Position: Technical Writer

Location: San Diego, CA 92121

Duration: 12 months

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:

• Experience 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.

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