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Engineer I, AV Access

Engineer I, AV Access

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Monday-Friday, 8am-5pm
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For more than 20 years, AlloSource’s allografts have been the biologic solutions our surgeon customers use to deliver better care to their patients. As one of the largest and most respected nonprofit tissue banks in the United States, AlloSource develops, processes and distributes over 200 types of life-saving and life-enhancing allografts for use in a variety of medical procedures. Our commitment to honoring the gift of tissue donation motivates us to develop innovative allografts and lead the way in cellular and tissue therapies.


Compliance Statement

Must comply and ensure adherence with FDA, CGTP, OSHA, AlloSource SOPs, work instructions & procedures, proper practices and techniques, AATB standards, and applicable company policies, training requirements, safety practices and regulatory requirements that are applicable to the job responsibilities.



The Engineer I is responsible for product and process related issues associated with sustaining engineering of current products. Responsibilities include equipment procurement and validation, process development, change management leadership, and point of contact in interfacing with Humacyte.


Essential Duties and Responsibilities:

  1. Supports initiatives in all product manufacturing aspects: Yield, Quality improvement, Process Improvement and Documentation.
  2. Develops sound understanding of products and focuses on ways to improve manufacturing as well as identify and implement yield improvements.
  3. Drafts and executes validation protocols for equipment and process validations.
  4. Gathers and analyzes manufacturing metrics and works closely with Quality organization to define and validate appropriate process changes.
  5. Utilizes statistical techniques to compile and analyze data and realize appropriate improvement initiatives.
  6. Collaborates with multiple departments to coordinate product changes and process improvements.
  7. Works with production management to ensure Technicians understand pertinent technical aspects of their assigned products and processes.



  • Bachelor’s degree in an Engineering discipline.
  • 0-3 years industry experience is required.
  • Proficiency in Microsoft Applications, specifically Excel, Word and Outlook


Preferred Experience:

  • Intern or work experience in biotech, med device, or related GMP regulated field.


Physical Requirements:

  • Lift up to 50 lbs (10lbs continuously), bend, stand, twist, push, pull, manual dexterity, visual acuity, type, repetitive motion of wrist and shoulder.
  • Will be exposed to florescent lighting, dust, fumes, chemicals, biohazardous materials, Aseptic environment, working in confined spaces, wearing personal protective equipment, and sharp tools/instruments.



For consideration you must apply online, submit a current resume and meet the minimum requirements. All offers are contingent upon a background check, drug screen and other contingencies may apply depending upon the position. Candidates within a 50 mile radius of the hiring zip code may receive first consideration. If you require special accommodations, please contact us at 720-873-0213.





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