Senior Engineer II, Quality Design Assurance Integra LifeSciencesSenior Engineer II, Quality Design AssuranceMassachusetts5 years of experience of working within a medical device or other regulated industry with knowledge of Risk Management (ISO 14971 2019), EU MDR, MDD (Medical Device Directive), IEC 62366, ISO 13485 (Quality Management Systems), FDA QSR and cGMP. Fulfill design control requirements compliant: software specifications, detailed design files, design verification and validation test plans, risk management, DHF, protocols, and reports in accordance with company procedures, FDA and ISO guidelines.
Creative Design Specialist Nichols CollegeCreative Design SpecialistDudley, MAResearch and manage stock photography and video; manage creative and digital graphics subscriptions; work with outside photographers, including Nichols College student staff; manage work study students as necessary. As the college's primary designer, the Specialist works closely with enrollment (admissions) and other key campus partners to communicate the value of a Nichols College education and contribute to strategic growth priorities.
Medical Device Complaint Trending Expert (Any Facility) Integra LifeSciences Holdings Corp.Medical Device Complaint Trending Expert (Any Facility)Mansfield, MA$81,650–$112,700 / yearThe individual partners cross functionally with Quality, Regulatory Affairs, Risk Management, R&D, Manufacturing, and Medical Safety to translate complex complaint data into actionable insights that support corrective and preventive actions (CAPA), regulatory submissions, and risk management decisions. The Medical Device Complaint Trending Expert is responsible for the end-to-end development, execution, and oversight of complaint data trending and signal detection activities to ensure timely identification of product quality, safety, and compliance risks.
NewSenior Oracle EBS Finance Functional Lead Integra LifeSciences Holdings CorpSenior Oracle EBS Finance Functional LeadMansfield, MAThe incumbent will partner with Finance and IT teams, translate business needs into functional solutions, and drive practical improvements across Record-to-Report value stream. The right person will help ensure Oracle EBS supports accurate close processes, costing, reconciliations, reporting, controls, and compliance in a regulated medical technology environment.
Sr Principal Engineer, Product Development Integra LifeSciences Holdings CorpSr Principal Engineer, Product DevelopmentMansfield, MA$166,750–$228,850 / yearMinimum of 10 years of progressive hands-on experience in medical device product development under FDA Quality System Regulation (21 CFR Part 820) and ISO 13485, with a demonstrated track record of successfully advancing complex electromechanical or electro-fluidic devices from concept through verification, validation, and commercialization. Effectively synthesize, condense, and communicate complex technical data, experimental results, trade-off analyses, and risk assessments through clear presentations, design reviews, and written reports for cross-functional audiences including R&D, Quality, Regulatory, Manufacturing, and senior leadership.
Senior Audit Program Specialist Integra LifeSciences Holdings Corp.Senior Audit Program SpecialistMansfield, MA$81,650–$112,700 / yearThis role is responsible for supporting the auditor team in coordinating and administering all stages of the corporate internal audit lifecycle, including audit scheduling, planning, execution logistics, report generation, review and approval facilitation, corrective and preventive action (CAPA) tracking, and performance metric reporting. The position ensures audits are conducted in compliance with corporate policies, FDA QMSR, ISO 13485, MDSAP, EU MDR, and other applicable global regulatory requirements.
Proposal Writer - {{Business Development Drug Manufacturing}} RPM ReSearchProposal Writer - {{Business Development Drug Manufacturing}}MassachusettsCoordinates and collaborates with key internal stakeholders on resource allocation areas such as FTE’s (labor utilization), Capital, etc., to allow the program design, proposal generation, resource and timeline estimates, and pricing required for a robust and strategic project proposal. The Proposal Services Specialist works alongside business development and scientific-technical professionals to respond to inbound requests for proposals (RFPs), requests for information (RFIs), due diligence questionnaires (DDQs), and other proposal services support requests.
Physical Therapist IVYREHAB Network IncPhysical TherapistMiddletown, RI$85,000–$100,000 / yearIvy''s rewarding work environment allows collaboration and mentorship while maintaining autonomy and growth that is specific to each of our clinicians'' passions and expertise. Our Physical Therapists treat a diverse orthopedic caseload, with opportunities to develop or expand expertise in: Orthopedics & Post-Surgical Rehab.
Staff Engineer, Quality Design & Reliability Assurance Integra LifeSciencesStaff Engineer, Quality Design & Reliability AssuranceMansfield, MA$109,250–$149,500 / yearCollaborates with internal customers and external design and development partners, participating on cross-functional project teams through all phases of the product and process development through commercialization, and supports technical teams with planning, execution, reporting and communication of Design and Reliability Assurance work products and deliverables. * 8 years of experience of working within a medical device or other regulated industry with knowledge of Risk Management (ISO 14971 2019), EU MDR, MDD (Medical Device Directive), IEC 62366, ISO 13485 (Quality Management Systems), FDA QSR and cGMP.
Machinist Technician I (2nd Shift) Integra LifeSciencesMachinist Technician I (2nd Shift)Mansfield, MA$23.28–$31.46 / hourAll 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. Subject to the terms of their respective policies and date of hire, Employees are eligible for the following https://jobs.integralife.com/total-rewards/.
Cleanroom Assembly Packaging Operator I Integra LifeSciences Holdings CorpCleanroom Assembly Packaging Operator IMansfield, MA$19.19–$25.43 / hourThe Cleanroom Assembly Packaging Operator I will be responsible for using equipment including computer-controlled equipment to assemble and test components and products as well as operating various pieces of manufacturing equipment including heat treat furnaces, automated cleaning and passivation equipment, media blast and hand deburring equipment and tools to established specifications and requirements. The Manufacturing Operator 1 will be responsible for using equipment including computer-controlled equipment to assemble and test components and products as well as operating various pieces of manufacturing equipment including heat treat furnaces, automated cleaning and passivation equipment, media blast and hand deburring equipment and tools to established specifications and requirements.
Senior Engineer II - Quality Design & Reliability Assurance Integra LifeSciences Holdings CorpSenior Engineer II - Quality Design & Reliability AssuranceMansfield, MA$82,000–$113,000 / year5 years of experience of working within a medical device or other regulated industry with knowledge of Risk Management (ISO 14971 2019), EU MDR, MDD (Medical Device Directive), IEC 62366, ISO 13485 (Quality Management Systems), FDA QSR and cGMP. Fulfill design control requirements compliant: software specifications, detailed design files, design verification and validation test plans, risk management, DHF, protocols, and reports in accordance with company procedures, FDA and ISO guidelines.
NewSupplier Quality Engineer II Integra LifeSciences Holdings CorpSupplier Quality Engineer IIMansfield, MA$71,300–$97,750 / yearThe position is responsible for supplier audits, supplier performance monitoring, CAPA and nonconformance management, supplier change control, quality agreement management, and validation activities while ensuring compliance with FDA 21 CFR Part 820, ISO 13485, and other applicable regulatory requirements. The ideal candidate will have experience working in a regulated medical device or life sciences environment and possess a strong understanding of supplier quality systems, root cause investigations, and quality engineering principles.
Senior Engineer, Quality Design Assurance Integra LifeSciencesSenior Engineer, Quality Design AssuranceMansfield, MA$81,650–$112,700 / year5 years of experience of working within a medical device or other regulated industry with knowledge of Risk Management (ISO 14971 2019), EU MDR, MDD (Medical Device Directive), IEC 62366, ISO 13485 (Quality Management Systems), FDA QSR and cGMP. For this Sr I role, ideal candidate will be a Subject Matter Expert with ISO11607, 10993, and functional cascading system requirements to component drawings, balancing the use of Y14.5 with the needs of the business.
Senior Quality Systems Engineer Integra LifeSciencesSenior Quality Systems EngineerMansfield, MA$81,650–$112,700 / yearPrimary responsibilities include driving improvements to the QMS, having oversight of and ensuring compliance to the CAPA, NC and Quality Planning (QP) processes, and providing experienced quality assurance support to manufacturing and product development teams as well as lower-level Quality Engineers. + Bachelors in a scientific discipline required with minimum of 5 years' experience preferably in the medical device industry; strong analytical skills, exceptional writing and interpersonal relationship skills or combination of relevant work experience and education.
Strategic Account Director (Remote) Cengage LearningStrategic Account Director (Remote)MassachusettsRemoteThis role blends new business development with deep post‑sale ownership, focusing on long‑term partnership success, customer value realization, and sustained revenue growth across all accounts including Cengage Unlimited Institutional Access (CU), Equitable Access (EA), and Inclusive Access (IA) business models. Operating as the point of strategic ownership for assigned accounts, the Strategic Account Director leads forecasting, multi‑year account planning, contract strategy, renewals, and expansion efforts while serving as a trusted advisor to senior academic and administrative stakeholders.
Sr Cost/FP&A Accountant Integra LifeSciencesSr Cost/FP&A AccountantMansfield, MA$81,650–$112,700 / yearPrimary responsibilities are to: + Oversee the day-to-day management of accounting activities related to general ledger accounts, including but not limited to inventories, prepaids, and other key balance sheet accounts. + Participate in the monthly financial close process for the local ledger, including preparation of the monthly journal entries, Account reconciliations and analysis on general ledger account balances.
Director, Legislative Affairs Ryan, LLCDirector, Legislative AffairsProvidence, RIThe Legislative Affairs Director assists the Principal and the Advocacy Services Practice with directing, implementing, managing, coordinating, overseeing, and supervising multistate legislative efforts of the Firm, or the Firm's clients as needed. Computer Skills: To perform this job successfully, an individual must have intermediate knowledge of Microsoft Word, Access, Excel, PowerPoint, Outlook, and Internet navigation and research.
Horticulture Crew Supervisor Mariani Premier GroupHorticulture Crew SupervisorMassachusettsThis employer participates in E-Verify and will provide the Social Security Administration (SSA) and, if necessary, the Department of Homeland Security (DHS), with information from each new employee's Form I-9 to confirm work authorization. Mariani Enterprises LLC is committed to pay transparency and equity among all employees and provides employees with an environment where pay transparency and dialogue on compensation are allowed.
NewSenior Director, Benefit/Risk Medical Adviser To The Qppv Regeneron PharmaceuticalsSenior Director, Benefit/Risk Medical Adviser To The QppvUxbridge, MAYou will combine clinical judgement with qualitative and quantitative approaches, including patient preferences, real-world data and epidemiological evidence, while partnering with colleagues across Global Patient Safety, Regulatory Affairs, Clinical Development and other functions. Partner across safety, regulatory, clinical, quality, legal, commercial, local pharmacovigilance and product supply functions while contributing to governance and inspection readiness.