Global Regulatory Strategist - Medical Devices
$140k - $185kScience
Science is seeking a Senior Regulatory Specialist to drive global regulatory strategies for our medical devices. This crucial role requires expertise in FDA submissions and EU MDR compliance to assure that our innovations reach patients safely. The position offers a competitive salary range of $140,000 to $185,000 annually, alongside equity and comprehensive benefits to support the well-being of our employees. #J-18808-Ljbffr Science
- A global healthcare leader is seeking a Regulatory Affairs Manager in Alameda, CA. This role involves end-to-end regulatory support within the Diabetes... ...The ideal candidate has significant experience in medical devices and possesses strong organizational as well as scientific...RegulatoryMedical device
- ...powered cardiac and pulmonary detection tools to market globally by leading regulatory strategy across the full product lifecycle. The Director... ...(FDA 510(k)/De Novo, CE Mark, Health Canada, PMDA) for medical device hardware and SaMD products, directly authoring technical...RegulatoryMedical device
- ...operations team and oversee end‑to‑end study execution for Class III medical devices. You will guide protocol development, budget planning, start... ...activation and vendor oversight while maintaining strict regulatory compliance. You will partner with hospitals, investigators,...RegulatoryMedical device
- Abbott is hiring a Senior Specialist for the Medical Events Group based in Alameda, CA. This role focuses on managing medical device reports and ensuring compliance with regulatory authority standards. The ideal candidate will have a Bachelor’s Degree in a related field...RegulatoryMedical device
$169.22k - $253k
...Position Summary The Director, Global Product Quality – Manufacturing Product Quality... ...in a controlled way in accordance with regulatory expectations and applicable cGMP/GDP quality... ..., or a related field. Experience with medical devices/combination products. At least 8 years...RegulatoryMedical deviceContract workTemporary workLocal areaFlexible hours$20.25 - $22.28 per hour
...Our client, a leader in the medical device manufacturing industry, is seeking a Light Assembler... ...manufacturing instructions, SOPs, and regulatory standards such as Federal QSR and ISO 1... ...® (NYSE: MAN), the leading global workforce solutions company, helps organizations...RegulatoryMedical deviceHourly payTemporary workMonday to FridayShift work- A global healthcare leader is seeking a qualified individual in Alameda, CA, to manage design control and quality oversight for medical devices. This role emphasizes compliance with regulatory standards while enhancing digital solutions for diabetes care. Candidates should...RegulatoryMedical device
- ...adaptive algorithms, and assistive devices to translate neural intent... ...re looking for a Director of Regulatory Affairs for our office in... ...outcomes. Define and own the global regulatory strategy, setting... ...experience in Regulatory Affairs for medical devices. 4+ years of...RegulatoryMedical deviceFull timeWork at office3 days per week
$40 - $45 per hour
Job Title: Regulatory Affairs Associate Location: Alameda, CA Work Arrangement: 100% Onsite... ...of experience in a regulated industry (Medical Device, Pharmaceutical, Nutrition, or Food).... ...with any employers without sponsorship. #J-18808-Ljbffr ManpowerGroup Global, Inc.RegulatoryMedical deviceHourly pay- ...validated, and maintained in compliance with regulatory, corporate and divisional requirements.... ..., validation, use, and maintenance of medical device software. Coordinate activities with... ...Insurance ~401(k) Abbott is a global healthcare leader that helps people...RegulatoryMedical deviceTemporary workFor contractorsFlexible hours
- ...Clinical Research Associate II Abbott is a global healthcare leader that helps people... ...and products in diagnostics, medical devices, nutritionals and branded generic medicines... ..., department procedures and applicable regulatory requirements. Responsible for assisting...RegulatoryMedical deviceContract workInterim roleWork at officeFlexible hours
$81.5k - $141.3k
...Abbott is a global healthcare leader that helps people live more fully at all stages... ...businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...that comply with brand standards and regulatory requirements. Manage the print and...RegulatoryMedical deviceWorldwide$90k - $180k
.... It involves reviewing complaints for regulatory compliance and patient safety impact, determining... ...assessment, and ensuring adherence to global standards such as ISO 13485 and FDA... ...and other global requirements. Write Medical Device Reports, MedWatch, Vigilance, and other...RegulatoryMedical device$114k - $228k
...Abbott Overview Abbott is a global healthcare leader that helps people live more fully... ...technologies spans diagnostics, medical devices, nutritionals, and branded generic medicines... ...critical role in ensuring product quality, regulatory compliance, and scalable delivery. What...RegulatoryMedical deviceWorldwide- ...A leading IT staffing company in Emeryville is looking for a qualified candidate to support the maintenance of their Global Regulatory Affairs filing system and RTS database. The role emphasizes effective organization, knowledge of compliance, and project execution skills...RegulatoryWork at office
$114k - $228k
...Employees can qualify for free medical coverage in our Health... ...scientists. The Opportunity This Regulatory Affairs Manager - APAC position... ...APAC region, creating robust global regulatory strategies,... ...prepare, and review medical device or IVD submissions to regulatory...RegulatoryMedical device- ...seeking a Quality Engineer II responsible for developing and implementing quality system elements to ensure product quality and regulatory compliance. You will collaborate with multiple teams to qualify products and improve testing methodologies. The role requires 2+...RegulatoryMedical device
$140k - $185k
...questions and most serious unmet medical needs. We work to restore... ...treatment options, creating devices aimed at restoring vision, cognition... ...Science Foundry. The Senior Regulatory Specialist will serve as the... ...domain. This role will drive global regulatory strategies for our...RegulatoryMedical deviceFull timeLocal areaRemote workFlexible hours- ...verification and validation across cloud and mobile platforms within a regulated medical device environment. This role is based in Alameda, CA and focuses on ensuring product quality and regulatory compliance throughout development. You will own end-to-end verification,...RegulatoryMedical device
$90k - $180k
Abbott is a global healthcare leader that helps people live more fully at all stages... ...businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...standards, ensuring compliance with regulatory and internal requirements. This is an...RegulatoryMedical deviceWorldwide$100 - $130 per hour
...an AI Platform Architect within a medical technologies firm. This is an exciting opportunity to work for a global leader in life‑saving medical devices with a strong corporate culture and... ...processes for AI/ML systems Clinical/regulatory data workflows Experience...RegulatoryMedical deviceHourly payContract workTemporary workLocal area- Exelixis is looking for a Regulatory Affairs professional in Alameda, California, responsible for developing and implementing global regulatory strategies. You will interact with regulatory authorities, oversee submissions, and ensure compliance with health regulations...Regulatory
- ...Programming to lead a team of statisti cal programmers supporting medical device clinical research. You will drive programming standards,... ...study outputs, and collaborate with Statistics, Data Management, Regulatory, and Clinical Study Management teams. You will develop...RegulatoryMedical device
$197.3k - $394.7k
About Abbott Abbott is a global healthcare leader that helps people live more fully. With products in diagnostics, medical devices, nutritionals, and branded generic medicines, we serve... ...internal functions such as BTS/IT, Regulatory, Quality, Commercial, and Global Strategic...RegulatoryMedical device- Exelixis is seeking a Regulatory Affairs specialist responsible for developing and implementing global regulatory strategies to align with corporate goals. The role includes ensuring the timely submission of regulatory documents, managing cross-functional teams, and maintaining...RegulatoryWork at office
$100k - $200k
Abbott is a global healthcare leader that helps people live more fully at all stages... ...businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...This Principal International Regulatory Operations Specialist will work on‑site...RegulatoryMedical deviceWorldwide- Eko is seeking a Director of Regulatory Affairs to lead global strategy for SaMD and hardware. You will own FDA/CE/Health Canada submissions, shape regulatory pathways, and partner with R&D, Quality, and Commercial teams to accelerate compliant market access. You will build...Regulatory
$114k - $228k
Abbott is a global healthcare leader that helps people live more fully at all stages... ...businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...market trends, consumer behaviors, regulatory environments, and competitive landscapes...RegulatoryMedical deviceWork at officeWorldwide- ...America Pharmaceutical Inc. is a global healthcare company with the... ...products to meet unmet medical needs and nutraceutical products... ...of pharmaceutical or medical device sales experience. ~ Prior experience... ..., an understanding of regulatory standards, and the ability to...RegulatoryMedical deviceTemporary workLocal areaWorldwideFlexible hoursNight shift
$130.7k - $261.3k
...Abbott is a global healthcare leader that helps people live more fully at all stages... ...businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...standards. Strong working knowledge of regulatory requirements for US, EU (EU MDR), and...RegulatoryMedical deviceWork experience placementShift work
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