<p>Job Title: PCR Analyst</p> <p>Job Description</p> <p>The PCR Analyst will be performing routine testing support and supporting projects. The routine testing consists of qPCR testing with samples that have a 7-hour turnaround time. It takes two people to do it in parallel, requiring an all-hands-on-deck team effort to turn around a sample. A sample shows up every 8 hours, which is why the team has to work around the clock. The analyst will be performing in-process testing and finished product testing. The in-process testing is on raw materials, usually from pig origin, that come in a tissue slurry, and the team is responsible for extracting RNA from the tissue. The finished product testing includes testing the final drug product, pancreatin powder. While the samples are running, the analyst will be performing contaminant monitoring, positive control environmental monitoring, calibration and maintenance of instruments, inventory, and reagent preparations. The analyst will be trained on validation tasks including validating basic centrifuges, spectrophotometers, and liquid handler robots, as well as software programming, validating lab spaces, and method drafting. The analyst will also be running speciation assays to identify and quantify different species within a sample.</p> <p>Responsibilities</p> <ul> <li>Perform routine qPCR testing with a 7-hour turnaround time. </li><li>Conduct in-process testing on raw materials and finished product testing on pancreatin powder. </li><li>Extract RNA from tissue samples. </li><li>Monitor contaminants and positive controls in the environment. </li><li>Calibrate and maintain instruments. </li><li>Manage inventory and prepare reagents. </li><li>Validate lab equipment including centrifuges, spectrophotometers, and liquid handler robots. </li><li>Run speciation assays to identify and quantify different species within samples. </li><li>Handle reporting for the specialty products division and test heparin for the Mobren site. </li></ul> <p>Essential Skills</p> <ul> <li>Experience with PCR, qPCR software, and thermo cyclers. </li><li>Knowledge of GMP, quality control, and environmental monitoring. </li><li>Strong understanding of molecular biology and microbiology. </li><li>Experience in pharmaceutical or related settings. </li><li>Bachelor's degree or above in Microbiology or related discipline preferred. </li></ul> <p>Additional Skills & Qualifications</p> <ul> <li>High School Diploma or G.E.D. required. </li><li>2+ years preferred PCR/Micro Lab experience for Associate QC Analyst. </li><li>2+ years required with GMP for QC Analyst, 5+ years preferred. </li><li>5+ years required with GMP for Sr QC Analyst, 10+ years preferred. </li></ul> <p>Work Environment</p> <p>This position requires working 3rd shift, Monday-Thursday, with 10-hour shifts starting at 9 pm. A 3rd shift differential of $1.50/hr is offered. The analyst will be working in a brand-new lab set to open in March 2025. The team will consist of 3 members per shift. The team culture is laid back, driven, and hard-working. Initial training will be conducted on the 1st shift for the first week, with the second week transitioning to the designated shift, and full transition by March 3rd.</p> <p>Pay and Benefits</p> <p>The pay range for this position is $22.00 - $43.26/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:</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 Madison,WI.</p> <p>Application Deadline</p> <p>This position is anticipated to close on Mar 28, 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>Diversity, Equity & Inclusion</p> <p>At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:</p> <ul> <li>Hiring diverse talent </li><li>Maintaining an inclusive environment through persistent self-reflection </li><li>Building a culture of care, engagement, and recognition with clear outcomes </li><li>Ensuring growth opportunities for our people </li></ul> <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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.</p>