Medical Devices H-1B Sponsorship Jobs in North Carolina
North Carolina's medical devices sector spans the Research Triangle Park corridor, Greater Charlotte, and the Triad region, with employers like Becton Dickinson, Teleflex, and Hologic operating significant facilities here. H-1B visa sponsorship is common for engineering, regulatory, and R&D roles, making North Carolina one of the more active states for international talent in this industry.
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Get Access To All JobsINTRODUCTION
Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives.
Pace® Life Sciences
Project Manager II – Pharmaceutical Analytical Outsourcing
Location: Morrisville, NC
Employment Type: Full-Time (Hybrid)
SUMMARY
The Project Manager II plays a critical role in delivering exceptional customer service and ensuring the successful execution of complex analytical testing projects. This position serves as the primary liaison between clients, laboratory teams, and sales staff, facilitating clear communication, managing project milestones, and ensuring all work is completed on time, within scope, and in compliance with industry standards.
The Project Manager II will oversee large and technically complex projects, coordinating cross-functional resources and maintaining a high level of scientific and operational understanding. This role supports multiple Pace® Life Sciences Analytical Outsourcing laboratories across Oakdale MN, Lebanon NJ, Morrisville NC, and San Germán PR.
ESSENTIAL FUNCTIONS
The following duties represent the core responsibilities of the role; additional tasks may be assigned as needed.
Project Leadership & Execution
- Develop and manage project plans, timelines, and budgets for analytical testing projects.
- Serve as the primary client contact for project updates, deliverables, issues, and scope changes.
- Support sample management for large or complex projects, ensuring regulatory and project-specific requirements are met.
- Update and maintain project status, cost details, and client information in the Laboratory Information Management System (LIMS).
- Approve testing to initiate laboratory work when required.
Client Engagement & Communication
- Lead client meetings, including preparing agendas and distributing meeting minutes.
- Host on-site client visits and support sales team activities as needed.
- Liaise with quoting and sales teams to initiate new quotes for scope changes or additional work.
- Provide specialized analysis and interpretation of data results to clients.
- Communicate project risks, issues, and progress to stakeholders with clear recommendations.
Quality & Compliance
- Ensure adherence to industry standards, regulatory requirements, and internal quality protocols.
- Collaborate with QA and clients to support timely completion of investigations and CAPAs.
- Maintain accurate and accessible project documentation.
Cross-Functional Collaboration
- Coordinate with laboratory, QA, sales, and operational teams to ensure efficient resource allocation and timely project completion.
- Track client account health and escalate concerns to management when necessary.
- Contribute to site forecasting by providing financial updates and projections for ongoing and upcoming work.
Leadership & Continuous Improvement
- Provide guidance and support to project team members, fostering a collaborative and high-performance environment.
- Identify opportunities for process improvements and support implementation of best practices.
- Promote a positive, cooperative work environment aligned with Pace® values and mission.
- Comply with all Environmental Health and Safety requirements.
QUALIFICATIONS
Education & Experience
- Bachelor’s Degree in Chemistry, Biology, Biochemistry, or related scientific field required; advanced degree preferred.
- PMP certification is a plus.
- Minimum of 4 years of experience in project management or technical operations, preferably in analytical testing or a laboratory environment.
- Equivalent combinations of education, training, and experience will be considered.
Knowledge & Skills
- Strong organizational and time management abilities with experience managing multiple complex projects.
- Excellent communication and interpersonal skills, with a commitment to customer service excellence.
- Proficiency in Microsoft Office Suite (Outlook, Word, Excel, PowerPoint).
- Extensive knowledge of analytical testing methodologies, instrumentation, and laboratory operations.
- Ability to interpret and communicate complex scientific data.
- Familiarity with pharmaceutical industry standards and analytical testing requirements preferred.
- Experience with regulatory compliance and quality systems (ISO, GLP) is a plus.
- Ability to work independently and collaboratively in a fast-paced environment.
- Demonstrated tact, discretion, and professionalism in client and team interactions.
OTHER REQUIREMENTS
- Performs all other duties as assigned.
- Supports and promotes the mission, values, and culture of Pace® Life Sciences.
Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work.
BENEFITS
When you join Pace®, you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft.
Equal Opportunity Employer
Pace® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
INTRODUCTION
Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives.
Pace® Life Sciences
Project Manager II – Pharmaceutical Analytical Outsourcing
Location: Morrisville, NC
Employment Type: Full-Time (Hybrid)
SUMMARY
The Project Manager II plays a critical role in delivering exceptional customer service and ensuring the successful execution of complex analytical testing projects. This position serves as the primary liaison between clients, laboratory teams, and sales staff, facilitating clear communication, managing project milestones, and ensuring all work is completed on time, within scope, and in compliance with industry standards.
The Project Manager II will oversee large and technically complex projects, coordinating cross-functional resources and maintaining a high level of scientific and operational understanding. This role supports multiple Pace® Life Sciences Analytical Outsourcing laboratories across Oakdale MN, Lebanon NJ, Morrisville NC, and San Germán PR.
ESSENTIAL FUNCTIONS
The following duties represent the core responsibilities of the role; additional tasks may be assigned as needed.
Project Leadership & Execution
- Develop and manage project plans, timelines, and budgets for analytical testing projects.
- Serve as the primary client contact for project updates, deliverables, issues, and scope changes.
- Support sample management for large or complex projects, ensuring regulatory and project-specific requirements are met.
- Update and maintain project status, cost details, and client information in the Laboratory Information Management System (LIMS).
- Approve testing to initiate laboratory work when required.
Client Engagement & Communication
- Lead client meetings, including preparing agendas and distributing meeting minutes.
- Host on-site client visits and support sales team activities as needed.
- Liaise with quoting and sales teams to initiate new quotes for scope changes or additional work.
- Provide specialized analysis and interpretation of data results to clients.
- Communicate project risks, issues, and progress to stakeholders with clear recommendations.
Quality & Compliance
- Ensure adherence to industry standards, regulatory requirements, and internal quality protocols.
- Collaborate with QA and clients to support timely completion of investigations and CAPAs.
- Maintain accurate and accessible project documentation.
Cross-Functional Collaboration
- Coordinate with laboratory, QA, sales, and operational teams to ensure efficient resource allocation and timely project completion.
- Track client account health and escalate concerns to management when necessary.
- Contribute to site forecasting by providing financial updates and projections for ongoing and upcoming work.
Leadership & Continuous Improvement
- Provide guidance and support to project team members, fostering a collaborative and high-performance environment.
- Identify opportunities for process improvements and support implementation of best practices.
- Promote a positive, cooperative work environment aligned with Pace® values and mission.
- Comply with all Environmental Health and Safety requirements.
QUALIFICATIONS
Education & Experience
- Bachelor’s Degree in Chemistry, Biology, Biochemistry, or related scientific field required; advanced degree preferred.
- PMP certification is a plus.
- Minimum of 4 years of experience in project management or technical operations, preferably in analytical testing or a laboratory environment.
- Equivalent combinations of education, training, and experience will be considered.
Knowledge & Skills
- Strong organizational and time management abilities with experience managing multiple complex projects.
- Excellent communication and interpersonal skills, with a commitment to customer service excellence.
- Proficiency in Microsoft Office Suite (Outlook, Word, Excel, PowerPoint).
- Extensive knowledge of analytical testing methodologies, instrumentation, and laboratory operations.
- Ability to interpret and communicate complex scientific data.
- Familiarity with pharmaceutical industry standards and analytical testing requirements preferred.
- Experience with regulatory compliance and quality systems (ISO, GLP) is a plus.
- Ability to work independently and collaboratively in a fast-paced environment.
- Demonstrated tact, discretion, and professionalism in client and team interactions.
OTHER REQUIREMENTS
- Performs all other duties as assigned.
- Supports and promotes the mission, values, and culture of Pace® Life Sciences.
Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work.
BENEFITS
When you join Pace®, you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft.
Equal Opportunity Employer
Pace® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
H-1B Medical Devices Job Roles in North Carolina
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Search Medical Devices Jobs in North CarolinaMedical Devices H-1B Sponsorship Jobs in North Carolina: Frequently Asked Questions
Which medical devices companies sponsor H-1B visas in North Carolina?
Several major medical devices employers with North Carolina operations have a track record of H-1B visa filings, including Becton Dickinson, Teleflex, Hologic, Labcorp, and Synecor. Contract manufacturers and smaller device startups in the Research Triangle Park area also file H-1B petitions regularly, particularly for engineering, quality assurance, and regulatory affairs positions. DOL LCA disclosure data is publicly searchable to verify specific employer filing history.
Which cities in North Carolina have the most medical devices H-1B sponsorship jobs?
The Research Triangle Park area, covering Raleigh, Durham, and Chapel Hill, concentrates the largest share of medical devices H-1B roles in North Carolina, supported by proximity to NC State, Duke, and UNC research ecosystems. Charlotte is a secondary hub, particularly for medical technology and diagnostics companies. Greensboro and the Triad region also host device manufacturing and R&D operations with documented H-1B sponsorship activity.
What types of medical devices roles typically qualify for H-1B sponsorship?
H-1B sponsorship in medical devices generally applies to specialty occupation roles requiring at least a bachelor's degree in a specific technical or scientific field. Common qualifying positions include biomedical engineers, regulatory affairs specialists, quality engineers, R&D scientists, software engineers developing embedded or clinical systems, and clinical applications specialists. Roles where a degree in a specific discipline is the standard industry requirement tend to have the strongest H-1B eligibility footing.
How do I find medical devices H-1B sponsorship jobs in North Carolina?
Migrate Mate is built specifically for international job seekers and filters medical devices H-1B sponsorship jobs in North Carolina by company, role type, and location. Rather than sorting through general job listings where sponsorship status is unclear, Migrate Mate surfaces roles from employers with verified H-1B sponsorship history, saving significant research time. It is the most direct way to identify North Carolina medical devices openings relevant to H-1B candidates.
Are there any state-specific or industry-specific considerations for H-1B sponsorship in North Carolina medical devices?
North Carolina does not impose state-level visa restrictions, so H-1B sponsorship follows standard federal USCIS requirements. Within the medical devices industry, roles touching FDA-regulated product development may require specific degree credentials that align with the specialty occupation standard, which can affect petition strength. Companies with established legal and HR infrastructure, particularly those based in Research Triangle Park, tend to have more streamlined H-1B sponsorship processes than smaller startups.
What is the prevailing wage for H-1B medical devices jobs in North Carolina?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.