- Endo International (Horsham, PA)
- …Description** **Responsibilities:** Material Resource Planning + On a regular basis, review the Materials Resource Plan (MRP) output and align material requirements. ... at each respective site informed of delivery changes that may impact production. + Review and update open purchased order report. + Convert planned orders to process… more
- Gilead Sciences, Inc. (Foster City, CA)
- …support for assigned brands, therapeutic area, and other projects. You may review and approve or co- review /approve promotional materials. You may manage ... requirements. You will assist or serve as the Promotional Review Committee (PRC) Chair for one or more brands...enforcement actions with regards to advertising and promotion of pharmaceutical products. + May initiate and/or contribute to local… more
- ThermoFisher Scientific (Middleton, WI)
- …to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or ... biological matrices. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product… more
- Marshfield Clinic (Rice Lake, WI)
- …The Pharmacy Buyer Technician is vital to maintaining a cost effective pharmaceutical supply chain for the Marshfield Clinic System and ensuring contract compliance ... related experience. Experience with microcomputers required. **Preferred/Optional:** Experience with pharmaceutical purchasing and inventory management is preferred. Experience with… more
- Mentor Technical Group (Juncos, PR)
- …MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices ... develop and maintain commissioning and qualification procedures and documents. + Write, review , and approve C&Q protocols and reports for various systems (eg, HVAC,… more
- Bristol Myers Squibb (Summit, NJ)
- …over to business area. + Support growing standardization efforts in the review and approval of Validation Deliverables. + Promotes and provides excellent customer ... documentation practices relating to systems, equipment, and instrumentation within the pharmaceutical industry. + Strong working knowledge of ISPE guidance and 21… more
- IQVIA (Boston, MA)
- …IQVIA Commercial Solutions. CSIH team members consult with manufacturers in the pharmaceutical and biotechnology industry to meet the challenges of today's complex ... the design, development and delivery of client solutions. + Leads teams to review and analyze client requirements or challenges and develops and costs associated… more
- AbbVie (North Chicago, IL)
- …+ Analytical science is not limited to chemical and structural R&D, pharmaceutical discovery and drug products. + Provides technical support to characterization to ... domains within neuroscience DMPK during pharmaceutical discovery and drug products. + Accountable for state...data protocols and reports in timely manner and occasionally review other protocols and reports. + Complete assigned tasks… more
- Lilly (Branchburg, NJ)
- …Pursue an injury free workplace and minimize our environmental impact. * Review and approve documentation related to areas of responsibility (Validation Lifecycle ... school diploma with a minimum of 5+ years of experience working with Pharmaceutical Manufacturing systems (eg Data solutions, LIMS systems, MES technologies such as… more
- McLaren Health Care (Lansing, MI)
- Under general direction, provides prescribed medications and pharmaceutical products for adequate patient care according to professional standards and practices. ... with medical staff, other health professionals, patients and families on pharmaceutical and patient care issues. **Responsibilities** : 1. Reviews prescriptions as… more