Quality Associate We are seeking a dedicated Quality Associate to ensure the document control of GMP Documents through paper-based data integrity. The ideal candidate will manage the controlled issuance and reconciliation of raw data form sheets, maintain files, and provide project support to identify process efficiencies. Additionally, this role involves revising and routing GMP documentation in the Document Management System and generating templates for quality processes to maintain efficiency. Ensuring all GMP documentation adheres to regulatory compliance is a key responsibility. Responsibilities + Ensure document control of GMP Documents via paper-based data integrity + Controlled Issuance and Reconciliation of Raw Data Form Sheets + Manage files including filing, tracking, and retrieving completed records such as complete batch records, protocols, logbooks, modules, and other GMP documentation + Provide project support and identify process efficiencies + Revise and route GMP documentation in the Document Management System + Generate templates for quality processes to maintain efficiency + Ensure all GMP documentation adheres to regulatory compliance Essential Skills + Experience with GMP documentation + Proficiency in document management + Knowledge of Microsoft Word + Experience with documentation control systems + 1-2 years of experience in GMP documentation Additional Skills & Qualifications + Bachelor's degree in a science field or equivalent experience in quality documentation within a GMP facility + 1+ years of experience in quality assurance and regulatory compliance Work Environment This position operates in an office setup, with working hours from Monday to Friday, 10:30 am to 6:30 pm. Pay and Benefits The pay range for this position is $21.00 - $23.00 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 Shawnee Mission,KS. Application Deadline This position will be accepting applications until Jan 31, 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. 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.