- Merck & Co. (Durham, NC)
- …of assigned activitiesComply with company health and safety procedures and practices. Author SOPs and technical documents Other duties as needed Education Requirement ... the pharmaceutical industry Demonstrated technical writing ability; able to author protocols and reports Demonstrated structured problem-solving skills; able to… more
- Merck & Co. (Rahway, NJ)
- …cell protein analysis.Represent the mass spectrometry group in project teams. Author regulatory submission sections and responses, technical reports and scientific ... as demonstrated through high impact scientific publications and presentations.- Preferred Experience and Skills Expertise in multiple reaction monitoring based… more
- Merck & Co. (Rahway, NJ)
- …responsibility. To accomplish these goals, the Senior Clinical Director may: Author detailed development documents, presentations, budgets, and position papers for ... therapeutic areas. Experience in late stage IBD trials and regulatory filing is preferred .Minimum of 3 years of clinical medicine experienceMinimum of 5 years of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …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 ... equivalent required and- Postgraduate training in TA or related specialty preferred Experience Qualifications- 4 or More Years industrial experience required Travel… more
- Aequor (Bothell, WA)
- …for method transfer and/or validation internally and externally for assigned program(s). Author or review protocols and reports for method transfer and/or method ... res DNA and host cell protein method experiences are preferred but not required. Good project management skills and...Reporting 3. Good understanding of analytical and biochemical methodology Preferred Skills: 1. Binding and Cell based assays 2.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …review global policies, inspections and audit CAPAs, and vendor audit documentation.- Author , update and maintain Global DX Computer System Validation policies and ... 1 or More Years Direct dealings with FDA, EMA, PMRA, other regulatory agencies. preferred - 1 or More Years Strong appreciation of the impact of regulatory bodies on… more
- Merck & Co. (Durham, NC)
- …inventories, and transports all required equipment, materials, supplies and products Author , review, and/or edit procedures and technical documents to support ... skills Able to lift 50 lbs. and work on elevated platforms Preferred (General) Demonstrated two to four years of leadership experience Minimum associate's… more
- Merck & Co. (Durham, NC)
- …direction and guidanceDeviation management, Review and approve Quality Notifications (QNs) Author , review, and approve SOPsTake on project management opportunities, ... or Technology or related disciplines with six (6) years of experience. Preferred Experience and Skills:Quality Assurance and/or cGMP experienceMinimum of 2 years… 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 ... in scientific discipline requiredMaster's Degree or other advanced degree preferred Experience Qualifications4+ years of pharmaceutical, biologicals an/or vaccines… 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, ... Chemical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field Preferred Experience and Skills: Knowledge of Investigational drug regulatory… more
- Novo Nordisk Inc. (Durham, NC)
- …FIFO, returns, etc. Participate actively in & support event response Review & author SOPs & other documents as required Identify, report & resolve quality issues ... based on the role. Qualifications High School Diploma or GED required Associate's degree preferred Minimum of one (1) year of experience in a manufacturing industry … more
- Aequor (Framingham, MA)
- …experimental work and results with appropriate supervision and documentation. Author high quality scientific and operational documentation and deliver scientific ... team-oriented environment with strong project management and communication skills (oral/written). Preferred Qualifications Relevant knowledge, coursework and/or hands-on experience in… more
- Merck & Co. (Rahway, NJ)
- …This role may support facility operations, support compliance investigations/change management, author GMP documentation and manage/lead engineers in any of our ... internal node for small molecule drug substance clinical manufacture, and as preferred site for first pilot of commercial small molecule processes, enabling gain… more
- Merck & Co. (North Wales, PA)
- …in his/her area of responsibility.To accomplish these goals, the Director may: Author detailed development documents, presentations, budgets, and position papers for ... well as the ability to function in a team environment are essential. Preferred :Board Certified or Eligible in Oncology (and/or Hematology)Prior specific experience in… more
- Insmed Incorporated (San Diego, CA)
- …standard and critical reagent programs, including creation, qualification, and inventory. Author GxP stability protocols, interim reports, and reports for stability ... and Change Controls. Drive related improvements.Position Requirements (Required and/or Preferred Skills, Experience and Education):Bachelor's Degree with minimum 8… more
- Insmed Incorporated (San Diego, CA)
- …the medical integrity of clinical study reports and data interpretation/communication. Author or oversee authorship of clinical sections of regulatory submissions ... years of management experience in ophthalmology clinical development.Pediatric experience preferred .Gene Therapy experience preferredClinical residency training in ophthalmologyExperience with… more
- University of Colorado (Aurora, CO)
- … preferred . + A record track of publications in reputable scientific journals (as first author or co- author ) is preferred . + Experience with in vivo tumor ... physiology or cancer biology, and experience characterizing mouse models is required. ** Preferred Qualifications:** + A record of oral and/or poster presentations at… more
- UCLA Fielding School of Public Health (Los Angeles, CA)
- …biostatistics is expected. The candidate is expected to have prior first author publications. Preferred qualifications Desired skills include experience in MRI, ... interventional procedures and ischemic/infarct modeling in large animals is preferred . The candidate is expected to have prior first.... The candidate is expected to have prior first author publications. The shared values of the DGSOM are… more
- Boston University (Boston, MA)
- …Now, our Business Intelligence team is looking for a Salesforce Dashboard Author who will transform complex data into meaningful visualizations and reports that ... meet but exceed its engagement and philanthropic goals. Salesforce Dashboard Author Reporting to the Senior Associate Director, Business Intelligence, the Salesforce… more
- University of Florida (Gainesville, FL)
- …letter of interest, CV, and two recent writing samples (at least one first author preferred ) to the Careers at UF website. For additional information, please ... Providers and Systems (CAHPS) surveys, and qualitative research methods are preferred . This position will supervise research support staff across multiple survey… more
