Fda Regulations Jobs in Somerville, NJ
Fda Regulations Jobs in Somerville, NJ

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Were not yesterdays IT department were Digital Technology. The world around us keeps changing and so do we. Were redefining what it means to be IT with a mindset centered on transformation experience AI-driven automation innovation and growth. Were all about delivering delightful secu More...
Were not yesterdays IT department were Digital Technology. The world around us keeps changing and so do we. Were redefining what it means to be IT with a mindset centered on transformation experience AI-driven automation innovation and growth. Were all about delivering delightful secu More...
Were not yesterdays IT department were Digital Technology. The world around us keeps changing and so do we. Were redefining what it means to be IT with a mindset centered on transformation experience AI-driven automation innovation and growth. Were all about delivering delightful secu More...
Clinical Research Project Manager Ii
Site: The General Hospital CorporationMass General Brigham relies on a wide range of professionals including doctors nurses business people tech experts researchers and systems analysts to advance our mission. As a not-for-profit we support patient care research teaching and community More...
Were not yesterdays IT department were Digital Technology. The world around us keeps changing and so do we. Were redefining what it means to be IT with a mindset centered on transformation experience AI-driven automation innovation and growth. Were all about delivering delightful secu More...
Title: Senior Director Technical Excellence Location: Washington DC or EGPAF Presence Country AfricaReports To: Vice President Program Management & Technical Excellence Classification: Full-time exemptClosing Date for Applications: Wednesday September 10 2025The Senior More...
Salary: $80000 - 90000/yearWe are seeking a highly experienced and detail-driven Quality Manager to lead quality assurance and quality control functions in an FDA-regulated manufacturing environment. The ideal candidate will ensure compliance with cGMP FDA ISO 13485 (if applicable) an More...
The Associate Director Statistics - Oncology provides statistical leadership for clinical development and life-cycle management strategies for assigned projects. Specific areas of work may include clinical trials patient safety and global medical affairs (GMA). The Associate More...
This position is responsible for designing planning and executing statistical components of plans for research studies that prove the clinical economic and humanistic value of pharmaceutical assets. Position uses sound statistical methodology to conduct studies develops/or applies sta More...
Whats In It for You:This is an exciting leadership opportunity for a person with passion and talent. The company believes that medical writing is a science that continuously evolves with new regulations and technologies. The role provides the ability to influence company leaders More...
About The Position The KIPP Foundation is seeking a Director of Transformation to drive strategic change and innovation across its operations. The Senior Director will be responsible for leading strategic transformation efforts across KIPP Foundation teams (i.e. Finance Schools T More...
AECOM is seeking a Senior CEQA/NEPA Manager for one of our offices in Sacramento CA. This job is open to remote work.JOB SUMMARYThis role provides critical oversight and coordination of environmental processes to ensure timely delivery of project clearances. This role supports the dev More...
The Senior Manager Regulatory Advertising and Promotion N.A. will be responsible for ensuring that product and disease communications comply with applicable laws regulations Sobi policies and regulatory requirements for both promotional and non-promotional materials related to assigne More...
Travel: 10% TravelThe Associate Director of Virtual Health will play a key leadership role in the development implementation and oversight of virtual care services across the organization. This individual will be responsible for supporting operational excellence driving clinical quali More...
Under the general direction of the Vice President manages the day-to-day operations and staff responsible for both external and internal engagement on all California state regulatory matters. For external engagement manages the ISOs participation in processes at the Califo More...
This role is located in Somerville MA - We are a hybrid work environment and are in the office 3 days/per week.Tulip the leader in frontline operations is helping companies around the world equip their workforce with connected apps leading to higher quality work improved efficiency an More...
Senior Manager Ngs Bioinformatics
Site: Mass General Brigham IncorporatedMass General Brigham relies on a wide range of professionals including doctors nurses business people tech experts researchers and systems analysts to advance our mission. As a not-for-profit we support patient care research teaching and communit More...
Senior Regulatory Affairs Manager OncologyPosition SummaryThe Senior Regulatory Affairs Manager - Oncology will provide direct regulatory support for Oncology IVD/CDx products (Guardant360 CDx and future products such as Tissue IVD/CDx) in all stages of the product lifecycle. Th More...
The Senior Regulatory Affairs Manager - Screening will provide direct regulatory support for IVD cancer screening products (Shield CRC and future blood-based cancer screening tests) in all stages of the product lifecycle. This role will actively lead and support development and implem More...
Senior Regulatory Affairs Manager OncologyPosition SummaryThe Senior Regulatory Affairs Manager will provide direct regulatory support for Oncology IVD/CDx products (Guardant360 CDx and future products such as Tissue IVD/CDx) in all stages of the product lifecycle. This role will act More...
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