Associate Project Engineer

FUJIFILM Healthcare Americas Corporation is on a mission to innovate for a healthier world, and they are seeking an Associate Project Engineer to provide remote assistance to the Project Engineering team and customers. This entry-level position involves handling various tasks related to software deployments, monitoring processes, and ensuring high-quality product solutions.

Responsibilities:

• Works closely with MI Project Management (PM) and Project Engineering teams to deliver high quality Synapse product solutions
• The expectation of this role is to maintain the knowledge that is known and absorb the knowledge provided through training, mentorship, and initiative to develop your skillsets and start your career as part of the FUJIFILM team
• This engineer also works on 3rd party hardware, software, and network related issues that are sold or supported by FUJIFILM
• Works cross-functionally with other Synapse teams/products as required and handles other duties as assigned
• Maintains a high level of success with yearly goals provided by your manager and metrics defined on a team level
• Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that all job duties inherent in the position description are performed in accordance with established policies and procedures
• Comply with all applicable U.S. Food and Drug Administration (U.S. FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all other applicable laws, regulations and standards

Requirements:

• Trade School Certification, 2 Year Degree, or Industry Experience Equivalent in computer systems or related fields
• 0 to 3 years' experience in internships or on the field, preferred
• Superior communication and interpersonal skills, excellent phone manner
• Ability to achieve results and meet goals in a fast-paced, team environment
• Ability to make independent decisions based on interpretation of technology data and product knowledge
• Excellent organizational and multi-tasking skills
• Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that all job duties inherent in the position description are performed in accordance with established policies and procedures
• Comply with all applicable U.S. Food and Drug Administration (U.S. FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all other applicable laws, regulations and standards
• Basic knowledge of Microsoft and VMware operating systems
• Basic knowledge of Networking and Storage
• Basic knowledge of clinical data transfer protocols and interfaces (HL7 and DICOM)