Axogen is committed to building and maintaining a strong and gratifying company culture that fosters professional growth. Our hands-on and personal approach makes transitioning to a new job a seamless and enjoyable process.

Benefits

are effective on day one! Axogen is an equal opportunity employer and does not discriminate against applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or veteran status.

package effective on date of hire Educational assistance available for all employees Matching 401(k) retirement plan Paid holidays, including floating holidays, to be used at your discretion Employee Stock Purchase Plan Referral incentive program Axogen Mission and Business Purpose Our business purpose is to restore health and improve quality of life by making restoration of peripheral nerve function an expected standard of care. We aim to lead the markets we serve by always requiring the solutions we offer patients and caregivers provide an improved benefit-to-risk profile as compared to existing standards of care. To ensure we deliver improved benefit-to-risk solutions, we will guide and expect the market and design requirement specifications underlying our engineering, business development, and clinical research activities, objectively target advancements in standards of care.

Job Summary of the Quality Analyst The Quality Analyst performs quality control (QC) inspections and dispositions of materials and products according to specifications. This role will perform QC inspection using measuring instruments (when applicable) and inspection methods. The role ensures any non-conforming materials or products that are identified are managed according to Axogen’s Quality System.

The Quality Analyst is responsible for following all Axogen policies and procedures to ensure compliance with applicable with FDA, state OSHA and ISO regs and standards. Employees within this role will performs a variety of tasks under limited supervision.

Requirements

of the Quality Analyst Bachelor’s Degree in a Life Science discipline, engineering, or in a related field preferred. High School Diploma and minimum of 0-2 years of relevant industry experience within a Medical Device, Pharmaceutical, or Tissue commercial organization. 4-2003, c=0 and AQL methodologies preferred Experience in an FDA-regulated environment, particularly medical device, human tissue or pharmaceutical manufacturing preferred.

Experience with Microsoft Excel Experience writing Standard Operating Procedures and Work Instructions Experience with Quality System elements for CAPA, Non-Conforming Reports (NCRs) and Deviations.

Provides QMS Operations related support to all CGMP departments. Performs Quality Control activities at Axogen’s processing or distribution sites. The Quality Analyst will be responsible for incoming material inspections, in-process inspections and finished product inspections.

Products include Medical Devices, sterile processed Human Tissue-Based Products, unprocessed human tissue, components supplies and labeling materials. The Quality Analyst will maintain accurate and complete records of Quality Control activities, following Good Documentation Practices.

Responsibilities

of the Quality Analyst The specific duties of the Quality Analyst include but are not limited to: Performs reviews of batch production records and manufacturing records as part of lot release activities. Coordinates and tracks CAPA, NCR and Deviation records, ensuring tasks are completed on time. Assists teams in coordination of problem solving and root cause analysis for associated quality events.