- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders.Summary The Associate Director, RACMC Portfolio Products, will be responsible for regulatory CMC ... regulatory process optimizations on relevant topics.Responsibilities- Supports CMC regulatory compliance activities for portfolio biologics to meet US, International… more
- Aequor (West Greenwich, RI)
- …to written procedures and cGMP requirements. Alert management of quality, compliance , supply and safety risks. Complete required assigned training to permit ... execution of required tasks. Responsible for being in clean room space for majority of time on shift which includes gowning in and out of frocks and coveralls. Communicating and collaborating with the PQA shift to ensure required tasks are completed Preferred… more
- Aequor (Thousand Oaks, CA)
- …as appropriate as well as any updates/amendments, ensuring template and version compliance . Manages the set-up of third-party vendors, assessing initial statement of ... work and budget, as well as the change order process. Prepares presentation material for meetings and newsletters. Contributes to review of new/amended/unique SOPs and guidance documents. more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for developing and continually growing strong relationships with DS internal senior stakeholders to assess, develop, implement and drive execution of Strategic ... procurement technology and knowledge management tools. Closely partners with senior Business stakeholders to design optimal processes and sourcing solutions… more
- Merck & Co. (North Wales, PA)
- …for current and future indications. This role will report to the Associate Director, Oncology Market Access.The Senior Specialist, Oncology Market Access ... that help us revolutionize how our medicines create value in society.The Senior Specialist, Oncology Market Access role will work closely with agency partners,… more
- Merck & Co. (Rahway, NJ)
- …the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the ... the world.Looking for someone with a growth mindset.Position Description: The Senior Director, Global Regulatory Lead, is responsible for development and… more
- Aequor (Athens, GA)
- …manner. Interfaces with relevant stakeholder groups as needed to ensure compliance . Provide training for team members in assigned areas of responsibility. ... within the regulatory department and stakeholder groups relative to regulatory compliance of BIAH products and processes. With minimum guidance and supervision,… more
- Merck & Co. (Rahway, NJ)
- …Manager COM , Clinical Research Manager CRM and Clinical Research Associate CRA. And the person collaborates with finance/budgeting representatives to manage ... payments (to investigators, vendors, grants)Ensure adherence to financial and compliance proceduresMonitor and track adherence and disclosures,Maintain tracking toolsObtain… more
- Aequor (Athens, GA)
- …and guidance. Interfaces with relevant stakeholder groups as needed to ensure compliance . Provide training for team members in assigned areas of responsibility. ... within the regulatory department and stakeholder groups relative to regulatory compliance of BIAH products and processes. With minimum guidance and supervision,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …listings, SAP, Data Mgmt plan; Reviews patient population and protocol compliance for consistency with study strategy; Develops biomarker strategy in collaboration ... between CRO / vendors / AROAdditional non-study related activities: Occasional senior management interactions at FIHC, WDC; Initiates contact w/KOL and prepares… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …an ability to balance needs spanning customer service, operations, marketing and compliance . Relationships This role reports to the Associate Director-Patient ... Solutions across multiple therapeutic areas at Novo Nordisk Inc., (NNI). The Senior Manager Patient Solutions will be responsible for delivering the vision spread… more
- Merck & Co. (Millsboro, DE)
- …Delaware seeks to add an Attending Veterinarian in the role of Associate Director.This position will have overall responsibility for oversight and administration of ... at our company's Millsboro Animal Health facilities. This role is highly compliance -driven in accordance with State and Federal regulations as applicable to the… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Director Market Access will work closely with agency partners, internal brand colleagues, promotions, internal communications, pricing, ... indications. This role will report to the Director, Oncology Market Access.The Associate Director Market Access will be responsible for supporting market access… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Director, US Payer Marketing/ Oncology Market Access - Alliances will work closely with cross functional teams, alliance partners, ... will report to the Director, Oncology Market Access - Orals & AlliancesThe Associate Director, US Payer Marketing/ Oncology Market Access will be responsible for… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Device Development Associate Principal Scientist - Development Strategy, Design Controls and Risk Management Our company's ... Development and with external suppliersUnderstand and apply regulatory / compliance requirements relative to design controls and risk management activities.Lead… more
- Merck & Co. (North Wales, PA)
- …and ensure that customers are at the center of every business decision. Associate Director, Customer Experience Management Strategist will report to the Director of ... help coach and guide team members; communicate progress and potential challenges to senior team members as they arise.Culture: Support a culture of learning, smart… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …schedule requirements. At the direction of the Supervisor and more Senior Engineers, provide support including facilities engineering, design, project coordination, ... thorough understanding of cGMP's, established manufacturing practices and procedures, and compliance with GMP, QS, and ISO regulations and guidelines Understanding… more
- Eisai, Inc (Nutley, NJ)
- …and corporate goals, as well as commit to meet all compliance and reporting requirements. Requirements Bachelor's degree required; MBA preferred.Experience using ... contract operations.Demonstrated critical thinking analytical skills.Ability to communicate to senior leadership and lead cross functional teams.Motivate and guide… more
- HITT Contracting (Falls Church, VA)
- …our vision to create extraordinary experiences, you belong at HITT. Quality Control Senior AssociateJob Description: The Senior Associate , Quality Control is ... installations, and supporting the Site Ops Teams with issue/punch list resolution. The Senior Associate , Quality Control will assist the Quality Control Manager… more
- Eisai, Inc (Louisville, KY)
- …is your profile, we want to hear from you. Job Summary The Senior Oncology Sales Specialist is responsible for meeting/exceeding sales goals through promoting ... within an assigned territory in a compliant and appropriate manner. The Senior Oncology Sales Specialist represents and promotes assigned brand(s) in the oral… more
