- Hologic (Marlborough, MA)
- Medical Device Reporting Specialist Marlborough, MA, United States We are seeking a detail-oriented and proactive Medical Device Reporting ... for treatment **Experience:** + 2-5 years progressive quality experience in Medical Device or related Industry. + Bachelor's Degree in Medicine, Nursing or… more
- Kelly Services (Portage, MI)
- ** Medical Device Labeling Specialist (QMS)** + **Location** : Portage, Michigan (49002) + **Duration:** 6 month assignment (Contract extension potential) + ... and healthcare staff in global markets. + Labels must comply with medical device regulations, standards, and business requirements. **Key Responsibilities** +… more
- Amgen (Cambridge, MA)
- …and transform the lives of patients while transforming your career. Engineer I - Medical Device Design Control Documentation Specialist **What you will do** ... Management - ISO 13485; Risk Management - ISO 14971; EU Medical Device requirements - Council Directive 93/42/EECStrong background in documenting requirements… more
- PCI Pharma Services (Bedford, NH)
- …our global network to pioneer and shape the future of PCI. The **QA Operations Specialist I - Medical Device Floor Support** is responsible for providing ... of Manufacturing and Visual Inspection activities for clinical and commercial medical device products in a GMP facility. The work scope includes on-the-floor… more
- Actalent (St. Paul, MN)
- …on sustaining engineering. The team is responsible for managing changes to medical devices after commercialization, ensuring that any changes in raw materials do ... standards. Responsibilities + Manage and sustain engineering changes for commercialized medical devices. + Ensure product integrity amidst changes in raw materials.… more
- Kelly Services (Dublin, CA)
- **Sr. Process Engineer ( Medical Device Transfer Specialist )** + **Location** : Dublin CA 94568 + **Duration:** 12 months (contract extension potential) + ... **MUST HAVE:** + Engineering - Electrical or Mechanical preferable. + Medical Device experience in manufacturing: preferably electrical mechanical devices.… more
- Fujifilm (Bismarck, ND)
- …activities. + Keep abreast of new legislation and enforcement matters relevant to the medical device industry as well as industry and compliance best practices. ... Degree. + 2 to 3 years of corporate compliance experience in the medical device and/or pharmaceutical industry and working knowledge of healthcare related… more
- Actalent (Davis, CA)
- …a candidate that has at least 2-5 years of regulatory experience within Medical Device Class II. MUST HAVE: Regulatory experience, Experience with international ... Job Title: Regulatory Affairs Specialist Must be LOCAL to Davis or at...Regulatory Affairs and Quality Assurance within the diagnostic or medical device industry. + In-depth knowledge of… more
- Henry Ford Health System (Detroit, MI)
- …Machine Learning Engineer Additional Information + Organization: Corporate Services + Department: Ascension MEDICAL DEVICE SECUR + Shift: Day Job + Union Code: ... to the Emerging Technology Security Manager, the AI Integrity Specialist is a technical role that works collaboratively across...Ford is one of the nation's most respected academic medical centers and is leading the Future of Health:… more
- West Pharmaceutical Services (Exton, PA)
- Senior Specialist , Regulatory Affairs - Medical Device Requisition ID: 69746 Date: May 13, 2025 Location: Exton, Pennsylvania, US Department: Regulatory ... regulatory requests. **Essential Duties and Responsibilities** + Develop and implement medical device regulatory strategies for West's administration and safety… more
Related Job Searches:
Device,
Device Specialist,
Medical,
Medical Device,
Medical Device Clinical Specialist,
Medical Specialist,
Specialist