- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Job Summary: Provide leadership and guidance as the lead statistician dedicated to safety on one or more safety monitoring team(s), accountable for all ... methodological and statistical aspects for safety signal detection and characterization for ongoing studies and compound level pooled clinical trial data of… more
- Eisai, Inc (Exton, PA)
- …difference. If this is your profile, we want to hear from you. The Associate Director of Biologics Operations Upstream and Downstream is responsible for leading and ... as supporting technology transfer to external partners (as required). The Associate Director sets strategic directions and project priorities, providing scientific… more
- Aequor (Thousand Oaks, CA)
- …or GED and two years of relevant work or military experience, though an associate 's degree with six months of experience is also acceptable. A bachelor's degree is ... General understanding of aseptic techniques, cGMPs, gowning, sampling procedures and safety guidelines Work as a team player and/or independently Multi-task and… more
- Genmab (NJ)
- …feel like a fit? Then we would love to have you join us!Role:The Associate Director acts as a statistical expert supporting the clinical development of compounds as ... trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and plans.Responsibilities:Compound/Indication… more
- Merck & Co. (Durham, NC)
- …Operations, Drug Delivery Systems and Devices within our Manufacturing Division ( Associate Director).-This role serves as a Virtual Plant Manager - responsible ... to deliver Pharmaceutical, Biologic, and Vaccine Products. Our team works with a " Safety First, Quality Always" mindset.-As the primary point of contact for all… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Associate Director, Clinical Programming must have expertise in addressing technical challenges in the ... technical skills in SAS systems and application development and experience. The Associate Director must be a highly specialized individual contributor or functional… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a Warehouse Operations Associate III as part of the Technical Operations team based in Raritan, NJ. ... warehouse space. This individual will assist in regulatory inspections, perform safety and quality audits, and answer relevant questions about packaging, methods,… more
- Aequor (West Greenwich, RI)
- …training compliance and proficiency. 8. At all times, comply with safety guidelines, cGMPs/CFRs and other applicable regulatory requirements. Shift: Saturday - ... preferred.Basic Qualifications: Science related background, lab experience Bachelor's degree OR Associate 's degree and 4 years of experience OR High school diploma… more
- Insmed Incorporated (San Diego, CA)
- …and Best Medium Workplaces™ lists.OverviewInsmed is seeking a Senior Research Associate with significant experience with droplet digital PCR (ddPCR). This individual ... assays to third party contractors. Depending on experience, the Sr Research Associate will expand molecular and product specific assay development working with the… more
- Merck & Co. (Rahway, NJ)
- …in Rahway, New Jersey.The Sterile Process Engineer role at the Associate Director level will leverage the individual's leadership, technical, and communication ... change management.Familiarity with United States and European Union GMP and Safety compliance regulations.Ability to convert new drug product attributes and process… more
- Insmed Incorporated (San Diego, CA)
- …Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Research Associate will expand molecular and product specific assay development working ... novel medicines to the clinic.Strict adherence to environmental, health, and safety guidelines.Salary Range$68,000 - $90,467 a yearCompensation & BenefitsAt Insmed,… more
- Insmed Incorporated (San Diego, CA)
- …lead on a PDT as required by the business.ResponsibilitiesThe Analytical Development Operations associate director is responsible for building a team to take care of ... technology transfers and mentoring junior staff. Maintaining laboratory equipment, ensuring safety and regulatory compliance, and supporting audits are also part of… more
- Aequor (North Creek, WA)
- …(Required): Position Summary: We are seeking an experienced, highly motivated Research Associate to join our Manufacturing Science and Technology (MSAT) lab team in ... to collaborate with others in a dynamic environment Adherence to laboratory safety guidelines and, SOPs, and other regulatory requirements Must be willing and… more
- Genmab (NJ)
- …to have you join us!The Global Regulatory Labeling, Policy and Intelligence Associate Director will primarily 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
- Merck & Co. (Rahway, NJ)
- …support business objectives, with focus on Process Design and Process Safety for Small Molecule High Potency/Containment Projects. Develop project scope, front-end ... Participate in development and review of engineering guidelines, standards, safety /environmental policies, and change requests. Define intent in Front-End Loading,… more
- Aequor (Walkersville, MD)
- …procedures and instructions for all activities in which the team participates. Safety Responsibility Is knowledgeable and complies with all pertinent safety ... and regulations. Ensure that all team members comply with safety rules and regulations. Job Scope Works on problems...from others is primarily internal. Work in a fast-paced, safety -oriented team environment. Working Conditions A majority of the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …as R shiny apps for data surveillance, visualization, modeling and simulations, and safety signal detection. Lead the development and validations of R package and/or ... R capabilities and implementations. Collaborate with CSPV to enable/effectively support safety signaling detections and across compounds safety reviews (ie,… 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
- Merck & Co. (Rahway, NJ)
- …enhance performance.Maintain a strong focus on compliance and Environmental Health and Safety (EHS) to drive supply excellence.Serve as the primary technical contact ... Clinical Manufacturing, Compliance Reviews, Data Analysis, Environment Health and Safety , Interpersonal Relationships, Lean Manufacturing, Manufacturing Processes, Manufacturing Support,… more
- AUROBINDO (Durham, NC)
- …to the ware house department as requested.Follow company policies, cGMP's, safety and Standard Operating Procedures. Qualifications - Skills & RequirementsAbility to ... instructions precisely and perform basic math calculation.Understanding/knowledge of cGMP, safety criteria or the ability to learn.Basic computer knowledge.Ability… more
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