<p>Job Title: QC Micro Investigator IIJob Description</p> <p>The Quality Investigator/Scientist II operates in a high-throughput environment, completing investigations primarily for QC Micro. This role involves leading multiple investigations simultaneously and ensuring their timely completion through dedication, tenacity, and building relationships with partners in QA and various testing groups. As a strong individual contributor, the Quality Engineer/Scientist III maintains a steady record closure rate while working on moderate complexity investigations.</p> <p>Responsibilities</p> <ul> <li>Stay current with training in Success Factors. </li><li>Conduct RAPID meetings with QA and QC staff occasionally. </li><li>Use TrackWise software to author investigations. </li><li>Be responsible for compliance-related deliverables including audit support, presentations to senior management and site leadership, and generating trend reports. </li><li>Support compliance culture initiatives and assist in implementing changes. </li><li>Develop the team through creation and delivery of proactive and reactive trainings. </li><li>Assist with the development of tools and resources to improve the investigative process. </li><li>Assist Scientist I investigators when needed. </li><li>Average 3-4 deviation/OOS/CAPA record closures per month based on complexity. </li><li>Complete overdue assessments and file record extensions as required. </li><li>Author and revise SOPs as needed. </li><li>Assist with formulating continuous improvement strategies and timelines. </li><li>Perform other job duties as assigned. </li></ul> <p>Essential Skills</p> <ul> <li>Knowledge of GMP regulations. </li><li>Experience in QC Microbiology. </li><li>Aseptic technique. </li><li>USP compendia methods. </li><li>OOS/OOT investigations. </li></ul> <p>Additional Skills & Qualifications</p> <ul> <li>Bachelor's degree in a science-related field with 3-4 years of industry experience. </li><li>Experience in a Pharmaceutical FDA/GMP regulated environment. </li><li>Experience with Endotoxin and Bioburden testing. </li><li>TrackWise and TapRooT experience is a plus. </li><li>Knowledge of Good Laboratory Practices (GLP) and Good Documentation Practices (GDP). </li><li>Strong computer skills including SmartSheet, PowerBI, MS Excel, Word, and PowerPoint. </li><li>Strong communication skills including active listening and facilitation. </li><li>Ability to inspire innovation and team effectiveness. </li></ul> <p>Work Environment</p> <p>The position is primarily onsite for training and will offer the opportunity to work one day from home once trained. Laboratory spaces require wearing gloves and other PPE. The role involves extended periods of desk and meeting time, working within a team of three and a supervisor.</p> <p>Job Type & Location</p> <p>This is a Contract to Hire position based out of Berkeley, MO.</p> <p>Pay and Benefits</p> <p>The pay range for this position is $32.00 - $35.00/hr.</p> <p>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)</p> <p>Workplace Type</p> <p>This is a fully onsite position in Berkeley,MO.</p> <p>Application Deadline</p> <p>This position is anticipated to close on Mar 12, 2026.</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>