- 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 ... assigned job duties. **Qualifications:** + Bachelor's degree in biomedical engineering , healthcare, computer science or registered nurse, sonographer, technologist -… more
- Integra LifeSciences (Braintree, MA)
- …field preferred. + 5+ years GMP/GLP laboratory experience in a medical device , pharmaceuticals, Quality/Regulatory Compliance, or other regulated industry ... to the continuous improvement of processes. Works collaboratively with Manufacturing, Engineering , Quality Assurance, and other functional experts to support all… more
- Consolidated Precision Products (Burlington, MA)
- …reduce greenhouse gas emissions. Job Summary: As part of manufacturing process operations, the Quality Control Technician is responsible for hands-on inspection ... and quality standards. + Communicate effectively with production, quality, and engineering teams to resolve quality issues. + Support continuous improvement… more
- Sanofi Group (Framingham, MA)
- …on different facets of drug product development, including formulation and process development, compatibility in-use studies and drug- device compatibility, ... and Manufacturing organization, supporting biologic drug product formulation and process development. The Co-Op/Intern will be exposed to laboratory-based studies… more
- J&J Family of Companies (Raynham, MA)
- …+ Experience leading cross-functional change-management initiatives + Knowledge of global medical - device competitive and regulatory landscapes Other: + This ... & Johnson, procedures and guidelines, this position: + **Digital ecosystem & process automation** - Drive organizational change from manual, siloed activities to an… more
- Sanofi Group (Cambridge, MA)
- …commercial team members + Knowledge of the pharmaceutical / biotech / medical device industry(ies), especially product development and/or commercialization + ... a given therapeutic area or functional area** + Help drive deal process + Contribute to and/or lead cross-functional teams including senior scientific, technical,… more
- Philips (Cambridge, MA)
- …You've acquired 10+ years of experience working in Regulatory Affairs within the medical device industry; Experience with software-enabled medical devices, ... and all key stakeholders including R&D, Product Management, Quality, Medical & Clinical Affairs, and other functions at all...a bachelor's degree or higher, in an Informatics or Engineering field preferred. + You must be able to… more
- Abbott (Burlington, MA)
- …spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues ... you dream of. + Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO...This role has responsibility for complaint handling and is process owner for clinical and regulatory decision making. This… more
- Philips (Cambridge, MA)
- …a plus. + You have 4+ years in a role associated with healthcare and/or medical device and software development in a regulated environment. + You have experience ... objectives. **Your role:** + Oversee the End-to-end (E2E) lifecycle management process to align with strategic objectives, ensuring value propositions and business… more
- Amazon (North Reading, MA)
- …The benefits that generally apply to regular, full-time employees include: 1. Medical , Dental, and Vision Coverage 2. Maternity and Parental Leave Options 3. ... experience - Bachelor's degree in Computer Science or Electrical Engineering - 3+ years of programming with C/C++, Java,...for motion control - Knowledge of Linux kernel and device -driver development - Familiarity with common bus protocols such… more