Technical Writer - Medical Devices
Sunrise Systems, Inc.San Diego, CA, USjob_description.job_card.variable_days_ago
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- serp_jobs.job_card.full_time
job_description.job_card.job_descriptionExperience working in a regulated industry such as medical devices or pharmaceuticals. Extensive experience with regulatory compliance processes. Strong background in supporting regulatory requirements to ensure adherence to regulatory guidelines. Demonstrated ability to be highly collaborative with marketing, clinical, quality, and regulatory reviewers. Five or more years writing and editing hardware / software user guides (print and online) and other technical product documentation. Ability to effectively manage the delivery of prioritized tasks. Ability to demonstrate a high level of initiative to gather information for developing documentation. Ability to work independently with minimal supervision. Effective at thinking independently and solving problems with product core team members. Ability to work under compressed deadlines and must be able to deal with unresolved situations, frequent project changes, delays, or other events. Ability to handle multiple projects with excellent follow-up and project management skills. Familiarity with electro-mechanical concepts and software application usage. Experience in device labeling and / or packaging content development. Familiarity with large company engineering change control processes and Agile software development methodologies. Experience with SAP, Oracle, or similar enterprise resource planning (ERP) system is a plus. Experience in version control systems (VCS) such as, Perforce, Apache Subversion, Microsoft Team Foundation Server, or GitHub. Knowledge of photography and photo editing software such as Adobe Photoshop. Skilled in both electronic and hard copy markup (Acrobat, tracked changes in Microsoft Word, standard editorial and proofreading symbols). Knowledge and experience with desktop publishing (DTP) software applications (MadCap Flare, Adobe FrameMaker, Adobe InDesign, Adobe Illustrator, XML, DITA) as applicable for technical documentation.
Job Description
Our client, a leading medical devices manufacturing company, is looking for a Technical Writer – Medical Devices. This is for an initial duration of 12 months and is located in San Diego, CA.
Job Type : Contract (Candidates must be able to work on W2 without VISA sponsorship)
Job Summary :
- The Technical Writer will be responsible for developing, writing, and maintaining comprehensive technical documentation for our Class II medical devices.
- This role requires a detail-oriented professional with strong writing skills and a deep understanding of regulatory requirements.
- The ideal candidate will have extensive experience in the medical device industry and the ability to work effectively with cross-functional teams.
Qualifications :
Compensation : The hourly rate for this position is between $47-$50 per hour.
Factors which may affect starting pay within this range may include [geography / market, skills, education, experience and other qualifications of the successful candidate].
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