Packaging Engineer Green Card Jobs
Packaging Engineer roles qualify for employment-based green card sponsorship under EB-2 or EB-3, depending on the position's degree requirements and your credentials. Employers file a PERM labor certification with DOL before sponsoring permanent residency, making these roles a path to lawful permanent residency rather than a temporary visa.
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Date: May 1, 2026
Location: Morrisville, NC, US
Company: Teleflex
Expected Travel: Up to 10%
Requisition ID: 13758
About Teleflex Incorporated
As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.
Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ – trusted brands united by a common sense of purpose.
At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.
Global Operations
Global Operations is a complex and diverse organization within the company which is responsible for product fulfilment to all our customers from end to end. We pride ourselves on being totally Customer Centric in our unrelenting focus on Improving Quality, Service and Value as perceived by our customers. Our employees are dedicated to the Global Operations Enterprise Excellence journey. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients’ lives.
Position Summary
Responsible for and/or assist in the design, testing and validation of sterile and non-sterile packaging for medical products for the Global Teleflex Packaging team. Package design activities include risk analysis, design input, design output, design verification and validation, and design transfer per the Teleflex Design Control policies and procedures, and adherence to all applicable global package integrity and protection standards. Support process development, validation, and implementation activities within Teleflex manufacturing sites, contract manufacturers or strategic suppliers as required. Assist or lead updates to the design history files (DHF) or internal SOPs/Work Instructions in compliance with the Teleflex Quality System.
Principal Responsibilities
- Work as a Subject Matter Expert in many aspects of medical packaging.
- Work with cross-functional teams to develop medical device packaging, specifications, and processes with input from the packaging industry, physicians, marketing, and manufacturing, adhering to the design control process.
- Lead the redesign of existing packaging systems and manufacturing processes to improve quality, utilize automated production techniques, optimize process capabilities, and produce higher quality products in a more cost-effective manner.
- Interface with suppliers, Strategic Sourcing, R&D, Marketing, Quality and Regulatory Affairs to deliver projects.
- For in-house manufactured and purchased packaging systems/components, manage the design control activities for the new/replacement and existing product packaging and components.
- Lead and drive the development/improvement of packaging design & processes by utilizing tools such as DOE and statistical analysis, assist in implementation with appropriate controls and metrics.
- Conduct or coordinate package testing in the internal Teleflex Packaging Lab or with external testing service providers.
- For both in-house and purchased packaging systems/components, coordinate the transfer of parts, assemblies, documentation, and processes from prototype stage, through pilot to production. Generate product, process, and experimental activity specifications for the Device Master Record as required.
- Lead and support project teams in meeting project objectives, milestones, and target dates. Update and review project progress with leadership.
- As requested, work with the Product Performance Team and R&D personnel to lead investigation of product complaints involving packaging to determine the root cause and implement corrective action.
- Understand and utilize the requirements of and operate in a medical device manufacturing environment.
- Have a strong understanding and skill set in project management and technical writing.
- Direct efforts of drafts people, technicians, tradespeople, and lab personnel in the development of packaging related products, processes, test fixtures, equipment, test procedures, and documentation.
- Participate and lead design and technical phase reviews.
- Support packaging assessments, review of industry standards updates, product regulatory submissions, and/or limited market evaluations/clinical trials as required.
- Ensure projects are developed and documented in compliance with the Teleflex Quality System.
- Adhere to and ensure the compliance of Teleflex's Code of Ethics, all Company policies, rules, procedures, and housekeeping standards.
Education / Experience Requirements
Bachelor of Science or Professional Engineer (PE) Certification - Engineering or technical discipline (Packaging Science or equivalent degree).
- Minimum 8 years of medical device packaging experience.
- Advanced knowledge of ISO11607 standards.
- Strong analytical and problem-solving skills.
- Medical Device Package design, equipment, and testing knowledge.
- Effective verbal and written communication skills.
- Team player with good interpersonal skills.
- Proficient in Microsoft Office Suite and computerized analysis applications.
Specialized Skills / Other Requirements
Self-motivated, high energy, collaborative, positive attitude individual with the initiative and drive for timely completion of goals.
- Able to travel domestically and internationally
Working Conditions / Physical Demands
TRAVEL REQUIRED: 10 %
WORKING ENVIRONMENT:
- Office/Professional Plant/Manufacturing Remote/Field Laboratory
At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.
Teleflex Incorporated is an equal opportunity employer. Applicants will be considered without regard to age, race, religion, color, national origin, ancestry, sexual orientation, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: 877-880-8588 or Talent@Teleflex.com.
Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.
© 2026 Teleflex Incorporated. All rights reserved.

Date: May 1, 2026
Location: Morrisville, NC, US
Company: Teleflex
Expected Travel: Up to 10%
Requisition ID: 13758
About Teleflex Incorporated
As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.
Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ – trusted brands united by a common sense of purpose.
At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.
Global Operations
Global Operations is a complex and diverse organization within the company which is responsible for product fulfilment to all our customers from end to end. We pride ourselves on being totally Customer Centric in our unrelenting focus on Improving Quality, Service and Value as perceived by our customers. Our employees are dedicated to the Global Operations Enterprise Excellence journey. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients’ lives.
Position Summary
Responsible for and/or assist in the design, testing and validation of sterile and non-sterile packaging for medical products for the Global Teleflex Packaging team. Package design activities include risk analysis, design input, design output, design verification and validation, and design transfer per the Teleflex Design Control policies and procedures, and adherence to all applicable global package integrity and protection standards. Support process development, validation, and implementation activities within Teleflex manufacturing sites, contract manufacturers or strategic suppliers as required. Assist or lead updates to the design history files (DHF) or internal SOPs/Work Instructions in compliance with the Teleflex Quality System.
Principal Responsibilities
- Work as a Subject Matter Expert in many aspects of medical packaging.
- Work with cross-functional teams to develop medical device packaging, specifications, and processes with input from the packaging industry, physicians, marketing, and manufacturing, adhering to the design control process.
- Lead the redesign of existing packaging systems and manufacturing processes to improve quality, utilize automated production techniques, optimize process capabilities, and produce higher quality products in a more cost-effective manner.
- Interface with suppliers, Strategic Sourcing, R&D, Marketing, Quality and Regulatory Affairs to deliver projects.
- For in-house manufactured and purchased packaging systems/components, manage the design control activities for the new/replacement and existing product packaging and components.
- Lead and drive the development/improvement of packaging design & processes by utilizing tools such as DOE and statistical analysis, assist in implementation with appropriate controls and metrics.
- Conduct or coordinate package testing in the internal Teleflex Packaging Lab or with external testing service providers.
- For both in-house and purchased packaging systems/components, coordinate the transfer of parts, assemblies, documentation, and processes from prototype stage, through pilot to production. Generate product, process, and experimental activity specifications for the Device Master Record as required.
- Lead and support project teams in meeting project objectives, milestones, and target dates. Update and review project progress with leadership.
- As requested, work with the Product Performance Team and R&D personnel to lead investigation of product complaints involving packaging to determine the root cause and implement corrective action.
- Understand and utilize the requirements of and operate in a medical device manufacturing environment.
- Have a strong understanding and skill set in project management and technical writing.
- Direct efforts of drafts people, technicians, tradespeople, and lab personnel in the development of packaging related products, processes, test fixtures, equipment, test procedures, and documentation.
- Participate and lead design and technical phase reviews.
- Support packaging assessments, review of industry standards updates, product regulatory submissions, and/or limited market evaluations/clinical trials as required.
- Ensure projects are developed and documented in compliance with the Teleflex Quality System.
- Adhere to and ensure the compliance of Teleflex's Code of Ethics, all Company policies, rules, procedures, and housekeeping standards.
Education / Experience Requirements
Bachelor of Science or Professional Engineer (PE) Certification - Engineering or technical discipline (Packaging Science or equivalent degree).
- Minimum 8 years of medical device packaging experience.
- Advanced knowledge of ISO11607 standards.
- Strong analytical and problem-solving skills.
- Medical Device Package design, equipment, and testing knowledge.
- Effective verbal and written communication skills.
- Team player with good interpersonal skills.
- Proficient in Microsoft Office Suite and computerized analysis applications.
Specialized Skills / Other Requirements
Self-motivated, high energy, collaborative, positive attitude individual with the initiative and drive for timely completion of goals.
- Able to travel domestically and internationally
Working Conditions / Physical Demands
TRAVEL REQUIRED: 10 %
WORKING ENVIRONMENT:
- Office/Professional Plant/Manufacturing Remote/Field Laboratory
At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.
Teleflex Incorporated is an equal opportunity employer. Applicants will be considered without regard to age, race, religion, color, national origin, ancestry, sexual orientation, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: 877-880-8588 or Talent@Teleflex.com.
Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.
© 2026 Teleflex Incorporated. All rights reserved.
See all 162+ Packaging Engineer jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Packaging Engineer roles.
Get Access To All JobsTips for Finding Green Card Sponsorship as a Packaging Engineer
Document your specialty occupation credentials early
Gather transcripts, professional certifications, and letters confirming your packaging engineering responsibilities before applying. PERM requires your employer to verify your qualifications meet the job's minimum requirements, so gaps in documentation slow the process.
Target manufacturers with dedicated immigration support
Consumer goods, pharmaceutical, and food and beverage manufacturers regularly sponsor packaging engineers and often have in-house HR teams familiar with PERM filings. Smaller contract packagers rarely have the infrastructure to manage a multi-year green card process.
Distinguish EB-2 from EB-3 eligibility for your role
Packaging Engineer positions requiring only a bachelor's degree typically fall under EB-3. If your employer defines the role as requiring an advanced degree or you have specialized credentials, EB-2 may apply and can reduce your priority date wait for most nationalities.
Search green card sponsoring employers on Migrate Mate
Filter by Packaging Engineer roles where employers have active PERM or I-140 filing history. Migrate Mate surfaces this data so you can focus outreach on companies already committed to employment-based sponsorship rather than cold-pitching employers unfamiliar with the process.
Confirm the prevailing wage tier before accepting an offer
Use the OFLC Wage Search to look up the prevailing wage for packaging engineer roles in the employer's metro area. Your offered salary must meet at least the Level I wage certified on the LCA, and a low tier designation can create complications during DOL audit.
Packaging Engineer jobs are hiring across the US. Find yours.
Find Packaging Engineer JobsPackaging Engineer Green Card Sponsorship: Frequently Asked Questions
Does a Packaging Engineer role qualify for EB-2 or EB-3 green card sponsorship?
Most Packaging Engineer positions qualify under EB-3 as skilled workers requiring a bachelor's degree in packaging science, mechanical engineering, or a related field. EB-2 applies when the employer genuinely requires an advanced degree or when you qualify for a National Interest Waiver. Your employer's job description and your credentials together determine which category fits.
How does green card sponsorship differ from H-1B sponsorship for packaging engineers?
H-1B is a temporary nonimmigrant status capped at 85,000 per year and subject to the annual lottery. EB-3 green card sponsorship has no annual cap on petitions filed, though visa numbers for certain nationalities face backlogs. Green card sponsorship leads to lawful permanent residency, not a time-limited work authorization, and begins with a PERM labor certification rather than a lottery registration.
What does the PERM process look like for a Packaging Engineer?
Your employer recruits U.S. workers through DOL-mandated recruitment steps, documents that no qualified U.S. applicants are available, then files the PERM application with DOL. Once certified, they file an I-140 immigrant petition with USCIS. The entire sequence commonly takes 18 to 36 months before you can file for adjustment of status, depending on your nationality and priority date.
How do I find employers who sponsor green cards for Packaging Engineer roles?
Search Migrate Mate to identify companies with confirmed PERM or I-140 filing history for packaging engineering positions. Targeting employers who have already sponsored similar roles reduces the friction of convincing a hiring team to start the process from scratch, which is where many sponsorship conversations stall.
Can my employer start PERM sponsorship while I'm on a work visa?
Yes. Employers can begin the PERM process while you hold H-1B or another nonimmigrant status. Filing early matters because PERM and I-140 approval establishes your priority date, which determines when you can file for adjustment of status. USCIS also allows H-1B extensions beyond six years once your I-140 is approved and your priority date is not yet current.
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