Manufacturing Technician (Sterile Processing)

Induce Biologics USA Inc. is proud to be the appointed representative for Red Rock Regeneration Inc. in the United States, overseeing the manufacture, marketing, and distribution of their innovative regenerative medicine products. This collaboration places us at the forefront of delivering cutting-edge solutions to patients within the U.S. healthcare market. By joining Induce Biologics USA Inc., you’ll be part of a mission-driven team working with revolutionary technology that’s reshaping the future of bone regeneration—and making a real difference in patients’ lives. The Sterile Processing and Materials Management Technician is responsible for the day-to-day operations of the sterile processing department, which includes processing, sterilization, and preparation of materials and components required for daily manufacturing activities. This role will also be responsible for management of manufacturing inventory and support manufacturing by coordinating the receipt, inspection, transfer of donor tissue, raw materials, supplies and finished products where needed. Essential Functions and Responsibilities: Sterile Processing Responsible for the daily activities of sterile processing, ensuring compliance with all relevant policies, procedures, and regulations. Ensure the workflow processes of decontamination, cleaning, assembly, packaging, sterilization, storage, and distribution of tissue processing instrumentation and equipment. Ensure proper sterilization procedures and monitoring processes, including daily biological and chemical indicator verification. Maintain accurate and original records of sterilization procedures, equipment maintenance, and inventory levels. Operation and maintenance of reprocessing equipment, including ultrasonic baths, washer decontaminators, and autoclaves, ensuring proper function and maintenance. Promote and maintain a safe sterile environment, adhering to strict infection control protocols and procedures. Responsible for manufacturing support and controlled environment maintenance during routine production. Material & Inventory Management Receive, inspect, and verify incoming donor tissue, reagents, and processing supplies to ensure compliance with tissue banking standards. Accurately log all incoming and outgoing materials using inventory management systems to maintain traceability. Monitor stock levels of critical materials such as cleanroom supplies, sterile packaging, and lab consumables, and communicate with the Supply Chain Manager as needed. Conduct routine cycle counts and support physical audits to ensure inventory accuracy and regulatory compliance. Logistics & Material Transfer Coordination Coordinate the timely transfer of raw materials, parts, and finished products between suppliers, warehouses, cleanrooms, laboratories, and production areas. Prepare materials for shipment, including labeling, packaging, and ensuring compliance with cold chain logistics or other storage conditions as needed. Arrange and track shipments with third-party logistics providers, ensuring timely and accurate delivery. Warehouse and Storage Management Monitor and manage inventory levels of supplies, reagents and equipment, ensuring adequate stock and timely replenishment. Organize and maintain warehouse and storage areas for efficient material retrieval and workflow. Operate pallet jacks and other material handling equipment as needed. Ensure proper storage conditions (e.g., refrigerated or frozen storage) for temperature-sensitive materials. In collaboration with Manufacturing and Supply Chain Management, troubleshoot and resolve inventory discrepancies, material shortages, and storage capacity issues. Cross-Functional Coordination Collaborate with Manufacturing, Quality, and Supply Chain teams to meet material demands and production schedules. Support product traceability efforts by ensuring accurate lot tracking and chain of custody documentation. Participate in process improvements to enhance material flow, inventory accuracy, and efficiency. Education/Experience Required High school diploma or GED. 2+ years of experience in material handling, warehouse/manufacturing operations, or inventory management in hospital, surgery center or regulated GMP biotech environment. Thorough knowledge of sterile processing principles, procedures, and regulations. Education/Experience Preferred Associate’s or Bachelor’s degree in biotechnology, life sciences, supply chain, or logistics is a plus Certified in Sterile Processing, e.g., CST, CSPD, or RCST Prior experience in a biotech, pharmaceutical, tissue banking, or regenerative medicine company is highly preferred Ability to operate specialized material handling equipment (e.g., , biohazard containment units, cleanroom carts). Familiarity with handling biological materials, cryopreserved products, and controlled-temperature shipments (e.g., fresh/frozen tissues, stem cells, or other human-derived materials). Prior experience working under FDA 21 CFR Part 1271 regulations and AATB (American Association of Tissue Banks) Basic understanding of regulatory requirements, such as GMP, GDP, and other industry standards. Skills, Knowledge, and Abilities Strong attention to detail for material tracking, documentation, and compliance reporting. Strong communication and teamwork skills to collaborate with manufacturing, purchasing, and customer service. Knowledge of ISO 13485 and FDA regulations preferred. Ability to work in a fast-paced, evolving environment, with flexibility to adapt to new processes. Must be able to adhere to Health, Safety and GMP requirements. Ability to work weekends, overtime, and holidays, if required. Proficient in using MS Office suite. Physical & Enviromental Factors Lifting: Will regularly lift or move items weighing up to 45 pounds unassisted. Comfortable handling delicate biological material. Mobility: Must be able to sit, stand, or walk for extended periods. Manual Dexterity: Ability to use computer, phone, and other standard office equipment for extended periods. Vision: Close vision required for working on a computer and reviewing detailed documents. This position requires frequent or continuous exposure to chemicals and/or solvents. The base pay range for this position is $25.00 to $27.00 / hour. The pay for the successful candidate will depend on various factors (e.g., qualifications, skills, education, certifications, and prior experience). Induce Biologics participates in E-Verify, a program that allows employers to confirm the employment eligibility of all newly hired employees through the U.S. Department of Homeland Security (DHS) and the Social Security Administration (SSA). Induce Biologics is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or any other characteristic protected by law. Third-Party Recruiters Please note that Induce Biologics does not accept unsolicited resumes or inquiries from third-party recruiters or staffing agencies. Any resumes submitted to our team without a prior agreement will be considered the property of Induce Biologics, and we will not be obligated to pay any fees related to unsolicited submissions. Job Type: Full-time Pay: $25.00 - $27.00 per hour Benefits: 401(k) 401(k) matching Dental insurance Flexible spending account Health insurance Life insurance Paid time off Vision insurance Work Location: In person