Systems Engineer - Medical Device
Systems Engineer - Medical Device
Intellectt Inc
Westbrook, ME
See who Intellectt Inc has hired for this role
Role: Systems Engineer - Medical Device
Location: Columbia, MD - 21046
Duration: 6 Months on W2
Work Site/Location: Columbia, MD. Hybrid.
Expected to report to the office 3 days a week.
Work Schedule: Typical workday hours. (9-5 with 1 hour lunch).
Must Have Skill
Location: Columbia, MD - 21046
Duration: 6 Months on W2
Work Site/Location: Columbia, MD. Hybrid.
Expected to report to the office 3 days a week.
Work Schedule: Typical workday hours. (9-5 with 1 hour lunch).
Must Have Skill
- CAD experience (SolidWorks creation of part files, drawings files)
- GD&T
- Experience with starting/ process change order in PLM system (Agile)
- Project management (meeting delivery expectation, forecasting roadblock
- Effective communication and time management skills
- Organizational skills
- Authoring of specifications (material and purchasing specs).
- Experience in equipment qualification (IQ, OQ , PQ)
- 2-5 years of Solidworks experience required creating parts and drawing files, must understand and implement GD&T methodology.
- The ability to work a wide range of personalities in a team setting required
- Technical writing skills required
- Experience with a variety of sensing and measurement technologies (thermocouples, photoelectric, vision, laser, etc.)
- Familiarity with a variety of manufacturing processes (machining, injection molding, additive manufacturing, sheet metal, welding, etc.)
- Experience in product verification via test equipment development and equipment validation (IQ/OQ/PQ) within an FDA regulated or other regulated industry (i.e. medical device/pharma, aerospace, etc.)
- Experience interfacing with documentation control systems
- Bachelor's Degree in engineering plus 3-5 years (of engineering experience in design and analysis within the medical device or another design-intensive industry Responsibilities
- Participates as a team member on product packaging design teams and performs related design functions; including equipment design and troubleshooting, analysis, and technical writing
- Analyzes problems in design, process, and test development
- Recommend/implement solutions
- Prepares and presents oral and written project updates and technical discussions
- Writes and approves protocols and reports
- Manages testing outlined in protocols and test methods
- Manages/develops validation studies on equipment and processes in on-site packaging lab.
- Maintains a professional working relationship with internal and external customers and support staff
- Initiates new or revised documentation and tracks through appropriate approval cycles and implementation through PLM systems
- Understands and follows company procedures and regulatory requirements
- Develops and implements procedures/policy
- Provides mid-level engineering activities of an organization's information systems.
- Typical Functions: Plans, designs, develops, evaluates, tests, and integrates an organization's systems infrastructure, including the implementation and design of hardware and software. Captures, understands, translates, and documents customer requirements.
- Defines system and product requirements; and generates mechanical, electrical, and software performance and reliability specifications and requirements. Creates and maintains programmatic and technical documentation to ensure efficient planning and execution.
- Manages and documents system configurations and oversees all transitions into production.
- Performs troubleshooting and remediation, ensures successful project implementation, and performs post project end user support. 3-5 years of experience.
- Soft skills include organizational, time management, action-oriented, and communication.
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Seniority level
Entry level -
Employment type
Contract -
Job function
Information Technology -
Industries
Medical Equipment Manufacturing and Biotechnology Research
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