Technical Writer

TAE Technologies•Irvine, CA

6d•Onsite

About The Position

Do Epic Science TAE is the world’s first private fusion energy company, founded in 1998 to commercialize the cleanest, safest, most affordable, and sustainable form of carbon-free power. We are applying science and engineering to design transformational technologies. Whether it's harnessing fusion through the science of stars, making exponential leaps in power efficiency, or innovating medical care with a novel cancer treatment: We're turning the promise of science into reality. We’re looking for candidates who are passionate about realizing our mission: A future where all people have affordable access to reliable, abundant, and environmentally friendly fusion-generated electricity. About The Role Collaborate with a team to create technical documentation, specification writing, technical &engineering specifications, product manuals, IFUs, service and operation manuals. Work closely with engineers and scientists at different levels to assist in deploying world changing mechanical/electronic systems. Keep technical documentation on projects according to ISO 9001/13485 quality management system requirements. Work with engineers and physicists to review drawings and compile specifications that can be sent to procurement. Support various tasks to document design, testing, requirement traceability and inspection. Maintain documents and drawings in an organized manner according to Document Control and Quality Assurance principles.

Requirements

Minimum 3 years of experience in technical writing.
Excellent Technical writing skills for a variety of mechanical, electrical, and various other high-tech products.
Practical knowledge of concepts of Quality Assurance and Document Control.
Ability to work with others and seek out necessary information to make effective Part Specifications.
Experience working with industrial vendors to get component information, design specifics, quality documents, testing certifications, etc.
Hands-on experience in managing technical documentation according to ISO 9001 quality management system requirements.
Adobe Software
Basic knowledge of CAD systems for mechanical design (AutoCAD, SolidWorks).
Good verbal and communication skills
Ability to work independently as well as a member of a team
Ability to cooperate in a fast-paced, team environment
Ability to liaise with others to achieve company goals
Organizational skills to include project documentation, SOP’s, and training
Knowledge of the medical industry quality systems (ISO 13485)
Mechanical and/or electrical drawing checking
Manufacturing Instruction Writing
Familiarity with equipment testing (Verification & Validation) and documentation

Nice To Haves

Medical background preferred.
Ability to utilize a database or write macros to optimize data entry is a plus.

Responsibilities

Create technical documentation, specification writing, technical & engineering specifications, product manuals, IFUs, service and operation manuals.
Work closely with engineers and scientists at different levels to assist in deploying world changing mechanical/electronic systems.
Keep technical documentation on projects according to ISO 9001/13485 quality management system requirements.
Work with engineers and physicists to review drawings and compile specifications that can be sent to procurement.
Support various tasks to document design, testing, requirement traceability and inspection.
Maintain documents and drawings in an organized manner according to Document Control and Quality Assurance principles.