- Granville Medical Center (Oxford, NC)
- …Overview: The Director of Pharmacy oversees all aspects of pharmacy operations including regulatory compliance and financial performance. Position ... to secure competitive pricing terms. *Oversees the implementation and compliance of the 340B Drug Pricing Program,...the procurement of medications; knowledge and understanding of pharmaceutical principles, drug therapy, and medication… more
- Granville Health System (Oxford, NC)
- …Overview: The Director of Pharmacy oversees all aspects of pharmacy operations including regulatory compliance and financial performance. Position ... to secure competitive pricing terms. #Oversees the implementation and compliance of the 340B Drug Pricing Program,...the procurement of medications; knowledge and understanding of pharmaceutical principles, drug therapy, and medication… more
- Bristol Myers Squibb (Princeton, NJ)
- …both verbal and written + He or she should have an understanding of pharmaceutical drug development including clinical development, regulatory, life cycle ... their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director (AD) for US Medical Pulmonary will provide deep...management of pharmaceutical products, and knowledge … more
- AbbVie (Mettawa, IL)
- …in the pharmaceutical industry or academia or equivalent. At least 5 years of experience within the pharmaceutical industry preferred. + MD: Minimum of ... or academia or equivalent. At least 5 years preferred. At least 2 years of experience within the pharmaceutical industry preferred. Completion of residency… more
- Fujifilm (Holly Springs, NC)
- **Position Overview** The Associate Director of Commissioning, Qualification, and Validation (CQV) is responsible for leading and executing CQV activities for a ... and Risk-based Validation approach. This role exists to guarantee the integrity and compliance of production systems and to mitigate risks associated with the… more
- AbbVie (Mettawa, IL)
- … of pipeline development and on-market product + Typically 3+ years of clinical development experience in the pharmaceutical industry, CRO, academia or ... serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact...For problems surrounded by complex rules and regulations, the Director must be able to direct compliance … more
- Merck (Cambridge, MA)
- …As an Associate Director , you will represent QP2 on cross-functional teams of experienced scientists to discover and advance the clinical development of ... developer, with a strong, integrated understanding of the strategic elements of drug discovery and development. The Associate Director should demonstrate… more
- Eurofins (Louisville, KY)
- …efficiency. Position Overview : We are seeking an experienced and strategic Director of Oligonucleotide Manufacturing to oversee the day-to-day operations ... Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life… more
- Amgen (West Greenwich, RI)
- …these qualifications. **Basic Qualifications:** Doctorate degree and 4 years of pharmaceutical /biopharmaceutical Engineering, Manufacturing or a related ... technical discipline experience Or Master's degree and 8 years of pharmaceutical /biopharmaceutical Engineering, Manufacturing or a related technical discipline… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …and balance/influence cross-functional priorities, plans and objectives + Knowledge of medial/ compliance /legal review processes + Alliance partnership experience ... **Job Description** The Director , AAD HCP Lead is responsible for overall...responsible for overall HCP strategic direction and tactical execution of a major asset expecting FDA approval in 12-14… more