CDP) Team (which consists of functional leaders from within GCD e.g. Clin Pharm, Clin

The Certified Technician provides support to the pharmacist by reviewing, compounding and dispensing medications. All work is carried out under the supervision of a licensed Pharmacist. Responsibilities 1. Compounds and/or prepares medications (sterile products, oral, topical, controlled substances, etc.) including high risk medication processes as defined by the entity,

The Certified technician provides general support to the pharmacist by receiving, reviewing, compounding and dispensing medications. All work is carried out under the supervision of a licensed Pharmacist. Responsibilities 1. Receives and accurately transcribes orders from prescribers under the supervision of a pharmacist. Process prescriptions in a timely order and manner

Manufacturing Specialist 3 Drug Product Job Locations US NC Holly Springs Requisition ID 2024 26613 Category Manufacturing Company (Portal Searching) FUJIFILM Diosynth Biotechnologies Overview Follow Your Genki to North America's largest, state of the art Life Science Manufacturing Facility & CDMO The work we do at FDB has never been more important and we are looking for

Under the supervision of a Pharmacist, performs all aspects of fulfilling medication orders and distributing medications, including preparing, charging, prepackaging, delivering, outdating, ordering, and receiving. Assists the Pharmacist in providing drug information, overseeing and monitoring safe medication use, controlling drug distribution and security, and tracking o

Manufacturing Specialist 1 Job Locations US NC Holly Springs Requisition ID 2024 26587 Category Manufacturing Company (Portal Searching) FUJIFILM Diosynth Biotechnologies Overview Follow Your Genki to North America's largest, state of the art Life Science Manufacturing Facility & CDMO The work we do at FDB has never been more important and we are looking for talented cand

Compounder 8 Sanford, NC To manufacture and preweigh bulk batches and receive raw materials. Adhere to HR, S&H policies, respect GMPs (Good Manufacturing Practices), and follow departmental procedures with respect to manufacturing, preweigh, and receiving. Contribute positive results to the bulk department key objectives (QA Index, GCM, S&H, RFT). In this role you will be

M F Business Hours Primary responsibilities for this position include performing tasks associated with method validations and transfers. The analyst will be responsible for ensuring that Seqirus validation samples are tested and reviewed according to quality requirements and results reported are valid, accurate, and documented per applicable regulatory and corporate requi

Responsible for the regulatory review and submission of advertising and promotional materials for all Chiesi Global Rare Disease products in the United States. This position is also responsible for providing input to risk management activities, managing the labeling control process, including generation of new labeling and changes to existing labeling, and submission of l

1. Verbalizes and/or demonstrates knowledge of clinical information and practices essential to assuring provision of age specific care to all age groups. 2. Verifies patient identification, confirms physician orders, obtains patient history / forms, assesses patient condition, explains procedures, provides patient education, and addresses patient concerns prior to perform