Senior Facilities Maintenance Technician Integra LifeSciences Holdings CorpSenior Facilities Maintenance TechnicianBraintree, MA$29.86–$40.91 / hourThe Senior Facilities Maintenance Technician is responsible for maintaining, troubleshooting, and repairing both facility systems and production equipment supporting a regulated medical device manufacturing environment, including ISO-classified cleanrooms. Maintain and repair facility systems including HVAC, cleanroom AHUs, HEPA filtration, boilers, chillers, compressors, wastewater, and building automation systems.
EHS Specialist Integra LifeSciences Holdings Corp.EHS SpecialistBraintree, MA$71,300–$97,750 / yearThe EHS Specialist partners with operations, facilities, engineering, and leadership teams to proactively identify hazards, reduce environmental impact, and improve overall workplace safety and compliance performance. Operating within a GMP-regulated environment, the EHS Specialist partners closely with Facilities, Manufacturing, Quality, and Engineering to ensure that safety and environmental controls are effectively integrated into daily operations.
Director, Supplier Quality Engineering ZOLL MedicalDirector, Supplier Quality EngineeringChelmsford, MassachusettsRemote$190,000–$210,000 / yearThe position oversees both day-to-day supplier quality activities and the development of long-term supplier quality strategies, processes, and organizational capabilities that improve supplier performance, reduce risk, and lower the Cost of Poor Quality (COPQ) at suppliers. The Director of Supplier Quality Engineering reports to the Vice President of Procurement and provides strategic and operational leadership for the Supplier Quality Engineering organization supporting manufacturing operations in the United States and China.
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.
Facilities Engineering Technician II Integra LifeSciences Holdings CorpFacilities Engineering Technician IIBraintree, MA$26.21–$35.38 / hourThe Facilities Engineering Technician II is responsible for performing preventive maintenance, troubleshooting, repair, installation, and continuous improvement activities on manufacturing equipment, production machinery, and facility support systems. Experience supporting automated manufacturing equipment in medical device, pharmaceutical, biotechnology, or other regulated manufacturing environments preferred.
Sr Principal Engineer, Product Development Integra LifeSciences Holdings Corp.Sr 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 Oracle EBS Finance Functional Lead Integra LifeSciences Holdings Corp.Senior Oracle EBS Finance Functional LeadMansfield, MA$109,250–$149,500 / yearThe 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.
Supervisor Quality Control, Analytical Laboratory Integra LifeSciences Holdings Corp.Supervisor Quality Control, Analytical LaboratoryBraintree, MA$81,650–$112,700 / yearOversee and coordinate analytical testing of raw materials, in-process materials, finished products, validation samples, stability samples, and special studies in support of manufacturing operations and product release. Ensures compliant laboratory operations, data integrity, testing execution, inventory control, personnel development, and inspection readiness while partnering with Manufacturing, QA, Engineering, Product Development, and external laboratories.
Supplier Quality Engineer II Integra LifeSciencesSupplier Quality Engineer IIMassachusettsThe 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.
Engineer II, Quality Integra LifeSciences Holdings CorpEngineer II, QualityBraintree, MA$71,300–$97,750 / yearThe Quality Engineer II (QE II) is responsible for independently supporting manufacturing and engineering operations to ensure the manufacture of safe, compliant, and high‑quality medical devices. This role maintains and improves quality system effectiveness through ownership of investigations, CAPAs, risk management activities, and validation support, while ensuring compliance with applicable regulatory requirements and corporate policies.
Director, Regulatory Writing Entrada TherapeuticsDirector, Regulatory WritingBoston, MassachusettsRemote$220,000–$249,711 / yearReporting to the Senior Vice President, Regulatory Affairs, the successful candidate will support the development of strong internal processes, be the key liaison with external writing providers, serve as a lead author and document specialist, and support documentation planning and submission activities. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51).
Corporate Counsel MKS IncCorporate CounselAndover, MA$155,250–$258,750 / yearThe successful candidate will report to the Company's Vice President, Associate General Counsel & Secretary, and will work on a team with responsibility for a broad range of securities, corporate governance, and other corporate legal matters, including SEC disclosure, debt refinancings/restructurings, equity plan management, tax reorganizations and global subsidiary management. 5+ years' focused experience with securities and corporate governance matters, developed through advising public company clients at a large law firm and/or supporting the securities function of a public company as an in-house lawyer.
NewDirector/Senior Director, Human Resources, Commercial Xenon PharmaceuticalsDirector/Senior Director, Human Resources, CommercialNeedham, MassachusettsThe role advises leaders on organizational structure, workforce planning, leadership capability, talent strategies, and organizational readiness while ensuring the organization has the capabilities, talent, and workforce plans required to support successful commercialization. Our Total Rewards program includes base salary, target bonus, and stock options, as well as a full range of benefits including medical, dental, vision, short-& long-term disability, accidental death & dismemberment, and life insurance programs, Employee Assistance Program, travel insurance, and retirement savings programs with company matching contributions.
NewSenior Medical Director, Clinical Development (Psychiatry) Xenon PharmaceuticalsSenior Medical Director, Clinical Development (Psychiatry)Needham, MassachusettsExperience with developing study concepts for clinical development and clinical trial designs with cross functional input, including biostatistics, observational research and patient reported outcomes in Phase 3 clinical trials experience, including experience with clinical trials from concept to clinical study report is required. The Senior Medical Director, Clinical Development will have medical knowledge of psychiatry and preferably neurology, recent development advances in psychiatric therapeutics landscape, relevant drug development experience, be a collaborative, inspirational, resilient leader, have a broad strategic view of therapeutic area and be well-versed in high quality trial execution.
NewDirector/Senior Director, Corporate Communications Xenon PharmaceuticalsDirector/Senior Director, Corporate CommunicationsNeedham, MassachusettsIn partnership with the Senior Vice President of Corporate Affairs and the broader Corporate Affairs team, this role will work with corporate, commercial, medical, and senior leaders to execute the Corporate and Product Communications strategy, and effectively develop messaging and communications around our clinical, regulatory, and commercial progress for various stakeholder groups, including investors and media, healthcare professionals, and the patient community. Collaborate with Corporate Affairs, the Executive Leadership team, and leaders in Commercial and Medical Affairs to craft clear, consistent messaging and execute communications strategies related to company strategy, the late-stage/future commercial product portfolio, and milestones, including regulatory, commercial and data milestones for azetukalner.
Senior Quality Compliance Specialist Integra LifeSciencesSenior Quality Compliance SpecialistBraintree, MA$81,650–$112,700 / yearBachelor's degree in Engineering, Life Science, or a related field with 5+ years' experience in QA/Compliance within the medical device or similar industry or equivalent education and years of experience. This position will support the Quality Compliance team and supports the site CAPA program, Quality Management Review preparation, Quality metrics, and the internal audit program.
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/.
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.
NewCleanroom Assembly Packing Operator Integra LifeSciences Holdings CorpCleanroom Assembly Packing OperatorMansfield, MA$19.19–$25.43 / hourThis Manufacturing Operator - Assembly & Packaging (Neurosurgical Perforators) Assembled precision neurosurgical perforators and related medical devices in a controlled cleanroom environment following detailed work instructions and engineering specifications. Manufacture 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.
Medical Assistant UMass Memorial HealthMedical AssistantWorcester, Massachusetts$20.60–$32.82 / hourExceptional patient care, academic excellence and leading-edge research make UMass Memorial the premier health system of Central Massachusetts, and a place where we can help you build the career you deserve. Under the direction of the appropriate licensed clinician, the Medical Assistant I (MA I) provides clinical care and performs clerical duties to support office/clinic functions.