Integra Lifesciences Green Card Visa Sponsorship Jobs USA
Integra Lifesciences sponsors Green Cards for skilled professionals in the medical devices industry, typically supporting engineers, regulatory specialists, and research roles through the EB-2 and EB-3 pathways. The company has an established sponsorship program, making it a worthwhile target for candidates building long-term U.S. careers in med-tech.
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INTRODUCTION
Changing lives. Building Careers.
Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.
ROLE AND RESPONSIBILITIES
The Manufacturing Operator 1 - 2nd Shift, performs post-formulation processing such as product cutting, inspection, defect identification, packaging, machine packaging operations, and labeling and boxing to produce the finished good. Also performs sub assemble post chemical processing such as cross linking required to produce collagen-based products. All work streams include responsibility in the setup, operation, and cleaning of all clean room manufacturing equipment. All chemical processing operations are performed in ISO Class 5 or ISO Class 7 areas and require proper Clean Room gowning. All processing is performed in compliance with Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOP’s) and Health and Safety requirements. Operate in a team environment focused on daily milestones and quality throughout.
This is a second shift role. (3:00 p.m. - 11:30 p.m.)
ESSENTIAL DUTIES AND RESPONSIBILITIES
- Operate, maintain, and troubleshoot process equipment utilized in the collagen business, and be able to make minor equipment adjustments as needed.
- Responsible for performing precise measurements and using measurement equipment to accurately add chemicals to batches.
- Responsible for the cross linking, cutting, packaging, and boxing of the product in its finished goods form, which includes performing visual product and component inspections to identify and remove defects.
- Pass and maintain gowning qualification to perform Gowning Requirement for ISO Class 5 Clean room operations or ISO Class 7 Clean room operations.
- Responsible for accurately maintaining legible and accurate records, required logs, books, records, and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOP’s), and Health and Safety requirements.
- Interface with QA/QC/Material departments during course of work to coordinate inspections and efficient flow of subassemblies and completed product.
- Enter and record production activities in Oracle MRP systems to issue material and labor hours to specific work orders.
- Follow applicable Standard Operating Procedures, Quality System Regulations, and ISO 13485 requirements.
BASIC QUALIFICATIONS
The requirements listed below are representative of the knowledge, skill, and/or ability required for this position.
- High School diploma or equivalent. Degree in a related science a plus.
- 0 - 2 years of chemical processing experience or batch mixing in Medical Device or Pharmaceutical manufacturing industry. Production experience is highly desirable.
- Basic computer skills for email and data entry.
- Must read, write, and speak in English, and communicate clearly and concisely.
- Fundamental understanding of mathematics and chemistry.
- Able to participate in a team-oriented environment, willingness to assist and train others.
- Able to work independently with minimal supervision.
- Ability to operate, maintain and troubleshoot process equipment, and make minor adjustments as needed.
- Ability to gown to ISO Class 5 and 7 Clean Room standards.
- Able to work overtime.
- Support department and plant Safety goals by continuously demonstrating safe behavior.
- Maintain a clean and orderly work area.
- Ability to work flexible shifts, and flexible days within the week to meet batch milestone requirements.
- Perform other manufacturing activities as assigned by the department leadership.
TOOLS AND EQUIPMENT USED
- Lyophilizers, Autoclave, homogenizers, grinder, vacuum pump, pH meters, thermometers, balances (scales), water bath circulators, sonicators, humidity cabinet, mixers, centrifuge, blenders, air gun, drop indicator, Filamatic filling machines, slicer machines, scalpels, temperature recorders, Crosslinking chamber, humidification chamber, compression unit, cutting table, sealing machines, shrink wrap machines.
Physical Requirements
The physical requirements listed in this section include, but are not limited, to the motor/physical abilities and skills require of position to successfully undertake the essential duties and responsibilities of this position. In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to empower individuals with disabilities to undertake the essential duties and responsibilities of the position.
- While undertaking the essential duties and responsibilities of the position, the employee must repeatedly sit, listen, speak, and write/type. The employee must be able to stand for 8 hours, lift to 60lbs and climb ladders without assistance. The employee is required to go to all areas of the company.
- Must be able to bend and lift 30 to 60 lbs without assistance daily.
- Ability to gown to ISO Class 5 type Clean Room standards and/or additional clean room clothing.
- Ability to gown to ISO Class 7 type Clean Room standards and/or additional clean room clothing.
- Ability to stand for 8 hours.
- Must be able to climb step ladders without assistance.
- Vision: Requires eyesight correctable to 20/25 to detect any defect in product/materials. Visual acuity adequate to perform job duties, including meeting all of quality reclassification. Requires normal color perception.
COMPENSATION
- Salary Pay Range: $19.19 - $25.43 USD Hourly
Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or training. In addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensation. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.
Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance, and savings plan (401(k)).
Subject to the terms of their respective policies and date of hire, Employees are eligible for the following benefits.
Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.
This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices: EEO Is the Law | EOE including Disability/Protected Veterans
Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA. If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers@integralife.com.
Unsolicited Agency Submission
Integra LifeSciences does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidate’s name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails.

INTRODUCTION
Changing lives. Building Careers.
Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.
ROLE AND RESPONSIBILITIES
The Manufacturing Operator 1 - 2nd Shift, performs post-formulation processing such as product cutting, inspection, defect identification, packaging, machine packaging operations, and labeling and boxing to produce the finished good. Also performs sub assemble post chemical processing such as cross linking required to produce collagen-based products. All work streams include responsibility in the setup, operation, and cleaning of all clean room manufacturing equipment. All chemical processing operations are performed in ISO Class 5 or ISO Class 7 areas and require proper Clean Room gowning. All processing is performed in compliance with Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOP’s) and Health and Safety requirements. Operate in a team environment focused on daily milestones and quality throughout.
This is a second shift role. (3:00 p.m. - 11:30 p.m.)
ESSENTIAL DUTIES AND RESPONSIBILITIES
- Operate, maintain, and troubleshoot process equipment utilized in the collagen business, and be able to make minor equipment adjustments as needed.
- Responsible for performing precise measurements and using measurement equipment to accurately add chemicals to batches.
- Responsible for the cross linking, cutting, packaging, and boxing of the product in its finished goods form, which includes performing visual product and component inspections to identify and remove defects.
- Pass and maintain gowning qualification to perform Gowning Requirement for ISO Class 5 Clean room operations or ISO Class 7 Clean room operations.
- Responsible for accurately maintaining legible and accurate records, required logs, books, records, and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOP’s), and Health and Safety requirements.
- Interface with QA/QC/Material departments during course of work to coordinate inspections and efficient flow of subassemblies and completed product.
- Enter and record production activities in Oracle MRP systems to issue material and labor hours to specific work orders.
- Follow applicable Standard Operating Procedures, Quality System Regulations, and ISO 13485 requirements.
BASIC QUALIFICATIONS
The requirements listed below are representative of the knowledge, skill, and/or ability required for this position.
- High School diploma or equivalent. Degree in a related science a plus.
- 0 - 2 years of chemical processing experience or batch mixing in Medical Device or Pharmaceutical manufacturing industry. Production experience is highly desirable.
- Basic computer skills for email and data entry.
- Must read, write, and speak in English, and communicate clearly and concisely.
- Fundamental understanding of mathematics and chemistry.
- Able to participate in a team-oriented environment, willingness to assist and train others.
- Able to work independently with minimal supervision.
- Ability to operate, maintain and troubleshoot process equipment, and make minor adjustments as needed.
- Ability to gown to ISO Class 5 and 7 Clean Room standards.
- Able to work overtime.
- Support department and plant Safety goals by continuously demonstrating safe behavior.
- Maintain a clean and orderly work area.
- Ability to work flexible shifts, and flexible days within the week to meet batch milestone requirements.
- Perform other manufacturing activities as assigned by the department leadership.
TOOLS AND EQUIPMENT USED
- Lyophilizers, Autoclave, homogenizers, grinder, vacuum pump, pH meters, thermometers, balances (scales), water bath circulators, sonicators, humidity cabinet, mixers, centrifuge, blenders, air gun, drop indicator, Filamatic filling machines, slicer machines, scalpels, temperature recorders, Crosslinking chamber, humidification chamber, compression unit, cutting table, sealing machines, shrink wrap machines.
Physical Requirements
The physical requirements listed in this section include, but are not limited, to the motor/physical abilities and skills require of position to successfully undertake the essential duties and responsibilities of this position. In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to empower individuals with disabilities to undertake the essential duties and responsibilities of the position.
- While undertaking the essential duties and responsibilities of the position, the employee must repeatedly sit, listen, speak, and write/type. The employee must be able to stand for 8 hours, lift to 60lbs and climb ladders without assistance. The employee is required to go to all areas of the company.
- Must be able to bend and lift 30 to 60 lbs without assistance daily.
- Ability to gown to ISO Class 5 type Clean Room standards and/or additional clean room clothing.
- Ability to gown to ISO Class 7 type Clean Room standards and/or additional clean room clothing.
- Ability to stand for 8 hours.
- Must be able to climb step ladders without assistance.
- Vision: Requires eyesight correctable to 20/25 to detect any defect in product/materials. Visual acuity adequate to perform job duties, including meeting all of quality reclassification. Requires normal color perception.
COMPENSATION
- Salary Pay Range: $19.19 - $25.43 USD Hourly
Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or training. In addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensation. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.
Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance, and savings plan (401(k)).
Subject to the terms of their respective policies and date of hire, Employees are eligible for the following benefits.
Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.
This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices: EEO Is the Law | EOE including Disability/Protected Veterans
Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA. If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers@integralife.com.
Unsolicited Agency Submission
Integra LifeSciences does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidate’s name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails.
Job Roles at Integra Lifesciences
How to Get Visa Sponsorship in Integra Lifesciences Green Card Visa Sponsorship Jobs USA
Target roles in engineering and R&D
Integra Lifesciences most consistently sponsors Green Cards for technical and scientific roles. Focus your applications on positions in biomedical engineering, product development, and regulatory affairs, where the company has a clear pattern of long-term workforce investment.
Understand the EB-2 vs. EB-3 distinction
Integra files Green Cards under both EB-2 and EB-3. EB-2 typically applies to roles requiring advanced degrees or specialized expertise. Knowing which category your role falls under helps you set realistic timeline expectations and prepare the right documentation from the start.
Start the conversation before you accept an offer
Green Card sponsorship at large medical device companies like Integra often requires internal approval. Raise it during the offer negotiation stage rather than after onboarding. HR teams are more receptive when it is framed as a retention tool, not a last-minute request.
Use Migrate Mate to find verified sponsoring roles
Not every Integra Lifesciences job listing will mention Green Card sponsorship explicitly. Migrate Mate surfaces verified sponsors so you can filter by real sponsorship history, helping you focus your applications on roles where sponsorship is genuinely on the table.
Demonstrate long-term value in the medical devices field
Integra sponsors Green Cards for employees it views as long-term contributors. Candidates with niche expertise in regulatory compliance, FDA submissions, or advanced manufacturing processes are stronger sponsorship candidates given the company's focus in med-tech.
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Get Access To All JobsFrequently Asked Questions
Does Integra Lifesciences sponsor Green Card visas?
Yes, Integra Lifesciences sponsors Green Card visas for eligible employees. The company files petitions under the EB-2 and EB-3 preference categories, primarily for skilled professionals in technical, engineering, and scientific roles. Sponsorship is typically initiated after an employee has demonstrated strong performance and is seen as a long-term fit for the organization.
Which roles and departments at Integra Lifesciences are most likely to receive Green Card sponsorship?
Green Card sponsorship at Integra Lifesciences tends to concentrate in technical and highly specialized functions. Biomedical engineers, regulatory affairs specialists, quality assurance professionals, and R&D scientists are among the profiles most commonly supported. Roles that require niche expertise in the medical devices industry, particularly those tied to FDA-regulated processes, are strong candidates for sponsorship.
How do I start the Green Card sponsorship process at Integra Lifesciences?
The process typically begins with a conversation between the employee, their manager, and HR. Integra would then initiate a PERM labor certification filing with the Department of Labor, followed by an I-140 immigrant visa petition with USCIS. Employees should raise sponsorship intent early, ideally during the offer stage or shortly after starting, rather than waiting until a visa deadline is approaching.
How long does the Green Card process take at Integra Lifesciences?
The timeline depends on the visa category and the applicant's country of birth. For most applicants, the PERM and I-140 stages together can take one to two years. Nationals from countries with visa backlogs, particularly India and China, may face significantly longer waits for a visa number to become available after I-140 approval. Starting early is critical.
How do I find Green Card jobs at Integra Lifesciences?
Not all Integra Lifesciences job postings explicitly state that Green Card sponsorship is available, which makes it difficult to identify qualifying roles through general job boards. Migrate Mate tracks verified sponsorship history at companies like Integra, so you can search specifically for roles where Green Card sponsorship has been extended to candidates in the past, saving significant research time.
What is the prevailing wage for Green Card sponsorship at Integra Lifesciences?
Employers sponsoring a Green Card through the PERM labor certification process must pay at least the prevailing wage for the role. The Department of Labor determines this rate based on the specific job title, location, and experience level. The prevailing wage is locked in during the PERM filing and applies through the entire Green Card process. You can look up current rates using the DOL's OFLC Wage Search tool.
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