- Astellas Pharma (Cambridge, MA)
- …of this exciting work, you belong at Astellas! Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We ... and contributions to Astellas Clinical Development include: -Guide development of, review and approve clinical study designs, new and amended protocols for… more
- Endo International (Horsham, PA)
- …Management + Regularly assess material inventory levels at all plants. + Review MRP with respective team members and order/adjust, orders and ordering patterns, ... as required. + Review safety stock levels, inventory turns, and slow-moving inventory. + Storage capacity modeling and planning. Cross-Functional Support + Develop… more
- Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
- …aspects of downstream process technology transfers to CDMOs, including documentation review , gap analysis, and risk assessment. + Provide expert technical oversight ... of downstream manufacturing operations at CDMOs, including review of batch records, deviation investigations, and change controls. + Lead or significantly contribute… more
- Otsuka America Pharmaceutical Inc. (Augusta, ME)
- …aspects of upstream process technology transfers to CDMOs, including documentation review , gap analysis, and risk assessment. + Provide expert technical oversight ... of upstream manufacturing operations at CDMOs, including review of batch records, deviation investigations, and change controls. + Lead or significantly contribute… more
- Burns & McDonnell (Chicago, IL)
- **Description** The Senior Architect - Process will lead in the development of pharmaceutical and life science projects teams to create world-class designs for Life ... are set forth by clients and project colleagues. + Develop, modify, and review production drawings for Life Science facilities. + Participate in the development of… 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 ... visual factory + Required to read, understand, follow, and review GMP documents + Leads area continuous improvement activities...degree or higher preferred + 3 years of direct pharmaceutical manufacturing experience + 3 years of GMP experience… more
- Cambrex High Point (High Point, NC)
- …ability to manage projects on-time without supervision. + Ability to author and review comprehensive reports at the conclusion of projects for internal and customer ... and ability to support initiatives within the department. + Technical Documentation and Review : Ability to author and review key technical documents with minimal… more
- Bozeman Health (Bozeman, MT)
- Position Summary: The Pharmacist - Inpatient role helps provide high quality pharmaceutical services that foster efficacious, safe and cost effective drug use for ... clinical and distributive services. Primary duties include performing clinical review and order verification, following pharmacy clinical protocols/policies, completing… more
- AristaCare (Cherry Hill, NJ)
- …committee meetings of the facility (ie, Infection Control, Policy Advisory, Pharmaceutical , Quality Assessment, etc.) as required. + Assist in preparing written ... dress codes, are followed by all departmental personnel. + Review complaints and grievances made or filed by department...and/or to assist in the improvement of services. + Review and evaluate your department's work force and make… more
- Lilly (IN)
- …reporting of adverse events as mandated by corporate patient safety; the review process for protocols, study reports, publications and data dissemination for ... trials (for example, sample size, patient commitment, timelines, grants, and governance review interactions). + Review and approve risk profiles to ensure… more