- Merck & Co. (Rahway, NJ)
- …to the Director responsible for this area, you will partake in medical device assembly and process development using semi-automated and automated equipment, ... as needed. Key Responsibilities: Experience with, and a fundamental understanding of medical device assembly equipment to enable development of product specific… more
- Merck & Co. (Rahway, NJ)
- …robust scientific methodology we collaborate to discover and develop the next medical breakthrough. Our Company's success is backed by ethical integrity, forward ... portfolio. Within Biologics and Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team… more
- Merck & Co. (Rahway, NJ)
- …required; advanced degree (Master's or PhD) preferred.Minimum of 10 years of experience in medical device or combination product engineering , with at least 5 ... Job DescriptionJob Summary: -The Director , Combination Product Commercialization is a key leadership...technical leadership in Technology Transfer and Design Transfer for medical device and combination product component manufacturing,… more
- Merck & Co. (Durham, NC)
- …Experience and Skills: Manufacturing - Injection Molding and Automated Assembly of Medical Device Components. Final Assembly and Packaging of Combination ... Delivery Systems and Devices within our Manufacturing Division (Associate Director ).-This role serves as a Virtual Plant Manager -...development and manufacturing for MDCP (21 CFR Part 4, Medical Device Reporting, ISO 13485:2016, EU … more
- Merck & Co. (Rahway, NJ)
- …stability manufacturing by designing, developing, and scaling-up the formulation, device , and manufacturing process.- Driving drug product design from the ... to transform drug delivery and manufacturing technology to positively impact patients.The Director of Oral Formulation Sciences will lead a team of scientists and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …of experience in GxP-regulated IT system implementation, validation, and compliance in pharma/biotech/ medical device industry - Required 4+ years of proven ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- TransMedics (Andover, MA)
- …(IEC 60601, RTCA DO-160, etc.). In-depth knowledge of and experience with medical device development across the entire product development lifecycle from ... utilization of donor organs in the US. As our Director of Electrical & Systems Engineering at...concept to commercialization. Class II or III Medical device experience under IEC 60601 Proven… more
- Intuitive (Sunnyvale, CA)
- …producibility, and cost Planning, decision-making and negotiation Experience navigating medical device risk analysis Required Education: Bachelor of ... Class II medical product experience Experience with FDA regulations and medical device design control Working knowledge of sterilization processes and… more
- Eli Lilly and Company (Indianapolis, IN)
- …better for people around the world. The Global Process Automation and Control Engineering (GPACE) function within the Engineering Tech Center is primarily ... and process control. In addition, GPACE champions the automation engineering discipline across manufacturing by providing global discipline leadership, training,… more
- Cognizant Technology Solutions (Chicago, IL)
- Experience Partner - Life Sciences (Pharma / BioTech / Medical Device ) Associate Director - Chicago/Midwest Remote Who we are: We are Cognizant Moment ... clinical/drug discovery, Global Pharmaceutical market and industry, including BioTech, Medical Device , Traditional Rx, enabling technologies and… more
- Jones Lang LaSalle IP, Inc. (Chicago, IL)
- …we have integrated our occupier businesses into a single global division. The Account Director role, which creates and drives the account plan to exceed the clients' ... expectations, creating opportunity for growth and renewal. The Team The Account Director will lead a team of talented individuals to deliver integrated, innovative… more
- Merz North America (Racine, WI)
- About the Business: Merz is a family-owned medical device and pharmaceutical company headquartered in Germany. Our Global Technical Operations based in WI ... can live better, feel better, and look better. The Director IT Operations plays a pivotal role in leading...to drive operational and security objectives. Knowledge of the Medical Device regulations (ISO13485, ISO 14971, 21CFR… more
- Merz North America (Franksville, WI)
- About Us: Merz is a family-owned medical device and pharmaceutical company headquartered in Germany. Our Global Technical Operations based in WI manufactures, ... better, feel better, and look better. A Brief Overview As the Director , Manufacturing Operations, you'll be the driving force behind strategic supplier partnerships,… more
- PTC (Boston, MA)
- …team to drive the strategy and roadmap for our Windchill Quality Management and Medical Device solutions, including key concepts such as ISO quality processes, ... prospective candidate should have a keen interest in quality engineering and the medical technology industry as...such as APQP, 8D, FRACAS and FMEA *Experience in medical device manufacturing and the ISO 13485… more
- Leica Biosystems (Miami, FL)
- …driving innovation and excellence in the Biopharma sector.This position reports to the Director , Regulatory Affairs and is part of the Global Regulatory Affairs and ... regulations on the development and registration activities for the respective medical productsDevelop and manage regulatory submissions (eg, 510(k), PMA, EU… more
- Atrium Medical (Hudson, NH)
- …the changes in compliance with Quality Systems Regulations (QSR), the Medical Device Directives, CMDR, and other International regulations. Participates ... compliance activities working under the direction of the Regulatory Affairs Director . Assists the Regulatory Affairs Director with regulatory strategy/plans… more
- Beckman Coulter Diagnostics (Miami, FL)
- …plus if you also possess:Experience working in FDA-regulated industries or medical device manufacturing environments.Professional certifications such as CQE, ... for Beckman Coulter Diagnostics can provide.This position reports to the Sr. Director of Global Supplier Quality responsible for global supplier quality strategy. If… more
- University of Utah (Salt Lake City, UT)
- …16 - May 15) Career-line faculty position in the area of Regulatory Affairs, Medical Device Design and Regulatory Science. The anticipated start date is August ... and strong interest in teaching Regulatory Affairs, Regulatory Science, and medical device design courses. Practical experience in regulatory affairs/regulatory… more
- Becton, Dickinson and Company (Brea, CA)
- … devices marketed in all regions throughout the world. Expertise in failure investigation and medical device CAPA process. Experience in medical device ... Summary Sr Design Quality Systems Manager reports to the Director , Quality Management, WWIPD. The Sr Design Quality Systems...of possible BD is one of the largest global medical technology companies in the world. Advancing the world… more
- Zscaler (San Jose, CA)
- …for our Digital Experience Monitoring (DEM) solution. Reporting to the Sr. Director of Product Marketing, you will be responsible for: Leading product marketing ... features into compelling customer value, including latency visualization, network analysis, device telemetry, and SaaS performance insights Defining buyer and user… more
