- Takeda Pharmaceuticals (Lexington, MA)
- …Sourcing) may also contribute actively to cross functional teams as required. + Lead Global Clinical Supply Chain group initiatives including the development and ... strategies, including requirements associated with controlled substances, compliance to global trade standards, and in-country investigational product regulatory … more
- Takeda Pharmaceuticals (Boston, MA)
- …or a related specialty, disease mechanisms and plasma derived/related therapies + Regional/ global Regulatory requirements + GCP/ICH + Emerging research in plasma ... to clinical development, taking into consideration the medical, scientific, regulatory and commercial perspectives. They will lead ...across the organization or external to the company. May lead PDT R&D internal teams and global … more
- Pfizer (Cambridge, MA)
- …data management, result interpretation, and providing statistical support and leadership in global regulatory submission activities, as well as implementing new ... will plan, direct, and coordinate specialized and complex global development projects led by the Rheumatology group within... submissions. + Provide input to the Statistics Group Lead (Senior Director or Executive Director… more
- Bristol Myers Squibb (Cambridge, MA)
- …development including analytical validation, clinical development, manufacturing, US and global regulatory submission, and commercialization of diagnostics. ... medicine and R&D. We have an exciting opportunity for a Senior Director to join the Precision Medicine, Bioanalytical and Translational Sciences organization, where… more
- Takeda Pharmaceuticals (Lexington, MA)
- …Design (AQbD) principles, aligning with ICH Q14, ICH Q2(R2), and global regulatory expectations for biologics. + Lead technical assessments and risk analyses ... a Brighter Future to people worldwide. As an Associate Director in Analytical Development, you will lead ...strategies. + Solid knowledge of late-stage analytical development, including global regulatory requirements for Biologics (US, EU,… more
- Sumitomo Pharma (Boston, MA)
- …ensure the successful delivery of SMPA's commercial portfolio of products. The Executive Director will lead the RSM/API department, by alignment with business ... in bringing clinical molecules to successful commercial products within different Global Markets, including leading regulatory filings. + Successfully executed… more
- Santander US (Boston, MA)
- …practices, ensuring the program's effectiveness, scalability, and alignment with evolving regulatory expectations and industry standards. The Director will ... Director , AML Enhanced Due Diligence Program Country: United...procedures, and standards, ensuring their effectiveness and alignment with regulatory requirements. + Lead the day-to-day operations… more
- Pfizer (Cambridge, MA)
- …data-driven decision-making, and driving innovation across these critical domains. The Senior Director will lead a multidisciplinary team of data engineers, ... our organization. In this pivotal leadership role, the Senior Director , Data Engineering will define and execute the vision...problems within a Division or Global Business Unit/ Global Operating Unit + Sponsor and Lead … more
- Hologic (Marlborough, MA)
- …as the primary point of contact for privacy-related inquiries, investigations, and regulatory requests. + Lead privacy impact assessments, data mapping, and ... Senior Director of Privacy, Information Security United States Marlborough,...to join us on our mission to make our global security platform a solid differentiator in the Medical… more
- Sanofi Group (Cambridge, MA)
- …of Sanofi's Global Medical Device and Packaging organization is to lead the industry in device-mediated therapies, with the ambition to develop, launch and ... **Job Title:** Director - Packaging Technology **Location** : Cambridge, MA,...and deploy robust manufacturing solutions. May act as Manufacturing Lead on large scale global projects. +… more