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Position Status Full Time Posting Number 24FA0689 Posting Open Date 06/27/2024 Posting Close Date 07/26/2024 Qualifications Minimum Education and Experience Terminal degree in the biological sciences (e.g., PhD, DSc), plus at least 5 years’ experience post-degree; or terminal professional degree in the medical or veterinary sciences plus at least 10 years’ experience post-degree.
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BS degree plus minimum 6 years or Master degree plus minimum 4 years of experience OR PhD plus 1 year of experience in Pharmaceutics, Chemistry, Biomedical Engineering, Chemical Engineering, or related field with a strong background in nanoparticle-based formulation development & analytical characterization.
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Experience and solid knowledge of Pharmacovigilance specificallyProficiency in one or more of these additional areas is a plus: CMC/Mfg., Clinical development and trial execution, Regulatory, Real-World Data and Real-World Evidence, Cell and Gene Therapy, Medical Device, IVD/CDxExperienced in understanding and interpreting regulatory guidelines and documents.
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Familiarity with other BI tools (e.g., Tableau, QlikView) is a plus. Job Summary: The Power BI Developer will be responsible for designing, developing, and maintaining interactive and visually compelling dashboards and reports using Microsoft Power BI. This role involves collaborating with stakeholders to understand business requirements, translating them into technical specifications, and delivering high-quality BI solutions that drive data-driven decision-making.
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Previous experience working with or for a Civil Society Organisation or an NGO involved in social impact work would be a plus. Proficiency in a second language, preferably French, is a plus.
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Experience in pharmacovigilance databases and adverse event reporting systems is a plus. Experience in quality assurance, preferably in life sciences or pharmaceutical industry is a plus.
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Bachelor’s degree in Civil Engineering, Environmental Science, Biology, Ecology, Natural Resources, or an earth science-related field or relevant degree with a focus on transportation plus six (6) years of experience of demonstrated equivalency of experience and / or education or demonstrated equivalency of experience and education.
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Health care experience a plus including: BONENT Certified, Certified Hemodialysis Technician (CHT), Certified Nursing Assistant (CNA), Certified Medical Assistant (CMA), or Phlebotomy certification.
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Experience with optical spectroscopies such as Raman and PL is a plus. Experience with instrument control software such as LabView is a plus. Associate's degree in science or technology from two-year College or technical school plus 1 to 3 years of related experience and/or training.
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Job Summary: We are seeking a talented Full Stack Developer with expertise in Drools and Java as the primary skill, along with experience in Angular and RDBMS. Knowledge or experience in claims or insurance is a plus.
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Experience with Veeva (Quality Docs, QMS and Training modules) a plus. Global Pharmaceutical company, with US HQ in Central New Jersey, focused in Metabolics, Endocrinology and Oncology is expandingLooking for a strong Quality Assurance Manager for the entire North American manufacturing and quality organization.
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Intermediate knowledge of Microsoft Word, Microsoft Excel and Adobe AcrobatKnowledge of cGMP/GDP regulations, ICH Guidelines, and CMC (Chemistry and Manufacturing Controls) recommendedExcellent communication, organizational, interpersonal and computer skillsExcellent Oral/Written Communication SkillsDemonstrated ability to manage multiple competing prioritiesSolid organizational skills and attention to detail.
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Create, route and track controlled records within documents management system, Veeva. This includes documentation control, change control, deviation management, and CAPA (Corrective and Preventive Action) systems.
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Position requires on-site presence at companies' HQ Essential Duties and Responsibilities Conducting Training: Developing and conducting training programs for personnel on GMP and GDP requirements, quality systems, and relevant procedures to ensure understanding and compliance throughout the organization.
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Developing and Maintaining Quality Systems: Establishing and maintaining comprehensive quality systems in compliance with GMP and GDP regulations. Sets and manages audit schedule – collaborating with Tech Ops and internal QA to ensure audit reporting reflects current state of compliance at COs and to help address issues requiring remediation.
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plus job Title: manager national in Bridgewater, NJ
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