• Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …clinical or basic research in a pharmaceutical company, a medical device /Diagnostic company, Academic Research Organization (ARO) or Contract Research Organization ... (CRO). preferredCRA experience preferred.Time spent directly in a medical environment (eg as a Study Site Coordinator) preferred.Familiarity to a Japan-based organization preferred.Physical Requirements: In-house office position that may require occasional… more
    HireLifeScience (05/22/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …clinical or basic research in a Pharmaceutical company, a Medical device /Diagnostic company, Academic Research Organization (ARO) or Contract Research Organization ... (CRO). CRA experience is preferred. Clinical Project Management experience required. Time spent directly in a medical environment (eg as a Study Site Coordinator) is also considered relevant. preferred Familiarity to a Japan-based organization is desirable.… more
    HireLifeScience (05/18/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …and/or post marketing in Clinical research, Pharmaceutical company, CRO or Medical Device setting preferred- 4 or More Years Experience in oncology Therapeutic Area ... and/or in late phase projects is preferred Travel Ability to travel up to 20% domestically and internationally. Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without… more
    HireLifeScience (05/17/24)
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  • BioAgilytix (Durham, NC)
    …for Medical Devices, ISO 13485, FDA and (New) EU Medical Device requirementsCE Mark product certifications experienceDemonstrated project coordination and management ... skills; strong experience in a QMS functionAbility to achieve results and function independently in a fast-paced environment; ability to self-motivate with strong work ethicExcellent oral and written communication skillsStrong interpersonal skills with the… more
    HireLifeScience (05/07/24)
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  • Novo Nordisk Inc. (Charlottesville, VA)
    …of Obesity management through HCP/staff education, patient education, patient device training, employer education, health system education and community education ... (support groups, partnership with weight management centers) Seeks new avenues to heighten awareness and action within each unique territory utilizing approved resources and Standards of Care in Obesity Management on how to better manage patients respective… more
    HireLifeScience (04/17/24)
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  • Tris Pharma (Monmouth Junction, NJ)
    …Quality Manager, Engineer or AuditorExperience with drug- device combination products (highly desirable)Travel requirements0%Physical requirementsOffice ... based position Tris Pharma, Inc. offers a highly competitive compensation package. To build and enhance our diverse workforce, we encourage applications from individuals with disabilities, minorities, veterans and women, etc. Tris Pharma, Inc. is an Equal… more
    HireLifeScience (04/02/24)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    …and experience with the following is required: Instrumentation & Control Device operation and troubleshooting Programmable Logic Controllers Supervisory Control & ... Data Acquisition Systems (SCADA) Variable Speed Drives Electrical systems such as 120 VAC, 24 VDC, 480 VAC NFPA codes related to Automation & Electrical work Some knowledge of the Microsoft Office Suite (Word, Excel, Visio, Project, & PowerPoint) Excellent… more
    HireLifeScience (03/29/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …A minimum of two (2) years related experience in medical device , biopharmaceutical, or pharmaceutical industry. Solid understanding of regulatory requirements, ... policies and guidelines. Experience with Quality Control document reviews and regulatory inspection processes. Working knowledge of Quality systems. Experience in management of retain samples using electronic systems (eLIMS). Candidates must be able to… more
    HireLifeScience (03/28/24)
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  • Exela Pharma Sciences, LLC (Lenoir, NC)
    …and quality and regulatory requirements important to pharmaceutical and medical device manufacturing labs.Able to write detailed investigation summary memos that ... meet the requirements of the Quality Organization and the expectations of regulatory agencies.Understand how to implement investigation strategies and apply root cause failure analysis.Education RequirementsBachelor's degree Master's Degree/Bachelor's degree… more
    HireLifeScience (03/21/24)
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  • Beth Israel Deaconess Medical Center (Boston, MA)
    …highly complex EP interventions, including 3D mapping, sophisticated ablation techniques, device implants, and lead extractions. The structural heart program is a ... national leader in transcatheter valve replacement (TAVR), valvuloplasty, PFO, ASD and VSD repair. Our fast-paced Interventional Cardiology unit performs cardioversions and TEE procedures and provides highly specialized pre and post-procedure care. Our… more
    Radancy (06/17/24)
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