- UPMC (Monroeville, PA)
- …of improving clinical pharmacy services by monitoring processes, analyzing data , implementing interventions, and evaluating the effectiveness of those interventions. ... therapeutic interchange protocols, and promoting rational drug therapy selection. + Review , maintain, and screen patient medication records and profiles for… more
- Boehringer Ingelheim (Charleston, SC)
- …opportunities that meet both territory and brand tactics. + Utilizes sales data and supporting analysis to plan activity, monitors literature use, and maintains ... Associate Director. + Develops a personal development plan and ensures twice annual review with Associate Director. + Demonstrates a complete knowledge of BIPI ILD… more
- Curia (Albuquerque, NM)
- …organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At ... initiatives + Will provide quality training related to batch review , sitewide + Read/interpret SOPs to ensure compliance +...(3) years of GMP experience in an FDA regulated pharmaceutical environment + Minimum of two (2) years of… more
- Dr. Reddy's Laboratories (Princeton, NJ)
- …sites, prepare diligence reports summarizing findings from the diligence process, review and revise key assumptions following due diligence findings, and update ... Finance, Business Development in Pharma Industry **Skills & attributes:** + ** Pharmaceutical Industry Expertise:** Deep understanding of the pharmaceutical … more
- ThermoFisher Scientific (Greenville, NC)
- …**Key Responsibilities:** + Lead the validation of test methods for pharmaceutical raw materials and finished products for strength, impurities, identity, potency, ... Write and complete validation protocols in accordance with regulatory guidelines + Review and interpret analytical test results; make recommendations based on … more
- Sumitomo Pharma (Scranton, PA)
- Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... in the area of urology and women's health through review of the scientific literature and attendance at key...- 3 years of relevant experience in biotech or pharmaceutical industry + 1-3 years of MSL experience in… more
- The County of Los Angeles (Los Angeles, CA)
- …packaging, storing, and distribution and control of drugs and other pharmaceutical products. Positions also supervise licensed personnel providing expert information ... principles of supervision governing personnel administration to plan, direct, and review work of staff. Essential Job Functions Establishes, maintains, and revises… more
- J&J Family of Companies (Athens, GA)
- …humanity. Apply today for this exciting opening to support us at our pharmaceutical plant! The Senior CQV Engineer is responsible for supporting the qualification of ... cleanroom facilities and large process equipment at pharmaceutical manufacturing sites in Athens, GA. They will also be responsible for hands-on writing and… more
- Novo Nordisk (Bloomington, IN)
- …6 weeks paid family medical leave + Free access to Novo Nordisk-marketed pharmaceutical products + Tuition Assistance + Life & Disability Insurance + Employee ... to the Manager to be added as required + Review all activities within the Master Batch Record (MBR)...degree or higher preferred + 2 years of direct pharmaceutical manufacturing experience + 2 years of GMP experience… more
- Otsuka America Pharmaceutical Inc. (Little Rock, AR)
- …of integrated brand strategy and plans + Represents Global Medical Affairs on Copy Review governance committee + Is a core member of the Global Medical Affairs ... the field to obtain feedback on clinical aspects of products and new data generation, interpretation and dissemination and advocates for Otsuka prominence in CNS… more