- J&J Family of Companies (Santa Clara, CA)
- …with a diverse team of Design Engineers, Development Engineers, Quality Engineers, Regulatory Affairs , Marketing, and Clinical. + Meet with Quality management ... Previous quality engineering related experiences. + Knowledge of FDA or regulatory guidance. + Medical related experience (previous co-op at medical device… more
- UPMC (Mechanicsburg, PA)
- …Assists at other UPMC Radiation Oncology locations if the need arises. + Regulatory Affairs Management: Participates in regulatory compliance activities and ... and radiation delivery systems. Our board-certified radiation oncologists and medical physicists work in collaboration with referring physicians and… more
- Abbott (Abbott Park, IL)
- …cross functional relationships with internal departments such as R&D, Manufacturing, Quality Control, Regulatory Affairs and Operations. + Be able to work with a ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Teleflex (Morrisville, NC)
- …* Ability to work with colleagues across cross-functional teams (Sales, R&D, Operations, Regulatory Affairs etc.) to drive consensus on campaigns, collateral and ... the medical device new product development processes and the medical regulatory environment * Self-starter, knows how to approach the job, passionate about… more
- Kelly Services (Las Vegas, NV)
- …local opinion leaders + Work closely with colleagues in other functions including, Regulatory Affairs , Clinical Operations and Patient Engagement + Lead and ... commitment to careful planning and execution in accordance with regulatory compliance. Due to their continued growth, we are...clinical direction to the study team **Requirements:** + Current medical license in the state of hire + Current… more
- Abbott (Atlanta, GA)
- …integrate information from varied disciplines including Clinical Medicine, Engineering, Marketing and Regulatory Affairs + Ability to work within a team and ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- University of Pennsylvania (Philadelphia, PA)
- …comply with all policies relating to UPHS, JCAHO, GCP and other regulatory standards. Job Description Job Responsibilities Clinical Research Nurse C Responsibilities ... Principal Investigator (PI) for assessment and review, and communicate with medical staff regarding protocol-specific management of toxicities and adverse events. +… more
- Sutter Health (Los Altos, CA)
- …Division currently generates $4.5 billion in revenue, with the Palo Alto Medical Foundation (PAMF) accounting for nearly $3.5 billion-making it the largest ... and Ambulatory Surgery. These ancillary operations represent 1/3 of the Palo Alto Medical Foundation's (PAMF) annual revenue. As the foundation enters a period of… more
- Takeda Pharmaceuticals (Boston, MA)
- …of experience in GCP Quality/Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA, EU, MHRA, ... for clinical deviation management, and Serious Breaches investigation and reporting to regulatory agencies. + Act as strategic partner to Clinical Program Quality… more
- Terumo Neuro (Aliso Viejo, CA)
- …Stakeholder Management + Collaborate closely with cross-functional teams, including R&D, regulatory affairs , manufacturing, quality assurance, and marketing, to ... Professional (PMP) certification is highly desirable. 3. Strong knowledge of medical device development processes, regulatory requirements, and quality… more