- Merck & Co. (Rahway, NJ)
- Job DescriptionOur company's Device Development and Technology (DD&T) Team designs, develops, and commercializes novel biologic/drug/vaccine - device enabled ... their intended site of action.- The DD&T Team manages the development of the device constituent of our company's pipeline of combination products across a variety of… more
- Merck & Co. (Rahway, NJ)
- …formulation science, preclinical and clinical research.In-depth knowledge of medical device development, regulatory requirements, and quality standards, with ... Job DescriptionPosition Description: Early Device Program Strategy and Due Diligence The Principal...Strategy and Due Diligence The Principal Scientist of Early Device Program Monitoring & Due Diligence will play a… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJob Summary: -The Director of Device Technology Transfer is a key leadership role within the Device Development and Technology Organization. This ... launch in alignment with the company's business goals, and quality and regulatory compliance.-Essential Duties and Responsibilities:Program Leadership and Technical… more
- Aequor (Thousand Oaks, CA)
- …protocol development and execution Experience with combination product / medical device quality systems verification Process equipment knowledge - cell ... to have process/utility Engineering technical experience and not only be quality background driven. This engineering position supports projects that associated with… more
- Tris Pharma (Monmouth Junction, NJ)
- …knowledge or skills needed and/or licenses or certificates preferredCertified Quality Manager, Engineer or AuditorExperience with drug- device combination ... Junction, New Jersey, Tris has an immediate opening for a Manager, Quality Management Systems (QMS). Summary:The Manager, Quality Management Systems (QMS)… more
- Aequor (Thousand Oaks, CA)
- …combination of education and/or experience. Typically 2 plus years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical ... device industry. Evaluate documentation and operation according to company guidelines. Be self motivated, attentive to details and able to prioritize and meet… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …members. This position also monitors trends in functional performance via quality , time, and cost indicators, and makes recommendations for improvements. ... advanced experience working on Phase I-IV studies within the medical device and/or pharmaceutical industry across multiple therapeutic areas and actively… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of multiple myeloma.Legend Biotech is seeking QC Technician as part of the Quality Operations team based in Raritan, NJ. Company IntroductionFrom the very beginning, ... on the science. We came together as a team of experts, committed to quality , driven by excellence, and dedicated to experimentation. Though we faced many challenges,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Development Hub merges biotech speed and agility with large pharmaceutical company quality , resources, and stability, uniting the best of both worlds to develop ... content issues and questions arising during the writing process Assesses the quality of documents; provides findings and clear feedback to document authors… more
- Merck & Co. (Durham, NC)
- …Vaccines Manufacturing and Bulk Facilities (B101, B102, B130, B150 and B160), Quality Labs, Maintenance and Material Storage Facility (MMSF) and Teknika Facilities. ... and route engineering change requests through CMMS system.Manage pressure relief device spares for maintenance activities.This position is a 1st shift position… more
- Merck & Co. (Rahway, NJ)
- …other team members in delivering results collaborating with process, formulation and device .- You are expected to use your scientific expertise to find ingenious ... of connectivity between the functions supporting the pipeline (ie- quality , regulatory, clinical development; chemistry, manufacturing, and control (CMC); supply… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …evolve, so does our challenge to find better and more innovative ways to improve their quality of life. We're changing lives for a living. Are you ready to make a ... SOPs regarding collection, verification, and maintenance of adverse events (AE), device incidents, technical complaints, and other safety information for all Novo… more
- Merck & Co. (Austin, TX)
- …emerging technologies and industry best practices in network deployments, device onboarding, and automationAssisting in implementing DevOps and Infrastructure as ... Code principles to achieve velocity, better quality , and predictability in networking through automationContribute to process improvement efforts and opportunities… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Development Hub merges biotech speed and agility with large pharmaceutical company quality , resources, and stability, uniting the best of both worlds to develop ... and punctuation Demonstrated understanding of clinical research principles and the drug/ device development process Keen attention to detail to ensure the accuracy… more
- Strom Minnesota (Chaska, MN)
- …manufacturing high quality parts that are used in the medical device , agricultural and industrial industries. We've achieved this milestone because of our ... if necessary, create a new process sheet or set up instruction. Correct quality and cycle time deviations. Execute material handling functions as needed. Perform… more
- Regeneron Pharmaceuticals (East Greenbush, NY)
- We are currently looking to fill a Medical Device Quality Engineer position. This position will provide Quality Assurance oversight and ensure compliance in ... device risk management activities + You have a quality mind-set To be considered for this role you...work experience in combination device or medical device industry for each level: + Assoc Quality… more
- AbbVie (Irvine, CA)
- …Facebook, Instagram, YouTube and LinkedIn. Job Description Purpose: Manager, Medical Device Quality Systems is responsible for supporting the sustainment, ... improvement, and globalization of the AbbVie quality management system in support of AbbVie medical devices...to external regulators for ISO 13485 and other country-specific device audits under MDSAP. + Conducts Internal Audits to… more
- AbbVie (North Chicago, IL)
- …Facebook, Instagram, YouTube and LinkedIn. Job Description Purpose: Manager, Medical Device Quality Systems is responsible for supporting the sustainment, ... improvement, and globalization of the AbbVie quality management system in support of AbbVie medical devices...to external regulators for ISO 13485 and other country-specific device audits under MDSAP. + Conducts Internal Audits to… more
- Lilly (Durham, NC)
- …who are determined to make life better for people around the world. The Quality Assurance Representative for the Device Assembly & Packaging team provides daily ... Lead, mentor, and coach operations and support personnel on quality matters. + Ensure regular presence in device... quality matters. + Ensure regular presence in device assembly and packaging areas to monitor GMP programs,… more
- Amazon (Seattle, WA)
- …systems, workflows for Al-generated imagery, and lifestyle renders that scale in volume and quality . 3D device and lifestyle renderings play a critical role in ... CGI artists that understand Amazon customers and how to deliver high quality , photo-realistic device renders at scale. We respect each other and support each… more