A Technical Writer writes product instructions, user manuals or other material that helps to explain complex information or procedures. Writes help information available to customers online, or clear explanations of company policies. Supports internal communication among different technical, engineering and scientific specialists working on a project or product. Creates product documentation, and provides input for improving product design.
Kelly Science and Clinical FSP is currently seeking a Technical Writer for a remote opportunity supporting our Medical Device client. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you will be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You will also be eligible for paid time off, including holiday, vacation, and sick/personal time. The Sr. Technical Writer provides oversight and execution of Clinical Evaluation Reports (CER) and Summary of Safety and Clinical Performance Reports (SSCP)
DUTIES & RESPONSIBILITIES
Under supervision and in accordance with all applicable federal, state and local laws/regulations and Corporation's procedures and guidelines, this position is responsible for: Planning and writing CERs and SSCPs and mentoring junior technical writers. Conducting technical reviews to ensure document accuracy and compliance to local procedures, guidelines and regulatory requirements. Partnering with team members to address needs of each contributor. Managing daily activities to ensure timelines are met. Participating in workshops and other initiatives to help define and continuously improve process efficiency. Participating in continuous education activities to improve understanding of associated regulatory requirements and industry trends/practices. Supporting and, at times, acting as a subject matter authority during audits and inspections pertaining to processes and reports. Responsible for communicating business related issues or opportunities to next management level For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures Performs other duties assigned as needed
EXPERIENCE AND EDUCATION
• BA, BS, or BSN is required; advanced degree is preferred
REQUIRED
KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and
AFFILIATIONS
Experience within the medical device industry and knowledge of CER regulatory requirements, evidence generation, and CER document creation Strong verbal communication skills and interpersonal relationships Demonstrated knowledge and experience in clinical research, quality regulatory compliance, adverse event reporting, medical device risk management process, and common statistical methods is preferred
