- Merck & Co. (Upper Gwynedd, PA)
- … Associate Principal Scientist, CMC, R4 - Pharm Pre-approval Reporting to the Sr Director/Director/Principal Scientist/Sr Principal Scientist in Pre-approval ... Pharmaceutical CMC is responsible for developing and implementing CMC regulatory strategies for our company's pharmaceutical pipeline products in accordance with… more
- Merck & Co. (Rahway, NJ)
- …in West Point, PA / Rahway, NJ is seeking a curious and collaborative Associate Director to support our robust infectious disease and vaccines pipeline. - As an ... Associate Director, you will represent QP2 on cr o...vendors and partners, creating an aligned, quantitative and model-informed regulatory framework to impact strategies and decisions of drug… more
- Merck & Co. (North Wales, PA)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... predominantly includes the development and execution of statistical analysis and reporting deliverables (eg safety and efficacy analysis datasets, tables, listings,… more
- Merck & Co. (Rahway, NJ)
- …process validation, second generation process development and authoring of regulatory submissions.-Under the general scientific and administrative direction of the ... next generation process development and characterization, process validation, and regulatory submission authoringIn this role, the successful candidate will be… more
- Eisai, Inc (Nutley, NJ)
- … reporting , patient support, as well as other pharmaceutical regulatory counseling. Essential Functions: Provides proactive and day-to-day legal support, advice ... federal and state pricing-related laws and regulations, PhRMA Code and FDA regulatory guidelines.Serves as the legal representative for market access materials on… more
- Eisai, Inc (Exton, PA)
- …Development groups as well as with Facilities, Quality Assurance, Quality Control, Regulatory , and CMC Program Management departments.The Associate Director of ... 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… more
- Eisai, Inc (Nutley, NJ)
- …difference. If this is your profile, we want to hear from you. The Associate Director (AD), Global Medical Affairs Training and Education is responsible for the ... managers. Develop congress abstract tracker, assign MSL coverage, review MSL reporting responsibilities, collate and distribute Congress Report, execute pre- and… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Pediatrics will focus on driving strategy, development, and life-cycle ... the external community (Key Scientific Leaders, Patient Community, Payers, Regulatory Agencies)Responsible for managing, coaching, and mentoring Clinical Directors… more
- Eisai, Inc (Nutley, NJ)
- …a difference. If this is your profile, we want to hear from you. Associate Director, Medical Education - Oncology, is responsible for the strategic planning and ... input into CME budget and website portal as needed. Ensure compliance with regulatory and other ethical guidelines relevant to the pharmaceutical industry, and to… 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 ... for all dealings between our Company and the External Partner, the Associate Director External Manufacturing Operations is accountable for establishing a strong… more
- Aequor (Tampa, FL)
- …and interprets QC and microbial limits testing according to USP and regulatory requirements for raw materials, finished products, and stability samples. Perform ... from production or formulations development dept. Actively participates in customer and regulatory audits as area SME. Develops and executes validation protocols for… more
- Merck & Co. (North Wales, PA)
- …strategic statistical decision-making, development of study design and analysis and reporting through all phases of development including regulatory ... art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for… more
- Aequor (Thousand Oaks, CA)
- …of working Implement best practices in data collection, cleaning, and reporting including knowledge of Pinnacle 21, Centralized Statistical Monitoring, Quality by ... and ensure smooth integration into new and/or modified processes Regulatory Compliance and Quality Assurance: Ensure all data management...OR Bachelor's degree and 6 years of experience OR Associate 's degree and 10 years of experience OR High… more
- Santander Holdings USA Inc (Dallas, TX)
- CIB US Letters of Credit Transaction Management, Associate - Dallas/Miami Country: United States of America Your Journey Starts Here: Santander is a global leader ... Stakeholders. Answering or channeling questions to ensure the timely processing and accurate reporting of Trade and GTB products. Support the Back Office team on the… more
- Santander Holdings USA Inc (Boston, MA)
- Senior Digital Payments Risk Management Associate Country: United States of America Your Journey Starts Here: Santander is a global leader and innovator in the ... You! The Difference You Make: The Senior Digital Payments Risk Management Associate will be responsible for identifying, assessing, and managing operational risks… more
- Santander Holdings USA Inc (Dallas, TX)
- Technology Risk/Program Management, Sr Associate Country: United States of America Your Journey Starts Here: Santander is a global leader and innovator in the ... We Want to Talk to You! The Difference You Make: The Senior Associate , Technology Risk Management within the Technology and Information Risk Management organization… more
- System One Holdings, LLC (Tarrytown, NY)
- Job Title : Temp - Associate Director, Aggregate Reporting , GPS Type : Contract Compensation : $85 - $100 hourly (dependent on experience) Contractor Work Model ... , DSURs , RMPs , and other ICH-compliant safety reports . Familiarity with regulatory safety reporting guidelines (eg, EMA, FDA, ICH E2E). Demonstrated ability… more
- Goldman Sachs, Inc. (Dallas, TX)
- …Inventory Traceability, and (6) Issue Management. We are looking for a highly motivated Associate to join the Regulatory Inventory Traceability team with a focus ... financial market movements but can impact an organization's operations, reputation or regulatory standing. These risks include - operational risk, conduct risk, … more
- Abbott (San Diego, CA)
- …for diversity, working mothers, female executives, and scientists. The Opportunity This position, Associate Director Regulatory Affairs , works out of our San ... part of the RA New Product Introduction (NPI) team, reporting to the Director of Global NPI and US... to the Director of Global NPI and US Regulatory Affairs. We're empowering smarter medical and economic decision-making… more
- ADMA BIOMANUFACTURING LLC (Boca Raton, FL)
- …assists with documentation for inspections and audits, provides insight and guidance for regulatory reporting and follow up of any 483's or other identified ... consider ADMA Biologics. We currently have an exciting opportunity available for an Associate Director, Regulatory Affairs - Plasma Services in Boca Raton,… more
