Quality Analyst

Posted 3 Days Ago
Be an Early Applicant
Burleson, TX, USA
In-Office
57K-71K Annually
Junior
Healthtech
The Role
Perform QC inspections and dispositions for medical devices and human tissue products; review batch and manufacturing records; track and coordinate CAPA, NCRs, and Deviations; support root-cause analysis and batch release; maintain GDocP-compliant records; assist with equipment qualification, calibration/preventive maintenance reviews, gowning training, and onsite regulatory audits to ensure FDA/OSHA/ISO compliance.
Summary Generated by Built In

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. Most 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. 

 Why you’ll love working at Axogen: 

  • Friendly, open, and fun team culture that values unique perspectives 
  • Company-wide dedication to profoundly impacting patients’ lives 
  • Comprehensive, high-quality benefits 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.
  • Familiarity with ANSI/ASQ Z1.4-2003, 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.

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.
  • Provides input based on knowledge and experience with batch release requirements.
  • 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.
  • Provides support related to gowning qualification and training.
  • Interfaces with colleagues to ensure effective corrective and preventive actions are implemented for any recurring product/process discrepancies.
  • Assists in the review and approval of equipment qualifications.
  • Assists in the review of Calibration and Preventative Maintenance reviews.
  • Assists in hosing of onsite regulatory audits and inspections.

Location

300 Boone Road, Suites A2 & A3, Burleson, TX 76028

#LI-AC1

Benefits/Compensation

This position is eligible for an annual bonus.

Benefits offered for this position include Health, Dental, Vision, Matching 401K, Paid Time Off, 9 Paid Holidays + 3 Floating Holidays, Dependent Care Flexible Spending Accounts, Medical Flexible Spending Accounts, Tuition Reimbursement, Paid Parental Leave, Paid Caregiver Leave, Basic Life Insurance, Supplemental Life Insurance, Employee Stock Purchase Plan, and Disability Insurance, as described in more detail in summary plan descriptions.

Salary Range
$56,728$70,909 USD

Axogen follows healthcare system guidelines with respect to credentialing, vaccinations and other employment/compliance related requirements, as well as CDC guidance. Axogen reserves the right to amend its policies from time to time in its sole discretion.

Skills Required

  • High School Diploma and minimum of 0-2 years relevant industry experience within Medical Device, Pharmaceutical, or Tissue commercial organization.
  • Bachelor's Degree in a Life Science discipline, engineering, or related field.
  • 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.
  • 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.
  • Knowledge of FDA, state OSHA and ISO regulations and standards and ability to follow company policies to maintain compliance.
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The Company
HQ: Alachua, FL
365 Employees
Year Founded: 2002

What We Do

Axogen is the leading company focused specifically on the science, development and commercialization of technologies for peripheral nerve regeneration and repair. We are passionate about helping to restore peripheral nerve function and quality of life to patients with physical damage or discontinuity to peripheral nerves by providing innovative, clinically proven and economically effective repair solutions for surgeons and health care providers. Every day, people suffer traumatic injuries or undergo surgical procedures that impact the function of their peripheral nerves. Physical damage to a peripheral nerve, or the inability to properly reconnect peripheral nerves, can result in the loss of muscle or organ function, the loss of sensory feeling, or the initiation of pain. Axogen’s comprehensive portfolio of products focuses on helping patients touch, run, feel, kiss, smile and hug—some of the many things healthy peripheral nerves allow us to do.

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