SOFIE Gilroy, California Job Description Quality Assurance Specialist (QAS) I Title Quality Assurance Specialist I Department Quality & Compliance Reports To Regional Manager, Quality Assurance (or equivalent QA Manager) Overview The Quality Assurance Specialist I will be responsible for the oversight of the Quality Assurance program and the Quality Management System at the site level. Essential Duties and Responsibilitie |
SOFIE Sanford, Florida 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 Sterling,, Virginia Title Pharmacy Technician I Location Sterling, VA Department Network Operations, Pharmacy Reports To Pharmacist-in-Charge Overview The Pharmacy Technician will perform laboratory and pharmacy-related duties under the direct supervision of an authorized Nuclear Pharmacist. This job involves working in a clean room as well as occupational exposure to radiation. Essential Duties and Responsibilities |
SOFIE Somerset, Kentucky Description: Title Cyclotron-Support Engineer I Department Technical Services Reports To Field Service Engineer Overview The Cyclotron-Support Engineer I is accountable for the safe and routine operation, maintenance, and repair of one or more particle accelerators in SOFIE’s PET radiopharmacy, which manufactures PET diagnostics under 21 CFR 212 guidelines. Additionally, the Cyclotron-Support Engi |
SOFIE Romeoville, Illinois Cyclotron-Support Engineer II or III Title Cyclotron-Support Engineer II or III (Depending on experience) Location Somerset, NJ / Romeoville, Il Department Technical Services Reports To Field Service Engineer/Regional Service Manager Overview The Cyclotron-Support Engineer III is accountable for the safe and routine operation, maintenance, and repair of one or more particle accelerators in SOFIE’s |
SOFIE Oakwood Village, Ohio Overview The Pharmacy Technician will perform laboratory and pharmacy related duties under the direct supervision of an authorized Nuclear Pharmacist. This job involves working in a clean room as well as occupational exposure to radiation. Essential Duties and Responsibilities Perform the duties associated with compounding, dispensing, and distribution of FDG and NaF, including data entry with Pin |
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 |
Lonza Biologics Inc Hayward, California, 94545 BIOENGINEERING TECHNOLOGY SPECIALIST needed by Lonza Biologics Inc. in Hayward, CA to apply knowledge and experience globally across capital projects to drive harmonization and best practice utilization via creation and maintenance of design standards. BioEngi-neering Technology Specialist's earn between $148,408.00 to $163,000.00 yearly. Apply at email resume to John Segalla at resumes.ports mout |
Takeda Development Center Americas, Inc Lexington, Massachusetts, 02421 Takeda Development Center Americas, Inc. is seeking an Engineer IV in Lexington, MA to serve as a chemical engineer for biotherapeutics process development with a focus on protein (including monoclonal antibodies, fusion proteins, enzymes, protein-drug-conjugate molecules) purification, utilizing techniques that include affinity chromatography, ion-exchange chromatography, hydrophobic interaction |
Takeda Development Center Americas, Inc Lexington, Massachusetts, 02421 Takeda Development Center Americas, Inc. is seeking Senior Manager, Statistical Programming in Lexington, MA to Lead projects directly or indirectly related to GPTs or other functions. Up to 100% remote work allowed from anywhere in the U.S. Full time. $224,000 - $258,000 per year. Apply on-line at https://jobs.takeda.com and search for Req #R0134645. |
Takeda Development Center Americas, Inc Lexington, Massachusetts, 02421 Takeda Development Center Americas, Inc. is seeking a Manager, Global Regulatory Affairs CMC Submissions Management in Lexington, MA to establish global submission activities and timelines in partnership with global and cross-functional stakeholders in Pharmaceutical Science, GMS, Biologics and Small Molecule operating units, Regulatory Affairs, and QA. Up to 20% domestic travel required. Up to 50 |
Takeda Development Center Americas, Inc Cambridge, Massachusetts, 02142 Takeda Development Center Americas, Inc. is seeking a Product Manager in Cambridge, MA to drive the development of a product vision, strategy, and global roadmap taking into consideration key stakeholder capability and product needs. Up to 75% telecommuting allowed. Up to 20% domestic and international travel required. Full time. $224,100 - $255,600 per year. Apply on-line at https://jobs.takeda.c |
SOFIE Totowa, New Jersey Title Senior Product Development Specialist Position Note OPEN to any SOFIE locations Location Totowa, NJ Department Radiopharmaceutical Contract Manufacturing (RCM) Reports To Director, Radiopharmaceutical Contract Manufacturing (RCM) OVERVIEW The Senior Product Development Specialist will lead the development, implementation, and validation of manufacturing and analytical methods of new diagnost |
SOFIE Oakwood Village, Ohio Job Description Quality Assurance Specialist (QAS) I Title Quality Assurance Specialist I Department Quality & Compliance Reports To Regional Manager, Quality Assurance (or equivalent QA Manager) Overview The Quality Assurance Specialist I will be responsible for the oversight of the Quality Assurance program and the Quality Management System at the site level. Essential Duties and Responsibilitie |
SOFIE Sterling,, Virginia Title Junior Cyclotron-Support Engineer I Location Sterling, VA Department Network Operations / Technical Services Reports To Cyclotron-Support Engineer Overview The Junior Cyclotron-Support Engineer I is a training position with dual responsibilities to the Cyclotron-Support Engineer duties and the Network Operations Group within a SOFIE radiopharmacy. This training program provides readiness to |
SOFIE Totowa, New Jersey Title Nuclear Pharmacist I Department Network Operations, Pharmacy Reports To Pharmacist-in-Charge and Facility Manager Overview The Nuclear Pharmacist I will compound and dispense radiopharmaceuticals. This job involves working in a clean room as well as occupational exposure to radiation. While reporting into Network Operations, the Nuclear Pharmacist role is instrumental to the Quality Assuranc |
Jobot Piscataway, New Jersey, 08854 QC Scientist II / Amazing Benefits / $$$ / NJ This Jobot Job is hosted by: Brianna Volatile Are you a fit? Easy Apply now by clicking the "Quick Apply" button and sending us your resume. Salary: $70,000 - $110,000 per year A bit about us: We are currently seeking a dynamic and highly motivated QC Scientist II for our manufacturing industry. The successful candidate will play a pivotal role in our |
Pioneer Data Systems Conshohocken, Pennsylvania Our client, a world-leading Pharmaceutical Company in Conshohocken, PA is currently looking for a Process Engineer to join their expanding team. Position Details: Job Title: Process Engineer / Pharma-Biologics Manufacturing / Hybrid Work Duration: 14 months contract, extendable up to 24 months Location: Conshohocken, PA Hybrid role, 3 days in office, 2 days remote Note: The client has the right- |
Jobot New York, New York, 10065 Flow Cytometry experience required! Come join this amazing opportunity! This Jobot Job is hosted by: Luke Hoyt Are you a fit? Easy Apply now by clicking the "Quick Apply" button and sending us your resume. Salary: $55,000 - $65,000 per year A bit about us: We are one of the most comprehensive blood centers in the world, our focus is on cultivating excellence by merging cutting-edge innovation with |
Jobot New York, New York, 10065 Reputable Organization! Excellent Benefits! Growth Opportunity! This Jobot Job is hosted by: Juan Correa Are you a fit? Easy Apply now by clicking the "Quick Apply" button and sending us your resume. Salary: $60,000 - $65,000 per year A bit about us: We are one of the most comprehensive blood centers in the world, our focus is on cultivating excellence by merging cutting-edge innovation with dilig |
Belcherpharma LLC Largo, Florida, 33777 EDUCATION, EXPERIENCE, AND TRAINING REQUIREMENTS Education: Bachelors technical degree from a four year college or university, preferably In Pharmaceutical sciences, and/or chemistry. Advance course work or Master degree is preferred. Experience: Must have at least one year experience in Pharmaceutical product development. Knowledge: Specific knowledge of industrial chemistry pertaining to product |
Takeda Development Center Americas, Inc Lexington, Massachusetts, 02421 Takeda Development Center Americas, Inc. is seeking a Data Systems QA and Compliance Leader in Lexington, MA to serve as a subject matter expert in computer system validation requirements for systems used by Takeda’s global R&D organization. Up to 20% domestic & international travel required for R&D quality functions and activities. Full time. $177,500 - $186,000 per year. Apply on-line at https:/ |
Takeda Manufacturing USA, Inc Inman Square, Massachusetts, 02139 Takeda Manufacturing USA, Inc. is seeking a CMC Submissions Lead in Cambridge, MA to Lead the Global Chemistry, Manufacturing and Control (CMC) Submissions Team for regulatory submissions in all countries such as: Development submission (Investigational Medicinal Product Dossier / Clinical Trial Application / Investigational New Drug application); Global Marketing Applications (New Drug Applicatio |