- Merck & Co. (Rahway, NJ)
- …and regulatory postureDemonstrated working knowledge of FDA, ICH, and other regulatory requirements for CMC.- Strong experience in safety and environmental ... Capital Process having participated on a large capital project teamExperience in regulatory compliance expectations across all phases of product development to… more
- Genmab (NJ)
- …like a fit? Then we would love to have you join us!The Global Regulatory Labeling, Policy and Intelligence Associate Director will primarily be responsible for ... portfolio of products. The lead may also be responsible for supporting various regulatory policy and/or intelligence deliverables. This role will be within Global … more
- BioSpace (Boston, MA)
- …true to the best of my knowledge. Job Description About the role: The Associate Director, Clinical and Safety Quality Compliance is responsible for ensuring the ... quality of processes and product outputs. This role involves defining and specifying activities,...and monitoring processes, and ensuring compliance with corporate and regulatory standards. By maintaining high-quality standards, this role supports… more
- Merck & Co. (Durham, NC)
- …Safety Regulations, Quality Assurance, Risk Management, Deviation Management, Product Release, Change Control).- Supply Chain Management:-Manage coordination with ... Operations, Drug Delivery Systems and Devices within our Manufacturing Division ( Associate Director).-This role serves as a Virtual Plant Manager - responsible… more
- Merck & Co. (Rahway, NJ)
- …and change management.Familiarity with United States and European Union GMP and Safety compliance regulations.Ability to convert new drug product attributes and ... Sciences, Phytochemistry, Process Control Automation, Process Optimization, Process Simulation, Product Formulation, Safety Compliance, Standard Operating Procedure… 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
- Insmed Incorporated (San Diego, CA)
- …technology transfers and mentoring junior staff. Maintaining laboratory equipment, ensuring safety and regulatory compliance, and supporting audits are also ... 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… more
- Merck & Co. (Rahway, NJ)
- …and technical risks. You will also oversee External Partners during New Product Introductions and Technical Transfers, ensuring the success of our collaborative ... enhance performance.Maintain a strong focus on compliance and Environmental Health and Safety (EHS) to drive supply excellence.Serve as the primary technical contact… more
- Vera Therapeutics (Brisbane, CA)
- Job Description Title: Associate Director, Program Management Location: Brisbane , California About Us: Vera Therapeutics (Nasdaq: VERA), is a late clinical-stage ... in order to change the standard of care for patients. Vera's lead product candidate is atacicept, a fully humanized fusion protein self-administered at home as… more
- Ionis (Carlsbad, CA)
- …for review. Supports medical and commercial development for assigned products, including regulatory and medical strategies, product safety , product ... to our unique culture while you develop and expand your career! Associate Director/Director, Compliance Counsel SUMMARY: Reporting to the Director of Compliance, the… more
- Winn-Dixie Retail Stores (Tarpon Springs, FL)
- …food handling practices, sanitation and productivity are maintained. Adheres to all regulatory compliance requirements pertaining to food safety , United States ... necessary safety training. Ensures Hazardous Assessments are posted for associate reference and that Personal Protective Equipment is available and utilized by… more
- Takeda Pharmaceutical Company Limited (Round Lake, IL)
- …true to the best of my knowledge. Job Description About the role The Associate Director of Quality Control will lead the establishment of a state-of-the-art quality ... laboratory. Responsibilities include overseeing its design, construction, qualification, and regulatory approval. Collaborate with global teams to align with… more
- Mount Sinai Hospital (New York, NY)
- …Valley Health System is actively recruiting an Oncologist to join the team as Associate Chair for its Oncology Service Line. The Valley Medical Group (VMG) seeks an ... experienced Hematologic or Medical Oncology leader to serve as Associate Chair, Oncology Services, VMG, and Director, Hematology and Medical Oncology. Valley-Mount… more
- Planet Pharma (Raleigh, NC)
- Job Description The Associate Director, Quality Assurance, is responsible for the global strategic management and oversight of R&D Quality activities and associated ... EBD Medical Devices. Activities include, but not limited to general Product Development / Design Control customer input, specification development, verification and… more
- Eli Lilly and Company (Concord, NC)
- …now is the perfect opportunity! During the project phase, the Operations Associate (OA) will support commissioning, qualification, and validation of the Parenteral ... capacity planning). The PAR department will have ownership of product formulation, aseptic isolator barrier filling, and visual inspection...else, the role will lead by example with a safety first, quality always approach. As a site leader… more
- Sunnyside (South Beloit, IL)
- …we aim to lead the nation's cannabis industry with a focus on regulatory compliance, product consistency, and customer satisfaction. Our operations bring ... meets compliance regulations. Assist managers with organizing sales floor merchandise and product displays. Ensure security measures and safety compliance in the… more
- Arrowhead Pharmaceuticals (San Diego, CA)
- …bring new therapies to patients in need. The Position The Clinical Research Associate (CRA) provides support to Study Lead(s) in clinical study planning, execution ... oversight, and closeout activities in compliance with the clinical protocol, regulatory requirements, ICH GCP guidelines and governing policies & procedures.… more
- Bristol-Myers Squibb Company (New Brunswick, NJ)
- …data generation, insight generation and patients' access to medicine. The Regional Associate Director (RAD) role is field-based and focused on managing a team ... RAD oversees their regional team to ensure disease and product related medical needs in the region are being...Strategies, Objectives and FM Plans within boundaries established by regulatory and legal compliance in accordance with company policies… more
- BioMarin Pharmaceutical Inc. (San Rafael, CA)
- …preparation activities. Perform glassware/washing/autoclave services. Adhere to laboratory safety protocols, ethical guidelines, and regulatory requirements ... meaningful advances to patients who live with genetic diseases. The Operations Associate II, Laboratory Operations function is to support activities according to… more
- Forge Biologics (Columbus, OH)
- …new technologies and techniques to reduce costs, improve timelines, enhance safety , and improve regulatory compliance. What You'll Bring (Qualifications) ... and face to face meetings. About The Role We are currently seeking a Associate Scientist II, Manufacturing, Science & Technology (MS&T) to join the Forge Biologics… more
