a consolidated engineering design: creating well-defined mechanical components and system options; choose the optimal architecture, leveraging existing technology, establishment of milestones to implement components. Ensure good and up to date documentation of the architecture and implementation; use methods & tools for a structured approach.
Drive the accepted implementation of mechanical design; explain methods and convince other members of the team of the chosen approach. Perform validation and verification; work with other members of the team, including physicists and hardware engineers, to test the implementation of mechanical components. Participate in the definition of System Requirements
Specification, writes the functional requirement and specification for features, makes sure it is reviewed and approved. Qualifications: A Master's degree and 5 to 7 years of experience, or an equivalent combination of education and experience, required.
Design tools, e. g. Auto CAD, Inventor Mac OS X, i OS, Linux Experience with nuclear medicine imaging, PET technology Experience with data acquisition and computing hardware Experience with electrical and hydraulic systems Experience with industry standards for mechanical design and control processes Leadership skills - will help build an engineering team Team skills - will work with multi-disciplinary group of physicists, engineers,
and physicians Reference Number: 40-29050 Salary Grade: 029 Employment Type: Exempt Org: RA-Radiology Special Requirements: Job Family: I-Technical/Professional Research For more details: jobs-search.
org/architecture-construction_philadelphia-c445987/system-design-engineer-philadelphia_i1972601180
1-3 hours to complete and normally require a sign off form. Must have a clean driving record, dependable car, smart phone, and laptop. and be OK with traveling up to 300 milesweek. Background check and drug test is mandatory. pay rate $18-$25hr If interested, please reply with your resume. Thank you
processes and systems, including development of standards, processes, and training for clinical safety oversight for all CCI clinical trials. The Manager monitors adherence to regulatory requirements (ICH, FDA, NIH, NCI, etc. ) and GCP guidelines, leads efforts to identify potential compliance and quality risks to CCI safety management in clinical trials, and develops mitigation strategies with the assistance of clinical operations and QA personnel.
Qualifications: Bachelors degree and 5 to 7 years of experience in Clinical Safety Management, Clinical Development and Operations, and/or Clinical Quality Assurance or an equivalent combination of education and experience required. RN preferred
Experience in SOP and process design related to clinical safety management Extensive knowledge of FDA / global clinical trial regulations and ICH GCP Guidelines Understanding of the clinical development process and clinical safety documentation requirements Proactive approach to GCP clinical safety compliance Attention to detail, excellent communication skills and be able to work within a team under challenging and sometimes stressful conditions Exceptional knowledge of commonly-used clinical safety concepts, practices, and procedures within GCP area Ability to work independently with minimal direction.
Reference Number: 40-30037 Salary Grade: 028 Employment Type: Exempt Org: CI-Center
for Cellular Immunotherapy Special Requirements: Job Family: I-Technical/Professional Research For more details: jobs-search.
org/information-technology_philadelphia-c445987/clinical-safety-manager-philadelphia_i1972597088
