- Merck & Co. (Rahway, NJ)
- Job Description Summary, Focus and Purpose The Senior Engineer in Device Technology is a key member of our Device Development & Technology Team, with ... medical devices and combination products globally.- Experience in design controls, device risk management, medical device , complex combination product kits,… more
- Eisai, Inc (San Jose, CA)
- …profile, we want to hear from you. The Senior Oncology Sales Specialist is responsible for meeting/exceeding sales goals through promoting Oncology therapeutic ... territory in a compliant and appropriate manner. The Senior Oncology Sales Specialist represents and promotes assigned brand(s) in the oral markets with approved… more
- Eisai, Inc (Milwaukee, WI)
- …your profile, we want to hear from you.The Senior Oncology Sales Specialist is responsible for meeting/exceeding sales goals through promoting Oncology therapeutic ... assigned territory in a compliant and appropriate manner. The Senior Oncology Sales Specialist represents and promotes assigned brand(s) in the IV and oral markets… more
- Aequor (Devers, TX)
- …industry.Prior cGMP experience in biopharmaceuticals, pharmaceuticals, and/or medical device industry is highly preferred.Experience in SAP implementation and ... deployment in Procurement & Supply Planning is highly preferred.Strong Proficiency with SAP and/or other ERP systems is preferred.Strong proficiency in Microsoft Outlook, Word, and Excel. Experience using Infinity desired.Demonstrated independence with minimal… more
- Novo Nordisk Inc. (Durham, NC)
- …years of validation related discipline experience in pharmaceutical or medical device industry required Experience in quality concepts including technical & ... compliance review of validation & quality documents required Experience in one or more core validation areas (equipment, cleaning, process, or computer validation) preferred Experience in cGMP documentation practices & regulations required Basic computer… more
- Cytiva (Miami, FL)
- …which makes everything possible.The Contamination Control & Sterility Assurance Specialist is responsible for ensuring the integrity of environmental monitoring, ... and sterility assurance processes in a highly regulated medical device environment.This role involves conducting laboratory analyses, maintaining critical equipment,… more
- Cytiva (Miami, FL)
- …the Danaher Business System which makes everything possible.The Contamination Control Specialist is responsible to provide expertise and oversight for sterility ... and sterility assurance within the pharmaceutical, biotechnology, or medical device industries.In-depth knowledge of regulatory requirements and industry standards… more
- Integrated DNA Technologies (IDT) (Miami, FL)
- …delivery of solutions that safeguard and improve human health.The Stability Program Specialist is part of the Quality Assurance, Therapeutics Gene Editing department ... in a regulated environment or GMP compliant environment (Pharmaceutical, Medical Device , OTC Drug, Cosmetic, etc.)Experience with basic statistical analysis, and… more
- Cepheid (Miami, FL)
- …Danaher Business System which makes everything possible.The Senior Quality Systems Specialist is responsible for functioning as Lead Internal Auditor to schedule, ... well as other applicable global regulatory requirements, including Medical Device Single Audit Program (MDSAP) participating regulatory authorities Provide… more
- HonorHealth (AZ)
- …because it does. Learn more at HonorHealth.com. Responsibilities Job Summary The Cardiac Device Specialist team member provides comprehensive care based on the ... Implantable Electronic Devices (CIED) management will be done under the direction of a Device RN Manager or Provider & the Practice Manager. A team member has… more
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