- Legend Biotech USA, Inc. (Raritan, NJ)
- …many stakeholders.Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.Require minimal direction to complete ... an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Associate Director of Quality Project Management and Strategyas part of the … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and proficient in creation of process maps preferredExperience working with Quality Management systems preferredExperience with requirements related to global ... Director , Development SOP Management Join a Legacy of...and implementation of Development SOP activities to ensure regulatory compliance and cross functional cohesiveness across SOPs and related… more
- Tris Pharma (Monmouth Junction, NJ)
- …builds in-house analytical capabilities, when needed. The incumbent ensures timeline, quality and compliance with applicable Standard Operating Procedures ... guidance and provides technical guidance within and outside R&D for regulatory and quality matters.The Associate Director / Director , AR&D serves as Deputy to… more
- Merck & Co. (Rahway, NJ)
- …design verification testing, and process validation, with a strong understanding of quality management systems and regulatory compliance .Exceptional project ... products, with a focus on autoinjectors, prefilled syringes, and other drug delivery systems . The director will lead a team of engineers and technical… more
- Merck & Co. (North Wales, PA)
- Job DescriptionPrincipal Scientist / Director , GLOBAL REGULATORY CMC Biologics (R5)Under general supervision of an Executive Director /Senior Director , the ... support of their assigned projects. Position Description- The Principal Scientist / Director responsibilities include but are not limited to:Serve as a Regulatory… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …available for presenting at senior leadership meetings.Ensure and lead the establishment of the Quality Systems for the Research Quality area, and that all ... regulatory submissions and / or inspections Ensures that appropriate systems , processes are in place to enhance GLP/GCLP activities...a phase appropriate quality system that supports quality and compliance of Good Clinical Laboratory… more
- Aequor (Waltham, MA)
- …role - 3 days onsite, 2 days remote Position Summary: The IT Operations Director will oversee the operation of server systems , networking equipment, cloud ... Job description Job title - Director , IT Operations, and Infrastructure Location - Waltham,...cybersecurity best practices and experience in implementing security measures. Hands-on experience with GxP compliance and validated systems… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and immune disorders.Job Summary Deliver the development and implementation of informatics systems and programs to support the business functions of Daiichi Sankyo ... Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance, Regulatory/Risk Management, Quality Assurance, Medical Affairs, Translational Research, Research, Informatics Services,… more
- Merck & Co. (Rahway, NJ)
- …the Design Authority.- They will ensure the smooth operation of our SAP systems with a mindset towards continuous improvement.- Their expertise in SAP System ... and overall role administration. This role reports to Executive Director , SAP Platform Team. Primary Responsibilities: Leadership and StrategyProvide strategic… more
- Merck & Co. (North Wales, PA)
- …pipeline acceleration and uninterrupted supply of commercial products. The Associate Director , Large Molecule (LM) Critical Reagents (CR) Operations, is a leadership ... company's growing inline large molecule product portfolio. The LM CR Operations, Associate Director will lead a team responsible for the execution of material make,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …internally and with external parties. Ensure that all employees are in compliance with all contract requirementsSupport the Associate Director Global Strategy ... systems such as Sharepoint, LMS, Trackwise Digital and other quality management systems .Strong interpersonal, communication, technical writing, negotiation… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and Strategic Sourcing activities. This position will ensure the acquisition of high- quality goods/services at the best possible prices by negotiating and monitoring ... and/or strategic sourcing roles within the department. Relationships Reports to a Senior Director within the NNI Procurement Team and will interact with all NNI… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and Strategic Sourcing activities. This position will ensure the acquisition of high- quality goods/services at the best possible prices by negotiating and monitoring ... improvements and seek agreement through consensus management. Relationships Reports to an Associate Director / Director within the NNI Procurement Team and will… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …evolve, so does our challenge to find better and more innovative ways to improve their quality of life. We're changing lives for a living. Are you ready to make a ... Coordinates project activities and needs related to Patient Safety. Ensures compliance with Federal regulations and company SOPs regarding collection, verification,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and Strategic Sourcing activities. This position will ensure the acquisition of high- quality goods/services at the best possible prices by negotiating and monitoring ... improvements and seek agreement through consensus management.RelationshipsReports to an Associate Director / Director within the NNI Procurement Team and… more
- Merck & Co. (Rahway, NJ)
- …providing technical mentorship.Experience with Potent Compound processing and containment systems (eg, isolators).Experience with Quality systemsNOTICE FOR ... project management responsibility. The Specialist -Engineering position will report to the Associate Director , Engineering and will be a member of the EF Team at the… more
- Lovelace Biomedical Research Institute (Albuquerque, NM)
- …execution or resolution of study issues. The Laboratory Supervisor may review, perform quality control correct and give guidance to director reports. The ... of expertise. The work is performed in a highly regulated environment and compliance with documentation standards is required, will perform all other related duties… more
- Merck & Co. (Rahway, NJ)
- …by leveraging data analytics and understanding implications on global healthcare systems . Audit assignments are unique to each individual's skill set, professional ... Program (FLDP) will allow individuals to gain knowledge on products, healthcare systems , payors, and regulatory and reputational risks while working intimately with… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and compliance . Relationships This role reports to the Associate Director -Patient CRM Product Owner. Collaborates cross-functionally with internal teams, such as ... the vision spread across a multi-year roadmap for the CRM and Telephony systems . This role develops, manages, and prioritizes the product backlog, engages with the… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …improvements to prepare for launch, development and/or life cycle activities Health Systems strategy: Collaborates with medical affairs and market access teams to ... inform a health systems strategy to ensure system level acceptance and access...days remote. Approximately 20-30% overnight travel. Global Job level: Director Development of People Ensure that reporting personnel have… more
