- 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
- Merck (West Point, PA)
- **Job Description** **Summary, Focus and Purpose** The Senior Engineer in Device Technology is a key member of our Device Development & Technology Team, with ... and combination products globally. * Experience in design controls, device risk management, medical device , complex combination...manner are at the core of this position. The Senior Engineer will routinely face competing priorities, and must… more
- West Pharmaceutical Services (Exton, PA)
- …US Department: Regulatory Affairs Description: **Thank you for your interest in our Sr Specialist , Regulatory PM (Evergreen) position. Applicants of this role ... Sr . Specialist , Regulatory Project Management (Evergreen...and planet through our sustainability efforts. **Job Summary:** This Senior Specialist , Regulatory Project Management (RPM) role… more
- Chenega Corporation (Albuquerque, NM)
- Sr . Messaging Specialist Albuquerque, NM Join our Talent Network Sr . Messaging Specialist Albuquerque, NM Are you ready to enhance your skills and build ... experience in supporting, managing and architecting enterprise email systems, mobile device management (ie, MaaS 360) and working knowledge of Lotus Notes/Domino… more
- L3Harris (Rochester, NY)
- …Friday off Job Description: L3Harris' Communication Systems segment is currently seeking a Sr . Specialist , Software Engineer to join our team. This position will ... at our Rochester, NY facility and offers a 9/80 work schedule. The Sr . Specialist , Software Engineer, designs, develops and extensively tests complex engineering… more
- Amazon (Bellevue, WA)
- …Frames. Working as part of the Medical Devices Operational Compliance Team (MD-OCC), the Sr . Regulatory Affairs Specialist will be working to build best in class ... - . Knowledge and understanding of guiding principles in device and drug development such as benefit/risk...used to drive multi-million dollar businesses and reporting to senior leadership - . Regulatory Affairs Certification (RAPS) -… more
- Abbott (Temecula, CA)
- …Our location in **Temecula CA,** currently has an opportunity for a ** Senior Procurement Specialist ** **What you'll do:** Responsible for developing and/or ... adhering to a strict standard of business ethics and integrity **The Opportunity** The Sr . Specialist may have delegated authority to commit company funds as… more
- Houston Methodist (Houston, TX)
- At Houston Methodist, the Sr . Current Good Manufacturing Practices (cGMP) Specialist is responsible for adherence to Standard Operating Procedures (SOPs) and ... proper guidance of junior level team members. As a senior member of the department, this position will actively...or willingness to work in a highly regulated radiopharmaceutical drug manufacturing facility in compliance with FDA cGMP guidance.… more
- Danaher Corporation (Coralville, IA)
- …working in a GMP compliant facility such as biotech, pharma ( drug product or drug substance) or medical device manufacturing is required. It would be a plus ... improving IDT Tx's Quality Management System in accordance with cGMPs for drug substance manufacturing (ICH Q7, 21CFR210/211) and regulatory guidance documents. +… more
- Lilly (Lebanon, IN)
- …The Quality Control Laboratory assures patients worldwide receive safe and efficacious drug and drug / device combination products through effective execution ... of product testing. Position Description: The Technician -Environmental Monitoring (EM) is responsible for providing utility and classified clean room monitoring support for LP2 Operations. The technician is also responsible for performing routine and… more
