- Merck & Co. (Rahway, NJ)
- …activities in his/her area of responsibility.To accomplish these goals, the Senior Director may: Author detailed development documents, presentations, budgets, ... with talented and dedicated colleagues while developing and expanding your career.The Senior Director ( Senior Principal Scientist) has primary responsibility for… more
- Merck & Co. (Rahway, NJ)
- …activities in his/her area of responsibility. To accomplish these goals, the Senior Clinical Director may: Author detailed development documents, presentations, ... Job DescriptionThe Senior Clinical Director (Sr. Principal Scientist) has primary...in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of… more
- Insmed Incorporated (San Diego, CA)
- …batch records, SOPs, raw material specifications, GMP protocols, and author development reports.Demonstrate experience with process validation and scale-down models ... situations or data requires an in-depth evaluation of variable factors. Author Standard Operating Procedures, technical reports, process descriptions, including data… more
- Merck & Co. (Rahway, NJ)
- …in the program-specific design controls process and design history file development. Author and review relevant portions of the regulatory submissions (INDs, IMPDs, ... formal authority; ability to influence and present ideas to senior leadershipExcellent communication, presentation, negotiation, project management, and organizational… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders.Summary The Senior Director sits within Global Oncology Clinical Development, an organization ... narratives- May lead the development and updates of the Investigator's Brochure (IB): author the clinical section and lead the development of the other sections in… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. SummaryThe Senior Director sits within Global Oncology Clinical Development, an organization ... safety narrativesMay lead the development and updates of the Investigator's Brochure (IB): author the clinical section and lead the development of the other sections… more
- Aequor (Bothell, WA)
- …The Downstream Process Development group in Bioprocess R&D is seeking a Senior Associate Scientist contractor to support development and optimization of recovery and ... Transfer manufacturing processes to internal and/or external manufacturing facilities Author technical reports and make presentations to scientists and management… more
- Merck & Co. (Rahway, NJ)
- …ensure safety and quality of clinical supplies to augment and accelerate our products. Author and review GxP documentation including but not limited to batch records, ... specification, equipment qualifications, change records and deviations.Build partnerships by developing and leveraging relationships within and across work groups of formulators, engineers, safety and quality representatives.Foster culture of collaboration,… more
- Aequor (Thousand Oaks, CA)
- …sites and business partners 3) Manage complaint return sample inventory 4) Author technical assessment reports Requirements: Bachelor's Degree in Life Sciences or ... related field or the equivalent combination of education and/or experience. Typically 2 plus years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry. Evaluate documentation and operation according to… more
- Merck & Co. (North Wales, PA)
- …company's innovations and improve patient health outcomes. Under the guidance of a senior leader, this individual will serve as an Oncology, V&I, Outcomes Research ... to value evidence strategies for in-line and pipeline products. Obtain senior management approval of value evidence generation plans. Provide outcomes research… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to ensure the compliance for products marketed and/or distributed locally. May author or review stability studies protocol or reports. Provide the support for ... Quality Metrics in a periodical manner and communicate this to Senior Management handling Quality Meeting sessions, identifying potential quality issues and… more
- Boston University (Boston, MA)
- …only meet but exceed its engagement and philanthropic goals. Salesforce Dashboard Author Reporting to the Senior Associate Director, Business Intelligence, the ... Now, our Business Intelligence team is looking for a Salesforce Dashboard Author who will transform complex data into meaningful visualizations and reports that… more
- AECOM (Seattle, WA)
- …permitting, data collection and compilation, and/or GIS mapping. + Operating as primary author or senior reviewer, as appropriate. + Supervising personnel in the ... us. **Job Description** **AECOM** is actively seeking an experienced ** Senior Archaeologist/Project Manager** for immediate, full-time employment within our Cultural… more
- AECOM (Los Angeles, CA)
- …Delineation Reports, and/or Aquatic Resources Permit Applications. + Operates as primary author or senior reviewer. + Manages projects/tasks that include all ... Join us. **Job Description** **AECOM** is seeking a highly talented ** Senior Biologist/Project Manager** for immediate employment within our Southern California… more
- Abbott (St. Paul, MN)
- …software programs **Preferred Qualifications** + Has regularly appeared as first or senior author on peer-reviewed publications + Regularly presents at ... and ISO 10993 series. This is a manager and senior -level technical contributor responsible for serving as a leader...risk for manufacturing and life cycle management challenges + Author , review, approve, and provide guidance on risk assessments… more
- ThermoFisher Scientific (Greenville, NC)
- …and junior staff. External thought leadership. Contribute to abstracts and manuscripts as co- author and when possible, first/ senior author positions. Make ... depend on - now and in the future. The Senior Research Scientist (SRS), serves as the responsible person...project execution. The SRS, will also be responsible for senior oversight of project design, protocol and final study… more
- Jacobs (Bellevue, WA)
- …the western states; must be available for occasional travel. * WSDOT Biological Senior Author Certification * Certification as a Professional Wetland Scientist ... Jacobs' Bellevue office is seeking a Senior Wetland Biologist & Permitting Specialist who can provide leadership and support for public and private sector… more
- Jacobs (Bellevue, WA)
- …including traditional design-bid-build and progressive design-build delivery. - WSDOT Biological Senior Author Certification. - Certification as a Professional ... Jacobs' Bellevue office is seeking a mid- to senior -level Biologist & Environmental Permitting Project Lead who can provide leadership and support for public and… more
- Takeda Pharmaceuticals (Boston, MA)
- …+ Identify topics for initiatives and lead local/global initiatives on behalf of senior staff. + Author relevant sections of regulatory documents, validation ... and controlling high standards of purity and quality. The Senior Staff Engineer - Process Modeling will join a...Process Engineering & Technology Group. Join Takeda as a Senior Staff Engineer - Modeling where you will have… more
- University of Colorado (Aurora, CO)
- …peer-reviewed journals and contributions to the field as evidenced by first- and/or senior - author papers. + A strong record of successfully securing research ... journals and contributions to the field as evidenced by first- and/or senior - author papers. + A strong record of successfully securing research funding from… more
