- J&J Family of Companies (Boston, MA)
- Sr Clinical Research Associate - 2406209639W **Description** At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us ... Medtech companies is recruiting for a Sr Clinical Research Associate , located anywhere in the United States. For more...+ Provide coaching and training to junior employees. + Lead in the investigation of all discrepancies in study… more
- Bristol Myers Squibb (Cambridge, MA)
- …medical device , and/or translational development processes, with ability to lead supportive project management processes + Strong understanding of global ... the patients and health care providers we serve. The Associate Director, Technical Management, reports to the Technical Management...regulatory requirements for companion diagnostic device development… more
- Takeda Pharmaceuticals (Boston, MA)
- …order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director, Programming in Cambridge, MA, where you will oversee and direct ... applicable to the design, analysis of clinical trials and regulatory submissions. + Work with ICH-GCP guidelines for clinical...quality execution of the deliverables by assisting Programming CoE lead . + A SME in the special data types… more
- embecta (Andover, MA)
- …in Engineering or related field + 10+ years of post-educational experience in Medical Device Design highly desired + Experience as lead in the development of ... **The Staff Engineer, R&D - Verification and Validation, is the technical lead in the design verification or design validation of electromechanical medical devices… more
- embecta (Andover, MA)
- …in Engineering or related field. + 10+ years of post-educational experience in Medical Device Design highly desired. + Experience as lead in the development of ... Engineer, R&D - Verification and Validation, is the technical lead in the design verification or design validation of...medical devices developed by embecta. Reporting up to the Associate Director, R&D - Verification and Validation, the successful… more
- Pfizer (Andover, MA)
- …with 0+ years of experience + Experience in GMP Pharmaceutical or Medical Device Manufacturing environment or relevant regulatory experience (ie Board of Health) ... executed batch records and Logbooks to assure compliance with Site SOPs, Regulatory standards and filings. + Anticipate issues and escalate to appropriate management… more