Manufacturing Jobs at Globus Medical with Visa Sponsorship
Manufacturing jobs at Globus Medical span production, quality, and process engineering in medical device manufacturing, with an established record of supporting international workers through the sponsorship process. If you're targeting a hands-on or technical manufacturing role, Globus Medical is a credible path.
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INTRODUCTION
Branch Medical Group, a subsidiary of Globus Medical Inc., manufactures a wide range of implants for spinal and orthopedic applications as well as designs the instrumentation cases that house them. Our passion, combined with Globus’ world-class engineering, transforms clinical insights into tangible musculoskeletal solutions. We are constantly in pursuit of better patient care and understand that speed is critical because life cannot wait.
Position Summary:
The Supervisor is responsible for leading production personnel and overseeing daily manufacturing operations to ensure the consistent production of high-quality medical devices. This role supports site manufacturing strategy, drives operational efficiency, and ensures compliance with FDA regulations, quality system requirements, and company policies. The Supervisor provides direct leadership to line personnel and partners with cross-functional teams to achieve safety, quality, delivery, and productivity objectives.
Essential Functions:
- Supervise and coordinate daily production activities to meet quality, safety, and output targets
- Provide direct leadership to production and line personnel, including work assignment, coaching, performance feedback, and accountability
- Ensure production processes are executed in accordance with approved procedures, work instructions, and quality standards
- Monitor and improve operational efficiency, standardization, and adherence to established manufacturing processes
- Analyze production data, defects, scrap, yield, and productivity metrics; implement corrective and preventive actions as needed
- Lead and participate in structured problem-solving activities related to quality issues, complaints, scrap, downtime, or throughput
- Ensure compliance with applicable FDA regulations, ISO 13485 requirements, internal Quality Management System (QMS) procedures, and company policies
- Support and participate in internal and external audits, audits readiness activities, and follow-up actions
- Ensure team compliance with safety, health, and environmental requirements
- Collaborate with engineering, quality, and other cross-functional teams to support process improvements and manufacturing initiatives
- Support site energy policy initiatives by promoting efficient production processes and participating in improvement activities that optimize energy usage
- Maintain clean, organized, and compliant production areas
- Adhere to the letter and spirit of the company Code of Conduct, the AdvaMed Code, MedTech Code, and all other company policies
- Ensure compliance with applicable governmental laws, rules, and regulations, both in the United States and internationally, by completing introductory and annual training and maintaining knowledge of compliance as it applies to your role
- Represent the company in a professional manner and uphold the highest standards of ethical business practices and socially responsible conduct in all interactions with other employees, customers, suppliers, and other third parties
Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.
Qualifications
- Bachelor’s degree or an equivalent combination of education and relevant work experience required
- Minimum of three (3) to five (5+) years of experience in the medical device or regulated manufacturing industry required
- Minimum of three (3) years of experience in a supervisory or people-lead role required
- Experience analyzing, interpreting, and presenting detailed operational and quality metrics required
- Experience supporting or participating in internal and external quality system audits required
- Proficiency with manufacturing systems used to collect data and monitor or control processes required
- Demonstrated ability to effectively lead, influence, and motivate teams toward organizational goals required
- Strong working knowledge of FDA regulations, ISO standards, and quality system requirements required
- Excellent written and verbal communication skills required
- Strong organizational, time-management, and problem-solving skills required
- Ability to work effectively in a fast-paced, changing manufacturing environment required
- Ability to maintain regular and predictable attendance required
- Certifications relevant to medical device manufacturing or quality, such as CQE, Six Sigma Green or Black Belt, Lean certification, or structured problem-solving methodologies, preferred
- Knowledge of OSHA requirements and environmental, health, and safety standards preferred
Physical Demands:
The physical demands listed here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
- Required to sit; climb or balance; and stoop, kneel, crouch or crawl
- Required to regularly lift and/or move up to 15 pounds, and occasionally lift and/or move up to 25 pounds
- Required to possess specific vision abilities, including: close vision, distance vision, color vision, peripheral vision, depth perception and capacity to adjust focus.
Our Values:
Our Life Moves Us philosophy is built on four values: Passionate About Innovation, Customer Focused, Teamwork, and Driven.
- Passionate about Innovation: Improving patient care by delivering advanced technology to our customers is at the core of what we do. We are passionate about our role in improving the lives of patients by continuously developing better solutions.
- Customer Focused: We listen to our customers’ needs and respond with a sense of urgency.
- Teamwork: Working together, anything is possible. We value every person on our team and treat each other with respect. We are accountable to one another and support each other. Together, we make each other stronger.
- Driven: We pursue our mission with energy and passion. We are nimble, results-oriented and decisive. We overcome obstacles that arise in our quest to deliver solutions that will improve the lives of our customers and patients.
Equal Employment Opportunity:
Globus Medical is an equal opportunity employer. All applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, age, disability, marital status, pregnancy, national origin or citizenship. We are committed to a diverse workforce. We value all employees’ talents and support an environment that is inclusive and respectful.
Other Duties:
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.
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Get Access To All JobsTips for Finding Manufacturing Jobs at Globus Medical
Align your credentials to FDA manufacturing standards
Globus Medical operates under strict FDA quality system regulations. Before applying, make sure your resume reflects experience with GMP, ISO 13485, or similar quality frameworks, these signal day-one readiness for regulated medical device production environments.
Target roles requiring specialized technical qualifications
Manufacturing roles at Globus Medical that require a specific degree in engineering or a closely related field are the strongest candidates for H-1B specialty occupation classification. Roles where any general degree qualifies are harder to support through USCIS.
Use Migrate Mate to identify open manufacturing positions
Globus Medical posts manufacturing roles across production, quality, and process functions. Use Migrate Mate to filter specifically for Globus Medical openings that are flagged for visa sponsorship, so you're not applying blind to roles that won't support your status.
Clarify sponsorship scope during the offer stage
Before accepting an offer, confirm whether the company will support both initial H-1B filing and the longer-term EB-2 or EB-3 Green Card process. Some employers sponsor the work visa but leave PERM labor certification off the table until later.
Account for H-1B cap timing in your job search
If you're not currently in H-1B status, registrations open in March for an October 1 start. Plan your Globus Medical application timeline so an offer is in hand before the USCIS registration window, giving the employer time to file on your behalf.
Verify your work authorization documents are current
Globus Medical participates in E-Verify, so your Form I-9 documentation will be checked electronically on or before your first day. If you're on OPT or CPT, confirm your EAD and SEVIS record are accurate and your authorization end date covers the start date.
Frequently Asked Questions
Does Globus Medical sponsor H-1B visas for Manufacturing roles?
Yes, Globus Medical sponsors H-1B visas for manufacturing positions where the role qualifies as a specialty occupation under USCIS standards. Roles in process engineering, quality engineering, and manufacturing engineering tend to meet that threshold most cleanly. Production operator roles without a degree requirement are less likely to qualify for H-1B sponsorship.
Which visa types does Globus Medical support for Manufacturing positions?
Globus Medical has a track record of supporting H-1B transfers and new filings, F-1 OPT and CPT for recent graduates, TN visas for Canadian and Mexican nationals in qualifying engineering roles, J-1 visa for certain training arrangements, and immigrant pathways including EB-2 and EB-3 with PERM labor certification for longer-term permanent residency.
What qualifications does Globus Medical look for in Manufacturing candidates?
Most sponsored manufacturing roles at Globus Medical require a bachelor's degree in mechanical, industrial, biomedical, or manufacturing engineering. Hands-on experience with GMP environments, ISO 13485 quality systems, and medical device assembly or process validation is frequently listed. For senior roles, experience with FDA 21 CFR Part 820 compliance is a strong differentiator.
How do I apply for Manufacturing jobs at Globus Medical?
You can search for open manufacturing positions directly on Globus Medical's careers page or browse their visa-sponsoring roles through Migrate Mate, which filters specifically for employers with active sponsorship history. When applying, tailor your resume to reflect regulated manufacturing experience and confirm in your cover letter that you'll require visa sponsorship so the hiring team knows upfront.
How do I plan my timeline if I need H-1B sponsorship for a Globus Medical role?
If you need a new H-1B cap-subject filing, USCIS opens registration in March for an October 1 start date. You'll need an offer from Globus Medical before that window. If you're transferring an existing H-1B, the process can move faster since cap-exempt transfers can be filed year-round, often with a start date within 30 to 60 days of filing.