Job Title: Technical Writer Location: Franklin Lakes, NJDuration: 06+ Months QUALIFICATIONS:Required work sample of Technical writerBachelor’s degree in engineering or related technical field Need at least 4+ years of in medical devices.Ability to follow instructions accurately and work as a member of a team Has knowledge of theories, practices and procedures in medical device documentation high level of expertise with content publishing tools such as Microsoft Office software (Microsoft PowerPoint, Microsoft Word), screen capture software, graphics packages, Microsoft VISIO, etc. Excellent written, verbal and listening skills- must work well with others Strong attention to detail, accuracy Understanding of medical devices Ability to operate in a matrix environment with multiple competing priorities RESPONSIBILITIES: This function will work with R&D Core Team Members from multiple BDMPS-SAIS Sustaining and New Product Development project teams to create and modify project level documentation within tight timelines.The technical writer will contribute high quality documentation for the Design History Files within the guidance of PS procedures.Responsibilities include but are not limited to: Responsible for editing, rewriting, and authenticating program/projected related documentation including design control documentation, project timelines, charters, verification/validations plans/protocols/reports, following current PS procedures and templates Technical Writer will interface with technical professionals in the writing, editing, and publication of various types of technical product and process support documentation. Edit and format technical materials Meet deadlines so documentation is available as requested Ensures consistency, clarity, and quality in and across all types of documentation Engages in formatting, editing, and quality assurance on own work and the work of others Identify and correct problems as they arise Applies knowledge and skills to complete own work Depends on others for instruction, guidance and direction Develops competence in own area by performing routine work Send Supplier Approval/Notification of change to external vendors Label Approvals – route product labeling for approval via BDM-PS local procedure  Work with project team and functional/ business approvers to gather the appropriate documentation to manage the change Thanks & Regards,Nareshnaresh.v@stiorg.com609 232 8703