- Merck (Rahway, NJ)
- …integrator of all device development activities including engineering design, engineering analysis and testing, medical device design controls, risk ... of product and process development in the (bio)pharmaceutical and/or medical device industries to set tactical and...other key of our company's functions. + Lead the Device Development Engineering Core teams focused on… more
- Takeda Pharmaceuticals (Boston, MA)
- …company that will inspire you and empower you to shine? Join us as an Associate Director, Medical Device Safety Specialist in our Cambridge, MA office. ... vital contributor to our inspiring, bold mission. **OBJECTIVES:** The Medical Device Safety Specialist ( Associate ...Engineering . + Minimum of 5 years' experience in device safety or device quality assurance roles… more
- Merck (Rahway, NJ)
- …**Job description** This position will be responsible for leading and implementing medical device and combination product design controls for both new ... **Job Description** ** Device Development Associate Principal Scientist -...years of related experience + Has broad knowledge of medical device development, design controls and risk… more
- Merck (Rahway, NJ)
- …or PhD) preferred. + Minimum of 8 years of experience in pharmaceutical, biologic, medical device or combination product engineering , with at least 4 ... **Job Description** **Job Summary:** The Associate Director of Device Technology is...injection molding, automation, complex assembly and packaging operations for medical device or combination product component manufacturing,… more
- Sanofi Group (Cambridge, MA)
- …and bring hope to patients and their families. The strategic vision of Sanofi's Global Medical Device and Packaging organization is to lead the industry in ... **Job title** : Associate Principal Device Engineer **Location:** Cambridge,...You will be responsible for concept development of innovative medical device technologies, from ideation to proof… more
- Lilly (Indianapolis, IN)
- …oversight for quality system activities performed by Quality Assurance in the medical device complaint handling area. To support implementation and maintenance ... complaint investigations associated with use, design, and manufacturing investigations for medical devices and drug/ device combination products + Maintain key… more
- Merck (North Wales, PA)
- …and international regulations and guidance for combination products (Drug and Drug Device combinations). The Associate Principal Scientist is responsible for the ... **Job Description** This Associate Principal Scientist position is equivalent to an...+ Provide detailed, global regulatory assessments for changes to device and drug- device combination products according to… more
- Lilly (Indianapolis, IN)
- …are determined to make life better for people around the world. As an ** Associate Director - Indianapolis Device Manufacturing Supply Chain, you'll** play a ... Manufacturing (IDM) provides for and enables the reliable supply of devices and device components. The Supply Chain Associate Director provides the leadership… more
- Lilly (Durham, NC)
- …to make life better for people around the world. The Quality Assurance Associate - Device Assembly & Packaging team provides daily oversight, assistance, ... revisions, validations, batch disposition, commissioning, and qualification activities. The Associate - Quality Assurance position is essential for maintaining GMP… more
- Lilly (Concord, NC)
- …Concord, North Carolina which will house warehousing & logistics, parenteral operations, medical device assembly, and packaging, QC laboratories, and support ... now is the perfect opportunity! During the project phase, the Operations Associate (OA) will support commissioning, qualification, and validation of the Device… more
- Lilly (Indianapolis, IN)
- …Brand Description:** The Sr. Operations Associate (OA) will report to an Associate Director in Device Assembly or Packaging operations. The OA will be ... keeping department leadership informed of issues. Coordination with maintenance, engineering , automation, validation and technical services on projects is critical… more
- Amgen (Cambridge, MA)
- …transform the lives of patients while transforming your career. Engineer I - Medical Device Design Control Documentation Specialist **What you will do** Let's ... In support of Amgen's mission to serve patients, the Device Engineering group at Amgen is a...- ISO 13485; Risk Management - ISO 14971; EU Medical Device requirements - Council Directive 93/42/EECStrong… more
- Compass Group, North America (Mooresville, NC)
- …instructions to refer a friend to this position. Job Summary SUMMARY The Medical Device Cybersecurity Analyst will be involved in response to cybersecurity ... Crothall Healthcare Position Title: Tech, Admin Associate Crothall Healthcare is a Compass One Company...and provide subject matter expertise with Crothall resources for medical device cybersecurity. ESSENTIAL DUTIES AND RESPONSIBILITIES:… more
- Fujifilm (Bothell, WA)
- …and maintain test framework and software instrumentation hooks for our new and existing medical device products, by developing within a pure Ruby script test ... the Software Process & Quality team of our Software Engineering department, you will create, improve, and maintain our...to ensure software functionality and quality of our complex medical ultrasound device products. These works will… more
- Lilly (Indianapolis, IN)
- …Q support for newly launched products as requested by manager. + Apply knowledge of medical device governing standards and regulations (eg, 21 CFR Part 4, Part ... Parts 210/211, Part 820, QSR, ISO 13485, ISO 14971, Canadian MDR, EU Medical Device Directive, JPAL) to ensure organizational capability of prospective contract… more
- Cognizant (Chicago, IL)
- **Experience Partner - Life Sciences (Pharma / BioTech / Medical Device )** ** Associate Director - Chicago/Midwest Remote** **Who we are:** We are Cognizant ... clinical/drug discovery, Global Pharmaceutical market and industry, including BioTech, Medical Device , Traditional Rx, enabling technologies and… more
- Jabil (Albuquerque, NM)
- …seeking an experienced Change Coordinator to join our dynamic team in the medical device manufacturing sector. The ideal candidate will have experience managing ... to be a trusted partner for the world's top brands, offering comprehensive engineering , manufacturing, and supply chain solutions. With over 50 years of experience… more
- Lilly (Durham, NC)
- …leadership to a team of QA Specialists, while reporting directly to the Associate Director - DAP and Warehouse Quality. The Quality Assurance Floor Supervisor ... QA oversight to night shift GMP operations in the Device Assembly and Packaging (DAP) area. The QA Floor...Representatives on quality and operational issues. Escalates issues to Associate Director - DAP and Warehouse QA, when necessary.… more
- Kelly Services (Irvine, CA)
- …experience OR + Associate 's degree with 6+ years of experience. + Medical device industry experience is highly preferred. Technical & Software Proficiency: + ... For over a century, Johnson & Johnson has been at the forefront of medical device and pharmaceutical manufacturing. As production demand reaches new heights, we… more
- Lilly (Indianapolis, IN)
- …keeping department leadership informed of issues. Coordination with maintenance, engineering , automation, validation and technical services on projects is critical ... involvement in teams as directed by the Manager. Partners with Operations Associate Director for business planning. **Minimum Requirements:** + 3-5 years minimum… more
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