Job Title: Quality Associate - (Doc Control) Job Description We are seeking a diligent Quality Associate with expertise in document control to join our team. The role involves updating logs, databases, and catalogs of product, manufacturing, and regulatory compliance information. The successful candidate will coordinate the review and revision of procedures, specifications, and forms, prepare process and status reports, assign and monitor document numbers, and review documents for accuracy and completeness. Additionally, the role includes assisting in compiling regulatory filing documents and maintaining computerized files to support all documentation systems. Responsibilities * Update logs, databases, and catalogs of product, manufacturing, and regulatory compliance information. * Coordinate the review and revision of procedures, specifications, and forms. * Prepare process and status reports, assign and monitor document numbers, and review documents for accuracy and completeness. * Assist in compiling regulatory filing documents and maintaining computerized files to support all documentation systems. Essential Skills * Quality assurance * Medical device knowledge * Document control * Change control Additional Skills & Qualifications * 1-2 years of experience in a similar role * University degree or extensive practical knowledge gained through experience * Attention to detail in making evaluative judgments based on the analysis of factual information Work Environment This is an individual contributor role that requires the use of judgment in applying professional expertise and is expected to work independently with minimal supervision. The job requires an understanding and application of procedures and concepts of one's own discipline. The position offers 2 weeks of PTO and 10 paid holidays. Pay and Benefits The pay range for this position is $45.00 - $55.00/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 9, 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 [email protected] for other accommodation options.