Hybrid Global Regulatory Strategy Lead - Medical Devices
$130k - $150kHyperfine | AI-Powered Portable MRI
Hyperfine | AI-Powered Portable MRI is seeking a Senior Regulatory Affairs Specialist in Guilford, CT. This role involves advising regulatory strategies, ensuring compliance, and leading submissions for medical devices. The ideal candidate will have significant experience in regulatory affairs and must navigate the complexities of regulatory requirements. The position offers a hybrid work model and a competitive annual salary of $130,000 - $150,000. Candidates should possess a Bachelor’s degree and over 8 years in the medical device industry. #J-18808-Ljbffr Hyperfine | AI-Powered Portable MRI
$125k - $145k
A leading health technology company is seeking a Senior Regulatory Affairs Specialist in Guilford, CT or Palo Alto, CA. This hybrid role involves advising on regulatory strategy and ensuring compliance with domestic... ...requirements for medical devices. The candidate should...RegulatoryMedical device$130k - $150k
...revolutionize patient care globally through... ...Title: Senior Regulatory Affairs SpecialistLocation... ...Palo Alto, CA (Hybrid, 3 days/week)The... ...regulatory strategy for the company’s devices and ensures... ...and leadership.Lead the preparation... ...Strong knowledge of medical device labeling...RegulatoryMedical deviceWork experience placementWork at officeWorldwideWork visaNight shiftWeekend work3 days per week- ...Business Director to lead our newly created Emergency Medical Services... ...Director will oversee global commercial strategy, distributor management... ...fully remote or hybrid capable, locally... ..., operations, regulatory, and service) to... ...in EMS, medical devices, or related healthcare...RegulatoryMedical deviceCasual workRemote work3 days per week
- ...our Research & Development team in Guilford, Connecticut, onsite with hybrid flexibility. You will plan, design, develop, implement, and monitor validation strategies for next-generation medical devices. Collaborate across functions to create test protocols and deliver...Medical device
- ...in Guilford, CT seeks a Validation Engineer to join the R&D team onsite with hybrid flexibility. You will design, implement, and monitor validation strategies for next-generation medical devices, developing test protocols and reporting to support FDA and CE Mark...Medical device
- ...Guilford, Connecticut site, with hybrid flexibility. The Validation... ...and monitoring the validation strategies that support the release of next generation medical devices. In this role, you will... ...practices, company procedures, and regulatory requirements. Participates...RegulatoryMedical deviceWork at officeRemote work
$103.1k - $150k
...Description Site Quality Lead / Staff Quality... ...positive impact on a global scale. Join our colleagues... ...long-term quality strategy with day-to-day operational... ...with applicable regulatory and corporate quality... ...Quality experience in the medical device, IVD, biotechnology,...RegulatoryMedical deviceFull timeContract workTemporary workWork at officeDay shift$150k - $190k
Data Architect Hybrid / Full Time / Wayne,... ...influence enterprise-wide strategy, modernize data... ...across a global organization. ABOUT... ...Data Architect to lead the evolution of Novocure... ...operations, regulatory requirements, advanced... ..., biotechnology, medical device, or other...RegulatoryMedical deviceFull timeLocal area- ...in vitro diagnostic medical device and related infrastructure... ...in accordance with regulatory requirements specific... ...Actively leading and coordinating the... ...system level designs and strategies and leading definition... ...for local, remote or hybrid teams. Maintaining compliance...RegulatoryMedical deviceFor contractorsWork at officeLocal areaRemote work
- ...Compliance, and other areas as assigned. Hybrid Details: Onsite 3 days/week Duration:... ...role in a GxP-regulated biopharma, medical device, or similar industry. Bachelor s degree... ...retention schedules. Experience with GMP global regulatory requirements. Knowledge of archival...RegulatoryMedical deviceWork at office3 days per week
$107k - $123k
...to revolutionize patient care globally through transformational,... ...standards are achieved, applicable regulatory requirements are maintained,... ...and approval of Supplier Device History Records (DHRs) Collaborate... ...1 principles, and applicable medical device regulatory...RegulatoryMedical deviceWork visa$78k - $156k
...2026-08-28Abbott is a global healthcare leader that... ...spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and... ...and develops sales strategies for capital equipment... ...FDA) regulations, other regulatory requirements, company...RegulatoryMedical deviceFor contractorsWork experience placement$82k - $131.5k
...biorepository, oversight of regulatory and compliance... ...OnCore, or electronic medical record platforms. 2. Proficiency... ...large multi-site or global studies. Establish... ...and operational strategies and aspects of study that... ...contaminated medical supplies, devices and equipment,...RegulatoryMedical deviceWork at office$35 per hour
...role directly supports the production of medical device components and plays a critical part in... ...support consistent product quality and regulatory compliance. Job Type & Location... ...Aerotek is an Allegis Group company, the global leader in workforce and business solutions...RegulatoryMedical deviceWeekly payContract workTemporary work$260k - $300k
...speed of life.As a global leader in clinical... ...Senior Director, Medical & Scientific Affairs... ...business area and leading daily business... ...product development, regulatory submissions, and... ...and own the global strategies for health economics... ..., medical device, or pharmaceutical...RegulatoryMedical deviceFull timeRemote workWork from homeFlexible hours$130k
...initially, with potential hybrid flexibility after... ...with a premier, global med-tech... ...solutions for top medical Original Equipment... ...Manufacturing Engineer to lead process... ...ISO 13485 and FDA regulatory standards.Costing... ...ideally within medical device contract manufacturing...RegulatoryMedical deviceContract workRelocation packageFlexible hoursDay shift$143.5k - $165k
...to revolutionize patient care globally through transformational,... ...and monitoring of our fleet of devices and ingestion, storage, visualization... .... Implement comprehensive medical web application systems for... ...for internal and regulatory documentation. Participate in...RegulatoryMedical deviceWork experience placementRemote workWork visa$90k - $165.75k
...training and development, and regulatory compliance.The combined... ...Peabody Museum, one of the world’s leading institutions for research and... ...and preservation, and global heritage exchanges. Working with... ...implement the organization’s strategy. Understands and monitors external...RegulatoryFull timeWork at officeShift work- ...Middlefield, CT has been a global leader in designing and manufacturing... ...programs, spare parts strategies, and equipment reliability.... ...safety, environmental, and regulatory requirements, including LOTO... ..., semiconductor, aerospace, medical device, optics, or other high-technology...RegulatoryMedical deviceFor contractorsRelocation
- A leading medical device company is seeking an EMS Business Director to lead their newly created Emergency Medical Services Strategic Business... ...overseeing customer engagement, with options for remote or hybrid work from Guilford, CT. Candidates should have significant leadership...Medical deviceRemote job
- ...company in Guilford, Connecticut is seeking a VP of Software to lead software engineering for innovative diagnostic devices. This role involves overseeing the entire software development lifecycle, ensuring regulatory compliance, and collaborating across teams. The ideal...RegulatoryMedical device
$103.1k - $150k
...Description Site Quality Lead / Staff Quality... ...positive impact on a global scale. Join our colleagues... ...long-term quality strategy with day-to-day operational... ...with applicable regulatory and corporate quality... ...Quality experience in the medical device, IVD, biotechnology,...RegulatoryMedical deviceRemote jobFull timeContract workTemporary workWork at officeDay shift$105k
...here. Medtronic is a global leader in healthcare technology... ...developing innovative medical technologies that... ...focused outreach strategies in "hot" markets with... ...all company policies, regulatory guidelines, and ethical... ...roles within medical devices, medtech, healthcare,...RegulatoryMedical deviceContract workH1bWork at officeLocal areaImmediate startRemote workFlexible hours- ...improvement and innovation. Key Activities Lead and manage all plant operations,... ...compliance with safety, environmental, and regulatory standards. Drive operational... ...across the Packaging, Food and Beverage, Medical Devices, and Biotechnology industries. With 50+...RegulatoryMedical deviceFull time
- ...Engineering & Environmental Services seeks an Environmental Practice Lead to join its collaborative team in Boston, MA or New Haven,... ...compliance audits. You will lead a team, develop regulatory strategies, pursue new client opportunities, and contribute to the expansion...Regulatory
$68k - $120.5k
...study participants, and ensures regulatory and protocol requirements and... ...patient education and medical information to study participants... ...Duration Type Staff Work Model Hybrid Background Check Requirements... ...medical supplies, devices and equipment, surfaces, or air...RegulatoryMedical deviceFull timeWork at office- BCG Attorney Search seeks an Environmental Transactional and Regulatory Associate in New Haven, CT, with at least four years of experience... ...matters, with opportunities for professional development in a hybrid work environment. #J-18808-Ljbffr BCG Attorney SearchRegulatory
- ...Collaboration with paralegals and case managers is essential to ensure compliance with court orders and firm standards. The role emphasizes strategy development for mass tort matters, rigorous attention to procedural rules, and proactive coordination to advance settlements and...
- ...Manager, Expanded Access Program (EAP) to oversee global EAP portfolio operations and outsourced vendors, ensuring regulatory compliance and a high-quality experience for... .... You will partner with Clinical Development, Medical Affairs, Regulatory Affairs, Pharmacovigilance...Regulatory
- ...eligibility, and enroll participants while ensuring protocol and regulatory compliance. The role requires CT nursing licensure or... ...organizational skills, and experience with FDA/GCP guidelines. Hybrid work model and diverse responsibilities are offered. #J-18808-...RegulatoryWork at office
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