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- Manufacturing Engineering activities associated with the production of TransMedics Organ
- Work with production staff to develop manufacturing processes. Provide technical expertise
- Work hands on to develop manufacturing processes, participate in validation activities, data
- Complete continuous improvement project initiatives focused on improving product quality
- Provide mentorship and training to Jr level engineers and interns.
- Lead activities with the Engineering and Operations teams to identify opportunities to
- Work with cross functional teams to identify and resolve technical and quality related issues
- Serve as strong team player, supporting and assisting supervisor and colleagues when
- Perform other TransMedics tasks and duties as required.
- 8+ years of experience working in an FDA/ISO regulated Medical Device/ Medical Equipment
- Must have prior Process Development and/or Manufacturing Engineering experience including
- Must have prior experience leading the design, development, and validation of production
- Previous experience working directly with production staff to improve manufacturing
- Must have prior work experience leading the development of plastic assembly, hardware
- Ability to work with Solidworks, and/or Pro Engineer to create 3D models and drawings to
- Experience using Minitab or similar statistical evaluation software/tools, Lean Six Sigma
- Experience leading Root Cause Investigations and CAPAs.
- Proven track record of working in a fast-paced environment with demonstrated ability to adjust
- Must have ability to identify, prioritize, and resolve issues as they arise with minimal
Senior Manufacturing Engineer - Andover, United States - TransMedics
Description
JOB DESCRIPTION
Position:
Senior Manufacturing Engineer
Reports to:
Manufacturing Engineering Manager
DEPARTMENT OF MANUFACTURING ENGINEERING focuses on manufacturing of the Organ Care
System at our headquarters in Andover Massachusetts. The team works on developing, mainaining,
and improving manufacturing processes to support our initiavive to deliver the highest quality
technology to save patients' lives.
ESSENTIAL TASKS AND DUTIES:
production staff to improve, maintain, and provide support to such processes.
Creation of documentation including:
Manufacturing Instructions, Inspection procedures, Test
Protocols, Assembly drawings, equipment control documentation, and Component Drawings.
changes.
design activities, and regulatory submissions.
BACKGROUND AND QUALIFICATIONS:
and test equipment.
DocuSign Envelope ID:
B313FCCE-7775-4BBE-960F-64C45B794A313
engineering activities.
and excellent interpersonal skills.
EDUCATION:
BS in Engineering plus 8+ years of experience working in an FDA/ISO regulated Medical
Device/ Medical Equipment Industry, or equivalent education and years of experience
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