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3-5 years of experience in drug safety, pharmacovigilance, quality assurance, or a related field. This role requires a strong leader with a deep understanding of commercial patient services, pharmacovigilance, quality assurance, and regulatory compliance.
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A background of pharmaceutical manufacturing or quality control/quality assurance is a plus. The CMC Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports.
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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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In addition, this role will perform critical quality assurance activities such as Change Management, SOP Management, and Audit oversight. Experience with Veeva (Quality Docs, QMS and Training modules) a plus.
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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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The Quality Assurance (QA) Automation Engineer designs, builds, tests, and deploys effective test automation solutions for a myriad of Web and Windows applications. This position will report to the Manager of IT Quality Assurance in the Information Technology department.
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Quality Assurance: Conduct routine cleaning, testing, and monitoring of compounding equipment, cleanrooms, and laminar airflow hoods to ensure optimal performance and adherence to quality standards.
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Johnson and Johnson Innovative Medicine is recruiting for a Director, Global Real World Evidence (RWE) in our Global Commercial Strategy Organization (GCSO). Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
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The HORIBA Group of worldwide companies provides an extensive array of instruments and systems for applications ranging from automotive R&D, process and environmental monitoring, in-vitro medical diagnostics, semiconductor manufacturing, and metrology, to a broad range of scientific R&D and QC measurements.
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Description Kenvue is currently recruiting for: 2025 Customer Development Co-Op The Customer Development Co-Op Program is a full-time, six-month experience designed to help college students develop leadership, analytical and communication skills through practical business experience and ongoing training & development, coaching and mentorship.
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Among the key duties of this position are the following:Oversees various supervisory tasks including, but not limited to staff hiring, training and development, user support documentation and quality assurance.
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Participates in monitoring and auditing activities and investigations, and implementing quality assurance and performance improvement processes, as required. The RN Nursing Supervisor serves as a clinical operational liaison between the units and the CNE, ADON, and Unit Managers.
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This position will be focused on sustaining processing within SAP.Responsibilities Develop action plans with Production, Quality, Raw Materials, Warehouse, and Division Quality Assurance to ensure SAP processes are maintained.
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Responsibilities include hiring, training, scheduling, supervision of program staff, quality assurance and performance improvement oversight, as well as ensuring compliance with all licensing and accrediting bodies.
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DescriptionJohnson & Johnson is currently recruiting for Senior Manager, IT Procurement ADM (Application Development and Maintenance) located in Raritan, NJ or Tampa, FL. Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 130 years.
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assurance job Company: Johnson in Raritan, NJ
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