- Takeda Pharmaceuticals (Boston, MA)
- …asset programs in US + For US and with a global mindset, utilizes technical combination product knowledge, regulatory expertise and global regulatory lessons ... agencies and trade associations and acts as an advisor /liaison to senior management to plan, evaluate and recommend...management + Supports and/ or leads assigned device and drug -device combination aspects of US regulatory submissions… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …collaboration with Takeda teams and leadership through networks and enable CMC regulatory team's success in meeting goals/objectives on drug -device combination ... Sciences + Authors, reviews, provides critical assessments and gives input on drug -device combination regulatory strategies in regulatory filings through… more
- Lilly (Boston, MA)
- …Design and Development (SMDD) organization is responsible for the development of synthetic drug substances and drug products from the pre-clinical phase through ... commercialization. Our scientists and engineers develop innovative technical solutions to advance an exciting portfolio that includes small molecules, synthetic… more
- Intertek (Boxborough, MA)
- …opportunity to grow a versatile career in facilitating international trade and regulatory product testing on the Electrical Team! By joining Intertek, your ... of the specific cyber security standards, risk management practices, and regulatory requirements associated with IIoT and/or Medical Devices. How you'll make… more
- J&J Family of Companies (Boston, MA)
- …activities, and due diligence assessments. Responsibilities: + Serve as an experienced regulatory compliance advisor and Subject Matter Expert on key strategic ... requirements. + Experience working with, or for, the United States Food and Drug Administration (FDA) and other foreign regulatory agencies. + Demonstrated track… more
- Merck (Boston, MA)
- …clinical investigator brochures, clinical study reports, Worldwide Marketing Application/Common Technical Document (WMA/CTD) subsections, and regulatory agency ... collection processes. Applies knowledge of GCP, ICH guidelines and regulatory requirements for clinical development. Contributes to teams developing and/or… more
- Kelly Services (Cambridge, MA)
- …the Senior Director, In Vivo Gene Editing Discovery will serve as a scientific advisor and lead teams of scientists in the design of project strategies and plans ... In Vivo Gene Editing Discovery, you will be responsible for: + Leverage drug development experience and subject matter expertise in peripheral indication space to… more
- Editas Medicine (Cambridge, MA)
- …the Senior Director, In Vivo Gene Editing Discovery will serve as a scientific advisor and lead teams of scientists in the design of project strategies and plans ... In Vivo Gene Editing Discovery, you will be responsible for: + Leverage drug development experience and subject matter expertise in peripheral indication space to… more
- Bank of America (Boston, MA)
- …communicate and improve their business insight capabilities. Experience in supervising/leading technical or complex projects and managing to an outcome(directly or ... Advanced Analytics Team. The Client Quantitative Analytics Manger serves as a trusted advisor to the Consumer AML Leadership team directly. This role will: Improve… more
- Bank of America (Boston, MA)
- …**Job Description:** The Fiduciary Initiatives Executive will provide strategic and regulatory support to leadership and team members in connection with Fiduciary ... Team members and across the Merrill organization to tackle legal, compliance and regulatory issues as part of any strategic initiative or regulatory response.… more
- Black & Veatch (Burlington, MA)
- …all matters of the existing and proposed EPA regulations and will serve as a technical advisor to internal and external clients on all subjects related to LCRR. ... contracts, and amendments Project Execution: + Serve as a technical advisor with a deep understanding of...Share understanding of historical SL material selection based on regulatory requirements as it relates to building construction, local… more
- WSP USA (Boston, MA)
- …a part of a part of a rapidly expanding group that provides trusted advisor and engineer of record services to Hydropower and Utility clients throughout the United ... provides Civil Engineering and Project Management expertise, including high-level technical assistance and guidance for multi-site/phase due diligence, investigation,… more
- Pfizer (Cambridge, MA)
- …Advisor /Consultancy:** Provides well-informed advice, typically within a specific technical specialization, ensuring that it is properly understood and ... but are not limited to: + Responsible for delivering the solution architecture, technical and functional design for Digital Assistant products and services. + Manage… more
- WSP USA (Boston, MA)
- …a part of a part of a rapidly expanding group that provides trusted advisor and engineer of record services to Hydropower and Utility clients throughout the United ... latest electrical engineering techniques and practices. + Remain current with regulatory agencies and other bodies with jurisdiction over electrical power generation… more
- Merck (Boston, MA)
- …alignment with prioritized business requirements. + Demonstrate an eagerness to learn drug discovery & development processes and regulatory requirements as ... platforms, enhancing existing ones for expansion, efficiency and productivity across drug discovery modalities and clinical phases. You will collaborate with… more
- Intertek (Boxborough, MA)
- …to start or grow a versatile career, facilitating international trade and regulatory product testing on the Electrical Team! By joining Intertek, your contributions ... + Follow established test plan + Mentoring less senior technical personnel + Supply information for quotes such as...millions of people every day. Intertek is the trusted advisor to many of the world's leading brands, companies,… more
- Verista (Boston, MA)
- …groups. + Lead QA efforts to establish new programs to support Drug Product facility including start-up of assembly, packaging and label operations + ... + Review and approval of manufacturing documents. + Develop and deliver technical training programs + Supports drafting and revising Quality Agreements between… more
- Wolters Kluwer (Waltham, MA)
- …Clinical Effectiveness sales team working with our customers to offer expertise and advisor guidance to support the business and sales team in how our solutions ... will meet their unique needs. Major product brands include: UpToDate, UpToDate Lexi- Drug , Medi-Span and UpToDate Patient Engagement Solutions. The ideal candidate is… more