
1001 - 5000 employees
π Pharmaceuticals
π₯ Healthcare
𧬠Biotechnology
Pharmaceuticals β’ Healthcare β’ Biotechnology
Otsuka Pharmaceutical Companies (U. S. ) is a prominent player in the pharmaceutical manufacturing industry, dedicated to creating innovative products for better health worldwide. The company comprises two main entities: Otsuka America Pharmaceutical, Inc. (OAPI), which is focused on commercializing Otsuka-discovered and in-licensed products in North America, and Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC), which specializes in the clinical development and global registration of innovative healthcare solutions, particularly in the field of neuroscience.
π₯ 2 minutes ago
ποΈ New Jersey β Remote
π΅ $107.7k - $161k / year
β° Full Time
π‘ Mid-level
π Senior
π Manager
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1001 - 5000 employees
π Pharmaceuticals
π₯ Healthcare
𧬠Biotechnology
Pharmaceuticals β’ Healthcare β’ Biotechnology
Otsuka Pharmaceutical Companies (U. S. ) is a prominent player in the pharmaceutical manufacturing industry, dedicated to creating innovative products for better health worldwide. The company comprises two main entities: Otsuka America Pharmaceutical, Inc. (OAPI), which is focused on commercializing Otsuka-discovered and in-licensed products in North America, and Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC), which specializes in the clinical development and global registration of innovative healthcare solutions, particularly in the field of neuroscience.
β’ Support the development, implementation, continuous improvement and documentation of Otsuka Companiesβ Quality System β’ Support inspections including preparation for GxP inspections and responses to Regulatory Authorities β’ Manage global, regional and local Standard Operating Procedures (SOPs) and Working Practices (WPs) β’ Provide advice and act as project liaison for project activities
β’ Degree in natural science or equivalent number of yearsβ experience β’ 4+ years of clinical/industry/Regulatory Authority or otherwise relevant experience, preferably including Quality Management for Pharmacovigilance or Clinical Development or Computer System Validation β’ Advanced knowledge/experience in relevant regulations and guidance documents, e.g., in the area of Pharmacovigilance, Clinical Development, Medical Device, IMP management, Regulatory Affairs and Pharmacovigilance β’ Experience in Monitoring, Quality Assurance and/or Good Clinical Practices
β’ Comprehensive medical, dental, vision, prescription drug coverage β’ Company provided basic life, accidental death & dismemberment β’ Short-term and long-term disability insurance β’ Tuition reimbursement β’ Student loan assistance β’ A generous 401(k) match β’ Flexible time off β’ Paid holidays β’ Paid leave programs as well as other company provided benefits
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