Medical Devices TN Sponsorship Jobs in Delaware
TN visa sponsorship jobs in Delaware's medical devices sector connect Canadian and Mexican professionals with employers across Wilmington and the surrounding region. Companies like Siemens Healthineers and smaller contract manufacturers operating near the I-95 corridor regularly hire TN-eligible engineers, scientists, and regulatory specialists. Delaware's proximity to the Philadelphia biopharma cluster expands your options further.
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Provide product quality engineering support for on-market medical devices. This role will be responsible for performing evaluations, investigation, risk assessment and root cause analysis in relation to post market feedback and complaints from the field. Works with cross functional team in implementation of improvements or corrections based on the results of complaint investigations.
Essential Duties and Responsibilities
The incumbent may be asked to perform other function-related activities in addition to the below-mentioned responsibilities as reasonably required by business needs.
- Own Investigations and associated root cause analysis, including coordinating collaboration and communication with stakeholders.
- Provide input in prioritization of complaints and investigations based on product risk, data analysis and trending, and strategic impact.
- Partner with cross functional team and communicate root cause, determine if CAPA is required, recommended changes and scope effort to implement changes as needed.
- Partner with internal team to perform the Health Risk Assessment and coordinate with internal teams when needed; must demonstrate efficient and effective analysis of situation, including problem definition and impact.
- Participates in cross functional team implementation activities of improvements or corrections based on the results of complaint investigations.
- Perform data analysis and trending of data related to complaints and identified failure modes, identifying mitigations for any threshold risks and owning preparation and presentation of data and findings to internal stakeholders where applicable.
- Participate in projects to implement design or process change including drawing update, fixture and tooling update, performing testing and change control documentation, as applicable.
- Develop or improve testing methods used during complaint investigation and root cause activities.
- Support complaint intake team as needed to provide technical expertise and work through investigation activities.
- Assess changes of products for impact to design and risk management, determine supporting information required for implementation of changes.
- Provide Post-Market feedback, identified through complaint trending and other forums, to Operations, Engineering and R&D to improve design and manufacture of devices in the field and in development.
- Developing professional expertise, applying company policies and procedures to resolve a variety of issues. Normally receives general instructions on routine work, detailed instructions on new projects or assignments.
- Support PMQA team investigations in the field at customer sites, working to provide timely resolution of field quality issues while upholding the Hologic brand image and values.
- Support data analysis for product quality metrics to Leadership, providing root cause where applicable and recommending actions/resolutions.
- Active participation in internal and external audits, including but not limited to facility and supplier audits and Notified Body and FDA inspections.
- Supports monthly Quality Investigation Review boards, preparing and presenting material where applicable.
Qualifications
Education
- Bachelor’s Degree in Engineering (Mechanical, Electrical or Biomedical preferred)
Experience
- Bachelor's degree required in either Mechanical, Biomedical, Biomechanical, or Electrical Engineering with 0-2 years experience.
- Experience in an FDA regulated industry preferred.
- Experience in root cause analysis or product development/R&D is beneficial.
Skills
- Familiarity with FDA Quality System Regulations, especially Design Control requirements, ISO 13485, EU Medical Device Regulation, ISO 14970, Risk Management, GMP, and GDP.
- Ability to effectively work on project teams, including taking leadership role on critical tasks to assure appropriate and timely completion/resolution.
- Ability to appropriately assess written product and project documentation as an advocate for compliance, and ability to effectively communicate assessment.
- Knowledge of root cause analysis tools and ability to effectively participate in root cause activities for complaint investigations, NCs, CAPAs, etc.
-
Good communication and presentation skills.
-
Preferred:
- Familiarity with test method validation, root cause failure analysis, statistical methods, and design of experiment.
- Familiarity with Reliability, Electrical Safety, Sterilization, Packaging, and Biocompatibility standards and requirements.
- Working knowledge of verification and validation requirements for a regulated product.
- Familiarity with requirements analysis, including development of testable and measurable specifications. Knowledge of risk based and statistical analysis concepts.
The annualized base salary range for this role is $54,900 - 86,000 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, geography, education, business needs, and market demand.
Why Hologic?
We are committed to making Hologic the company where top talent comes to grow. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career.
If you have the right skills and experience, apply today!
LI-AV1
Agency and Third Party Recruiter Notice:
Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.
Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.
INTRODUCTION
Provide product quality engineering support for on-market medical devices. This role will be responsible for performing evaluations, investigation, risk assessment and root cause analysis in relation to post market feedback and complaints from the field. Works with cross functional team in implementation of improvements or corrections based on the results of complaint investigations.
Essential Duties and Responsibilities
The incumbent may be asked to perform other function-related activities in addition to the below-mentioned responsibilities as reasonably required by business needs.
- Own Investigations and associated root cause analysis, including coordinating collaboration and communication with stakeholders.
- Provide input in prioritization of complaints and investigations based on product risk, data analysis and trending, and strategic impact.
- Partner with cross functional team and communicate root cause, determine if CAPA is required, recommended changes and scope effort to implement changes as needed.
- Partner with internal team to perform the Health Risk Assessment and coordinate with internal teams when needed; must demonstrate efficient and effective analysis of situation, including problem definition and impact.
- Participates in cross functional team implementation activities of improvements or corrections based on the results of complaint investigations.
- Perform data analysis and trending of data related to complaints and identified failure modes, identifying mitigations for any threshold risks and owning preparation and presentation of data and findings to internal stakeholders where applicable.
- Participate in projects to implement design or process change including drawing update, fixture and tooling update, performing testing and change control documentation, as applicable.
- Develop or improve testing methods used during complaint investigation and root cause activities.
- Support complaint intake team as needed to provide technical expertise and work through investigation activities.
- Assess changes of products for impact to design and risk management, determine supporting information required for implementation of changes.
- Provide Post-Market feedback, identified through complaint trending and other forums, to Operations, Engineering and R&D to improve design and manufacture of devices in the field and in development.
- Developing professional expertise, applying company policies and procedures to resolve a variety of issues. Normally receives general instructions on routine work, detailed instructions on new projects or assignments.
- Support PMQA team investigations in the field at customer sites, working to provide timely resolution of field quality issues while upholding the Hologic brand image and values.
- Support data analysis for product quality metrics to Leadership, providing root cause where applicable and recommending actions/resolutions.
- Active participation in internal and external audits, including but not limited to facility and supplier audits and Notified Body and FDA inspections.
- Supports monthly Quality Investigation Review boards, preparing and presenting material where applicable.
Qualifications
Education
- Bachelor’s Degree in Engineering (Mechanical, Electrical or Biomedical preferred)
Experience
- Bachelor's degree required in either Mechanical, Biomedical, Biomechanical, or Electrical Engineering with 0-2 years experience.
- Experience in an FDA regulated industry preferred.
- Experience in root cause analysis or product development/R&D is beneficial.
Skills
- Familiarity with FDA Quality System Regulations, especially Design Control requirements, ISO 13485, EU Medical Device Regulation, ISO 14970, Risk Management, GMP, and GDP.
- Ability to effectively work on project teams, including taking leadership role on critical tasks to assure appropriate and timely completion/resolution.
- Ability to appropriately assess written product and project documentation as an advocate for compliance, and ability to effectively communicate assessment.
- Knowledge of root cause analysis tools and ability to effectively participate in root cause activities for complaint investigations, NCs, CAPAs, etc.
-
Good communication and presentation skills.
-
Preferred:
- Familiarity with test method validation, root cause failure analysis, statistical methods, and design of experiment.
- Familiarity with Reliability, Electrical Safety, Sterilization, Packaging, and Biocompatibility standards and requirements.
- Working knowledge of verification and validation requirements for a regulated product.
- Familiarity with requirements analysis, including development of testable and measurable specifications. Knowledge of risk based and statistical analysis concepts.
The annualized base salary range for this role is $54,900 - 86,000 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, geography, education, business needs, and market demand.
Why Hologic?
We are committed to making Hologic the company where top talent comes to grow. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career.
If you have the right skills and experience, apply today!
LI-AV1
Agency and Third Party Recruiter Notice:
Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.
Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.
TN Medical Devices Job Roles in Delaware
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Search Medical Devices Jobs in DelawareMedical Devices TN Sponsorship Jobs in Delaware: Frequently Asked Questions
Which medical devices companies sponsor TN visas in Delaware?
Delaware's medical devices employers include multinational manufacturers with regional offices in Wilmington and New Castle County, as well as contract manufacturers and laboratory services firms near the I-95 corridor. Companies in diagnostics, surgical instruments, and imaging equipment have historically filed TN visa-category Labor Condition Applications for engineering and scientific roles. Checking DOL OFLC disclosure data by employer name gives you a factual record of past sponsorship activity.
Which cities in Delaware have the most medical devices TN sponsorship jobs?
Wilmington is the primary hub for medical devices TN roles in Delaware, given its concentration of life sciences offices and proximity to the Philadelphia metro area. Newark, home to the University of Delaware's research partnerships, also attracts device and diagnostics employers. New Castle County overall accounts for the majority of medical devices hiring in the state, with some positions in Dover tied to clinical or regulatory functions.
What types of medical devices roles typically qualify for TN sponsorship?
TN visa eligibility in medical devices generally covers roles that map to USMCA's designated occupational categories. Engineers, including biomedical, electrical, and mechanical, qualify when the position requires a relevant bachelor's degree or higher. Scientific roles such as microbiologist, chemist, and medical laboratory technologist also qualify. Regulatory affairs specialists may qualify depending on how the position is defined and documented by the employer. Each case depends on how the job duties align with the USMCA occupation list.
How do I find medical devices TN sponsorship jobs in Delaware?
Migrate Mate filters medical devices job listings in Delaware specifically for TN-eligible roles, showing you which employers have active sponsorship history based on DOL filing records. This saves time compared to manually reviewing OFLC disclosure data for each company. Search by occupation category and location to surface biomedical engineering, regulatory affairs, and laboratory roles where Delaware employers have demonstrated TN sponsorship.
Are there any state-specific or industry-specific considerations for TN sponsorship in Delaware's medical devices sector?
Delaware has no state-level immigration surcharges or separate visa filing requirements, so the TN process follows standard USMCA procedures. However, medical devices roles in Delaware sometimes require FDA-regulated quality system knowledge, which can affect how employers write job descriptions for TN purposes. Biomedical and regulatory roles at device companies subject to 21 CFR quality requirements may need tightly scoped job duty letters to satisfy both the employer's compliance needs and the TN occupational category definition.