- Merck & Co. (Rahway, NJ)
- …to ensure compliance, scientific excellence, accuracy and completeness of submissionsPartner with Device Development, Device Quality , and other Drug ... Job DescriptionAs the Director/Principal Scientist in Devices and Drug- Device Combinations CMC (Chemistry, Manufacturing & Controls), you will report to the Director… more
- Merck & Co. (Rahway, NJ)
- …medical device and/or combination product space.In-depth knowledge of medical device development, regulatory requirements, and quality standards, with a ... Job DescriptionThe Associate Principal Scientist of Device Technology Assessment and Early Development will spearhead early-stage device technology evaluation… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Company's Device Product and Process Development (DPPD) Team is seeking a hands-on device characterization and design focused scientist.This ... will be responsible for technical interrogation of the various drug delivery device technology platforms supporting our pipeline to identify risks (ie when/how will… more
- Aequor (Durham, NC)
- …final assembly procedures to reduce build time and/or costs. Work closely with Quality Control Specialist to address device repairs. Assist manufacturing and ... equipment changes and ideas to improve the overall functionality and/or quality of operations between engineering and manufacturing. Work closely with engineering… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- Position SummaryThe Quality Engineer is responsible for overseeing the health of the manufacturing processes. This starts with proper risk analysis in manufacturing ... risk in process validations, and continues with overseeing risk using statistical quality control during manufacturing. In addition, addressing known issues with a… more
- Aequor (Thousand Oaks, CA)
- …available - admin hours 8-5 Mon - Friday. Ideal candidate: Experience with quality management systems and 5&plus YOE. Nice to have: Veeva knowledge. Ex candidates ... whether the complaint is associated with an adverse event or medical device , documentation of follow-up communication to complainants for additional information or… more
- Merck & Co. (Rahway, NJ)
- …(PSCS) deliverable which is the development of robust compositions, processes and device / packaging that enable patient centric products for patients. The successful ... team environment with key stakeholders across the organizations such as Quality , Regulatory CMC, and technical functions, to ensure timebound progression of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …teams, clinical safety and pharmacovigilance, CROs, and partners to ensure high quality coding deliverables are on time to support drug development processes and ... regulatory requirements. This position has experience working within the medical device and/or pharmaceutical industry across complex disease areas, and experience… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …together to contribute to a better tomorrow for our patients. Ethics and quality are held in the highest regard, and a patient-focused mindset guides everything ... assigned new capital improvement projects. Primary the system administrator and quality system interface for Siemens Building Management System (BMS) and… more
- Aequor (Cincinnati, OH)
- …equipment for the cGMP manufacture, particularly in pharmaceutical and medical device industries. Individual will work closely with and/or lead cross-functional ... teams including R&D, MS&T, Operations, Quality , and EHS to implement capital projects. Individual will be the host for vendors while onsite and ensure all… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …Engineer (Clean Utilities), you will provide cross-functional support to operations, maintenance, quality and project teams for site GMP utilities. You will be ... as well as closely monitoring the existing systems with respect to quality of final product and efficiency of operation. Responsibilities will include:Strong… more
- Merck & Co. (Rahway, NJ)
- …commercialization. -Our development teams ensure robust composition, primary packaging/ device , and process selection through deep fundamental understanding and ... for CMC.- Strong understanding of integration and partnering with Quality , Regulatory, Operations, Non-clinical, Clinical, and other functional areas.Demonstrated… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Digital Device Quality Expert - SaMD **Location:** Cambridge, MA **About the Job** At Sanofi, we're committed to providing the next-gen healthcare ... AI responsibly to search deeper and solve sooner than ever before. The Device Quality Expert will be accountable for the Software Quality Engineering, Risk… more
- AbbVie (North Chicago, IL)
- …Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose The Sr. 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
- Astrix Technology (St. Paul, MN)
- **Medical Device Quality Technician** Manufacturing St. Paul, MN, US Pay Rate Low: 22 | Pay Rate High: 27 + Added - 27/12/2024 Apply for Job _Our Quality ... is a great opportunity to work for a Medical Device company with an excellent working environment that offers...programs, etc.) + Safe work environment! + Growth opportunities! ** Quality Technician Daily Tasks** : + Set-up, adjust, align,… more
- Lilly (Indianapolis, IN)
- …is $118,500 - $173,800 **Position Brand Description:** The IDM (Indianapolis Device Manufacturing) Quality Assurance Associate Director is primarily responsible ... for quality assurance and quality control oversight of device contract manufacturing (CM) organizations including molding, sub-assembly and assembly… 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 (Sunnyvale, CA)
- …key features for device makers. Basic Qualifications - 6+ years of quality assurance engineering experience - 4+ years of delivering test automation, test tools, ... you will be responsible to innovate and drive new Quality initiatives, establish new test methodologies, frameworks and processes...new test methodologies, frameworks and processes for testing new device and OS, find ways to leverage and scale… more
- Integra LifeSciences (Boston, MA)
- …in a team environment. + Quality Engineering/ Quality Compliance/ Quality Assurance experience in the Medical Device or similar FDA regulated industry. ... outcomes and set new standards of care. The Staff Quality Engineer is a subject matter expert responsible for...5-7 years' direct QE experience in a regulated med device , life sciences or pharma industry with direct experience… 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
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