SOFIE Totowa, New Jersey Title Manager, Training and Learning Management Systems (LMS) Location Open / Remote within 50 miles of any SOFIE site Department Quality & Compliance Reports To Associate Director, Training Overview The Manager, Training and LMS , supports SOFIE by developing, overseeing, and managing the Learning Management System (LMS), by providing administrative support for SOFIE’s Training Program, such as c |
SOFIE Totowa, New Jersey, 07512 Title Manager, Training and Learning Management Systems (LMS) Location Open / Remote within 50 miles of any SOFIE site Department Quality & Compliance Reports To Associate Director, Training Overview The Manager, Training and LMS , supports SOFIE by developing, overseeing, and managing the Learning Management System (LMS), by providing administrative support for SOFIE’s Training Program, such as c |
SOFIE Totowa, New Jersey Facility Cleaning Technician The Facility Cleaning Technician will perform facility GMP and non-GMP cleaning, maintenance, and organization in support of all activities on the site. Responsibilities Follow company Standard Operating Procedures as well as current Good Manufacturing Practices Cleaning and disinfection of the ISO 7 cleanrooms daily, monthly, and quarterly or as needed Cleaning and di |
Zevacor Pharma Inc. Totowa, New Jersey, 07512 Job Description Manager, Pharmacy Compliance Title Manager, Pharmacy Compliance Department Quality/Compliance Reports To Director, Pharmacy Compliance Remote role Overview SOFIE aseptically manufactures and dispenses therapeutic and diagnostic radiopharmaceuticals across the US and is committed to all aspects of Quality and Compliance in the manufacture of these products. The successful candidate |
SOFIE Totowa, New Jersey Job Description Manager, Pharmacy Compliance Title Manager, Pharmacy Compliance Department Quality/Compliance Reports To Director, Pharmacy Compliance Remote role Overview SOFIE aseptically manufactures and dispenses therapeutic and diagnostic radiopharmaceuticals across the US and is committed to all aspects of Quality and Compliance in the manufacture of these products. The successful candidate |
SOFIE Totowa, New Jersey QC/Production Associate I Title QC/Production Associate I Department Network Operations Reports To Facility Manager Overview The QC/Production Associate I will operate the radiosynthesizers for the production of drug product, as well as operate analytical equipment for the quality control of drug product. Essential Duties and Responsibilities Perform FDG and NaF synthesis according to SOFIE Standa |
SOFIE Totowa, New Jersey, 07512 Title Distribution Technician I Department Network Operations Reports To Facility Manager Overview The Distribution Technician I is responsible for assisting with the production and distribution of drug product. This position requires administrative skills to accommodate the data entry requirements of the position along with being familiar with the area served, DOT regulations, ability to schedule |
SOFIE Totowa, New Jersey Distribution Technician I Title Distribution Technician I Department Network Operations Reports To Facility Manager Overview The Distribution Technician I is responsible for assisting with the production and distribution of drug product. This position requires administrative skills to accommodate the data entry requirements of the position along with being familiar with the area served, DOT regula |
SOFIE Totowa, New Jersey Title: Facility and Equipment Engineer II Location: NJ5-Totowa, New Jersey Department: Radiopharmaceutical Contract Manufacturing Overview: The Facility and Equipment Engineer for Radiopharmaceutical Contract Manufacturing is committed to ensuring the facility is maintained in compliance with cGMP, 21 CFR 211, and all Facility SOPs. They maintain, calibrate, and ensure proper operation of all equi |
SOFIE Totowa, New Jersey, 07512 Title: Facility and Equipment Engineer II Location: NJ5-Totowa, New Jersey Department: Radiopharmaceutical Contract Manufacturing Overview: The Facility and Equipment Engineer for Radiopharmaceutical Contract Manufacturing is committed to ensuring the facility is maintained in compliance with cGMP, 21 CFR 211, and all Facility SOPs. They maintain, calibrate, and ensure proper operation of all equi |