The Plasma-Derived Therapies (PDT) R&D Organization is dedicated to bringing forward new plasma-derived therapies for patients with immunologic, hematologic, and other complex diseases. There are two main drivers of innovation that are the focus of the PDT R&D organization:
Translational Pharmaceutical Sciences - a rapid-cycle innovation engine to develop improvements to existing products, develop new products, and improve yield. It combines translational research with pharmaceutical/manufacturing sciences, device development and clinical research.
Precision Medicine - a patient-centric research focus with the goal to develop comprehensive, value-oriented health care delivery packages around drug products targeted to maximize benefit and reduce risk to precise patient populations. In the process, this engine will drive innovation by practicing patient-centric R&D.
Lead the execution of the PDT global medical affairs activities and help develop an integrated medical strategy in collaboration with the Medical Unit Head and Global Medical Leads for assigned therapeutic area including scientific training, field medical resource development, medical conferences, and publications.
Scientific lead for assimilation, dissemination and archival of all content developed for the assigned therapeutic area
Provide accountability for medical aspects of the Commercial
Hobbs Brook Real Estate LLC is an innovative commercial real estate leader with a portfolio of forward-thinking, sustainable properties in the United States and Singapore. Shaping the market since 1952, the company acquires, develops, manages, and serves as a valued partner to a variety of stakeholders. Hobbs Brook Real Estate (HBRE) brings unique property visions to life with a commitment to improving both the environment and the community. For additional information, please visit www.hobbsbrook.com. HBRE is the real estate division of FM Global.
This Host opportunity is at our restaurant, One Bistro, located at the Four Points by Sheraton Hotel & Conference Center in Norwood, MA! One Bistro is a critically acclaimed, upscale casual dining restaurant. Our restaurant's success is driven by delicious, affordable, unpretentious food made from high quality, seasonal ingredients served in an atmosphere featuring beautifully lit, contemporary décor and open-kitchen energy.
The Host/Hostess primary responsibility is to greet and seat guests in a friendly, gracious manner to set a positive first impression of the restaurant as guests arrive. Other responsibilities include:
Must be skilled in using Open Table, Word and WordPress for updating spe
FM Approvals is an international leader in third-party testing and certification services. We test property loss prevention products and services for use in commercial and industrial facilities to verify they meet rigorous loss prevention standards of quality, technical integrity and performance. How? By employing a worldwide certification process that s backed by scientific research and testing, and over a century of experience.
The FM APPROVED mark is recognized and respected worldwide. Our certification instills confidence and commands respect in your marketplace.
The person in this position will be responsible for planning, conducting and directing testing and analysis of electronic equipment. This equipment is used primarily in fire protection and explosion prevention systems submitted for FM Approval. They will work in FM Global s Engineering and Research facility in Norwood, MA, with occasional travel to our state-of-the-art facility in West Glocester, RI, USA.
Duties will include, but are not limited to, the development of proposals, preparation of test plans, and supervision of tests. Additionally, project management, documentation of results, preparation of written reports and other complex tasks associated with third party certification.
The working environment includes both the office and laboratory.
Overnight travel is typically less than 25%. Travel will be to coordinate with customers, attend technical conferences and to conduct and monitor tests at test facilities.Qualifications:
Senior Manager, Non-Clinical Regulatory Writer
Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Senior Manager, Non-Clinical Regulatory Writer in our Cambridge, MA office.
At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
Here, you will be a vital contributor to our inspiring, bold mission. As a Senior Manager in the Non-Clinical Regulatory Writing and Submissions (NRWS) group within Preclinical and Translational Sciences (PTS), you will be empowered to contribute to this science driven, collaborative and dynamic environment, bringing experience to add further value to the NRWS contribution to the PTS organization and to Takeda, with involvement in a variety of projects of diverse scope and complexity, reflecting the breadth of Takeda's portfolio (e.g., Oncology, Gastrointestinal, Neuroscience, Rare Disease). The NRWS team is a goal- and results-driven team, and we are strong believers in innovation and streamlined processes. A typical day will include: