• Daiichi Sankyo, Inc. (Bernards, NJ)
    …areas centered around rare diseases and immune disorders. Summary The purpose of the Project Manager (RACMC) function is to lead and/or support complex filing ... activities, ensuring compliance with technical and regulatory standards. This role involves...resource management, and clear communication with stakeholders and the project team. The Project Manager more
    HireLifeScience (12/19/24)
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  • Exela Pharma Sciences, LLC (Lenoir, NC)
    …the organization, fostering innovation and supporting cross-functional teams. The Project Manager II is responsible for being in compliance with all safety ... Position Summary:The Project Manager II is responsible for...self and direct reports are trained and work in compliance with applicable SOPs, cGMPs, regulatory requirements, safety, environmental,… more
    HireLifeScience (12/18/24)
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  • Exela Pharma Sciences, LLC (Lenoir, NC)
    …coordination while working closely with cross-functional teams and leadership. The Project Manager I is responsible for being in compliance with all safety ... Position Summary:The Project Manager I supports the management...self and direct reports are trained and work in compliance with applicable SOPs, cGMPs, regulatory requirements, safety, environmental,… more
    HireLifeScience (12/18/24)
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  • Merck & Co. (Rahway, NJ)
    Job Description Job Description: - The drug development Project Manager is part of Global Project and Alliance Management (GPAM) which sits in the Research & ... company. - Position Description/Summary: - The GPAM Associate Director, Project Manager , is a core member of...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los… more
    HireLifeScience (01/03/25)
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  • Exela Pharma Sciences, LLC (Lenoir, NC)
    …complex projects under the guidance of a Project Manager . The Project Coordinator is responsible for being in compliance with all safety policies, cGMPs, ... Position SummaryThe Project Coordinator II manages small pharmaceutical projects independently...status reports and communicate updates to stakeholders.Maintain personal training compliance status and work in compliance with… more
    HireLifeScience (12/18/24)
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  • Merck & Co. (North Wales, PA)
    …of CMC and Clinical strategies . - Position Description/Summary: - The CIPM Associate Director, Project Manager , is a core member of DCTs , partnering with team ... Job DescriptionGlobal Project and Alliance Management (GPAM) sits in the...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los… more
    HireLifeScience (12/11/24)
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  • Merck & Co. (Durham, NC)
    …finished product, and laboratory testing for the BCG vaccine.The Quality Operations Laboratory Manager leads a team of analysts in the start-up and method transfer ... to work cross-functionally with existing Laboratories and organizations. The Laboratory Manager will be responsible for start-up testing in new laboratories using… more
    HireLifeScience (01/08/25)
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  • Genmab (Plainsboro, NJ)
    …Supply Manager , of the following tasks:Global Clinical Drug Supply Project /Trial ManagementObtain Project /Trial specific information to initiate drug supply ... is essential to fulfilling our purpose.Genmab is seeking a Clinical Drug Supply Manager to join our Global Clinical Drug Supply (GCDS) Operations Team in Princeton… more
    HireLifeScience (01/07/25)
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  • Merck & Co. (Durham, NC)
    …and patients on time, every time, across the globe. GENERAL SUMMARY: The Manager , Teknika QC laboratory, is responsible for managing a team of individual ... such as change control, deviation management, audits and regulatory inspections.- The Manager will be responsible for using principles of our Company Production… more
    HireLifeScience (01/08/25)
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  • Merck & Co. (North Wales, PA)
    …R&D division (our Research & Development Division ) is looking for Product Manager - PV Case Intake and Processing. Reporting into Product Line Lead Patient ... Safety and Quality & Compliance , this position will be responsible for managing the...responsibilities of a PV Case Intake & Processing Product Manager : Develop and implement PV strategies: Work with cross-functional… more
    HireLifeScience (01/07/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …possibilities for professional and personal development. Are you ready? The Position As Manager of Academy and Franchise within the NNI Employee Experience team, the ... journeys aligned with measurable business objectives. In addition, they need project management experience. The learning solutions developed should be innovative and… more
    HireLifeScience (12/14/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …research areas centered around rare diseases and immune disorders. Job Summary: The Manager of CRA Monitoring Oversight and Excellence is responsible for the support ... monitoring conduct across the DS portfolio. This position will serve to support the project plan of CRA Monitoring Oversight and Excellence and the CSOP as it… more
    HireLifeScience (01/06/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …members to ensure that the organization is in a perpetual state of compliance as follows:Support the Global Quality Lead(s) (GQLs) and Regional Quality Leads (RQLs), ... the status of Quality Events (QEs), CAPAs and GCP compliance matters raised to the GQLs and/or RQLs from...prioritize and focus on the delivery and execution of non- project initiatives within R&D Quality and Global RD/PV QA… more
    HireLifeScience (01/05/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …technical service providers to supplement in-house capabilities when necessary Evaluation, Compliance , and Improvement Conduct post- project evaluations to assess ... you ready to maximize your potential with us? The Position The Associate Manager of Technical Production will be responsible for overseeing the technical aspects of… more
    HireLifeScience (12/13/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …the treatment of multiple myeloma.Legend Biotech is seeking QA Batch Disposition Associate Manager as part of the Quality team based in Raritan, NJ. Role ... responsible for quality and maintaining the highest standards in compliance within company policies, procedures, and all applicable regulations.Key Responsibilities… more
    HireLifeScience (11/08/24)
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  • Genmab (Plainsboro, NJ)
    …area of clinical drug supply management.Oversee inspection readiness and ensure compliance with relevant regulations.Manage operational trial and project ... Role & DepartmentGenmab is seeking an experienced Senior Clinical Drug Supply Manager to join our Global Clinical Drug Supply Operations team.As Senior Clinical… more
    HireLifeScience (12/19/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …other research areas centered around rare diseases and immune disorders. Summary The Manager , Data Programmer is a member of the Biostatistics and Data Management ... Management, as necessary.Participates in the development of and ensure compliance to Standard Operating Procedures (SOPs), policies, and guidelines.Remain informed… more
    HireLifeScience (11/21/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …ensure business objectives are met Manages and monitors organizational compliance with all established supplier agreements Provides strategic procurement ... sourcing systems and tools: Follows up on system usage and proactively ensures compliance to system Interfaces with the Novo Nordisk Corporate Procurement to promote… more
    HireLifeScience (11/02/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …in cross-functional teams locally/globally to assure timely attainment of project milestones Develops solutions for process improvements; enhance quality and ... with respects to trial start up through trial closure Ensures contract compliance in accordance with established policies Ability to think strategically and initiate… more
    HireLifeScience (11/13/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …Regulatory Affairs, CMR, Supply Chain, and HQ colleagues regarding labeling compliance to accomplish company goals. External relationships may include interaction ... May participate in FDA submission planning meetings to ensure clear communication of the project plan, actions items, risks, and decisions to the team as it relates… more
    HireLifeScience (12/11/24)
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