- Boehringer Ingelheim (Ridgefield, CT)
- …competencies necessary to contribute to their respective functional area within a pharmaceutical company. The Fellow will be based at Boehringer Ingelheim's US ... of the broad range of opportunities available to a pharmacist in the pharmaceutical industry. As an employee of Boehringer Ingelheim, you will actively contribute to… more
- Centene Corporation (Chesterfield, MO)
- …and clinical monitoring activities. + Participate in decisions regarding the pharmaceutical services within assigned scope including: + Assessing the patient's ... general pharmaceutical needs + Planning for the pharmaceutical ...+ Assess responses to therapy, patient compliance, and ongoing review of drug regimens; report and manage adverse events… more
- Boehringer Ingelheim (Ridgefield, CT)
- …closely with staff and project/product responsible DRA colleagues to a) plan, review , approve required labeling components for filing of required information to FDA, ... individuals from other departments around package labeling generation and review . + Maintains excellent knowledge of applicable corporate/company SOPs, guidelines,… more
- Takeda Pharmaceuticals (Boston, MA)
- …Risk Management Scientist/Associate Director. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a ... Support the development of risk management plans (RMPs) in modular format, review RMPs) and ensure alignment with Good Pharmacovigilance Practices and other… more
- Lilly (Indianapolis, IN)
- …supporting the oversight of Insulin or Peptide Purification Active Pharmaceutical Ingredient (API) manufactured within Indianapolis Active Pharmaceutical ... + Exhibit cross-functional influence. + Maintain and improve quality systems. + Review and approve deviations, procedures, protocols, and change controls with focus… more
- Fujifilm (College Station, TX)
- …and perform assessments, gap confirmation and schedule stakeholder follow-up. + Review pre-purchase of systems and analyze to ensure Data Integrity Compliance. ... science concentration with 2+ years of experience of cGMP supporting pharmaceutical or biotechnology products or 1 year experience with FUJIFILM Biotechnologies… more
- Curia (Rensselaer, NY)
- …in or assist with test method validations + Evaluate data for trends and review data + Support supervisors in OOS Investigations and complete CAPA requirements + ... of activities and results on paperwork + Execute, author, and review SOPs, reports, protocols, investigations, change controls, and data summaries. Understand… 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 ... pieces of equipment, multiple end customers, duration between 1-3 months. + Review and verify validation documentation to ensure information is complete, accurate,… more
- Stantec (Roseville, CA)
- …compliance specialists delivering EHS and sustainability solutions to commercial, pharmaceutical , food and beverage, manufacturing, mining, oil and gas, power, ... Contractor Safety Program - Training plan recommendations and requirements - Safety Program review and recommended updates - Safety Culture assessment review and… more
- Sumitomo Pharma (Cheyenne, WY)
- 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 ... and Collaborative Research program. + Provide detailed and compliant medical review and approval of external resources, communications, and publications - ensuring… more