- University of Rochester (Rochester, NY)
- …determined by considering factors including, but not limited to, market data , education, experience, qualifications, expertise of the individual, and internal equity ... clinical trials business opportunities with Contract Research Organizations (CRO), pharmaceutical companies, biotech companies and other academic institutions. -… more
- Lilly (Indianapolis, IN)
- …involved in key activities for the development of synthetic active pharmaceutical ingredients (API) from pre-clinical phases through commercialization of drug ... technology transfer objectives. + Ability to integrate process (and property design) data based on a fundamental understanding of the underlying physical processes +… more
- ThermoFisher Scientific (Florence, SC)
- …and trains other employees on these techniques. + Provide thoughtful technical review of data collected by other employees. + Investigate out-of-specification ... or exceed the quality requirements from clients. + Collect reliable data through designed laboratory experiments with accurate, detailed documentation for… more
- Pfizer (Groton, CT)
- …+ In accordance with the Safety Review Plan, performs and documents regular review of individual subject safety data and performs review of cumulative ... driving change across all levels of the organization including senior management. + Data listing review experience + Experience working collaboratively in a… more
- Bristol Myers Squibb (Summit, NJ)
- …The Sr. Director a uthor s designated sections of regulatory filing s , review s all sections for clarity, technical persuasiveness , consistency and completeness , ... changes . + Drive timely and compliant completion of the Annual Product Quality Review ensuring coordination with leads of contributing . + Perform Quality review… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …of QCM [i.e., quality control and manufacturing] documents and other data received from pharmaceutical , ingredient and dietary supplement manufacturers ... evaluation of cGMP site audits/reports, QCM documentation/reports, and test data /results regarding facilities and products undergoing verification. In addition, you… more
- Bristol Myers Squibb (Warren, NJ)
- …as required in documentation review , SOP authoring and revision, and executed data review . **Excellent Customer Service and Support** + Regularly review , ... requirements and good documentation practices. + Advanced knowledge of pharmaceutical , manufacturing and laboratory systems and equipment that support cell… more
- Reckitt (Wilson, NC)
- …and data integrity standards. **Equipment Qualification** + Support qualification review of manufacturing and laboratory equipment (IQ/OQ/PQ). + Review and ... fully compliant and continually improve effectiveness. + Perform the Quality review and approval responsibility of projects associated with computer systems and… more
- AbbVie (Irvine, CA)
- …across assets with similar MOA + Leads and guide the safety physicians on data review (clinical and beyond) and interpretations across assets with similar MOA ... to effectively conduct safety surveillance + Responsible for safety surveillance for pharmaceutical / biological / drug -device combined products + Lead and set… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …delivery of digital capabilities. + Monitor IT service provider resource consumption, review demand and change requests for support work related to COTS/custom ... + Experience working in large and/or complex IT programs, preferably within the pharmaceutical development and quality control domains. + Must have experience in … more