<p>Quality Technician</p> <ul> <li>3rd shift * </li></ul> <p>Job Description</p> <p>The Quality Tech will primarily work on the production floor assisting the operations team with verifications, conducting general walkthroughs of the area, and performing onsite reviews and mini audits to ensure compliance. This role involves problem-solving tasks, such as initiating deviations, and reviewing various documents including executed batch records, cleaning records, and log books. Approximately 80-85% of the work will be conducted on the floor, with the remainder in the office. There are specific gowning requirements in certain areas ranging from wearing safety shoes to full gowning.</p> <p>Responsibilities</p> <ul> <li>Assist operations team with verifications and general area walkthroughs. </li><li>Perform onsite reviews and mini audits to ensure compliance. </li><li>Initiate deviations and contribute to problem-solving solutions. </li><li>Review and issue batch records, cleaning records, and log books. </li><li>Spend majority of time on production floor, with some office work. </li></ul> <p>Essential Skills</p> <ul> <li>Quality assurance expertise. </li><li>Familiarity with FDA regulations. </li><li>Experience in batch record review. </li><li>Knowledge of CAPA and audit processes. </li><li>Proficiency in document control. </li><li>Experience in pharmaceutical industry. </li></ul> <p>Additional Skills & Qualifications</p> <ul> <li>Bachelor's degree in any science discipline preferred. </li><li>2+ years of experience in regulated industry (GMP/FDA/ISO) for Specialist role. </li></ul> <p>Work Environment</p> <p>The majority of work is done on the production floor, with some office work involving interaction with the EQMS system. Dress code varies from safety shoes to full gowning depending on the area.</p> <p>Pay and Benefits</p> <p>The pay range for this position is $62000.00 - $90000.00/yr.</p> <p>Medical, dental, 401K, vision</p> <p>Workplace Type</p> <p>This is a fully onsite position in Madison,WI.</p> <p>Application Deadline</p> <p>This position is anticipated to close on Aug 26, 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>