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Manufacturing Engineer II

Simsurgical · Fenton, MO, 63026 · Active · JazzHR / ApplyToJob

Job facts

FieldValue
CompanySimsurgical
TitleManufacturing Engineer II
Normalized title-
Department / team-
LocationFenton, MO, United States
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerJazzHR / ApplyToJob
Posted / first seen2026-05-12 / 2026-05-30
Changed / last seen2026-05-30 / 2026-06-19

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Linked records

CompanySimsurgical
Source4bd687be-3863-4f24-8ebf-5c4b18bab633
ATS providerJazzHR / ApplyToJob

Description

Manufacturing Engineer II is a mid-level engineering role responsible for developing, validating, and improving manufacturing processes used in the production of medical devices. The individual will work cross-functionally with R&D, Quality, Operations, and Product Management to ensure robust, efficient, and compliant manufacturing operations. This role is expected to take ownership of projects, mentor junior team members, and contribute to the continuous improvement of processes and product quality. Responsibilities:   Develop and optimize manufacturing processes to improve quality and increase throughput through waste reduction risk prevention. Manage New Product Development (NPD) projects Generate full production documentation packages for Milling (3/5-axis), Swiss, and/or Metal Additive Mfg. methods. Uses Process Capability (Cp/Cpk) and Statistical Process Control (SPC) to ensure stable production. Independently lead moderate-scope projects supporting larger, cross-functional initiatives. Design, source, and implement fixtures, gages, molds, and tooling. Perform root cause analysis and corrective action planning related production issues. Analyze and interpret engineering drawings and specifications for manufacturability (DFM). Participate in process validations (IQ/OQ/PQ) and contribute to protocol generation and reporting. Provide technical input during design reviews for new products and design changes. Collaborate with machinists, technicians, and quality inspectors to resolve shop floor challenges. Assist in the development and refinement of SOPs, work instructions, and training materials. Participate in vendor selection and evaluation for outsourced manufacturing and tooling. Review and disposition Process Change Requests (PCR). Prepare project documentation and reports in compliance with QMS. Identify opportunities for new capital equipment to reduce costs or increase capacity. Utilize a risk-based approach to manufacturing using Lean/SixSigma tools (PFMEA, Pugh, etc.) Mentor or support Manufacturing Engineer I team members, as needed.  Requirements:   Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or a related field. 3–7 years of experience in a manufacturing engineering role, preferably in a medical device or regulated industry. Strong understanding of machining processes (CNC, EDM, milling, turning) and shop floor troubleshooting. Additive manufacturing experience a plus. Proficiency in SolidWorks or equivalent CAD software; capable of designing tooling and fixtures. Demonstrated experience with Mfg. NPD, DFM principles, GD&T, and reading complex prints and models. Working knowledge of quality systems, ISO 13485, and FDA regulations, 21 CFR 820. Hands-on experience with process validations, risk analysis (PFMEA), and statistical methods (DOE). Strong analytical skills and problem-solving abilities; ability to manage multiple priorities. Clear verbal and written communication skills and ability to work cross-functionally. Proficiency with Microsoft Office and familiarity with ERP or PLM systems.         Physical Requirements:                 The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.   Ability to stand, walk, climb, crouch, push, pull, and lift occasionally (up to 50 lbs). Regular use of hands and eyes for computer-based design and documentation tasks. Occasionally required to work in a manufacturing environment, exposed to noise, fumes, and moving machiner

Full job record

Job ID7f97dd9b824a05afb93bf07c077bf1a14b1eda6c
Org ID6dd1a48d-e9a2-4c05-ac2c-ddf013e881f1
Source ID4bd687be-3863-4f24-8ebf-5c4b18bab633
Board ID4bd687be-3863-4f24-8ebf-5c4b18bab633
Providerjazzhr
Provider Job Keysy5QikvHQA
TitleManufacturing Engineer II
Normalized Title—
Statusactive
Activeyes
Location TextFenton, MO, 63026
Department—
Team—
Employment Typefull_time
Workplace Type—
Remote Policy—
CountryUnited States
RegionMO
CityFenton
Salary Raw—
Salary Min—
Salary Max—
Salary Currency—
Salary Period—
Source URLhttps://simsurgical.applytojob.com/apply/sy5QikvHQA/Manufacturing-Engineer-II
Apply URLhttps://simsurgical.applytojob.com/apply/sy5QikvHQA/Manufacturing-Engineer-II
First Seen At2026-05-30 05:48:20Z
Last Seen At2026-06-19 10:59:53Z
Last Checked At2026-06-19 10:59:53Z
Last Changed At2026-05-30 05:48:20Z
Inactive At—
Source Posted At2026-05-12 00:00:00Z
Source Updated At—
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=jazzhr/board=simsurgical/date=2026-06-19/2026-06-19T10-59-53-238Z-77f3095488f4faca1efd303a07726d6c975ee82ac7f0bfe115fd420d6670d98f.json
Event Fields
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Extensions
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Native Structured
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    "description_html": "<span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Manufacturing Engineer II is a mid-level engineering role responsible for developing, validating, and improving manufacturing processes used in the production of medical devices. The individual will work cross-functionally with R&D, Quality, Operations, and Product Management to ensure robust, efficient, and compliant manufacturing operations. This role is expected to take ownership of projects, mentor junior team members, and contribute to the continuous improvement of processes and product quality.</span></span></span><br><br><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\"><b><u>Responsibilities:</u></b></span></span></span><br> <ul style=\"margin-top:2px;margin-bottom:2px;\"><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Develop and optimize manufacturing processes to improve quality and increase throughput through waste reduction risk prevention.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Manage New Product Development (NPD) projects</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Generate full production documentation packages for Milling (3/5-axis), Swiss, and/or Metal Additive Mfg. methods.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Uses Process Capability (Cp/Cpk) and Statistical Process Control (SPC) to ensure stable production.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Independently lead moderate-scope projects supporting larger, cross-functional initiatives.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Design, source, and implement fixtures, gages, molds, and tooling.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Perform root cause analysis and corrective action planning related production issues.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Analyze and interpret engineering drawings and specifications for manufacturability (DFM).</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Participate in process validations (IQ/OQ/PQ) and contribute to protocol generation and reporting.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Provide technical input during design reviews for new products and design changes.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Collaborate with machinists, technicians, and quality inspectors to resolve shop floor challenges.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Assist in the development and refinement of SOPs, work instructions, and training materials.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Participate in vendor selection and evaluation for outsourced manufacturing and tooling.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Review and disposition Process Change Requests (PCR).</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Prepare project documentation and reports in compliance with QMS.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Identify opportunities for new capital equipment to reduce costs or increase capacity.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Utilize a risk-based approach to manufacturing using Lean/SixSigma tools (PFMEA, Pugh, etc.)</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Mentor or support Manufacturing Engineer I team members, as needed.</span></span></span></li></ul><br><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\"><b> Requirements: </b></span></span></span><br> <ul style=\"margin-top:2px;margin-bottom:2px;\"><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or a related field.</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">3–7 years of experience in a manufacturing engineering role, preferably in a medical device or regulated industry.</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Strong understanding of machining processes (CNC, EDM, milling, turning) and shop floor troubleshooting. Additive manufacturing experience a plus.</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Proficiency in SolidWorks or equivalent CAD software; capable of designing tooling and fixtures.</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Demonstrated experience with Mfg. NPD, DFM principles, GD&T, and reading complex prints and models.</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Working knowledge of quality systems, ISO 13485, and FDA regulations, 21 CFR 820.</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Hands-on experience with process validations, risk analysis (PFMEA), and statistical methods (DOE).</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Strong analytical skills and problem-solving abilities; ability to manage multiple priorities.</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Clear verbal and written communication skills and ability to work cross-functionally.</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Proficiency with Microsoft Office and familiarity with ERP or PLM systems.</span></span></span></li></ul><br><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\"><b>        Physical Requirements: </b></span></span><br><br><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\"><b>                </b>The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.</span></span><br> <ul style=\"margin-top:2px;margin-bottom:2px;\"><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">Ability to stand, walk, climb, crouch, push, pull, and lift occasionally (up to 50 lbs).</span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">Regular use of hands and eyes for computer-based design and documentation tasks.</span></span></li></ul><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">Occasionally required to work in a manufacturing environment, exposed to noise, fumes, and moving machiner</span></span>",
    "description_text": "Manufacturing Engineer II is a mid-level engineering role responsible for developing, validating, and improving manufacturing processes used in the production of medical devices. The individual will work cross-functionally with R&D, Quality, Operations, and Product Management to ensure robust, efficient, and compliant manufacturing operations. This role is expected to take ownership of projects, mentor junior team members, and contribute to the continuous improvement of processes and product quality.\n Responsibilities:\n  Develop and optimize manufacturing processes to improve quality and increase throughput through waste reduction risk prevention.\n Manage New Product Development (NPD) projects\n Generate full production documentation packages for Milling (3/5-axis), Swiss, and/or Metal Additive Mfg. methods.\n Uses Process Capability (Cp/Cpk) and Statistical Process Control (SPC) to ensure stable production.\n Independently lead moderate-scope projects supporting larger, cross-functional initiatives.\n Design, source, and implement fixtures, gages, molds, and tooling.\n Perform root cause analysis and corrective action planning related production issues.\n Analyze and interpret engineering drawings and specifications for manufacturability (DFM).\n Participate in process validations (IQ/OQ/PQ) and contribute to protocol generation and reporting.\n Provide technical input during design reviews for new products and design changes.\n Collaborate with machinists, technicians, and quality inspectors to resolve shop floor challenges.\n Assist in the development and refinement of SOPs, work instructions, and training materials.\n Participate in vendor selection and evaluation for outsourced manufacturing and tooling.\n Review and disposition Process Change Requests (PCR).\n Prepare project documentation and reports in compliance with QMS.\n Identify opportunities for new capital equipment to reduce costs or increase capacity.\n Utilize a risk-based approach to manufacturing using Lean/SixSigma tools (PFMEA, Pugh, etc.)\n Mentor or support Manufacturing Engineer I team members, as needed.\n  Requirements:\n  Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or a related field.\n 3–7 years of experience in a manufacturing engineering role, preferably in a medical device or regulated industry.\n Strong understanding of machining processes (CNC, EDM, milling, turning) and shop floor troubleshooting. Additive manufacturing experience a plus.\n Proficiency in SolidWorks or equivalent CAD software; capable of designing tooling and fixtures.\n Demonstrated experience with Mfg. NPD, DFM principles, GD&T, and reading complex prints and models.\n Working knowledge of quality systems, ISO 13485, and FDA regulations, 21 CFR 820.\n Hands-on experience with process validations, risk analysis (PFMEA), and statistical methods (DOE).\n Strong analytical skills and problem-solving abilities; ability to manage multiple priorities.\n Clear verbal and written communication skills and ability to work cross-functionally.\n Proficiency with Microsoft Office and familiarity with ERP or PLM systems.\n         Physical Requirements:\n                 The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.\n  Ability to stand, walk, climb, crouch, push, pull, and lift occasionally (up to 50 lbs).\n Regular use of hands and eyes for computer-based design and documentation tasks.\n Occasionally required to work in a manufacturing environment, exposed to noise, fumes, and moving machiner",
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      "title": "Manufacturing Engineer II",
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      "datePosted": "2026-05-12",
      "description": "<span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Manufacturing Engineer II is a mid-level engineering role responsible for developing, validating, and improving manufacturing processes used in the production of medical devices. The individual will work cross-functionally with R&D, Quality, Operations, and Product Management to ensure robust, efficient, and compliant manufacturing operations. This role is expected to take ownership of projects, mentor junior team members, and contribute to the continuous improvement of processes and product quality.</span></span></span><br><br><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\"><b><u>Responsibilities:</u></b></span></span></span><br> <ul style=\"margin-top:2px;margin-bottom:2px;\"><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Develop and optimize manufacturing processes to improve quality and increase throughput through waste reduction risk prevention.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Manage New Product Development (NPD) projects</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Generate full production documentation packages for Milling (3/5-axis), Swiss, and/or Metal Additive Mfg. methods.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Uses Process Capability (Cp/Cpk) and Statistical Process Control (SPC) to ensure stable production.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Independently lead moderate-scope projects supporting larger, cross-functional initiatives.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Design, source, and implement fixtures, gages, molds, and tooling.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Perform root cause analysis and corrective action planning related production issues.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Analyze and interpret engineering drawings and specifications for manufacturability (DFM).</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Participate in process validations (IQ/OQ/PQ) and contribute to protocol generation and reporting.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Provide technical input during design reviews for new products and design changes.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Collaborate with machinists, technicians, and quality inspectors to resolve shop floor challenges.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Assist in the development and refinement of SOPs, work instructions, and training materials.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Participate in vendor selection and evaluation for outsourced manufacturing and tooling.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Review and disposition Process Change Requests (PCR).</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Prepare project documentation and reports in compliance with QMS.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Identify opportunities for new capital equipment to reduce costs or increase capacity.</span></span></span></li><li style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Utilize a risk-based approach to manufacturing using Lean/SixSigma tools (PFMEA, Pugh, etc.)</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Mentor or support Manufacturing Engineer I team members, as needed.</span></span></span></li></ul><br><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\"><b> Requirements: </b></span></span></span><br> <ul style=\"margin-top:2px;margin-bottom:2px;\"><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or a related field.</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">3–7 years of experience in a manufacturing engineering role, preferably in a medical device or regulated industry.</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Strong understanding of machining processes (CNC, EDM, milling, turning) and shop floor troubleshooting. Additive manufacturing experience a plus.</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Proficiency in SolidWorks or equivalent CAD software; capable of designing tooling and fixtures.</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Demonstrated experience with Mfg. NPD, DFM principles, GD&T, and reading complex prints and models.</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Working knowledge of quality systems, ISO 13485, and FDA regulations, 21 CFR 820.</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Hands-on experience with process validations, risk analysis (PFMEA), and statistical methods (DOE).</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Strong analytical skills and problem-solving abilities; ability to manage multiple priorities.</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Clear verbal and written communication skills and ability to work cross-functionally.</span></span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\">Proficiency with Microsoft Office and familiarity with ERP or PLM systems.</span></span></span></li></ul><br><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\"><b>        Physical Requirements: </b></span></span><br><br><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\"><b>                </b>The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.</span></span><br> <ul style=\"margin-top:2px;margin-bottom:2px;\"><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">Ability to stand, walk, climb, crouch, push, pull, and lift occasionally (up to 50 lbs).</span></span></li><li class=\"MsoListNumber\" style=\"margin-left:32px;margin-top:2px;margin-bottom:2px;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">Regular use of hands and eyes for computer-based design and documentation tasks.</span></span></li></ul><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">Occasionally required to work in a manufacturing environment, exposed to noise, fumes, and moving machiner</span></span>",
      "jobLocation": {
        "@type": "Place",
        "address": {
          "@type": "PostalAddress",
          "postalCode": "63026",
          "addressRegion": "MO",
          "addressLocality": "Fenton"
        }
      },
      "validThrough": "2026-08-10",
      "uniqueJobCode": "job_20260512051704_LGURBHHS7YEWFXVS",
      "employmentType": "FULL_TIME",
      "hiringOrganization": {
        "name": "Sim Surgical",
        "@type": "Organization",
        "sameAs": "http://www.simsurgical.com"
      },
      "experienceRequirements": "Mid Level"
    }
  },
  "list_job": {
    "id": "sy5QikvHQA",
    "title": "Manufacturing Engineer II",
    "detailUrl": "https://simsurgical.applytojob.com/apply/jobs/details/sy5QikvHQA?&"
  },
  "detail_errors": []
}
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