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Careers

Sterile Processing and Materials Management Technician

Irvine, CA

Job Type

Full time

Workspace

In-person

About the Role

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. 

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.  

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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.

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

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/or 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 & Environmental 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 a 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.

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For California, the base pay range for this position is $23.00 to $25.00 / hour. The pay for the successful candidate will depend on various factors (e.g., qualifications, skills, education, 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).

About the Company

Induce Biologics USA Inc. was founded to develop the next evolution of bone regeneration products. Its founders and management team have previously developed and launched several very successful orthobiologics (bone and tissue repair) products, including several bone graft substitutes.

Induce Biologics is commercializing a family of bioimplants that includes Natural Matrix Protein (NMP™) which replicates the body’s native healing capabilities in order to create natural bone regeneration. The NMP™ proprietary process unlocks the growth factors naturally found in bone, making them bioavailable.

Induce Biologics USA Inc. is a small business in Irvine, CA. We are professional, agile and innovative.

Our work environment includes:
- Modern office setting
- Growth opportunities

Benefits

  • 401(k)

  • Dental insurance

  • Health insurance

  • Paid time off

  • Vision insurance

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