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Integra LifeSciences
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  • Changing lives. Building Careers.Joining us is a chance to do importan... Read More
    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.The Director, Health Economics, is a strategic leader within Global Market Access responsible for advancing the economic value proposition of Integra’s portfolio across global markets. Reporting to the Global Head of Market Access, this role shapes and executes the company’s health economics and outcomes research (HEOR) strategy to enable reimbursement, accelerate adoption, and strengthen competitive differentiation.This leader will generate and translate robust economic and real-world evidence to demonstrate the clinical, financial, and system-level value of Integra’s technologies across priority therapeutic areas, including but not limited to Surgical Reconstruction, Advanced Wound Care, Neurosurgery, ENT, Regenerative Technologies]. The Director will integrate health economic theory, advanced statistical methods, epidemiology, and outcomes research to inform pricing strategy, payer engagement, coverage positioning, and portfolio optimization.SUPERVISION RECEIVED: Reports to Global Head of Professional Education and Market AccessSUPERVISION EXERCISED: NoneKEY RESPONSIBILITIES:• Develop and execute a comprehensive global health economics and outcomes research (HEOR) strategy aligned with enterprise growth priorities, reimbursement objectives, and lifecycle management plans.• Design and deliver robust economic models (cost-effectiveness, budget impact, cost-utility, and cost-consequence analyses) to quantify clinical and financial value across sites of care.• Lead the design and oversight of health economic endpoints within clinical trials and post-market studies.• Translate complex health economic and real-world evidence into clear, payer-relevant value narratives that support market access and commercial objectives.• Support development of global value dossiers, AMCP dossiers, and health technology assessment (HTA) submissions.• Support evidence generation roadmaps across priority therapeutic areas to support coverage, coding, payment, and value-based positioning.• Ensure methodological rigor through application of advanced biostatistics, epidemiology, and outcomes research methodologies.• Partner with regional Market Access leaders to inform payer engagement strategies and respond to economic evidence requirements.• Provide health economic insights to support coverage negotiations, value-based agreements, and risk-sharing arrangements.• Provide economic analyses to inform pricing strategy, reimbursement positioning, and competitive differentiation.• Support scenario modeling related to reimbursement reform, coding changes, and policy evolution.• Serve as the HEOR subject matter expert across Global Market Access, Commercial, R&D, Clinical Affairs, Medical Affairs, and Professional Education.• Integrate health economic evidence into launch planning, innovation pipelines, and early-stage product development.• Represent the company in external forums, advisory boards, and scientific congresses related to HEOR and value assessment.• Oversee publication strategy for economic and outcomes research in peer-reviewed journals and scientific meetings.• Build and maintain relationships with key academic institutions, health economists, and research partners.• Establish global HEOR standards, methodologies, and best practices across regions.• Manage external research vendors and academic collaborations to ensure high-quality and timely evidence generation.• Build scalable HEOR capabilities to support future pipeline growth and global expansion.DESIRED MINIMUM QUALIFICATIONS: • B.S./B.A. from an accredited university required.• Master’s required or Doctorate preferred in a related fi.• 7 – 10 years medical device/pharmaceutical health economics or HEOR experience.• Prior medical device industry experience strongly preferred.• Advanced expertise in health economic modeling, including cost-effectiveness, budget impact, cost-utility, and scenario analyses is required.• Proficiency in statistical and econometric methodologies, including regression analysis, survival analysis, longitudinal data analysis, and real-world evidence evaluation is strongly preferred.• Ability to form strong and constructive internal and external professional relationships.• Excellent collaboration skills and success working in matrix organizations at all levels• Proactive, results-oriented, self-starter motivated by an interesting and challenging task.• Excellent written and verbal presentation communication skills.• Must be able and willing to travel domestically and internationally up to 25%.TECHNICAL COMPETENCIES: • Demonstrated experience using statistical software such as SAS, R, Stata, or Python for analysis of claims, registry, and clinical trial data.• Experience with health economic modeling platforms (e.g., TreeAge Pro) and advanced Excel-based modeling for payer-facing tools.• Working knowledge of systematic literature review, meta-analysis, and indirect treatment comparison methodologies.• Strong capability in translating complex quantitative findings into clear, payer-relevant insights and value narratives.• Familiarity with global health technology assessment (HTA) frameworks and evidence requirements across U.S. and international markets.Salary Pay Range:$145,000.00 - $199,000.00 USD SalaryOur 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 Total Rewards | Integra LifeSciencesIntegra 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 VeteransIntegra 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 SubmissionIntegra 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.Integra - Employer Branding from Integra LifeSciences on VimeoSummaryLocation: US-xx-xx-NA-Home Office; US-NJ-Princeton-100-HeadquartersType: Full time Read Less
  • Manufacturing Operator I  

    - Hamilton County
    Manufacturing Operator Joining us is a chance to do important work tha... Read More
    Manufacturing Operator 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. The Manufacturing Operator follows established Standard Operating Procedures to perform functional testing. Operates CUSA tip testing consoles to ensure function of products. Operates the Cusa Bender. Uses multiple software platforms for completing work such as Windows, Agile, Oracle, and Excel. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Primary responsibilities are to: Ensures completion of tasks as directed by SOPs, routers, prints, work instructions, and manufacturing schedules. May package and test manufactured and purchased parts. May enter and transfer items in Oracle without assistance. Works closely with supervisor on any process challenges that require support from other departments. Follows standard operating procedures and Work Instructions to test manufactured and purchased parts. May operates CUSA Tip testing consoles for both internal and externally manufactured tips. Follows standard operating procedures to support general housekeeping in area. Always observes Company's safety procedures and policy. Performs other duties as required. May operate the Cusa Bender. Note: Other duties may be assigned as necessary. Qualifications The requirements listed below are representative of the knowledge, skill and/or ability required for this position. Education: High school diploma or GED required with 0 - 2 years of experience. Must be able to read and write in English. Must be able to demonstrate comprehension of written English by successfully completing unassisted written tests, including, but not limited to, Work Instructions and Standard Operating Procedures. Must be able to observe company policies and safety procedures at all times. Must be able to give and welcome constructive feedback; contribute to building a positive team spirit. Must be able to treat others with respect; work with integrity and ethically; uphold organizational values. Tools and Equipment Used CUSA tip testing consoles, Bending, and washing machines and personal computers. Use of Personal Protective Equipment (PPE) when required. Ability to utilize a desktop computer with typical business programs installed, including spreadsheets, word processing and Oracle systems. Strong computer skills are required. Knowledge and experience with MRP/ERP systems is a plus. Salary Pay Range: $16.68 - $22.12 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)). 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. Read Less
  • Lead Quality Inspector  

    - Middlesex County
    Lead Quality Inspector Joining us is a chance to do important work tha... Read More
    Lead Quality Inspector 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. The Lead Quality Inspector serves as a Lead Associate, Quality Inspector for the Plainsboro Manufacturing Site, Collagen Manufacturing Center (CMC). The lead associate is responsible for performing and/or scheduling quality assurance inspections on purchased components, manufactured sub-assemblies and final product. Expectations are to be familiar with and be able to measure critical dimensions as well as to train new quality inspectors and provide guidance to current quality inspectors. Lead Associate, Quality Inspector will perform all duties in accordance with the requirements of overall corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. This is for a Weekend Lead, the Shift is 12 hours on Friday, Saturday and Sunday from 6am to 6:30pm (will be compensated for 40 hours per week) Job Responsibilities Oversee daily activities in the QC department. Prepare the QC Inspection schedule to ensure that all manufacturing areas are covered in order to meet production schedule. Reports any non-conformances in timely manner. Support NCs and CAPA investigations as required. Assist with product flow between departments. Interface with Manufacturing department in order to coordinate inspections of completed product to ensure the inspections are done in a timely manner. Initiate and/or propose revisions to standard operating procedures involving new processes or process improvements. Train QC Inspectors as required. Perform inspections (incoming, in-process, first article, etc.) by using a variety of inspection measuring equipment to determine acceptance or rejection of material or parts. Interpret and work within the guideline of drawings, specifications, charts, procedures, and other data to determine product or material acceptance. Read and interpret sampling plan as per the American National Standard Institute (ANSI). Oversees physical and electronic quarantine locations. May also perform other related duties, responsibilities, and special projects as assigned. Desired Minimum Qualifications Minimum of 5+ years' experience in document and promotional materials management using electronic document management systems or with manual systems using electronic document storage. Minimum of 5+ years' experience in a Quality Systems / Regulatory Compliance environment with a working knowledge preferably in the medical device, diagnostics or pharmaceutical industries. Familiarity with FDA regulations and ISO series of quality standards preferred. Capable of both written and verbal effective communication skills. Proficient in the Microsoft Office suite of products. Proficient in Oracle R12/Agile preferred. Salary Pay Range: $26.21 - $35.38 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. 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)). 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. Read Less
  • Surgical Tissue Solutions Account Manager Joining us is a chance to do... Read More
    Surgical Tissue Solutions Account Manager 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. Job Description Responsible for driving sales growth in Surgical Tissue Solutions product line by executing territory plans, educating clinicians, and supporting operating room needs. The Account Manager will call on multiple call points/surgical specialties. Products include, but are not limited to: Plastic Hernia business or science-related degree preferred Experience Bachelor's Degree or an equivalent combination of education and/or experience is required; business or science-related degree preferred Minimum two years' experience business-to-business sales (or similar) Operating room experience is necessary; plastic surgery experience preferred. Minimum of two years of surgical device or other medical sales preferred Skills Read Less

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