Job Description
Top 3 things the manager is looking for:
- Problem-solver & Positive attitude
- Knowledge of authoring within a regulated environment (Medical Device/Pharma strongly preferred)
- Ability to manage multiple projects and stakeholders
Top 3 Tasks or Responsibilities in scope for this role:
- Working with SMEs to gather and develop content for Technical Literature
- Working within a CCMS content management system for authoring
- Working collaboratively to meet submission & launch deadlines with internal and external team
Education Required: Bachelor’s Degree
Years’ Experience Required: 4 years
Do they need to be local to any MDT office? No, May be asked to travel to Northridge (1-2 times per year)
Essentially we are looking for someone who has strong knowledge of working within a regulated environment to develop Technical Literature content that is patient-facing. The ideal candidate will be able to work well in gathering data from SMEs Regulatory Marketing Human Factors Quality and understand the critically of attention to detail and following processes and procedures. Some understanding of CAPA and Audit processes is favorable as they impact the role but this person will not likely drive these process.
- Creates develops plans writes and edits operational instructional maintenance or test procedures for paper multimedia web-based publications and user sites may produce content for embedded user assistance technology.
- Conducts interviews with various users and technical staff to gather data for documentation.
- Researches and translates technical information into manuals and/or web-based documents for nontechnical and technical users.
- May document engineering processes and specifications
- Recommends formats responsive to technical and customerrequirements.
- Produces products that conform to the company documentation and quality assurance standards.
Job Tags
Contract work, Local area,