- Novo Nordisk Inc. (Plainsboro, NJ)
- …grows. Relationships Reports to the Sr. Director, Patient Support Solution Quality/ Safety Associate Director. Interacts with colleagues within Patient Support ... future capabilities. We're responsible for regulating accounting, upholding workplace safety , managing our supply chain and sampling, supporting technological and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and Novo Nordisk Way. Qualifications Bachelor of Science degree; Advanced degree preferred 10 years of experience in Pharmacovigilance, Safety reporting, ... the head of Clinical, medical, Regulatory (CMR) Business Operations, the Associate Director (AD) is responsible for structuring facilitating and monitoring… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …degree requiredMaster's Degree preferred orPharmD preferred orRN degree preferred Experience Qualifications4 or More Years drug safety experience with ... to establish the strategy driving global Clinical Study Start-Up activities for PV Safety Operations. This position oversees the creation of SAE Flow Plans and may… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …processes, database business configuration, and data querying. Core Competencies Strongly preferred : Experience with administration of Argus Safety 8.4.x, 8.0.x ... configuration and associated validation activities of Daiichi Sankyo Pharmacovigilance Safety systems, and fulfillment of data change requests. ResponsibilitiesChange… more
- Merck & Co. (Rahway, NJ)
- …and Safety ), Engineering Firms, and Vendors to progress deliverables.The Associate Director is responsible for leading the planning, design, and implementation ... Product, Plant and Clean utilities), product equipment operation, vendor management, process safety and industry guidance are preferred .- Candidate should have… more
- Merck & Co. (Millsboro, DE)
- Job DescriptionOur company seeks to add an Associate Director. Veterinarian Services at our Millsboro, Delaware location. This position will have overall ... DEA, DNREC, etc.) of animal facilities and program reviews is required.PurposeThis Associate Director will report to the Site Quality Head/Director of Quality. They… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Associate Principal Statistical Programmer - Oncology (Hybrid) In BARDS (Biostatistics and Research Decision Sciences), a ... programming analysis and reporting deliverables for global stakeholders. The Associate Principal Programmer will gather and interpret user requirements for… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …as a process champion for an assigned special project as needed Follow all safety & environmental requirements in the performance of duties Performs all job duties ... Administration or related from an accredited university required May consider an associate 's degree in human resources, Business Administration or related field of… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …future capabilities. We're responsible for regulating accounting, upholding workplace safety , managing our supply chain and sampling, supporting technological and ... Are you ready to maximize your potential with us? The Position The Associate Director, Data & Analytics Governance is responsible for the governance of NNI… more
- Aequor (Devers, TX)
- Bio-Process Associate , 2nd Shift6 Months Contract - With high possibilities of extension100% Onsite in Devens, MA Please refer to the attached Work Schedule Shift ... maintains the area in a clean and orderly fashion.Recognizes and reports safety , maintenance, and operational variances to area management.Communicates the status of… more
- Aequor (Devers, TX)
- Bio-Process Associate - 1st ShiftLocation: Devens, MAWork Arrangement: 100% OnsiteContract Duration: 6 MonthsShift Hours: First Shift (5:00 AM - 5:00 PM)Additional ... and maintains area in a clean and orderly fashion.Recognizes and reports safety , maintenance, and operational variances to area management.Communicates the status of… more
- Merck & Co. (Rahway, NJ)
- …both analytical experimental design and biotherapeutic pipeline programs. Finally, this Associate Principal Scientist will be a partner in problem solving, building ... experiments.Mentor and share expertise across the Mass Spectrometry team.Champion compliance and safety as a leader both within and outside the laboratory. Education… more
- Merck & Co. (Durham, NC)
- Job DescriptionThe Associate Specialist, Quality Control participates in a team of analysts in the development, validation, and routine testing intermediate and ... requirementsProvides active support during audits and inspections (regulatory, internal, safety )Supports our Company's Manufacturing Division (MD) divisional and Quality… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …future capabilities. We're responsible for regulating accounting, upholding workplace safety , managing our supply chain and sampling, supporting technological and ... Are you ready to maximize your potential with us? The Position The Associate Manager of Technical Production will be responsible for overseeing the technical aspects… more
- Merck & Co. (North Wales, PA)
- …within pharmaceuticals life science industry as well as experience with Global Safety Case Intake, Processing, Management and Reporting. Preferred Capabilities: ... Manager - PV Case Intake and Processing. Reporting into Product Line Lead Patient Safety and Quality & Compliance, this position will be responsible for managing the… more
- Genmab (Plainsboro, NJ)
- …to fulfilling our purpose.The RoleThe Global Regulatory Labeling Strategy Sr Manager/ Associate Director will be responsible for leading the development and ... and maintain labeling documents including Company Core Data Sheets (CCDS), Core Safety Information (CSI), United States Package Inserts (USPI), Summary of Product… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Management, Regulatory Affairs, Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance, Regulatory/Risk Management, Quality Assurance, Medical ... required and- Master's Degree Life Science or Engineering or Information Systems preferred Experience Qualifications- 7 or More Years At least 7 years' experience… more
- Aequor (West Greenwich, RI)
- …month duration with possible extension.Ideal: Bachelor degree required, internship experience preferred but Academic experience is also fine. Candidates must have ... and /or implementing changes in controlled documents. Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …involving 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data Sheets ... scientific discipline requiredadvanced degree (eg, Masters, Pharm.D. or Ph.D.) preferred Experience Qualifications7 or More Years pharmaceutical industry experience… more
- Aequor (West Greenwich, RI)
- …and cGMP requirements. Alert management of quality, compliance, supply and safety risks. Complete required assigned training to permit execution of required ... with the PQA shift to ensure required tasks are completed Preferred Qualifications: Bachelor's degree and 2 years of Quality/Manufacturing work experience… more
