- Truist (Raleigh, NC)
- …(United States of America) **Please review the following job description:** The Head of Observability and Monitoring will lead the strategy, architecture, and ... skills to drive best-in-class monitoring solutions that align with regulatory and business requirements. **ESSENTIAL DUTIES AND RESPONSIBILITIES** **Technical… more
- Sanofi Group (Morristown, NJ)
- …or PhD in LifeScience; Law or Computer Sciences + **Pharmaceutical, biotech, medical device industry experience required** + Demonstrated experience in working ... **Job Title:** Head of Privacy, SpeCare and North America **Location:**...generate deeper insights to our Research, Marketing, commercial and medical activities. + Actively monitor North American privacy regulations/enforcements,… more
- Takeda Pharmaceuticals (Lexington, MA)
- …Operational, and Process Qualifications at Takeda to ensure compliance with GxP regulatory and quality standards while maintaining the integrity of data * Oversees ... related to engineering and qualifications * Provides expert support for regulatory inspections and responses to Health authorities regarding areas under this… more
- Amazon (Santa Clara, CA)
- …oriented Product Compliance leader to lead the compliance engineering strategy and global regulatory vision for AWS's hardware products. This role will manage a team ... requirements globally - Evaluating and mitigating product design and global regulatory risks related to safety, EMC, energy efficiency restricted substances, and… more
- BD (Becton, Dickinson and Company) (Warwick, RI)
- …+ Advance degree preferred. + Preferred minimum of 10-15 years of experience in the medical device industry, with at least ten years in a regulatory ... of United States, European, and international regulations and standards covering medical devices . + Demonstrated organizational, planning, and program management… more
- Sanofi Group (Cambridge, MA)
- …responsibilities. **About You** **Experience:** + 8+ years of experience within pharmaceutical or medical device Regulatory Affairs + Successful track record ... and direct reports. + In conjunction with the Sr. Director/Product Support Head , imparts senior regulatory guidance and advice during issues management… more
- Abbott (Sylmar, CA)
- …a diverse and growing portfolio of digital health products, including software as a medical device (SaMD), connected devices , and digital health platforms. ... of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines....years of proven experience in Connectivity development within the medical device / life sciences / digital… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …or other technical field + Minimum of 10 years of experience in Quality or Regulatory function within the medical device industry, including experience with ... technical product expertise (Design Assurance, Quality Operations, etc.) + Experience in full Medical Device product lifecycle. Ie Demonstrated medical … more
- Abbott (Sylmar, CA)
- …a diverse and growing portfolio of digital health products, including software as a medical device (SaMD), connected devices , and digital health platforms. ... of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines....This position reports directly to the Head of Technology, Digital Solutions and will be instrumental… more
- Abbott (St. Paul, MN)
- …and market success. + **Technical & Regulatory Acumen** : Deep understanding of medical device standards and regulatory frameworks (eg, IEC 60601, IEC ... of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines....are seeking a dynamic and strategic R&D leader to head our Global Product Development (GPD) function at our… more