- Daiichi Sankyo, Inc. (Bernards, NJ)
- …across all Medical Affairs programs. This role involves deputizing for the Sr. Director , representing the Quality organization at senior levels. The Director ... is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address...of excellence and compliance and working toward building a quality mindset with Medical Affairs.Support the Sr. Director… more
- Merck & Co. (Boston, MA)
- Job DescriptionWe are seeking an experienced Technical Product Manager to lead pharmaceutical process and meth od development data product portfolio. This unique - ... strong understanding of biopharma research, hands-on experience with- domains of pharmaceutical process , method development and tech transfer for commercial… more
- Cipla (Central Islip, NY)
- …Pay Range: 188k - 201k USDAbout Cipla: Cipla is a leading global pharmaceutical company, dedicated to high- quality , branded, and generic medicines. We are ... Job Title: Director - Procurement, Cipla North America Reports to:...acquisition of materials, services, and capital expenditures necessary for pharmaceutical operations across multiple manufacturing sites and Contract Manufacturing… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionReporting into the Director , Logistics and Distribution Technology the Associate Director , Logistics and Distribution Technology will be ... products for the benefit of patients. The Logistics and Distribution Technology Director is integral to this mission. The successful candidate will possess deep… more
- Merck & Co. (Rahway, NJ)
- …workflows.- - Required Skills and Experience: Knowledge of manufacturing, testing, quality , and supply chain processes from late clinical development through ... CMC regulatory content Understanding of CMC operations, technology transfer, control strategy development, and regulatory authoring requirements that inform… more
- Merck & Co. (Rahway, NJ)
- …Pharmaceutical Biology, Process Analytical Technology (PAT), Professional Networking, Quality Control Management, Regulatory Affairs Compliance, Regulatory ... microscopy and chromatography.Collaborate with cross-functional teams, including research, development, quality control , and regulatory affairs, to ensure… more
- Merck & Co. (Rahway, NJ)
- …Making, Drug Product Development, Estimation and Planning, General Safety, Manufacturing Quality Control , Mechanical Troubleshooting, Pharmaceutical Process ... Control Automation, Process Optimization, Product Formulation, Project Management, Quality Control Management, Regulatory Compliance, Regulatory Issues,… more
- Novo Nordisk Inc. (Boulder, CO)
- …rely on us. Our R&D hub merges biotech speed and agility with large pharmaceutical company quality , resources, and stability, uniting the best of both worlds ... to our patients Work effectively across all departments, such as Quality Assurance/ Control , Chemical Development, Program Management, Regulatory, Analytical… more
- Merck & Co. (Rahway, NJ)
- …DescriptionSr. Principal Scientist - Device Technical and Engineering Lead (Sr. Director Equivalent)Our company's Device Product & Process Development (DPPD) Team ... for applying their knowledge of product and process development in the (bio) pharmaceutical and/or medical device industries to set tactical and strategic direction… more
- Tris Pharma (Monmouth Junction, NJ)
- …in our Monmouth Junction, NJ facility for an experienced, hands-on SR. Director / Director , Procurement. Title and salary commensurate with experience. The ... Director / Senior Director , Procurement is responsible for...for multiple facets of the Procurement function within a pharmaceutical manufacturing environment including, but not limited to, purchasing,… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …demonstrated passion for creating new medicines.Experience with Engineering, Operations, Quality Control and Facilities Management.Experience in effectively ... entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize… more
- Insmed Incorporated (NJ)
- …external audits to ensure regulatory complianceManage technical ownership, change control , and documentation while ensuring system integrity and regulatory adherence ... alignment with business objectivesCollaborate closely with cross-functional teams including Quality Assurance, IT, CSV, and Compliance departmentsEnsure that Disaster… more
- Insmed Incorporated (NJ)
- …with regulatory requirements while maintaining operational excellence. The Executive Director , Cybersecurity & Risk Management plays a critical leadership role ... Committee and Board of Directors.Establish and maintain governance frameworks and control structures consistent with NIST and FDA data protection standards.Partner… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …methodologies, tools, and core deliverables. Relationships Reports to the Director , Sales Reporting & Forecasting. Position regularly interacts with members ... budget, per direction, and are internally consistent with group deliverable quality Systems and Data Management Responsible for gross-to-net forecast models, tools… more
- Insmed Incorporated (NJ)
- …for the future of science, we're in. Are you?About the Role:The Associate Director , Regulatory Affairs, CMC will be responsible for reviewing the CMC post approval ... programs.What You'll Do: Accountable for reviewing and approving all CMC change control documents and disposition of proposed changes and scheduling submissions as… more
- Cipla (Central Islip, NY)
- …General Shift: 9:00 AM - 5:30 PM (may vary based on business needs) Reports To: Quality Control Director Hourly Rate: $16.64 - $22.88Purpose: The content and ... outside of Cipla's US Subsidiaries or Affiliates. Job Title: Quality Control (QC) Lab Technician FLSA Classification:...to 35 pounds.About Cipla Cipla is a leading global pharmaceutical company, dedicated to high- quality , branded, and… more
- Insmed Incorporated (NJ)
- …possible for patients with serious diseases. Reporting to the Executive Director , Regulatory Operations, you'll be responsible for the publishing, management, and ... Veeva Submissions Vault, ensuring compliance with document management standards, version control , and audit readiness.Coordinate the intake, formatting, and QC of… more
- Merck & Co. (Rahway, NJ)
- …your skills and experience in audit through a career path in the pharmaceutical industry. Become part of a dynamic team that offers a flexible work ... programs, travel opportunities and workplace inclusion.We are a leading pharmaceutical company committed to improving health through innovative research, development… more
- JABIL CIRCUIT, INC (Hunt Valley, MD)
- Job Overview: In this role the Senior Director , Facilities & Engineering will be responsible for the Engineering, Maintenance, and Site Services for the ... buildings owned or leased by Pii (collectively 'the Site'). The Senior Director , Facilities & Engineering provides life cycle asset and facilities management… more
- Mercy (Ardmore, OK)
- …departments, to include: 1) supervising the development and implementation of quality control procedures as directed; 2) supervising a multi-disciplinary ... to oversee pharmacy operations and ensure the delivery of safe, effective, and compliant pharmaceutical care. Reporting to the Director of Pharmacy, this role is… more
