Quality Control Analyst

Job Description This role focuses on performing routine and project-based qPCR testing to support in-process and finished product quality control in a GMP pharmaceutical environment. The Quality Control Analyst conducts time-sensitive qPCR assays, handles raw material and finished product samples, supports method validation and development, and contributes to environmental and contaminant monitoring in a brand-new laboratory operating around the clock. QC Lab Analyst 3rd shift 4-10s (M-Thur) This role focuses on performing routine and project-based qPCR testing to support in-process and finished product quality control in a GMP pharmaceutical environment. The Quality Control Analyst conducts time-sensitive qPCR assays, handles raw material and finished product samples, supports method validation and development, and contributes to environmental and contaminant monitoring in a brand-new laboratory operating around the clock. Responsibilities Perform routine qPCR testing on samples with a 7-hour turnaround time, working in parallel with another analyst to ensure timely completion. Conduct in-process testing on raw materials, primarily pig-origin tissue slurries, including extraction of RNA from tissue samples. Perform finished product testing on final drug product and select specialty products, including some testing for additional sites. Run speciation assays to identify and quantify different species within a sample. Carry out contaminant monitoring and positive control environmental monitoring while samples are running. Perform calibration and routine maintenance of laboratory instruments, including centrifuges, spectrophotometers, and liquid handler robots. Prepare reagents, manage inventory, and ensure that all necessary materials are available and properly documented. Support validation activities, including validating basic centrifuges, spectrophotometers, liquid handler robots, laboratory software, and lab spaces. Assist with software programming related to qPCR and laboratory instruments as part of validation and method support. Draft and support laboratory methods, including method development and documentation in accordance with GMP and FDA expectations. Additional Skills & Qualifications Associates or Bachelor’s degree in Microbiology or a related discipline preferred for all levels. High School Diploma or G.E.D. required for all levels. Minimum of 1 year of working in a regulated laboratory environment. Experience with pipettes required. PCR experience from school or industry is preferred but not required. Open to different experience levels: Associate, Analyst, and Sr Work Environment The role is on third shift, Monday through Thursday, working 10-hour days starting at 9:00 p.m. Job Type & Location This is a Permanent position based out of Madison, WI. Pay And Benefits The pay range for this position is $45760.00 - $75000.00/yr. Competitive compensation; excellent benefits package - including Medical, Dental and Vision on Day 1; Life and AD&D Insurance, and Short and Long-term Disability; Health and Flexible Saving Account options; Employee Assistance Program, generous vacation; paid Holidays; 401k Workplace Type This is a fully onsite position in Madison,WI. Application Deadline This position is anticipated to close on Aug 17, 2026. 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. 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 process due to a disability, please email View email address on click.appcast.io for other accommodation options. San Francisco Fair Chance Ordinance Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI) We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools. #J-18808-Ljbffr Actalent