- Eisai, Inc (Baltimore, MD)
- …vendor management, and technical oversight to support the objectives of Global Regulatory Operations. The Associate Director will collaborate with the Heads ... If this is your profile, we want to hear from you. The Associate Director of Global Submission Management (GSM) is responsible for leading, managing, strategizing,… more
- Insmed Incorporated (NJ)
- …expand what's possible for patients with serious diseases. Reporting to the Associate Director, Regulatory Affairs, Tactical Implementation, you'll have a ... of science, we're in. Are you?About the Role:We're looking for a Manager, Regulatory Affairs, Tactical Implementation, on the Regulatory Affairs team to help… more
- Insmed Incorporated (NJ)
- …science, we're in. Are you?About the Role:We're looking for an In vivo Associate Scientist, Biology on the Research/Biologics Team to help us expand what's possible ... collection as part of Insmed's in vivo pharmacology team. The In vivo Associate Scientist will collaborate closely within the team and cross-functionally to plan and… more
- Eisai, Inc (Nutley, NJ)
- …Coordinates and provides reporting information for reports submitted to the regulatory agencies. Monitors adherence to protocols and determines study completion. ... other corporations when working under licensing agreements. Job Summary The Associate Director Operations, Global Medical Affairs, Strategic Planning and Operations,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director, Crisis & Issues Communications & Media, will play a critical role in advancing our Company's enterprise reputation and ... teams, Human Health Communications, and colleagues across the enterprise. The Associate Director will help shape and deliver clear, compelling narratives around… more
- Merck & Co. (Rahway, NJ)
- …DescriptionJOB DESCRIPTION SUMMARY Primary activities include but are not limited to: The Associate Principal Scientist is a DVM and/or PhD whose primary function is ... and report clinical laboratory and field studies that will support the regulatory approval of new companion animal and livestock products. The position requires… more
- Genmab (NJ)
- …fit? Then we would love to have you join us!The Role The Associate Director, External Data Quality Management, is a strategic leadership role supporting high-quality ... quality, and integrity of external data across the clinical programs.The Associate Director will guide cross‑functional teams, oversee external data quality and… more
- Cipla (Hauppauge, NY)
- …working outside of Cipla's US Subsidiaries or Affiliates. Job Title: QA Associate (IT) Location: Hauppauge, NY (Onsite) Employment Type: Full Time - Salaried/Exempt ... Range: $72,800-$93,600 Work Hours/Shift: 8:30AM - 5:00PM Job Overview: The QA Associate (IT) is responsible for review of batch production records, ensuring that… more
- Insmed Incorporated (NJ)
- …and for the future of science, we're in. Are you?About the Role:The Associate Director, Clinical Counsel will provide legal support to the clinical contracting team ... ering with internal cross-functional stakeholders to proactively apply legal and regulatory framework to business activity by understanding business goals and… more
- Cipla (Fall River, MA)
- Job Title QA QMS Associate Organization Name InvaGen Pharmaceuticals, Inc. Location 927 Currant Rd, Fall River, MA Shift General (8:30AM - 5:00PM) Employment Type ... employee discounts, and other benefits. Purpose The QA QMS Associate position is an individual contributor role and a...QMS in line with GMP (Good Manufacturing Practice) and regulatory requirements (eg, FDA, ). Maintain and ensure the… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Principal Scientist, Device Risk Management Lead, is a crucial member of our team, responsible for spearheading risk management efforts ... through launch and post-market surveillance. Key Responsibilities and Activities: The Associate Principal Scientist, Device System - Device Risk Management will be… more
- Bayer (Filer, ID)
- …diverse minds to make a real difference, there’s only one choice. Operations Associate This role contributes to the successful delivery of the Hybrid Wheat Breeding ... operation that is compliant with safety, plant health, quality and regulatory requirements. YOUR TASKS AND RESPONSIBILITIES The primary responsibilities of this… more
- Merck & Co. (Rahway, NJ)
- Job Description Associate Principal Scientist - Continuous & Expression Technologies in Large Molecule Downstream Processing - The Continuous & Expression ... the biologics and vaccine arenas. Specifically, CET is seeking an Associate Principal Scientist specializing in bioprocessing purification technologies for multiple… more
- Bayer (Urbandale, IA)
- Operations Associate At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where 'Health for all Hunger for none’ is ... diverse minds to make a real difference, there’s only one choice. Operations Associate Operations Associate is responsible for executing daily operations and… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Associate Senior Counsel, Privacy, is a strategic, business-minded, and hands-on attorney role whose ... In expanding and managing Eisai's US Privacy Program, the responsibilities of the Associate Senior Counsel, Privacy, include, but are not limited to, practical and… more
- Bayer (Filer, ID)
- …diverse minds to make a real difference, there’s only one choice. Operations Associate III (Field Nursery) YOUR TASKS AND RESPONSIBILITIES Operations Associate ... for the Hybrid Wheat Program. The primary responsibilities of this role, Operations Associate III (Field Nursery) , are to: Key Responsibilities Accountable for safe… more
- Aequor (Thousand Oaks, CA)
- …to current Good Manufacturing Practices (cGMP), safety guidelines, and regulatory requirements while supporting analytical testing, documentation, and laboratory ... is preferred but not required Preferred Qualifications Ability to follow regulatory requirements, written procedures, and safety guidelines Ability to review and… more
- Insmed Incorporated (NJ)
- …and for the future of science, we're in. Are you?About the Role:The Associate Director, Medical Review Committee (MRC) Operations is responsible for managing the ... operational execution of the company's Global We're looking for an Associate Director, Medical Review Committee Operations, on the Medical Review team to help us… 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.Role OverviewThe CAR-T Warehouse Operations Associate will be part of the Technical Operations team...optimization and efficient utilization of the warehouse space.Assist in regulatory inspections, perform safety and quality audits, and answer… more
- Aequor (Aliquippa, PA)
- …business and operations. Prepare for and support internal and external regulatory inspections and audits. Lead the development, revision, and lifecycle management ... or Business experience (preferably in the biotechnology or pharmaceutical industry) OR Associate 's Degree and 6 years of Life Science or Business experience… more
