Job Summary: The Senior Quality Specialist will be part of the Quality Assurance Department and will support Supplier Management activities at the Ridgefield site. This role is responsible for managing supplier-related quality processes, i...
Summary: The Senior Quality Specialist will be part of the Quality Assurance Department and will support Supplier Management activities at the Ridgefield site. This role is responsible for managing supplier-related quality processes, inclu...
Responsibilities: Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs. Be responsible for overall project delivery, including clinical trial reports and other regulatory submission delivera...
(M.S., MPH, Ph.D., or similar degree) in the health sciences, lifesciences, clinical sciences or biomedical engineering...
Job Description: We are seeking a detail-oriented Field Action Remediation Specialist to implement remote software and firmware deployments, configure devices in RSS, and perform other remediation activities. This role requires deep techn...
management, particularly in the oncology field. Requirements: Bachelor's degree in LifeSciences, Computer Science...
Roles & Responsibilities: 6+years of relevant experience in design utilizing 3-D modeling / drafting. 2+years of recent Revit Design Experience. 2+years of semiconductor experience. Proficiency in AutoCAD. Knowledge ...
successful 510(k) clearances and CE marking is required Strong understanding of medical device product life cycle and regulatory...
Job Summary: Manufacturing Project Manager responsible for leading, governing, and optimizing a diverse portfolio of strategic projects within a regulated medical device manufacturing environment. The role focuses on end-to-end project l...
Summary: Senior Process Engineer to support process and utility systems within a regulated biopharmaceutical manufacturing environment at our Holly Springs site. This role is fully onsite and requires strong hands-on technical expertise w...