Job Title: Technical WriterJob Description We are seeking a skilled Technical Writer to develop detailed and clear documentation for new processes within the Duplex department. This role involves creating step-by-step guides, standard operating procedures (SOPs), and quality control measures. The successful candidate will also assist in documenting and investigating nonconformances in the CFM department, creating reports that outline root cause analysis, corrective actions, and preventive measures. Additionally, the Technical Writer will be responsible for writing summary reports for new processes and nonconformance investigations, ensuring they are concise, accurate, and easily understandable by all stakeholders. Responsibilities + Develop detailed and clear documentation for new processes, including step-by-step guides, SOPs, and quality control measures. + Assist in documenting and investigating nonconformances, creating reports that include root cause analysis, corrective actions, and preventive measures. + Write summary reports for new processes and nonconformance investigations. + Collaborate closely with the Operations Manager, quality control teams, and other departments to gather necessary information and ensure documentation accuracy. + Contribute to continuous improvement of documentation practices and processes within the Operations department. Essential Skills + Technical writing + Root cause analysis + At least 3 years of experience with document creation and technical writing. + Experience with office and ERP systems. + Experience in supporting investigations from a writing perspective. Additional Skills & Qualifications + Experience working in an FDA regulated environment. + Document control knowledge. + Proficiency in Microsoft Office and ERP systems. Work Environment The work environment is dynamic and fast-paced, reflecting the high standards and demands of the medical device industry. The role is onsite from 8 am to 5 pm, within the Operations department, which consists of approximately 200 dedicated professionals. The environment thrives on collaboration and efficiency. Pay and Benefits The pay range for this position is $40.00 - $40.00/hr. 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. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision• Critical Illness, Accident, and Hospital• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available• Life Insurance (Voluntary Life & AD&D for the employee and dependents)• Short and long-term disability• Health Spending Account (HSA)• Transportation benefits• Employee Assistance Program• Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Irvine,CA. Application Deadline This position is anticipated to close on May 20, 2025. 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. 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 due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.