- Jabil (Hunt Valley, MD)
- …Summary: The Director of Validation will lead all validation activities across pharmaceutical and medical device manufacturing operations with a strong focus on ... objectives. + Direct personnel to the author, complete, and review all associated validation protocols (IQ, OQ, PQs). +...manufacturing equipment and processes; knows and complies with Safety Data Sheets and SOP requirements and trained in cGMP's.… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …resource allocations. + Reviews procedural documents, as requested. + Coordinates scheduling/ review of records as requested. + Participates in the monitoring program ... MS with 4-6 years of relevant experience within the pharmaceutical or healthcare industry, or a BS with 7-9...trial materials and materials for production, based on documentation review . + Decision-making where commitment is required on release… more
- Guthrie (Binghamton, NY)
- …must demonstrate growth and development of knowledge required to access data reflective of the patient's status, interpret the appropriate information needed ... to identify each patients requirements and to provide the pharmaceutical care needed, appropriate to the age of the patient and in accordance with appropriate… more
- Luke Staffing (Agana Heights, GU)
- …from a college or university accredited by the Accreditation Council on Pharmaceutical Education (ACPE). . **Experience:** Possess a minimum of 3 years' experience ... care support the progression of patient toward set outcomes. . Perform assessment/ data collection in an ongoing and systematic manner, focusing on physiological, and… more
- Walgreens (Houston, TX)
- …employees are trained on all required functions regarding payer and pharmaceutical contractual requirements (adverse event reporting, data and inventory ... the highest level of customer service (including patients, providers, and pharmaceutical and payer partners), and developing and protecting department assets. **Job… more
- GRAIL (Menlo Park, CA)
- …sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome one of medicine's greatest challenges. GRAIL ... United Kingdom. It is supported by leading global investors and pharmaceutical , technology, and healthcare companies. For more information, please visit grail.com… 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 ... of the Quality Operations team and is responsible for QA oversight, review , and quality approval of large-scale expansion project deliverables. This role supports… more
- Charles River Laboratories (Wayne, PA)
- …the Analytical lab, sample scheduling, coordination and testing. Also responsible for technical review of generated data and for refinement and development of ... cross- functional communication and laboratory activities as necessary. + Provide technical review of generated data . + Oversee/assist with refinement and… more
- Sanofi Group (Swiftwater, PA)
- …Responsibilities:** **Responsibilities monthly cycle:** + **Lead the monthly capability review :** clarify and validate key planning hypotheses/ bottlenecks to ensure ... rebalancing, launch priorities, ). + **Manage capacity** analysis, and capability review processes, for budgeting and strategic planning. + **Manage local APU… more
- Lilly (Indianapolis, IN)
- …safety; review process for protocols, study reports, publications and data dissemination for products; new and updated labels, documents and tools supporting ... interacting with government PRA agencies as needed), and leading in scientific data dissemination (leading and presenting at conferences, advisory boards, etc., and… more