Title: Technical Writer
Location: Plymouth, MN - 55442
Duration: 9 Months (Till end of year)
Description: The Technical Writer will support the Client Preclinical Engineering team with the creation, revision and proofreading of reports and technical content for bench and in vivo testing. These documents will be leveraged in regulatory submissions and will require specific compliance to formatting and content specifications.
Responsibilities: • Collaboration with Research & Development teams, including subject matter experts on Preclinical Engineering, Hardware and Ablation Catheter Design teams. • Coordinating document approval process according to team procedural requirements. • With limited supervision, drafting reports and technical content in the context of bench and in vivo preclinical studies.
Required Qualifications: • Bachelor's degree, with at least three years of relevant experience, preferably within the medical device or biomedical engineering fields.
Preferred Qualifications: • Bachelor's degree in communications, engineering, technical writing or within the realm of the physical or biological sciences. • Experience within a regulated industry (e.g., medical devices). • Strong writing, editing and communication skills. • Able to balance efficient authoring and editing of documents while maintaining a high standard in quality of work. • Proficiency in Microsoft Word and Excel.
Description: The Technical Writer will support the Client Preclinical Engineering team with the creation, revision and proofreading of reports and technical content for bench and in vivo testing. These documents will be leveraged in regulatory submissions and will require specific compliance to formatting and content specifications.
Responsibilities: • Collaboration with Research & Development teams, including subject matter experts on Preclinical Engineering, Hardware and Ablation Catheter Design teams. • Coordinating document approval process according to team procedural requirements. • With limited supervision, drafting reports and technical content in the context of bench and in vivo preclinical studies.
Required Qualifications: • Bachelor's degree, with at least three years of relevant experience, preferably within the medical device or biomedical engineering fields.
Preferred Qualifications: • Bachelor's degree in communications, engineering, technical writing or within the realm of the physical or biological sciences. • Experience within a regulated industry (e.g., medical devices). • Strong writing, editing and communication skills. • Able to balance efficient authoring and editing of documents while maintaining a high standard in quality of work. • Proficiency in Microsoft Word and Excel.