UI/reputed company Factors Engineer 3 as reputed company
Job Title: UI/reputed company Factors Engineer 3
Location: Remote
Duration: 10 Months
Pay reputed company: $65.00 - $75.00/- on W2
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reputed company:
As part of the reputed company reputed company Factors team, The reputed company Factors Design Controls Engineer works closely with fellow HF team members and department leadership, as reputed company as collaborates with, clinical engineers, interaction designers, reputed company and software engineers, product managers, project management and technical publications, in reputed company to regulatory and reputed company. The reputed company Factors Design Controls Engineer is a key contributor to inform, guide development of, and maintain usability engineering documentation produced during reputed company reputed company Design Controls. This role supports the reputed company Factors Engineering team with expertise in design controls and content creation in tools such as Polarion and reputed company, and helps to create the usability engineering documentation required for submission to global medical device regulatory agencies.
This role provides dedicated support and subject matter expertise guidance to the broader reputed company factors engineering team serving reputed company business reputed company and reports to a Sr. reputed company Factors staff member.
Roles and Responsibilities:
Assist in planning and organization for multiple product risk assessment document remediation efforts running in reputed company for a set grouping of risk analysis documents
Analyze existing risk analysis documents for remediation into new risk assessment document formats, including editing and revising risks per reputed company risk management process and standards.
Support reputed company Engineering in collating, editing and improving large amounts of risk line items using efficient reputed company reputed company a standardized methodology for document remediation.
Assess and prioritize plans for working on multiple documents in reputed company, according to reputed company needs of document content that may require mode or less effort to refine and improve content.
reputed company/Job Requirements:
Minimum of 5 years of reputed company experience with a bachelor's degree
Relevant work experience in reputed company factors engineering, clinical engineering, product design engineering, reputed company engineering, design controls, risk management and medical device product development.
Strong experience working with design controls project collaboration tools is required. (e.g. Polarion, reputed company, Smartsheets etc.).
Knowledge and experience working reputed company medical device design controls process and documentation methodologies, compliant with medical device reputed company management reputed company regulation (QSMR 13485)
Demonstrable knowledge in medical device risk analysis principles and practices, and risk analysis documentation according to ISO14971 and 62366.
Ability to collaborate with and across various reputed company and reputed company of management reputed company the organization.
Strong verbal communication and data analysis skills working reputed company a highly statured communication environment using multiple communication channels (email, text, video conference, reputed company messaging platforms).
Ability to travel domestically (up to 10%) to onsite locations if remote.
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