Key Responsibilities: - Develop and maintain technical documentation including forms procedures instructions for testing product and regulatory documents. - Translate complex technical information into clear concise and user-friendly content for various audiences including technicians and engineers. - Collaborate with cross-functional teams including R&D Quality Assurance and Process Owners to gather information and ensure accuracy. - Ensure all documentation complies with applicable internal policy standards. - Manage document version control and maintain documentation archives. - Participate in risk assessments and usability studies to inform documentation strategy. - Support the creation of training materials and internal SOP's. Key Skills: - Strong understanding of medical terminology and regulatory requirements. - Proficiency in document management systems and Microsoft Office. - Familiarity with Good Documentation Practices GDP and regulatory processes. - Excellent written and verbal communication skills. - Ability to manage multiple projects and meet tight deadlines. -5 years of experience in technical writing preferably in the medical device or healthcare industry. experience Education: Bachelors degree in English Communications Life Sciences Engineering or equivalent experience in Technical Writing. Pay and Benefits The pay range for this position is $30.00 - $45.00/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 Dallas,TX. Application Deadline This position is anticipated to close on Jul 1, 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.