Job Description 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 processes. + 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 customer requirements. + Produces products that conform to the company documentation and quality assurance standards. Top 3 things needed in a candidates experience: + 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 We reserve the right to pay above or below the posted wage based on factors unrelated to sex, race, or any other protected classification. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. This temporary role may be eligible for the following: + Medical, Dental & Vision + 401(k)/Roth + Basic/Supplemental Life & AD&D + Short and long-term disability + HSA & DCFSA + Transportation benefits + Employee Assistance Program + Company Paid Time off or State Sick Leave About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.