- Catalent Pharma Solutions (Chelsea, MA)
- …Control Analyst III** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to ... and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing...analytical test methods. The Quality Control Analyst III compiles data for documentation of test procedures that may include… more
- ThermoFisher Scientific (Boston, MA)
- …people and communities depend on - now and in the future. Thermo Fisher's clinical research business is a leading global contract research organization and world ... Conditions** Adherence to all Good Manufacturing Practices (GMP) Safety Standards **Job Description** At Thermo Fisher Scientific, you'll discover meaningful… more
- ThermoFisher Scientific (Boston, MA)
- …people and communities depend on - now and in the future. Thermo Fisher's clinical research business is a leading global contract research organization and world ... Conditions** Adherence to all Good Manufacturing Practices (GMP) Safety Standards **Job Description** At Thermo Fisher Scientific, you'll discover meaningful… more
- US Tech Solutions (Boston, MA)
- …Enrollment Specialist supports key areas business, quality and compliance support for a clinical Telehealth practice. + This is a 100% remote role, requiring 25-30 ... + Deliver credentialing, privileging, and payer enrollment services for clinical providers. + Provide administrative support for provider licensing and… more
- Bristol Myers Squibb (Cambridge, MA)
- …apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of ... (eg, Benchling Connect and MCP/Actions, orchestration across instruments and data platforms) to streamline experimental planning, automate routine steps, and… more
- Bristol Myers Squibb (Devens, MA)
- …apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of ... This position collaborates on these efforts with site and global stakeholders across manufacturing, quality, supply chain, information technology, facilities,… more
- Medtronic (Newton, MA)
- …of technical and operational excellence, and consistently deliver investigational, pre- clinical , and commercial software releases. At Medtronic, we bring bold ... teams to ensure full compliance with design controls, software lifecycle standards , and industry regulations. + Collaborate with cross-functional teams, including… more
- Medtronic (Boston, MA)
- …policies and procedures + Adheres to financial, regulatory, quality compliance standards and requirements. **Influence and Selling:** + Identify, establish and ... expectations and improves outcomes when supporting cases. + Engages physicians in clinical conversations about advantages of the therapy and products. + Conducts all… more
- Bristol Myers Squibb (Devens, MA)
- …partner with operational areas to ensure GxP compliance with Bristol-Myers Squibb policies, standards , procedures, and Global cGMP. In the capacity of QA Shop ... and represent function at cross functional meetings. + Share data /knowledge within and across team. Build & maintain strong...talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our… more
- Bristol Myers Squibb (Devens, MA)
- …activities at Devens in accordance with Bristol Myers Squibb (BMS) policies, standards , procedures, and Global current Good Manufacturing Practices (cGMPs). ... apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of… more
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