- Merck & Co. (Durham, NC)
- …management and staff to ensure on-time completion of assigned activitiesComply with company health and safety procedures and practices. Author SOPs and technical ... and patients on time, every time, across the globe.As part of our Company 's Quality Operations Organization, the Durham site Quality team is seeking a highly… more
- Insmed Incorporated (San Diego, CA)
- Company DescriptionInsmed is a global biopharmaceutical company on a mission to transform the lives of patients living with serious and rare diseases. Our most ... into innovative solutions for patients. That's why we were named the No. 1 company to work for in the biopharma industry in Science's Top Employers Survey for… more
- Merck & Co. (North Wales, PA)
- Job DescriptionJob Description:This position resides within our company 's Value and Implementation (V&I), Outcomes Research organization, which is responsible for ... generation and outcomes research to enable sustained patient access to our company 's innovations and improve patient health outcomes. Under the guidance of a… 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 ... HRBP or Talent Acquisition Advisor.Employees working in roles that the Company determines require routine collaboration with external stakeholders, such as… more
- Merck & Co. (Rahway, NJ)
- …appropriate corporate personnel is informed of the progress of studies of our company and competitors' drugs and internal and external expert opinion on scientific ... investigators who can assist in the development of our company 's investigational drugs in ImmunologyEstablishing collaborative relationships with external experts… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur company 's Device Development and Technology (DD&T) Team designs, develops, and commercializes novel biologic/drug/vaccine - device enabled ... The DD&T Team manages the development of the device constituent of our company 's pipeline of combination products across a variety of therapy areas and routes… more
- Merck & Co. (Durham, NC)
- …in Durham, NC. This state-of-the-art facility established in 2004, manufactures our Company lifesaving vaccines in bulk and finished forms.- Due to the importance ... of this facility in our Company Vaccine Manufacturing network, the facility has seen rapid...and transports all required equipment, materials, supplies and products Author , review, and/or edit procedures and technical documents to… more
- Merck & Co. (Durham, NC)
- …direction and guidanceDeviation management, Review and approve Quality Notifications (QNs) Author , review, and approve SOPsTake on project management opportunities, ... Talent Acquisition Advisor. VETJOBS #EBRGEmployees working in roles that the Company determines require routine collaboration with external stakeholders, such as… more
- Merck & Co. (Rahway, NJ)
- …development and clinical deliveries in a GMP piloting facility supporting our company 's research division.The Oral Solids Dosage (Non-Sterile) team at the FLEx ... processes, and ultimately to enable flexibility and speed of our company 's pipeline.This person will:Lead and strategically plan on-the-floor batch manufacturing to… more
- Merck & Co. (Rahway, NJ)
- …to enable flexibility and speed in the execution of the Company 's pipeline. This role may support facility operations, support compliance investigations/change ... management, author GMP documentation and manage/lead engineers in any of...Acquisition Advisor.#EligibleforERP #vetjobs #EBRGEmployees working in roles that the Company determines require routine collaboration with external stakeholders, such… more
- Merck & Co. (North Wales, PA)
- Job DescriptionOur company is a global health care leader with a diversified portfolio of prescription medicines, vaccines, and animal health products. Today, we are ... building a new kind of healthcare company - one that is ready to help create...his/her area of responsibility.To accomplish these goals, the Director may: Author detailed development documents, presentations, budgets, and position papers… more
- Insmed Incorporated (San Diego, CA)
- Company DescriptionInsmed is a global biopharmaceutical company on a mission to transform the lives of patients living with serious and rare diseases. Our most ... patients. That's why we were named the No. 1 company to work for in the biopharma industry in...the medical integrity of clinical study reports and data interpretation/communication. Author or oversee authorship of clinical sections of regulatory… 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 ... intra-department project/initiative or cross-functional teams in support of program and company goals. ORGANIZATIONAL RELATIONSHIPS: QC TT team QCSV-Portfolio PGS (… more
- Insmed Incorporated (San Diego, CA)
- Company DescriptionInsmed is a global biopharmaceutical company on a mission to transform the lives of patients living with serious and rare diseases. Our most ... into innovative solutions for patients. That's why we were named the No. 1 company to work for in the biopharma industry in Science's Top Employers Survey for… more
- Novo Nordisk Inc. (Durham, NC)
- …Vision Insurance - effective day one Guaranteed 8% 401K contribution plus individual company match option Family Focused Benefits including 12 weeks paid parental & ... Participate actively in & support event response Review & author SOPs & other documents as required Identify, report...longer good enough to aspire to be the best company in the world. We need to aspire to… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …to allow for analysis and trending.Documents are easily accessible by appropriate company personnel. Proprietary documents are secured and only made available to ... necessary personnel.Serves as the final Quality Reviewer/Approver for internal company documentation [e.g., Standard Operating Procedures (SOPs), Facility Maps,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …validation strategy by considering regulatory requirements, industry best practices and company policies and procedures. Provide expertise and solutions to CSV ... review global policies, inspections and audit CAPAs, and vendor audit documentation.- Author , update and maintain Global DX Computer System Validation policies and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …international regulations and guidelines satisfying DS requirements and supporting the company 's vision. Ensure proactive planning and completion for QA Agreements ... to ensure the compliance for products marketed and/or distributed locally. May author or review stability studies protocol or reports. Provide the support for… more
- Aequor (Bothell, WA)
- …access reviews), coordinating with system owners and Quality in accordance with company procedures and regulatory requirements. Author , review and/or approve ... applicable CSV documentation Assist Business Owners and Technical Owners during test execution, document test failures and ensure testing aligns with internal procedures Assist Business Owners and Technical Owners to develop requirements and specifications for… 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 ... pharmaceutical or medical device industry. Evaluate documentation and operation according to company guidelines. Be self motivated, attentive to details and able to… more
