- Merck & Co. (Rahway, NJ)
- …Source Management Business Operations Lead is expected to understand the end-to-end regulatory submission process. The main focus will be on document production ... Bachelor's degree with a minimum of 10 years of industry experience, at least 6 of those in a... experience, at least 6 of those in a regulatory and/or compliance area and experience with technical systems… more
- Merck & Co. (Rahway, NJ)
- …related industry .Demonstrated success in leading global marketing initiatives and managing teams.Strong analytical skills with the ability to interpret data and ... Job DescriptionRole Overview:The Customer Marketing Director will be responsible for shaping and spearheading the development and global deployment of the… more
- Merck & Co. (Rahway, NJ)
- …pipeline programs using fed-batch and continuous manufacturing platforms. The Director , Biologics Process Development (BPD) within the Biologics Process Research ... 3-6 programs at various stages of development. The key accountabilities include managing the work and personal development of direct reports while effectively… more
- Merck & Co. (Boston, MA)
- …development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director ... Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for...plans, settings) based on these clinical development strategiesMonitoring and managing the conduct of ongoing or new clinical trials… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Pharmacovigilance, handling and processing of raw data and external data, CDASH/SDTM, industry best practices, and relevant regulatory requirements is essential. ... areas centered around rare diseases and immune disorders. Job Summary: The Director of Data Management (DM) Reporting provides leadership in Data Management… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …5 of those working in or supporting a clinical, medical and/or regulatory organization, in the pharmaceutical industry (Pharma/Biotech/CRO) Experience in leading ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...automation, and continuous improvement. Relationships Reports to the Executive Director , PS & GxP Business Operations. Accountable for establishing… more
- Cipla (Central Islip, NY)
- …resolve any issues or disputes that may arise. Ensure compliance with regulatory requirements, industry standards, and company policies. Ensure procurement ... Job Title: Director - Procurement, Cipla North America Reports to:...activities adhere to regulatory requirements, industry standards, and company policies.… more
- Tris Pharma (Monmouth Junction, NJ)
- …success.We have an opening in our Monmouth Junction, NJ facility for a Director , Information Technology - Infrastructure LeadThe Director , Infrastructure Lead is ... have hands-on technical expertise combined with leadership experience in managing complex infrastructure environments.Key ResponsibilitiesLead the infrastructure team responsible… more
- Legend Biotech USA, Inc. (Philadelphia, PA)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Sr. Director of Toxicology as part of the Clinical Development team based in ... NJ. Role OverviewWe are seeking a highly experienced and strategic Senior Director of Toxicology to lead and oversee all nonclinical safety assessment activities… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across our company ... (as a lead GCS Planning program representative) such as clinical development, regulatory , quality and other supply chain areas to negotiate timelines, strategies and… more
- Merck & Co. (Rahway, NJ)
- …inspection readiness at all times. The Director should be well engaged with regulatory and industry trends and have thorough working knowledge of GMPs, ICH, ... Job DescriptionRaw Materials & Medical Device Director , Small Molecule Analytical Research & Development The...not required, the ideal applicant would have prior experience managing a GMP lab that supports raw material, excipient,… more
- Merck & Co. (Rahway, NJ)
- …motivated and experienced Anatomic Pathologist (MD) for the role of Principal Scientist ( Director ) to join our innovative team. This position will play a crucial ... pathology within our company's clinical therapeutic pipeline.The Principal Scientist ( Director ) will have the following responsibilities: Engage in providing… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionReporting into the Director , Logistics and Distribution Technology the Associate Director , Logistics and Distribution Technology will be ... Goods globally.-The Packaging Technical Operations organization aims to be an industry leader in problem-solving, delivering robust and pragmatic technical solutions… more
- Merck & Co. (Rahway, NJ)
- …Packaging Shipping Systems (Logistics and Distribution Technology)Reporting into the Director Packaging Distribution, Components and Systems COE the Director ... globally.- The Packaging Technical Operations organization aims to be an industry leader in problem-solving, delivering robust and pragmatic technical solutions to… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionReporting into the Executive Director Packaging Technical Operations the Director Packaging Distribution, Components and Systems Center of ... and systems.The Packaging Technical Operations organization aims to be an industry leader in problem-solving, delivering robust and pragmatic technical solutions to… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From healthcare provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
- Merck & Co. (North Wales, PA)
- … Distribution Channels, Market Analysis, Marketing, Oncology, Pharmaceutical Industry , Product Management, Sales Target Achievement, SAP Enterprise Resource ... and Vaccine customer channels.- This role is responsible for utilizing and managing SAP, Microsoft Office systems and, via third party vendor relationships,… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Associate Director , Engineering as part of the Technical Operations team based in ... Raritan, NJ. Role OverviewThe Associate Director of Engineering is a strategic and operational leader...and systems support business goals and comply with safety, regulatory , and sustainability standards. This position is a key… more
- Formation Bio (New York, NY)
- …Advancements in AI and drug discovery are creating more candidate drugs than the industry can progress because of the high cost and time of clinical trials. ... our values are the driving force behind our mission to revolutionize the pharma industry . Every team and individual at the company shares these same values, and… more
- Eisai, Inc (Nutley, NJ)
- …Knowledge/ Expertise, Critical Thinking & Business Agility, Drafting and Negotiation, Industry / Regulatory Knowledge, Legal & Reputational Risk Management, ... profile, we want to hear from you. The Associate Director , Compliance Operations will be a key member of...primary point of contact for Eisai's US monitoring activities, managing in-house efforts and third-party vendor engagements. The Associate… more
