- American Honda Motor Co Inc (Marysville, OH)
- …PurposeSupports the NA Region Risk Management Secretariat and the NA Region Compliance Secretariat, along with the Company Risk and Compliance Officers, ... as a member of the NA Region Governance, Risk, Compliance & Ethics Office, with the execution of the...Care Support* Wellbeing Program* Community Service and Engagement Programs* Product Programs* Free Drinks OnsiteHonda is an equal opportunity… more
- Merck & Co. (Durham, NC)
- …providing documentation to support the approval of licensure supplements and new product license registrations Collaborate with Durham Laboratory Compliance to ... Job DescriptionPosition Description: Specialist , Quality Control Our Company is expanding its...robustness, work standardization and lean six sigma initiatives Ensuring compliance in the laboratory for equipment and facility function… more
- Merck & Co. (Durham, NC)
- … product inspection, and quality control laboratories.The Quality Assurance Specialist will support this expansion. Project activities requiring support include ... Job DescriptionPosition Description: Specialist , Quality Assurance Our Company will construct a new manufacturing facility to significantly expand its production… more
- American Honda Motor Co Inc (Marysville, OH)
- …to join our team to Bring the Future!Job PurposeThe Senior Contract Specialist will be responsible for managing the organization's contracts, ensuring compliance ... and regulatory standards, and aligning with company policies. The Senior Contracts Specialist is responsible for reviewing contract requests of medium and high… more
- Merck & Co. (Austin, TX)
- Job Description RESPONSIBILITIES: Provide special Mobile Apps compliance and SOP Audit input and compliance reviews.Engage Markets and requestors on Mobile Apps ... related to mobile listings, Apps feedback and compliance .Manage vulnerability and technical scanning of mobility applications and ensure applications meet required… more
- Merck & Co. (Rahway, NJ)
- …Center located in Rahway, New Jersey includes a state-of-the-art sterile drug product cGMP clinical supply manufacturing facility known as FLEx Sterile that is ... clinical pipeline to patients across the globe throughout a range of product modalities which includes sterile small molecule, biologics, vaccines, antibody drug… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …manufacturing facility produces a global supply of our hemophilia and growth hormone product lines, as well as our next generation of cutting-edge medications. What ... will review manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all NNUSBPI products. This… more
- Eisai, Inc (Sacramento, CA)
- …to work cross-functionally while adhering to all of Eisai's ethics and compliance standards. Senior Neurology Account Specialist (Sr NAS) Responsibilities ... the midst of an approved launch of a new product in the US focused on educating HCPs on...Alzheimer's disease (AD) or mild AD. TheSenior Neurology Account Specialist (Sr NAS) will be part of a diverse… more
- Merck & Co. (Durham, NC)
- …facility will be used to produce the bulk active ingredient, finished product , and laboratory testing for vaccines.The Specialist , Quality Control participates ... Laboratory Specialist performs laboratory testing on a variety of product samples, including bulk vaccine, filled vaccine, and media. The successful candidate… more
- Eisai, Inc (San Diego, CA)
- …want to hear from you. Job Summary The Sr. Oncology Sales Specialist is responsible for meeting/exceeding sales goals through promoting Oncology therapeutic products ... in a compliant and appropriate manner. The Oncology Sales Specialist represents and promotes assigned brand(s) in the oral...etc. learn about the efficacy and safety of Eisai's product (s) consistent with FDA approved label. Works with office… more
- Legend Biotech USA, Inc. (Memphis, TN)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a Sr. Cell Therapy Account Specialist - Memphis, TN as part of the Commercial team that will be based ... Remotely within the territory. Role OverviewThe Sr. Cell Therapy Account Specialist is responsible for representing Legend's products and services to a defined… more
- Eisai, Inc (Louisville, KY)
- …want to hear from you. Job Summary The Senior Oncology Sales Specialist is responsible for meeting/exceeding sales goals through promoting Oncology therapeutic ... a compliant and appropriate manner. The Senior Oncology Sales Specialist represents and promotes assigned brand(s) in the oral...etc. learn about the efficacy and safety of Eisai's product (s) consistent with FDA approved label. Works with office… more
- Merck & Co. (Durham, NC)
- …timely resolution of issues.Utilizes monitoring, performance tools and systems to ensure product quality, drive Right First Time and compliance standards.Able to ... responsible for activities that support Good Manufacturing Practice and regulatory compliance during product manufacturing:Direct in-line Quality support for all… more
- Aequor (Thousand Oaks, CA)
- …ATO FACILITY. Manufacturing Specialist Job Description: Part of the Drug Product New Product Introduction Team at Thousand Oaks, Building 20. Building ... patients worldwide. Responsibilities include, but are not limited to: New Product Introductions (NPI) program management and non-capitol project management. The… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Maintenance Specialist as part of the Technical Operations team based in Raritan, New ... to drive effective and robust production, testing and release of product to patients.Key Responsibilities Diagnoses, troubleshoot, repair, maintain, all types of… more
- Insmed Incorporated (San Diego, CA)
- …Workplaces™ lists.OverviewReporting to the Associate Director, Quality Assurance GMP, the QMS Specialist , Quality Assurance, will play a key role in managing QA and ... Regulatory Compliance activities for Insmed Gene Therapy. This role directly influences Insmed GMP compliance through QA oversight, monitoring and review of… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of multiple myeloma.Legend Biotech is seeking a QA Warehouse Incoming Raw Material Specialist as part of the Quality team based in Raritan, NJ. Role OverviewThe ... QA Warehouse Incoming/Raw Material Specialist is an exempt level position with responsibility to...materials required for manufacturing and release of patient material/final product of CAR-T at Raritan, NJ Legend manufacturing site.Key… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist as part of the Quality Operations team based in Raritan, New Jersey. Role ... OverviewThe QA Shop Floor Specialist is an exempt level position responsible for the...responsible for quality and maintaining the highest standards in compliance within company policies, procedures, and all applicable regulations.Key… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …Assurance. Essential Functions Reviews all manufacturing and support records to certify compliance with specifications and procedures Releases product based on ... a global supply of our hemophilia and growth hormone product lines, as well as our next generation of...of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all NNUSBPI… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a Technical Equipment Specialist as part of the Technical Operations team based in Raritan, NJ. Role ... OverviewThe Technical Equipment Specialist will be responsible for ensuring equipment/systems required to...and having an understanding of next generation equipment and product roadmaps.Collaborate with process development team to identify as… more
