- Fujifilm (Boston, MA)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... + Analyzes and designs clinical workflow and utilizes change management techniques tofacilitate process improvement to include: + Order Entry and creation as well as… more
- Fujifilm (Boston, MA)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... efficiently uses the FUJIFULM knowledge resources available to help in the troubleshooting process . + Collaborates with peers and other team members when working on… more
- ConvaTec (Lexington, MA)
- …activities to develop new products as well as examine the interaction between our medical device components and the biological tissues they contact. The role ... Pioneering trusted medical solutions to improve the lives we touch:...of data-driven decision making for the Biointerfaces and Regenerative Engineering team. **Key Responsibilities:** Responsible for conducting and/or managing… more
- Fujifilm (Boston, MA)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... the troubleshooting of issues and follows the TAC escalation process to move cases to the next level engineer....articles. + Maintains an expert working knowledge of current medical imaging products and related technologies. + Engineers must… more
- Actalent (Billerica, MA)
- …work instructions Ability to read and interpret documents related to medical device sterilization and cleanrooms Including: International standards regulations ... Expertise in cGMPrsquos and quality systems as related to terminally sterilized medical devices. Knowledge in compendial AAMI USP ISO methodologies and techniques… more
- Takeda Pharmaceuticals (Lexington, MA)
- By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... Although the role supports all modalities, expertise in small molecule process and product development is a prerequisite. + **Inbound** licensing/partnering… more
- Mentor Technical Group (Boston, MA)
- …the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, ... calculation + Experience in Calibration system assessment + Strong knowledge in process tolerance evaluation. + Process Instrumentation/ Calibration to manage… more
- Meta (Boston, MA)
- …for our AR, VR, and wearable devices, working on low-level systems software, device drivers, and connectivity protocols such as Wi-Fi, Bluetooth, and Core Android ... Experience in large-scale C/C++ code base 12. Embedded software engineering experience 13. Currently has, or is in the... experience 13. Currently has, or is in the process of obtaining a Bachelor's degree in Computer Science,… more
- Hologic (Marlborough, MA)
- …Supplier Quality Engineering roles. + 5+ years of experience in medical device manufacturing or related industries. + Hands-on experience with manufacturing ... and performance standards, define and approve Production Part Approval Process (PPAP) requirements, and oversee corrective actions, continuous improvements, and… more
- Actalent (Billerica, MA)
- …work instructions + Ability to read and interpret documents related to medical device sterilization and cleanrooms Including: International standards regulations ... for this temporary role may include the following: * Medical , dental & vision * Critical Illness, Accident, and...2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help… more