Axogen Corporation logo

Sr. Engineer, Supplier Quality

Axogen Corporation

Vandalia, OHJobSeen 1 day agoSeen in employer's feed 1 day ago

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At a glance

Compensation
No compensation found
Location
Vandalia, OH
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Axogen seeks a Sr. Engineer, Supplier Quality to lead implementation, management, and compliance of the GxP Supplier Quality Management program, conduct supplier audits, and support quality assurance for contract service provider selection, ensuring adherence to FDA, EMA, Health Canada, ISO, and other regulatory requirements.

Skills & qualifications

RequiredNice to have

Skills

AuditingSupplier Quality ManagementGxP Operations21 CFR ComplianceISO StandardsICH GuidelinesCommercial Drug Product OperationsBiologics ManufacturingAPI ManufacturingExcipient ManufacturingAnalytical TestingIndependent Decision MakingOral CommunicationWritten CommunicationCollaborationInterpersonal SkillsInfluencing OthersFacilitating Team InteractionsPartnering With Stakeholders

Qualifications

Bachelor's Degree in Sciences5+ Years Pharmaceutical or Biopharmaceutical Experience in GMP Environment2+ Years Auditing Experience in Pharmaceutical or Medical Device IndustryQuality Auditor Certification

Benefits

401(k) Match

Full job description

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 Sr. Engineer, Supplier Quality This position reports to the Staff Engineer I, Supplier Quality and is responsible for the implementation, management, and compliance of the GxP Supplier Quality Management (SQM) Program, Supplier Audits, and Quality Agreements. This role ensures a robust and compliant SQM process that complies with FDA, EMA, Health Canada, ISO, and other applicable regulatory requirements and company procedures. The position is responsible for executing the SQM strategy and facilitating SQM integration with cross- functional processes. The role will also provide Quality Assurance support and oversight to contract service provider selection and qualification processes. Requirements of the Sr. Engineer, Supplier Quality * Bachelor's degree in the sciences (biology, chemistry, biochemistry, or chemical engineering) with 5+ years of pharmaceutical or biopharmaceutical experience in a GMP environment. * Experienced auditor with minimum 2 years auditing in pharmaceutical or medical device industry. Quality auditor certification is preferred. * Working experience managing a supplier quality management program. * Demonstrated understanding of Quality principles, industry practices, and standards (21 CFR, ISO, GxP, ICH, etc.) and ability to apply these to GxP operations internally and contract service providers. * Experience with commercial drug product operations including biologics, finished goods production, API and excipient manufacturing, and analytical testing. Combination product or medical device experience is a plus. * Independent decision making with a high degree of initiative. * Strong oral and written communication, collaboration, and interpersonal skills with the ability to influence others, facilitate team interactions, and partner with key stakeholders.

How this job compares

Set against the 629 open Supplier Quality Engineer jobs on Olive Jobs, counted November 3, 2026.

Pay
  • This postingNot listed
  • US median$98–154K/yr374 salary ranges
  • US median$40–48/hr28 hourly ranges
Openings
Olive Jobs lists 20 open Supplier Quality Engineer jobs in Ohio and 629 across the US. 6% of them nationwide are listed as remote or flexible.
Hiring the most in Ohio
Experience
This posting asks for at least 5 years of experience; Supplier Quality Engineer postings that state a minimum ask for 4 years at the median (538 postings).
Education
This posting asks for a bachelor's degree; 339 of the 629 open Supplier Quality Engineer jobs (54%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on November 3, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

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