Technical Writer II

The Contingent Plan

San Diego, CA

JOB DETAILS
SKILLS
Biotech and Pharmaceutical, Communication Skills, Current Good Manufacturing Practice (cGMP), Data Collection, Detail Oriented, Documentation, Establish Priorities, ISO (International Organization for Standardization), Medical Equipment, Multitasking, Organizational Skills, Presentation/Verbal Skills, Procedure Development, Project/Program Management, Regulatory Requirements, Technical Recruiting, Technical Writing, Time Management, Writing Skills
LOCATION
San Diego, CA
POSTED
Today
Technical Writer Opportunity

The Contingent Plan is actively recruiting an experienced technical writer for a client in the San Diego area. This is a 6 month assignment that may be renewed. This full-time role is an immediate need and the client will move quickly with the right candidates. Responsibilities include collaborating with multiple departments to establish standardized procedures and work instructions in accordance with PIL, PQMS, and Excellence Process Framework requirements. You will also be responsible for collecting data by interviewing specialists, technicians, reviewing written materials, and observing users. Effective communication with team members and other groups is essential to ensure consistent and complete requirement documentation. Additionally, you will escalate issues to management as appropriate and in a timely fashion. The role requires the ability to embed images, system screenshots in procedures to illustrate documentation, author and revise QMS documentation, participate in project teams, and manage complex, multiple projects from concept to release under tight deadlines. Adaptability and the ability to respond to changes in environment and priorities are crucial. Participation in the development of training material to support system deployment is also required.

Requirements include a Bachelor's degree or equivalent combination of education and experience. Pharmaceutical and/or medical device experience is preferred, along with an understanding of cGMP, ISO13485, and regulatory requirements. Three years of experience working as a technical writer, project management experience preferred, exceptional technical writing skills, excellent verbal communication skills, well-organized, efficient, and able to prioritize work and meet deadlines. A can-do attitude and commitment to stay in the organization more than 90 days are essential. The ability to work independently, detail-oriented to generate accurate and precise work, and collaborate and work with all levels of management and staff is required. Benefits include medical, dental, and vision.

About the Company

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The Contingent Plan