Company Name:
Category:
Administrative & Support Services
Status:
Part-Time
Contact Email:
hr@photonicareinc.com
Description:
PhotoniCare, Inc. is looking for a technical writer to support the production, regulatory (FDA and other agencies), and usability documentation for a regulated medical device. This is a contract position.
PhotoniCare, Inc. (www.photoni.care) is a medical device manufacturer located in EnterpriseWorks at U of I Research Park, Champaign, IL. Our mission is to improve child health and reduce healthcare costs by empowering physicians with better information. We are starting by developing technology that will change the standard of care for middle ear disease.
Responsibilities:
- Be responsible for drafting a selected subset of documents for the regulatory submission and production of a medical device
- Learn the usage of a device, engineering specification and/or manufacturing processes depending on the document type and category
- Learn and implement regulatory, compliance, and company requirements on documentation
- Use common language and document design skills to enhance readability and impression of end-user documents such as Instruction for Use, User Manual, brochures, etc
Minimum Qualifications:
- BS degree in engineering, communication or related field
- Excellent written and verbal communication skills
- Excellent word processor software skills (MS Word, Google Doc, etc.)
- Ability to learn new concepts quickly and independently
- Ability to work in a timeline and milestone driven R&D environment
Preferred Qualifications:
- Experience in a regulated clinical environment is a plus
How to Apply: Please respond with cover letter, resume and 2 technical writing samples to hr@photonicareinc.com