Posted in Other 30+ days ago.
Type: Full Time
Axogen is committed to building and maintaining a strong and gratifying company culture that fosters a work-life balance and 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 the leading company revolutionizing the science of nerve repair. We are passionate about helping to restore function and quality of life to patients with physical damage or discontinuity to peripheral nerves.
Contribute to positively impacting lives while working for a company that respects, recognizes, and values all team members!
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
- Flexible working hours
- Paid holidays, including floating holidays, to be used at your discretion
- Employee Stock Purchase Plan
- Referral incentive program
If you want to see how you can impact lives at Axogen, take a look at these inspiring patient stories:
Axogen is hiring Manufacturing Process Engineers in Dayton, OH!
Job Summary of the Manufacturing Process Engineer
The Manufacturing Process Engineer will provide focused technical and engineering support to operations with emphasis on yield improvements, capacity analysis, cost reduction, and validations.
Requirements of the Manufacturing Process Engineer
- Bachelor's degree in engineering or science required.
- Minimum of two years of experience in a manufacturing environment.
- Ability to analyze complex processes and systems, present improvement ideas, and drive improvements through to completion.
- Excellent documentation skills. Proven ability to analyze yields, document yield improvements, and create data sets to justify and implement yield improvements. Ability to write, execute, and complete validations (IQ/OQ/PQ). Ability to write procedures, specifications, and other manufacturing documents that are clear, concise, and ensure the appropriate audience has the correct information.
- Computer proficiency in Microsoft office. Proficiency in other engineering software's preferred.
- Excellent organizational skills. The ability to organize one's own tasks, documents, and projects as well as manage projects and tasks for others involved in implementing improvements.
- Excellent communication skills. The ability to assess a situation and communicate in a manner that is most effective to the receiver for a variety of levels of education, job role, and behavioral tendencies.
- Proven ability to work on multiple projects simultaneously in a fast-paced environment with minimal supervision.
- Experience in medical device, biologics, or tissue processing preferred.
- Lean, six sigma, or similar experience preferred.
- Experience in tissue recovery yield improvements preferred.
Responsibilities of the Manufacturing Process Engineer
The specific duties of the Manufacturing Process Engineer, but are not limited to:
- Works with tissue recovery staff and agencies to identify and implement yield improvements. May involve up to 25% travel.
- Supports continuous improvements of productivity, quality, cost, cycle time, and yield of raw material.
- Analyzes product and/or equipment specifications and performance requirements to determine feasibility of new plant equipment or modifying existing equipment.
- Assesses and implements improvements to manufacturing process efficiency and effectiveness.
- Supports and collaborates with R&D and Quality Management on new product launches.
- Leads continuous improvement projects.
- Analyzes and prepares recommendations for capital equipment investments.
- Provides cross-functional project management support to other areas of the business.
- Provides expertise and technical communications on quality issues.
- Utilizes root cause analysis methods and statistical tools to resolve processing issues.
- Uses statistical methods to determine in-control/out-of-control processes.
- Develops and implements methods and procedures for inspecting, testing, and evaluating products for acceptability.
- Participates in developing and executing equipment installation and operational qualifications.
- Participates in developing and executing process validations.
- Participates in developing and maintaining support systems for production work processes.
- Supports integration of new business work processes.
- Maintains the calibration program.
- Complies with all company policies, procedures, and SOPs.
- Works with Quality Assurance to ensure compliance with all international, federal, state, FDA, and AATB regulations.
- Support compliance with FDA Current Good Manufacturing Practices (CGMP) consistent with the Code of Federal Regulations for Tissue, Medical Device, Pharmaceuticals and Biologics.
- Performs other duties as assigned by Supervisor.
If you know someone who would be a great candidate for this position, just copy and send this link!
Location
Dayton Processing Center (APC)
913 Industrial Drive Place
Vandalia, OH 45377
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