QC Analyst I, QC - Micro & EM(2nd Shift)

Forge Your Future with Us: At Forge Biologics, we believe in turning bold ideas into life-changing realities. Our mission is simple yet powerful: to enable access to life-changing gene therapies and help bring them from ideas into reality. We partner with scientists, physicians, biotech and pharma innovators, and patient communities — all united by one goal: improving lives. If you’re driven by purpose and excited to make a tangible impact, this is where your journey begins. Our team works out of The Hearth, a state-of-the-art, 200,000-square-foot cGMP facility in Columbus, Ohio. Here, you won’t just watch innovation happen — you’ll be part of it. Whether you’re scaling AAV manufacturing, collaborating on cutting-edge therapies, or supporting complex technical projects, you’ll play a key role in bringing hope to patients with genetic diseases. What sets Forge apart is our culture of H.O.P.E. We are hardworking , showing up each day with determination and grit. We are open , creating a space where ideas flow freely, and every voice is valued. We are purpose-driven , with every task directly tied to changing lives. And we are engaged , energized by the challenges we face and the milestones we achieve together. At Forge, your growth matters. We’re committed to helping you expand your skills, take on new challenges, and develop your career through mentorship, hands-on learning, and opportunities for advancement. Our people are our greatest investment, and we’re proud to see team members grow with us. Position Overview: QC Analyst I (EM &Micro) will be a supporting contributor to the Environmental Monitoring (EM) program, supporting the aseptic manufacturing environment and ensuring compliance with GMP standards. The Analyst I will support EM initiatives and QC microbiology lab routine testing. This position also requires a good understanding of cleanroom behavior, sterile gowning, and aseptic sampling. Responsibilities: • Performs EM sampling that incorporates application of GMP principles and methodologies.  • Conduct environmental monitoring activities including air, surface, and personnel inside the sterile manufacturing areas.  • Support trending of EM data using software’s eg: JMP and LIMS. • Performing microbial testing including but not limited to: Gram-stain, Growth promotion, Endotoxin, Bioburden, Osmolality, pH, etc.  • Supports thorough investigations to determine root cause of OOS investigations in the implementation of appropriate corrective and preventative actions in a timely manner.  • Trains junior staff in laboratory skills and scheduling EM sampling.  • Plans work to meet production and schedule requirements from clients (internal and external).  • Prepares EM data forms, EM labels, and executes the EM testing.  • Deliver results in a fast-paced environment.  • Participates in Media Fill/Aseptic Process Sims (APS) qualifications.  • Perform other duties as assigned Qualifications: • Minimum of a High School Diploma or GED equivalent required. Bachelor’s degree in microbiology, Biology, or a related scientific field preferred.  • Minimum 1-2 years’ experience in a GMP or QC environment is strongly preferred.  • Must be self-motivated, organized, and proactive.  • Strong technical aptitude, including demonstrated experience in applying scientific reasoning to solve complex problems.  • Ability to work hours necessary to support QC and production  • Job activities require long periods of standing and use of controlled movements as well as aseptic techniques/behaviors in the sterile filling suites.  • Knowledge of aseptic techniques preferred.  • Ability to work in confined spaces like clean rooms and near operating equipment.  • Ability to work in loud noise environments and in Personal Prot