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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Get Access To All JobsINTRODUCTION
The Senior Supplier Quality Engineer is responsible for supporting the Supplier Quality organization by overseeing components, materials, and services provided by suppliers. This role ensures that suppliers meet all regulatory and quality requirements, collaborates with internal teams, and drives continuous improvement in supplier performance.
KNOWLEDGE
- Working knowledge of Medical Device Regulations/In Vitro Diagnostic Regulation (as applicable), cGMP, CFR 820, ISO-13485, ISO-14971, ISO-9001
- Quality System Regulation and risk management
- Validations (IQ, OQ, PQ) and root cause analysis (CAPA process)
- Project management techniques
- Measurement system analysis (GR&R, AAA)
- Statistical Process Controls (SPC) and statistical sampling
- PPAP (Production Part Approval Process) knowledge (desirable)
- Familiarity with applicable regulations (FDA, Canada, Brazil, Japan, etc.)
SKILLS
- Effective written and verbal communication at all organizational levels
- Proficiency in problem-solving tools (SPC, TQM, etc.)
- Analytical skills to evaluate data and situations, translating them into actionable plans
- Ability to communicate ideas and approaches through proposals, plans, and presentations
- High proficiency with Microsoft Office suite for reporting and data analysis
- Ability to manage multiple complex projects simultaneously
- Ability to work independently and collaboratively
- ISO 13485 lead auditor certification (preferred)
- Proficiency in English (written and oral); a second language is a plus
- Familiarity with tools such as Project, Visio, MiniTab, and Agile (desirable)
BEHAVIORS
- Collaborative approach with suppliers and internal teams
- Strong organizational and follow-up skills
- Commitment to continuous improvement and regulatory compliance
- Willingness to travel domestically and internationally as needed
- Adherence to safety protocols, including wearing safety shoes in designated areas
Experience
- Minimum of 5 years of professional experience in similar roles with responsibility for decision-making and problem-solving
- Recognized expertise within a similar organization
- Bachelor’s degree in an engineering field (specific discipline may vary based on business needs)
- ASQ Supplier Quality Engineer Certificate is a plus
WHY JOIN Hologic?
We are committed to making Hologic the destination for top talent. 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.
The annualized base salary range for this role is $98,500 - $154,000 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, education, business needs and market demand.
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
The Senior Supplier Quality Engineer is responsible for supporting the Supplier Quality organization by overseeing components, materials, and services provided by suppliers. This role ensures that suppliers meet all regulatory and quality requirements, collaborates with internal teams, and drives continuous improvement in supplier performance.
KNOWLEDGE
- Working knowledge of Medical Device Regulations/In Vitro Diagnostic Regulation (as applicable), cGMP, CFR 820, ISO-13485, ISO-14971, ISO-9001
- Quality System Regulation and risk management
- Validations (IQ, OQ, PQ) and root cause analysis (CAPA process)
- Project management techniques
- Measurement system analysis (GR&R, AAA)
- Statistical Process Controls (SPC) and statistical sampling
- PPAP (Production Part Approval Process) knowledge (desirable)
- Familiarity with applicable regulations (FDA, Canada, Brazil, Japan, etc.)
SKILLS
- Effective written and verbal communication at all organizational levels
- Proficiency in problem-solving tools (SPC, TQM, etc.)
- Analytical skills to evaluate data and situations, translating them into actionable plans
- Ability to communicate ideas and approaches through proposals, plans, and presentations
- High proficiency with Microsoft Office suite for reporting and data analysis
- Ability to manage multiple complex projects simultaneously
- Ability to work independently and collaboratively
- ISO 13485 lead auditor certification (preferred)
- Proficiency in English (written and oral); a second language is a plus
- Familiarity with tools such as Project, Visio, MiniTab, and Agile (desirable)
BEHAVIORS
- Collaborative approach with suppliers and internal teams
- Strong organizational and follow-up skills
- Commitment to continuous improvement and regulatory compliance
- Willingness to travel domestically and internationally as needed
- Adherence to safety protocols, including wearing safety shoes in designated areas
Experience
- Minimum of 5 years of professional experience in similar roles with responsibility for decision-making and problem-solving
- Recognized expertise within a similar organization
- Bachelor’s degree in an engineering field (specific discipline may vary based on business needs)
- ASQ Supplier Quality Engineer Certificate is a plus
WHY JOIN Hologic?
We are committed to making Hologic the destination for top talent. 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.
The annualized base salary range for this role is $98,500 - $154,000 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, education, business needs and market demand.
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.
Medical Devices Job Roles in Delaware
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Search Medical Devices Jobs in DelawareMedical Devices 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.