<p>Job Title: QC Associate II</p> <p>Job Description</p> <p>We are seeking a motivated QC Associate II to join our team, where you will play a crucial role in testing and validating assays, implementing change controls, and conducting stability and raw material testing. You will also be responsible for thorough documentation and quality management systems.</p> <p>Responsibilities</p> <ul> <li>Conduct testing using ELISA assays, PCR, SDS-Page, Gel Electrophoresis, and Microbiological assays. </li><li>Validate assays to ensure accuracy and reliability. </li><li>Manage change controls and contribute to stability and raw material testing. </li><li>Maintain detailed documentation and adhere to Quality Management Systems (QMS). </li><li>Revise Standard Operating Procedures (SOPs) as needed. </li></ul> <p>Essential Skills</p> <ul> <li>Proficiency in ELISA assays, validation, and documentation. </li><li>Experience with Quality Control processes. </li><li>Familiarity with PCR, Gel Electrophoresis, and Microbiological assays. </li><li>Ability to document test data accurately. </li><li>Understanding of Good Manufacturing Practices (GMP). </li></ul> <p>Additional Skills & Qualifications</p> <ul> <li>Bachelor's degree in a science-related field. </li><li>Experience in a late-stage clinical trial environment or commercial setting is helpful. </li></ul> <p>Work Environment</p> <p>This role requires working in both office and lab settings, offering a dynamic environment for growth and development as we prepare for phase 3 of clinical trials. Exciting opportunities await as we embark on the next round of manufacturing and testing.</p> <p>Pay and Benefits</p> <p>The pay range for this position is $37.00 - $44.00/hr.</p> <p>Eligibility requirements apply to some benefits and may depend on your job</p> <p>classification and length of employment. Benefits are subject to change and may be</p> <p>subject to specific elections, plan, or program terms. If eligible, the benefits</p> <p>available for this temporary role may include the following:</p> <ul> <li>Medical, dental & vision </li><li>Critical Illness, Accident, and Hospital </li><li>401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available </li><li>Life Insurance (Voluntary Life & AD&D for the employee and dependents) </li><li>Short and long-term disability </li><li>Health Spending Account (HSA) </li><li>Transportation benefits </li><li>Employee Assistance Program </li><li>Time Off/Leave (PTO, Vacation or Sick Leave) </li></ul> <p>Workplace Type</p> <p>This is a fully onsite position in Los Angeles,CA.</p> <p>Application Deadline</p> <p>This position is anticipated to close on Jul 25, 2025.</p> <p>About Actalent</p> <p>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.</p> <p>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.</p> <p>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 for other accommodation options.</p>