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Process Engineer-Converting
F3CF2E6F06D96C7D42AC218710A77851 · PPC - Pleasant Prairie - Pleasant Prairie, WI 53158; 10101 78th Avenue, Pleasant Prairie, WI, 53158, USA · Deleted · Paycom ATS
Job facts
| Field | Value |
|---|---|
| Company | F3CF2E6F06D96C7D42AC218710A77851 |
| Title | Process Engineer-Converting |
| Normalized title | - |
| Department / team | - |
| Location | Pleasant Prairie, WI, United States |
| Work model | - |
| Employment type | Full Time |
| Salary | - |
| Status | deleted |
| ATS provider | Paycom ATS |
| Posted / first seen | 2026-04-16 / 2026-05-31 |
| Changed / last seen | 2026-06-06 / 2026-06-04 |
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| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from F3CF2E6F06D96C7D42AC218710A77851. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through Paycom ATS. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Pleasant Prairie. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | F3CF2E6F06D96C7D42AC218710A77851 |
| Source | 3cb780d8-6be3-46d2-91e2-7cc80fcdee60 |
| ATS provider | Paycom ATS |
Description
Description
The Converting Process Engineer is responsible for Execution and implementation of projects of great impact for the organization, related to R&D and New Product Introduction. We are seeking a highly skilled and innovative Converting Process Engineer to lead process development, optimization, and technical innovation in blown film extrusion and converting for medical device and medical packaging applications. This role is central to our R&D and New Product Introduction (NPI) initiatives, supporting cutting-edge projects from concept through commercialization while ensuring compliance with regulatory standards and industry best practices.
The ideal candidate will bring deep expertise in polymer processing, film manufacturing, and converting technologies, coupled with experience in regulated environments (ISO 13485, FDA, GMP). Will work cross-functionally with R&D, Quality, Manufacturing, and Commercial teams to drive product and process excellence.
Process Engineering & Development
Supports Engineers, technicians and operators during process development work.
Lead the design, development, and optimization of blown film extrusion processes for multilayer medical-grade films.
Define and implement process parameters, tooling design, material selection, and quality control strategies.
Develop robust converting processes (slitting, printing, pouching, laminating, etc.) tailored for sterile barrier systems and medical device packaging.
Research & Development (R&D)
Drive process innovation to support new materials, multilayer film structures, and proprietary packaging technologies.
Collaborate with product development teams to ensure process capabilities align with product performance requirements and regulatory expectations.
Conduct trials and scale-up activities to validate new materials and processes on pilot and production lines.
New Product Introduction (NPI)
Serve as the technical lead during the NPI lifecycle, from feasibility to design transfer and commercialization.
Develop and execute process validation (IQ/OQ/PQ), design of experiments (DOE), and risk assessments (PFMEA).
Provide hands-on support for equipment commissioning, tooling procurement, and technology transfer.
Quality & Compliance
Ensure processes and documentation comply with ISO 13485, FDA 21 CFR Part 820, and applicable medical packaging standards (e.g., ISO 11607).
Collaborate with Quality and Regulatory Affairs to develop and maintain technical files, validation protocols, and work instructions.
Support root cause investigations, CAPA, and continuous improvement initiatives.
Project Management & Leadership
Manage multiple technical projects concurrently with minimal supervision.
Mentor junior engineers and technicians; promote knowledge sharing and best practices.
Interface with suppliers, equipment manufacturers, and customers to support technical objectives.
Qualifications
Candidate Requirements:
Bachelor’s degree in engineering or scientific discipline.
7+ years of relevant experience in process engineering, with a strong focus on blown film extrusion and film converting.
At least 3 years of direct experience in a Medical Device or Healthcare packaging environment.
Expert level experience with integrated extrusion systems, Test Method development, protocol generation, execution, and reporting.
Proven track record in R&D and NPI projects within a regulated manufacturing setting.
GMP and ISO 9000 training.
Experience with tooling design with advanced SolidWorks CAD knowledge.
Six Sigma Green belt or equivalent certification beneficial but not required.
20% travel.
Competencies/Skills
Self-motivation and hands-on skills to simplify complex processes.
Professional experience in exploration of new technologic prospects.
Capability to establish change and encourage the inter-organizational exchange of skills.
Exceptional problem-solving, organizational, analytical, and critical thinking skills including high discretion/judgment in decision-making.
In-depth knowledge of blown film extrusion (co-extrusion, die design, resin rheology, cooling, winding).
Proficiency in converting processes such as slitting, die cutting, heat sealing, laminating, and pouch manufacturing.
Strong understanding of polymer behavior, film characterization, and testing methods.
Experience with statistical analysis tools (Minitab, JMP), DOE, SPC, and process validation methodologies.
Familiarity with medical packaging standards such as ISO 11607, ASTM F88, F1929, etc.
Excellent communication and interpersonal skills for cross-functional collaboration.
Demonstrated leadership and project management capabilities.
Experience with cleanroom manufacturing and Class I/II/III medical device packaging.
Knowledge of sustainability trends in polymer materials and biodegradable films.
Experience with ERP and document control systems (e.g., IQMS, Agile).
Full job record
| Job ID | 1466f77a02c04bcc9aa47857523c68e61eafb1b5 |
| Org ID | 968c2664-c111-4130-9156-2f81599b2773 |
| Source ID | 3cb780d8-6be3-46d2-91e2-7cc80fcdee60 |
| Board ID | 3cb780d8-6be3-46d2-91e2-7cc80fcdee60 |
| Provider | paycom |
| Provider Job Key | 761317 |
| Title | Process Engineer-Converting |
| Normalized Title | — |
| Status | deleted |
| Active | no |
| Location Text | PPC - Pleasant Prairie - Pleasant Prairie, WI 53158; 10101 78th Avenue, Pleasant Prairie, WI, 53158, USA |
| Department | — |
| Team | — |
| Employment Type | full_time |
| Workplace Type | — |
| Remote Policy | — |
| Country | United States |
| Region | WI |
| City | Pleasant Prairie |
| Salary Raw | Description The Converting Process Engineer is responsible for Execution and implementation of projects of great impact for the organization, related to R&D and New Product Introduction. We are seeking a highly skilled and innovative Converting Process Engineer to lead process development, optimization, and technical innovation in blown film extrusion and converting for medical device and medical packaging applications. This role is central to our R&D and New Product Introduction (NPI) initiatives, supporting cutting-edge projects from concept through commercialization while ensuring compliance with regulatory standards and industry best practices. The ideal candidate will bring deep expertise in polymer processing, film manufacturing, and converting technologies, coupled with experience in regulated environments (ISO 13485, FDA, GMP). Will work cross-functionally with R&D, Quality, Manufacturing, and Commercial teams to drive product and process excellence. Process Engineering & Development Supports Engineers, technicians and operators during process development work. Lead the design, development, and optimization of blown film extrusion processes for multilayer medical-grade films. Define and implement process parameters, tooling design, material selection, and quality control strategies. Develop robust converting processes (slitting, printing, pouching, laminating, etc.) tailored for sterile barrier systems and medical device packaging. Research & Development (R&D) Drive process innovation to support new materials, multilayer film structures, and proprietary packaging technologies. Collaborate with product development teams to ensure process capabilities align with product performance requirements and regulatory expectations. Conduct trials and scale-up activities to validate new materials and processes on pilot and production lines. New Product Introduction (NPI) Serve as the technical lead during the NPI lifecycle, from feasibility to design transfer and commercialization. Develop and execute process validation (IQ/OQ/PQ), design of experiments (DOE), and risk assessments (PFMEA). Provide hands-on support for equipment commissioning, tooling procurement, and technology transfer. Quality & Compliance Ensure processes and documentation comply with ISO 13485, FDA 21 CFR Part 820, and applicable medical packaging standards (e.g., ISO 11607). Collaborate with Quality and Regulatory Affairs to develop and maintain technical files, validation protocols, and work instructions. Support root cause investigations, CAPA, and continuous improvement initiatives. Project Management & Leadership Manage multiple technical projects concurrently with minimal supervision. Mentor junior engineers and technicians; promote knowledge sharing and best practices. Interface with suppliers, equipment manufacturers, and customers to support technical objectives. Qualifications Candidate Requirements: Bachelor’s degree in engineering or scientific discipline. 7+ years of relevant experience in process engineering, with a strong focus on blown film extrusion and film converting. At least 3 years of direct experience in a Medical Device or Healthcare packaging environment. Expert level experience with integrated extrusion systems, Test Method development, protocol generation, execution, and reporting. Proven track record in R&D and NPI projects within a regulated manufacturing setting. GMP and ISO 9000 training. Experience with tooling design with advanced SolidWorks CAD knowledge. Six Sigma Green belt or equivalent certification beneficial but not required. 20% travel. Competencies/Skills Self-motivation and hands-on skills to simplify complex processes. Professional experience in exploration of new technologic prospects. Capability to establish change and encourage the inter-organizational exchange of skills. Exceptional problem-solving, organizational, analytical, and critical thinking skills including high discretion/judgment in decision-making. In-depth knowledge of blown film extrusion (co-extrusion, die design, resin rheology, cooling, winding). Proficiency in converting processes such as slitting, die cutting, heat sealing, laminating, and pouch manufacturing. Strong understanding of polymer behavior, film characterization, and testing methods. Experience with statistical analysis tools (Minitab, JMP), DOE, SPC, and process validation methodologies. Familiarity with medical packaging standards such as ISO 11607, ASTM F88, F1929, etc. Excellent communication and interpersonal skills for cross-functional collaboration. Demonstrated leadership and project management capabilities. Experience with cleanroom manufacturing and Class I/II/III medical device packaging. Knowledge of sustainability trends in polymer materials and biodegradable films. Experience with ERP and document control systems (e.g., IQMS, Agile). |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://www.paycomonline.net/v4/ats/web.php/jobs/ViewJobDetails?job=761317&clientkey=F3CF2E6F06D96C7D42AC218710A77851 |
| Apply URL | https://www.paycomonline.net/v4/ats/web.php/jobs/ViewJobDetails?job=761317&clientkey=F3CF2E6F06D96C7D42AC218710A77851 |
| First Seen At | 2026-05-31 19:05:11Z |
| Last Seen At | 2026-06-04 10:02:22Z |
| Last Checked At | 2026-06-06 20:00:47Z |
| Last Changed At | 2026-06-06 20:00:47Z |
| Inactive At | 2026-06-06 20:00:47Z |
| Source Posted At | 2026-04-16 00:00:00Z |
| Source Updated At | — |
| Raw Payload Uri | s3://bluework-jobs-prod-raw-590183727216/raw/provider=paycom/board=F3CF2E6F06D96C7D42AC218710A77851/date=2026-06-04/2026-06-04T10-02-19-490Z-1de92d7db421961e1f47fbbdc7fa7ea454bd06035333471804e0606dbe3d5c15.json |
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"description": "<p style=\"margin-right:3px; margin-left:3px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:Roboto\"><span style=\"color:black\">The Converting Process Engineer is responsible for <span style=\"background:white\">Execution and implementation of projects of great impact for the organization, related to R&D and New Product Introduction. </span>We are seeking a highly skilled and innovative Converting Process Engineer to lead process development, optimization, and technical innovation in blown film extrusion and converting for medical device and medical packaging applications. This role is central to our R&D and New Product Introduction (NPI) initiatives, supporting cutting-edge projects from concept through commercialization while ensuring compliance with regulatory standards and industry best practices.</span></span></span></span></span></span></span></p>\r\n\r\n<p style=\"margin-right:3px; margin-left:3px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:Roboto\"><span style=\"color:black\">The ideal candidate will bring deep expertise in polymer processing, film manufacturing, and converting technologies, coupled with experience in regulated environments (ISO 13485, FDA, GMP). Will work cross-functionally with R&D, Quality, Manufacturing, and Commercial teams to drive product and process excellence.</span></span></span></span></span></span></span></p>\r\n\r\n<p style=\"margin-right:3px; margin-left:3px\"> </p>\r\n\r\n<p style=\"margin-right:3px; margin-left:3px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"font-family:Aptos,sans-serif\"><b><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Process Engineering & Development</span></span></span></b></span></span></span></span></p>\r\n\r\n<ul style=\"margin-bottom:11px; list-style-type:square\">\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"background:white\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Supports Engineers, technicians and operators during process development work.</span></span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"background:white\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Lead the design, development, and optimization of blown film extrusion processes for multilayer medical-grade films.</span></span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Define and implement process parameters, tooling design, material selection, and quality control strategies.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Develop robust converting processes (slitting, printing, pouching, laminating, etc.) tailored for sterile barrier systems and medical device packaging.</span></span></span></span></span></span></span></span></li>\r\n</ul>\r\n\r\n<p style=\"margin-right:3px; margin-left:3px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"font-family:Aptos,sans-serif\"><b><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Research & Development (R&D)</span></span></span></b></span></span></span></span></p>\r\n\r\n<ul style=\"margin-bottom:11px; list-style-type:square\">\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Drive process innovation to support new materials, multilayer film structures, and proprietary packaging technologies.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Collaborate with product development teams to ensure process capabilities align with product performance requirements and regulatory expectations.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Conduct trials and scale-up activities to validate new materials and processes on pilot and production lines.</span></span></span></span></span></span></span></span></li>\r\n</ul>\r\n\r\n<p style=\"margin-right:3px; margin-left:3px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"font-family:Aptos,sans-serif\"><b><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">New Product Introduction (NPI)</span></span></span></b></span></span></span></span></p>\r\n\r\n<ul style=\"margin-bottom:11px; list-style-type:square\">\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Serve as the technical lead during the NPI lifecycle, from feasibility to design transfer and commercialization.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Develop and execute process validation (IQ/OQ/PQ), design of experiments (DOE), and risk assessments (PFMEA).</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Provide hands-on support for equipment commissioning, tooling procurement, and technology transfer.</span></span></span></span></span></span></span></span></li>\r\n</ul>\r\n\r\n<p style=\"margin-right:3px; margin-left:3px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"font-family:Aptos,sans-serif\"><b><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Quality & Compliance</span></span></span></b></span></span></span></span></p>\r\n\r\n<ul style=\"margin-bottom:11px; list-style-type:square\">\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Ensure processes and documentation comply with ISO 13485, FDA 21 CFR Part 820, and applicable medical packaging standards (e.g., ISO 11607).</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Collaborate with Quality and Regulatory Affairs to develop and maintain technical files, validation protocols, and work instructions.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; 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margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Mentor junior engineers and technicians; promote knowledge sharing and best practices.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Interface with suppliers, equipment manufacturers, and customers to support technical objectives.</span></span></span></span></span></span></span></span></li>\r\n</ul>\r\n",
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"summary": "The%20Converting%20Process%20Engineer%20is%20responsible%20for%C2Execution%20and%20implementation%20of%20projects%20of%20great%20impact%20for%20the%20organization%2C%20related%20to%20R%26D%20and%20New%20Product%20Introduction.%C2We%20are%20seeking%20a%20highly%20skilled%20and%20innovative%20Converting%20Process%20Engineer%20to%20lead%20process%20development%2C%20optimization%2C%20and%20technical%20innovation%20in%20blown%20film%20extrusion%20and%20converting%20for%20medical%20device%20and%20medical%20packaging%20applications.%20This%20role%20is%20central%20to%20our%20R%26D%20and%20New%20Product%20Introduction%20%28NPI%29%20initiatives%2C%20supporting%20cutting-edge%20projects%20from%20concept%20through%20commercialization%20while%20ensuring%20compliance%20with%20regulatory%20standards%20and%20industry%20best%20practices.%0D%0A%0D%0AThe%20ideal%20candidate%20will%20bring%20deep%20expertise%20in%20polymer%20processing%2C%20film%20manufacturing%2C%20and%20converting%20technologies%2C%20coupled%20with%20experience%20in%20regulated%20environments%20%28ISO%2013485%2C%20FDA%2C%20GMP%29.%20Will%20work%20cross-functionally%20with%20R%26D%2C%20Quality%2C%20Manufacturing%2C%20and%20Commercial%20teams%20to%20drive%20product%20and%20process%20excellence.%0D%0A%0D%0A%C2%0D%0A%0D%0AProcess%20Engineering%20%26%20Development%0D%0A%0D%0A%0D%0A%09Supports%20Engineers..."
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"googleJobJson": "{\"@context\":\"https://schema.org/\",\"@type\":\"JobPosting\",\"title\":\"Process Engineer-Converting\",\"identifier\":\"J0VI76761317\",\"url\":\"https://www.paycomonline.net/v4/ats/web.php/portal/F3CF2E6F06D96C7D42AC218710A77851/jobs/761317\",\"image\":\"https://www.paycomonline.net/v4/ats/web.php/application/style/logo?clientkey=F3CF2E6F06D96C7D42AC218710A77851\",\"datePosted\":\"2026-04-16\",\"description\":\"Job DetailsJob Location: PPC - Pleasant Prairie - Pleasant Prairie, WI 53158Position Type: Full TimeThe Converting Process Engineer is responsible for Execution and implementation of projects of great impact for the organization, related to R&D and New Product Introduction. We are seeking a highly skilled and innovative Converting Process Engineer to lead process development, optimization, and technical innovation in blown film extrusion and converting for medical device and medical packaging applications. This role is central to our R&D and New Product Introduction (NPI) initiatives, supporting cutting-edge projects from concept through commercialization while ensuring compliance with regulatory standards and industry best practices.\\r\\n\\r\\nThe ideal candidate will bring deep expertise in polymer processing, film manufacturing, and converting technologies, coupled with experience in regulated environments (ISO 13485, FDA, GMP). Will work cross-functionally with R&D, Quality, Manufacturing, and Commercial teams to drive product and process excellence.\\r\\n\\r\\n \\r\\n\\r\\nProcess Engineering & Development\\r\\n\\r\\n\\r\\n\\tSupports Engineers, technicians and operators during process development work.\\r\\n\\tLead the design, development, and optimization of blown film extrusion processes for multilayer medical-grade films.\\r\\n\\tDefine and implement process parameters, tooling design, material selection, and quality control strategies.\\r\\n\\tDevelop robust converting processes (slitting, printing, pouching, laminating, etc.) tailored for sterile barrier systems and medical device packaging.\\r\\n\\r\\n\\r\\nResearch & Development (R&D)\\r\\n\\r\\n\\r\\n\\tDrive process innovation to support new materials, multilayer film structures, and proprietary packaging technologies.\\r\\n\\tCollaborate with product development teams to ensure process capabilities align with product performance requirements and regulatory expectations.\\r\\n\\tConduct trials and scale-up activities to validate new materials and processes on pilot and production lines.\\r\\n\\r\\n\\r\\nNew Product Introduction (NPI)\\r\\n\\r\\n\\r\\n\\tServe as the technical lead during the NPI lifecycle, from feasibility to design transfer and commercialization.\\r\\n\\tDevelop and execute process validation (IQ/OQ/PQ), design of experiments (DOE), and risk assessments (PFMEA).\\r\\n\\tProvide hands-on support for equipment commissioning, tooling procurement, and technology transfer.\\r\\n\\r\\n\\r\\nQuality & Compliance\\r\\n\\r\\n\\r\\n\\tEnsure processes and documentation comply with ISO 13485, FDA 21 CFR Part 820, and applicable medical packaging standards (e.g., ISO 11607).\\r\\n\\tCollaborate with Quality and Regulatory Affairs to develop and maintain technical files, validation protocols, and work instructions.\\r\\n\\tSupport root cause investigations, CAPA, and continuous improvement initiatives.\\r\\n\\r\\n\\r\\nProject Management & Leadership\\r\\n\\r\\n\\r\\n\\tManage multiple technical projects concurrently with minimal supervision.\\r\\n\\tMentor junior engineers and technicians; promote knowledge sharing and best practices.\\r\\n\\tInterface with suppliers, equipment manufacturers, and customers to support technical objectives.\\r\\n\\r\\nQualificationsCandidate Requirements:\\r\\n\\r\\n\\r\\n\\tBachelor’s degree in engineering or scientific discipline.\\r\\n\\t7+ years of relevant experience in process engineering, with a strong focus on blown film extrusion and film converting.\\r\\n\\tAt least 3 years of direct experience in a Medical Device or Healthcare packaging environment.\\r\\n\\tExpert level experience with integrated extrusion systems, Test Method development, protocol generation, execution, and reporting.\\r\\n\\tProven track record in R&D and NPI projects within a regulated manufacturing setting.\\r\\n\\tGMP and ISO 9000 training.\\r\\n\\tExperience with tooling design with advanced SolidWorks CAD knowledge.\\r\\n\\tSix Sigma Green belt or equivalent certification beneficial but not required.\\r\\n\\t20% travel.\\r\\n\\r\\n\\r\\nCompetencies/Skills\\r\\n\\r\\n\\r\\n\\tSelf-motivation and hands-on skills to simplify complex processes.\\r\\n\\tProfessional experience in exploration of new technologic prospects.\\r\\n\\tCapability to establish change and encourage the inter-organizational exchange of skills.\\r\\n\\tExceptional problem-solving, organizational, analytical, and critical thinking skills including high discretion/judgment in decision-making.\\r\\n\\tIn-depth knowledge of blown film extrusion (co-extrusion, die design, resin rheology, cooling, winding).\\r\\n\\tProficiency in converting processes such as slitting, die cutting, heat sealing, laminating, and pouch manufacturing.\\r\\n\\tStrong understanding of polymer behavior, film characterization, and testing methods.\\r\\n\\tExperience with statistical analysis tools (Minitab, JMP), DOE, SPC, and process validation methodologies.\\r\\n\\tFamiliarity with medical packaging standards such as ISO 11607, ASTM F88, F1929, etc.\\r\\n\\tExcellent communication and interpersonal skills for cross-functional collaboration.\\r\\n\\tDemonstrated leadership and project management capabilities.\\r\\n\\tExperience with cleanroom manufacturing and Class I/II/III medical device packaging.\\r\\n\\tKnowledge of sustainability trends in polymer materials and biodegradable films.\\r\\n\\tExperience with ERP and document control systems (e.g., IQMS, Agile).\\r\\n\\r\\n\",\"responsibilities\":\"The Converting Process Engineer is responsible for Execution and implementation of projects of great impact for the organization, related to R&D and New Product Introduction. We are seeking a highly skilled and innovative Converting Process Engineer to lead process development, optimization, and technical innovation in blown film extrusion and converting for medical device and medical packaging applications. This role is central to our R&D and New Product Introduction (NPI) initiatives, supporting cutting-edge projects from concept through commercialization while ensuring compliance with regulatory standards and industry best practices.\\r\\n\\r\\nThe ideal candidate will bring deep expertise in polymer processing, film manufacturing, and converting technologies, coupled with experience in regulated environments (ISO 13485, FDA, GMP). Will work cross-functionally with R&D, Quality, Manufacturing, and Commercial teams to drive product and process excellence.\\r\\n\\r\\n \\r\\n\\r\\nProcess Engineering & Development\\r\\n\\r\\n\\r\\n\\tSupports Engineers, technicians and operators during process development work.\\r\\n\\tLead the design, development, and optimization of blown film extrusion processes for multilayer medical-grade films.\\r\\n\\tDefine and implement process parameters, tooling design, material selection, and quality control strategies.\\r\\n\\tDevelop robust converting processes (slitting, printing, pouching, laminating, etc.) tailored for sterile barrier systems and medical device packaging.\\r\\n\\r\\n\\r\\nResearch & Development (R&D)\\r\\n\\r\\n\\r\\n\\tDrive process innovation to support new materials, multilayer film structures, and proprietary packaging technologies.\\r\\n\\tCollaborate with product development teams to ensure process capabilities align with product performance requirements and regulatory expectations.\\r\\n\\tConduct trials and scale-up activities to validate new materials and processes on pilot and production lines.\\r\\n\\r\\n\\r\\nNew Product Introduction (NPI)\\r\\n\\r\\n\\r\\n\\tServe as the technical lead during the NPI lifecycle, from feasibility to design transfer and commercialization.\\r\\n\\tDevelop and execute process validation (IQ/OQ/PQ), design of experiments (DOE), and risk assessments (PFMEA).\\r\\n\\tProvide hands-on support for equipment commissioning, tooling procurement, and technology transfer.\\r\\n\\r\\n\\r\\nQuality & Compliance\\r\\n\\r\\n\\r\\n\\tEnsure processes and documentation comply with ISO 13485, FDA 21 CFR Part 820, and applicable medical packaging standards (e.g., ISO 11607).\\r\\n\\tCollaborate with Quality and Regulatory Affairs to develop and maintain technical files, validation protocols, and work instructions.\\r\\n\\tSupport root cause investigations, CAPA, and continuous improvement initiatives.\\r\\n\\r\\n\\r\\nProject Management & Leadership\\r\\n\\r\\n\\r\\n\\tManage multiple technical projects concurrently with minimal supervision.\\r\\n\\tMentor junior engineers and technicians; promote knowledge sharing and best practices.\\r\\n\\tInterface with suppliers, equipment manufacturers, and customers to support technical objectives.\\r\\n\\r\\n\",\"employmentType\":\"FULL_TIME\",\"hiringOrganization\":{\"@type\":\"Organization\",\"name\":\"Spectrum Plastics Group\",\"logo\":\"https://www.paycomonline.net/v4/ats/web.php/application/style/logo?clientkey=F3CF2E6F06D96C7D42AC218710A77851\"},\"jobLocation\":{\"@type\":\"Place\",\"address\":{\"streetAddress\":\"10101 78th Avenue\",\"addressLocality\":\"Pleasant Prairie\",\"addressRegion\":\"WI\",\"postalCode\":53158,\"addressCountry\":\"USA\"}},\"qualifications\":\"Candidate Requirements:\\r\\n\\r\\n\\r\\n\\tBachelor’s degree in engineering or scientific discipline.\\r\\n\\t7+ years of relevant experience in process engineering, with a strong focus on blown film extrusion and film converting.\\r\\n\\tAt least 3 years of direct experience in a Medical Device or Healthcare packaging environment.\\r\\n\\tExpert level experience with integrated extrusion systems, Test Method development, protocol generation, execution, and reporting.\\r\\n\\tProven track record in R&D and NPI projects within a regulated manufacturing setting.\\r\\n\\tGMP and ISO 9000 training.\\r\\n\\tExperience with tooling design with advanced SolidWorks CAD knowledge.\\r\\n\\tSix Sigma Green belt or equivalent certification beneficial but not required.\\r\\n\\t20% travel.\\r\\n\\r\\n\\r\\nCompetencies/Skills\\r\\n\\r\\n\\r\\n\\tSelf-motivation and hands-on skills to simplify complex processes.\\r\\n\\tProfessional experience in exploration of new technologic prospects.\\r\\n\\tCapability to establish change and encourage the inter-organizational exchange of skills.\\r\\n\\tExceptional problem-solving, organizational, analytical, and critical thinking skills including high discretion/judgment in decision-making.\\r\\n\\tIn-depth knowledge of blown film extrusion (co-extrusion, die design, resin rheology, cooling, winding).\\r\\n\\tProficiency in converting processes such as slitting, die cutting, heat sealing, laminating, and pouch manufacturing.\\r\\n\\tStrong understanding of polymer behavior, film characterization, and testing methods.\\r\\n\\tExperience with statistical analysis tools (Minitab, JMP), DOE, SPC, and process validation methodologies.\\r\\n\\tFamiliarity with medical packaging standards such as ISO 11607, ASTM F88, F1929, etc.\\r\\n\\tExcellent communication and interpersonal skills for cross-functional collaboration.\\r\\n\\tDemonstrated leadership and project management capabilities.\\r\\n\\tExperience with cleanroom manufacturing and Class I/II/III medical device packaging.\\r\\n\\tKnowledge of sustainability trends in polymer materials and biodegradable films.\\r\\n\\tExperience with ERP and document control systems (e.g., IQMS, Agile).\\r\\n\\r\\n\",\"experienceRequirements\":\"Candidate Requirements:\\r\\n\\r\\n\\r\\n\\tBachelor’s degree in engineering or scientific discipline.\\r\\n\\t7+ years of relevant experience in process engineering, with a strong focus on blown film extrusion and film converting.\\r\\n\\tAt least 3 years of direct experience in a Medical Device or Healthcare packaging environment.\\r\\n\\tExpert level experience with integrated extrusion systems, Test Method development, protocol generation, execution, and reporting.\\r\\n\\tProven track record in R&D and NPI projects within a regulated manufacturing setting.\\r\\n\\tGMP and ISO 9000 training.\\r\\n\\tExperience with tooling design with advanced SolidWorks CAD knowledge.\\r\\n\\tSix Sigma Green belt or equivalent certification beneficial but not required.\\r\\n\\t20% travel.\\r\\n\\r\\n\\r\\nCompetencies/Skills\\r\\n\\r\\n\\r\\n\\tSelf-motivation and hands-on skills to simplify complex processes.\\r\\n\\tProfessional experience in exploration of new technologic prospects.\\r\\n\\tCapability to establish change and encourage the inter-organizational exchange of skills.\\r\\n\\tExceptional problem-solving, organizational, analytical, and critical thinking skills including high discretion/judgment in decision-making.\\r\\n\\tIn-depth knowledge of blown film extrusion (co-extrusion, die design, resin rheology, cooling, winding).\\r\\n\\tProficiency in converting processes such as slitting, die cutting, heat sealing, laminating, and pouch manufacturing.\\r\\n\\tStrong understanding of polymer behavior, film characterization, and testing methods.\\r\\n\\tExperience with statistical analysis tools (Minitab, JMP), DOE, SPC, and process validation methodologies.\\r\\n\\tFamiliarity with medical packaging standards such as ISO 11607, ASTM F88, F1929, etc.\\r\\n\\tExcellent communication and interpersonal skills for cross-functional collaboration.\\r\\n\\tDemonstrated leadership and project management capabilities.\\r\\n\\tExperience with cleanroom manufacturing and Class I/II/III medical device packaging.\\r\\n\\tKnowledge of sustainability trends in polymer materials and biodegradable films.\\r\\n\\tExperience with ERP and document control systems (e.g., IQMS, Agile).\\r\\n\\r\\n\",\"validThrough\":\"2027-04-16\"}",
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"qualifications": "<p style=\"margin-right:3px; margin-left:3px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"font-family:Aptos,sans-serif\"><b><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Candidate Requirements:</span></span></span></b></span></span></span></span></p>\r\n\r\n<ul style=\"margin-bottom:11px; list-style-type:square\">\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Bachelor’s degree in engineering or scientific discipline.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">7+ years of relevant experience in process engineering, with a strong focus on blown film extrusion and film converting.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">At least 3 years of direct experience in a Medical Device or Healthcare packaging environment.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Expert level experience with integrated extrusion systems, Test Method development, protocol generation, execution, and reporting.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Proven track record in R&D and NPI projects within a regulated manufacturing setting.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">GMP and ISO 9000 training.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Experience with tooling design with advanced SolidWorks CAD knowledge.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Six Sigma Green belt or equivalent certification beneficial but not required.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">20% travel.</span></span></span></span></span></span></span></span></li>\r\n</ul>\r\n\r\n<p style=\"margin-right:3px; margin-left:3px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"font-family:Aptos,sans-serif\"><b><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Competencies/Skills</span></span></span></b></span></span></span></span></p>\r\n\r\n<ul style=\"margin-bottom:11px; list-style-type:square\">\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Self-motivation and hands-on skills to simplify complex processes.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Professional experience in exploration of new technologic prospects.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Capability to establish change and encourage the inter-organizational exchange of skills.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Exceptional problem-solving, organizational, analytical, and critical thinking skills including high discretion/judgment in decision-making.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">In-depth knowledge of blown film extrusion (co-extrusion, die design, resin rheology, cooling, winding).</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Proficiency in converting processes such as slitting, die cutting, heat sealing, laminating, and pouch manufacturing.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Strong understanding of polymer behavior, film characterization, and testing methods.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Experience with statistical analysis tools (Minitab, JMP), DOE, SPC, and process validation methodologies.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Familiarity with medical packaging standards such as ISO 11607, ASTM F88, F1929, etc.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Excellent communication and interpersonal skills for cross-functional collaboration.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Demonstrated leadership and project management capabilities.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Experience with cleanroom manufacturing and Class I/II/III medical device packaging.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Knowledge of sustainability trends in polymer materials and biodegradable films.</span></span></span></span></span></span></span></span></li>\r\n\t<li style=\"margin-right:3px; margin-left:11px; margin-bottom:11px\"><span style=\"font-size:12pt\"><span style=\"background:white\"><span style=\"line-height:normal\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:Aptos,sans-serif\"><span style=\"font-size:11.0pt\"><span style=\"font-family:"Calibri",sans-serif\"><span style=\"color:black\">Experience with ERP and document control systems (e.g., IQMS, Agile).</span></span></span></span></span></span></span></span></li>\r\n</ul>\r\n",
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