Medical Devices Visa Sponsorship Jobs in North Carolina
North Carolina's Research Triangle Park hosts major medical device companies like Becton Dickinson, Cook Medical, and Teleflex, creating substantial visa sponsorship opportunities. The state's biotech corridor spans Raleigh-Durham-Chapel Hill, with additional manufacturing hubs in Charlotte and Greensboro. Strong university partn visaerships with Duke, UNC, and NC State provide talent pipelines for international professionals.
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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.
ABOUT THE JOB
Project Manager I – Pharmaceutical Analytical Outsourcing
Location: Morrisville, NC
Employment Type: Full-Time (Hybrid)
SUMMARY
The Project Manager I plays an important role in supporting the successful execution of analytical testing projects, while developing the skills and experience necessary for independent project management. This position begins with supporting the project management team through project coordination and administrative responsibilities, including project tracking, documentation management, and coordination of project activities.
As knowledge and proficiency are gained, the Project Manager I progressively assumes responsibility for managing a portfolio of their own client projects, and then begins serving as the primary liaison between the clients, laboratory teams, and sales staff. In this capacity, the Project Manager I facilitates clear communication, manages project milestones, and helps ensure work is completed on time, within scope, and in compliance with industry standards.
This role supports the Pace® Life Sciences Analytical Outsourcing laboratory in Morrisville NC.
ESSENTIAL FUNCTIONS
The following duties represent the core responsibilities of the role; additional tasks may be assigned as needed:
Project Leadership & Execution
- Support Project Managers in the planning, coordination, and execution of analytical testing projects, ensuring project requirements and timelines are tracked effectively.
- Assist with client communications by providing project updates, coordinating deliverables, documenting discussions, and escalating issues as needed.
- Coordinate sample management activities for assigned projects, ensuring project-specific and regulatory requirements are accurately documented and communicated.
- Maintain project status, cost information, and client records within the Laboratory Information Management System (LIMS) and other project management tools.
- Review project documentation and testing requests to support the timely initiation of laboratory work and project execution.
- Develop the knowledge and skills necessary to progressively assume responsibility for managing a portfolio of client projects under the guidance of senior project management staff.
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.
Continuous Improvement
- Provide support to project team members, fostering an inclusive, 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.
- PMP certification is a plus.
- Minimum of 2 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).
- Knowledge of analytical testing methodologies, instrumentation, and laboratory operations.
- Ability to 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.
- Demonstrates 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.
ABOUT THE JOB
Project Manager I – Pharmaceutical Analytical Outsourcing
Location: Morrisville, NC
Employment Type: Full-Time (Hybrid)
SUMMARY
The Project Manager I plays an important role in supporting the successful execution of analytical testing projects, while developing the skills and experience necessary for independent project management. This position begins with supporting the project management team through project coordination and administrative responsibilities, including project tracking, documentation management, and coordination of project activities.
As knowledge and proficiency are gained, the Project Manager I progressively assumes responsibility for managing a portfolio of their own client projects, and then begins serving as the primary liaison between the clients, laboratory teams, and sales staff. In this capacity, the Project Manager I facilitates clear communication, manages project milestones, and helps ensure work is completed on time, within scope, and in compliance with industry standards.
This role supports the Pace® Life Sciences Analytical Outsourcing laboratory in Morrisville NC.
ESSENTIAL FUNCTIONS
The following duties represent the core responsibilities of the role; additional tasks may be assigned as needed:
Project Leadership & Execution
- Support Project Managers in the planning, coordination, and execution of analytical testing projects, ensuring project requirements and timelines are tracked effectively.
- Assist with client communications by providing project updates, coordinating deliverables, documenting discussions, and escalating issues as needed.
- Coordinate sample management activities for assigned projects, ensuring project-specific and regulatory requirements are accurately documented and communicated.
- Maintain project status, cost information, and client records within the Laboratory Information Management System (LIMS) and other project management tools.
- Review project documentation and testing requests to support the timely initiation of laboratory work and project execution.
- Develop the knowledge and skills necessary to progressively assume responsibility for managing a portfolio of client projects under the guidance of senior project management staff.
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.
Continuous Improvement
- Provide support to project team members, fostering an inclusive, 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.
- PMP certification is a plus.
- Minimum of 2 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).
- Knowledge of analytical testing methodologies, instrumentation, and laboratory operations.
- Ability to 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.
- Demonstrates 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.
Medical Devices Job Roles in North Carolina
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Search Medical Devices Jobs in North CarolinaMedical Devices Jobs in North Carolina: Frequently Asked Questions
Which medical devices companies sponsor visas in North Carolina?
Major sponsors include Becton Dickinson (BD) in the Research Triangle, Cook Medical with manufacturing operations, Teleflex for interventional devices, and Viant Medical Technology. Smaller innovators like Abiomed (acquired by Johnson & Johnson) and various startups in RTP also sponsor H-1B visa and other work visas for engineering, regulatory affairs, and clinical roles.
How to find medical devices visa sponsorship jobs in North Carolina?
Use Migrate Mate to filter medical devices positions specifically in North Carolina cities like Raleigh, Durham, Charlotte, and Greensboro. The platform shows verified sponsorship employers and includes both established companies in Research Triangle Park and emerging biotech firms throughout the state's medical corridor.
Which visa types are most common for medical devices roles in North Carolina?
H-1B dominates for engineering, regulatory affairs, and quality assurance positions. TN visas work well for Canadian and Mexican professionals in biomedical engineering roles. Some companies sponsor O-1 visas for senior researchers with notable achievements, while L-1 visa transfers occur for international companies with North Carolina operations.
Which cities in North Carolina have the most medical devices sponsorship jobs?
Raleigh-Durham leads with Research Triangle Park concentration, hosting BD, Cook Medical, and numerous startups. Charlotte follows with medical technology companies and regional headquarters. Chapel Hill contributes through university-affiliated research positions, while Greensboro and Winston-Salem offer manufacturing and operations roles.
What are the prevailing wage considerations for medical devices jobs in North Carolina?
North Carolina's lower cost of living compared to California or Massachusetts means competitive prevailing wages while maintaining attractive real purchasing power. Research Triangle Park commands premium wages similar to other major biotech hubs, with H-1B LCA requirements typically met easily for engineering and regulatory positions in the medical devices sector.
What is the prevailing wage for sponsored 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.