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Axogen

Specializes in peripheral nerve repair devices

Quality Analyst

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeVandalia, OH, USAIn-person

About the Job

Requirements

  • A high school diploma and 0–2 years of relevant industry experience within a medical device, pharmaceutical, or tissue commercial organization are required.
  • A bachelor's degree in a Life Science discipline, engineering, or a related field is preferred.
  • Ability to work the third shift, 11 p.m. to 7:30 a.m., Sunday night through Friday morning, is required.
  • Familiarity with ANSI/ASQ Z1.4-2003, c=0, and AQL methodologies is preferred.
  • Experience in an FDA-regulated environment, particularly medical device, human tissue, or pharmaceutical manufacturing, is preferred.
  • Experience with Microsoft Excel is required.
  • Experience writing Standard Operating Procedures and Work Instructions is required.
  • Experience with Quality System elements for CAPA, Non-Conforming Reports, and Deviations is required.

Responsibilities

  • Perform reviews of batch production records and manufacturing records as part of lot release activities.
  • Coordinate and track CAPA, NCR, and Deviation records, ensuring tasks are completed on time.
  • Pick, maintain, and regulate the custody and movement of biologic finished goods.
  • Assist teams in coordinating problem solving and root cause analysis for associated quality events.
  • Provide input based on knowledge and experience with batch release requirements.
  • Provide QMS Operations-related support to all CGMP departments.
  • Perform Quality Control activities at processing or distribution sites, including incoming material inspections, in-process inspections, and finished product inspections.
  • Maintain accurate and complete records of Quality Control activities, following Good Documentation Practices.
  • Provide support related to gowning qualification and training.
  • Interface with colleagues to ensure effective corrective and preventive actions are implemented for recurring product or process discrepancies.
  • Assist in the review and approval of equipment qualifications.
  • Assist in the review of calibration and preventative maintenance reviews.
  • Assist in hosting onsite regulatory audits and inspections.

Desired Qualifications

  • Familiarity with ANSI/ASQ Z1.4-2003, c=0, and AQL methodologies.
  • Experience in an FDA-regulated environment, particularly medical device, human tissue, or pharmaceutical manufacturing.

About the Company

Axogen

Specializes in peripheral nerve repair devices

AxoGen develops and sells surgical solutions for peripheral nerve repair. Its core products include Avance Nerve Graft, a processed human nerve allograft that bridges nerve gaps without a second surgical site, and Axoguard devices for nerve coaptation, protection, and neuroma reduction. The products are distributed directly to hospitals and surgical centers, targeting plastic, hand, and oral/maxillofacial surgeons. The goal is to improve nerve repair outcomes and grow a sustainable business in the U.S. nerve repair market by offering clinically proven, FDA-cleared tissue grafts and devices.

Company size
501-1,000
Company stage
IPO
Headquarters
Alachua, FL
Founded
2002

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