- 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
- Novo Nordisk Inc. (Plainsboro, NJ)
- …you ready to make a difference? The Position We are looking to hire an Associate Director of Clinical Operations. This is a unique opportunity to work in a growing ... Operations Department that manages multiple early to late-stage clinical programs. The Associate Director role will be responsible for all aspects of clinical trial… more
- Merck & Co. (Rahway, NJ)
- …Product, Plant and Clean utilities), product equipment operation, vendor management, process safety and industry guidance are preferred .- Candidate should have ... DescriptionReporting to a Technology Director in Global Engineering Solutions (GES), the Associate Director will be part of a high performing team, accountable for… 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. (Durham, NC)
- Job DescriptionWe are seeking a Growth and Improvement minded Associate Specialist Automation Technician who can help drive our Strategic Operating Priorities.- The ... proposes solutions.Learns and supports all Good Manufacturing Practices (GMPs), safety , and environmental regulations.-Participates in investigations of automation incidents… more
- Aequor (South San Francisco, CA)
- Job Title : Research Associate I Location : South San Francisco, CA Duration : Until 12/24/2025 Job Description: This position is focused on the daily performance, ... setting. Ability to adhere to established policies, procedures and safety requirements. Independently establishes new procedures/methods/assays, and effectively communicates… 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. (Plainsboro, NJ)
- …future capabilities. We're responsible for regulating accounting, upholding workplace safety , managing our supply chain and sampling, supporting technological and ... maximize your potential with us? The Position As the Associate Director of Strategic Market Insights, the functional responsibilities...required, preferably in a science discipline. Master 's degree preferred A minimum of eight (8) years ' related… more
- Aequor (Bothell, WA)
- …independentlyCommunication skillsAttention to detail Job Summary:The primary focus of the QC Associate position is to perform GMP testing to support product release ... and gram-staining.Demonstrated experience with basic laboratory techniques and laboratory safety practices.Identify and facilitate continuous improvement projects.Experience with LIMS… more
- Aequor (West Greenwich, RI)
- …PHD. Ideally looking for candidates with at least 2 years of an associate degree combined with 2 years of General lab experience/lab background, GDP/GMP experience ... training compliance and proficiency. 8. At all times, comply with safety guidelines, cGMPs/CFRs and other applicable regulatory requirements. Shift: Tuesday -… more
- Novo Nordisk Inc. (Durham, NC)
- …all Novo Nordisk policies, procedures, and Novo Nordisk Way Follow all safety and environmental requirements in the performance of duties Other accountabilities, as ... relevant field of study from an accredited university required May consider an associate 's degree in engineering or relevant field of study from an accredited… 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 ... overnight travel required. Qualifications Bachelor's degree or equivalent required, MBA- preferred 2+ years of progressive brand management/marketing and/or sales/operations… more
- Novo Nordisk Inc. (Los Angeles, CA)
- …Drives the understanding and delivery of quality clinical research (patient safety , rights and wellbeing; data reliability; scientific integrity; regulatory and ... Initiation, Monitoring, and Closure) for assigned sites and clinical trials Verifies safety reporting and the proper handling, monitoring and storage of trial… 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 ... overnight travel required. Qualifications A Bachelor's degree required; Advanced degree preferred . A minimum of 10 years of marketing/sales reporting and analysis… 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
- 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
- Merck & Co. (Rahway, NJ)
- …projects as the leader of a cross-functional team.--Champion compliance and safety ; promote a culture of diversity, inclusion, and equity. Minimum Education ... maximize talent development and utilization.Excellent interpersonal and communication skills Preferred Experience and Skills Experience in leadership of CMC… more
- Merck & Co. (North Wales, PA)
- …the development and execution of statistical analysis and reporting deliverables (eg safety and efficacy analysis datasets, tables, listings, figures), the span of ... multiple stakeholder groups which include clinical development, outcomes research and safety evaluation.The position is a key collaborator with statistics and other… more
- BAXTER (Medina, NY)
- …that is never the same from one day to the next. As a Quality Associate II, you are unafraid of navigating through necessary internal processes to facilitate a ... if needed. You take pride in getting things done quickly without sacrificing safety or quality.Your Team at BaxterWithin Quality, every role makes a difference.… more
