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Manager, Quality Assurance

Axogen Corporation

Vandalia, OHJobSeen todaySeen in employer's feed today

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At a glance

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

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Job overview

The Manager, Quality Assurance establishes, administers, and maintains quality processes and systems for tissue, biologic, and medical device products in compliance with applicable practices and standards. The role manages quality departments at Axogen facilities, partners with Operations, and develops quality strategies and scalable processes to support compliance and continuous improvement across manufacturing, processing, testing, and distribution.

Skills & qualifications

RequiredNice to have

Skills

Quality AssuranceQuality EngineeringPeople LeadershipProject ManagementRegulatory AuditsSix SigmaLean Manufacturing

Qualifications

Bachelor's in Life Science or Engineering or Related Field5+ Years Quality Assurance Experience3+ Years Leading Others or Project ManagementCertified Quality Engineer

Benefits

Tuition Assistance
401(k) Match
Paid Time Off

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 Manager, Quality Assurance The Manager, Quality Assurance is responsible for establishing, administering, and maintaining Quality Assurance (QA) processes, systems, and tasks in compliance with current Good Manufacturing Practice (cGMP), current Good Distribution Practice (cGDP), and applicable domestic and international standards for tissue, biologic, and medical device products. The Manager, Quality Assurance manages quality departments at Axogen's facilities, including Processing Centers (DPC or APC) or the Burleson Distribution Center (BDC). The Manager, Quality Assurance collaborates closely with Operations to provide Quality Assurance (QA) support, ensuring that the organization maintains high standards of compliance and fosters a culture of continuous improvement in manufacturing, processing, systems, testing, and product distribution functions. This role is responsible for developing and executing quality strategies that align with company goals and industry best practices. By working cross-functionally, the Manager, Quality Assurance helps implement scalable processes that support organizational growth and ensure quality standards are met for receiving, storage, processing, shipping, and distribution activities. Requirements of the Manager, Quality Assurance * Bachelor's Degree in Life Science or Engineering discipline and/or a related field. * Minimum of 5 years Quality Engineering/Quality Assurance experience in medical device, pharmaceutical, or biotech manufacturing. * Minimum 3 years of leading others or project management, direct people management preferred. * Experience leading external regulatory audits (e.g., FDA, ISO). * Proficiency in Six Sigma or Lean Manufacturing is desirable. * Certified Quality Engineer preferred. * Travel Req

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