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Careers at NuvOx

Quality Assurance and Document Control Specialist

NuvOx Pharma


Job Description

NuvOx Pharma is a biotechnology company located in Tucson, Arizona developing a novel oxygen therapeutic to treat life-threatening diseases where hypoxia plays a role. The company is in the clinical stage for stroke and oncology, and will be in clinical stage for ARDS/COVID.


We are currently hiring a Quality Assurance and Document Control Specialist to join our team of dedicated professionals.  The primary function of the position is to ensure quality adherence to GMP.


 Primary duties may include, but are not limited to:

  • Refining QMS - Assist in improving the consistency, control, and quality of manufacturing/operation.

  • Ensure doc control; Lead quality reviews

  • Identify operational risk and propose solutions/corrections

  • Write and review SOPs


Required Experience:

Understanding of manufacturing process and equipment; Understanding of chemistry/chemical engineering; Familiar with QMS and doc control principles; Analytical skills and critical thinking skills; Sharp attention to details, especially critical details; Team player and “can do” attitude. Sense of urgency and solution driven; Proficient in MS Word, Excel and PowerPoint.


Preferred Experience:

Good understanding of life science/pharmaceutical industry and possible consequences/requirements associated with the industry; 3-5 years’ experience in pharma/biotech/medical device industries in quality assurance and documentation capacity; Ideally proficient in analytical/statistical tools.


Education: A bachelor’s degree in chemistry or engineering, and/or the equivalent experience in life sciences, health services or related field.


Employment Type: Full time/flexible


Location: Tucson, AZ; Other locations in AZ acceptable if willing to travel


Please submit your resume to

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