Russell Tobin
Responsibilities
You will write product design requirements, specifications, interface descriptions, and other formal design and test documentation based on input from Process Development team members and cross-functional collaborators.
You will release formal documentation by creating and submitting change orders to company's PLM system.
You will create informal documentation for development and test teams, including process guides and "how to" instructions, using Confluence and other tools.
You will create technical diagrams to support both formal and informal documentation using tools such as Gliffy or Lucidchart.
You are responsible for planning writing processes and accurately setting and communicating timelines and completion dates.
You will provide editing support to ensure content flow, simplicity, and succinctness, and adjust copy as necessary for grammar and spelling.
You will perform other related duties as assigned.
Qualifications
You have previous experience writing technical documents.
You have the ability to run self-directed projects, maintain timelines, transfer technology, and execute projects in an R&D environment.
You can deal with ambiguity and uncertainty, and you are willing to try new and challenging things.
You have proven ability to work in a fast-paced environment.
You have previous direct involvement in the medical device industry.
You are detail-oriented with strong time management skills.
You have excellent communication (written and verbal) and personal interaction skills.
Required Skills
Experience navigating PLM systems
Experience writing technical documents
Seniority level
Associate
Employment type
Contract
Job function
Writing/Editing and Information Technology
Industries
Pharmaceutical Manufacturing
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You will write product design requirements, specifications, interface descriptions, and other formal design and test documentation based on input from Process Development team members and cross-functional collaborators.
You will release formal documentation by creating and submitting change orders to company's PLM system.
You will create informal documentation for development and test teams, including process guides and "how to" instructions, using Confluence and other tools.
You will create technical diagrams to support both formal and informal documentation using tools such as Gliffy or Lucidchart.
You are responsible for planning writing processes and accurately setting and communicating timelines and completion dates.
You will provide editing support to ensure content flow, simplicity, and succinctness, and adjust copy as necessary for grammar and spelling.
You will perform other related duties as assigned.
Qualifications
You have previous experience writing technical documents.
You have the ability to run self-directed projects, maintain timelines, transfer technology, and execute projects in an R&D environment.
You can deal with ambiguity and uncertainty, and you are willing to try new and challenging things.
You have proven ability to work in a fast-paced environment.
You have previous direct involvement in the medical device industry.
You are detail-oriented with strong time management skills.
You have excellent communication (written and verbal) and personal interaction skills.
Required Skills
Experience navigating PLM systems
Experience writing technical documents
Seniority level
Associate
Employment type
Contract
Job function
Writing/Editing and Information Technology
Industries
Pharmaceutical Manufacturing
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