- Sokol Materials & Services (Skillman, NJ)
- …+ Strong interest in pursuing a career in CQV within the pharmaceutical , biotechnology, or medical device industries. + Excellent organizational skills and attention ... to detail. + Ability to analyze data and communicate findings effectively. + Effective team collaboration...and Engineering, to coordinate and execute CQV activities. * Review validation documentation under the guidance of senior team… more
- University of Colorado (Aurora, CO)
- …emergency unblinding procedures for clinical trials + Participate in protocol review committees, site initiation visits, and feasibility assessments from the ... research environment. + **Attention to detail and commitment to data integrity** , particularly in maintaining investigational drug accountability records,… more
- HCA Healthcare (Panama City, FL)
- …of daily medicines; responsible for the safe, accurate and rational distribution of pharmaceutical agents to patients of all ages, employees and designated areas of ... + Documents clinical interventions. + Reviews/interprets culture and susceptibility data for antibiotic appropriateness and recommends changes as needed. +… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Director, Product Management Team Lead, and part of the larger Pharmaceutical Development and Manufacturing (PDM) organization, the Director, Product & Project ... activities and their status + Organize preparation of high-quality documents for review by governance committee in collaboration with the PDMProduct Team + Identify… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Drive development and implementation of new systems to improve project execution and data management + Lead collaborations with Gilead PDM functions such as Quality ... within the organization + Support regulatory filings by guiding the draft, review , and approval of CMC sections; support associated agency interactions and… more
- Sanofi Group (Richmond, VA)
- …including attendance at relevant symposium, scientific workshops, preceptorships, and review of key journals, and successful completion of internal training ... Sciences/ Nursing + 3-5 years of Industry experience + Experience in biotechnology/ pharmaceutical industry + Prior product launch experience + Ability to present to… more
- Medexus Pharma (AZ)
- …2025 Description **Company Bio:** Medexus Pharmaceuticals Inc. is a leading specialty pharmaceutical company with a focus on the therapeutic areas of rheumatology, ... including the provision of guidance on the publication and presentation of clinical data , in accordance with company policies. + Support the creation of Medical… more
- Merck (West Point, PA)
- …molded Device Components, Device Constituents, and Medical Devices used to deliver Pharmaceutical , Biologic, and Vaccine Products. Our team works with a "Safety ... Reliability, and Lifecycle Management). - Lead Periodic Business and Operations Review Meetings (with External Partner). . **Compliance:** Achieve compliance goals… more
- Takeda Pharmaceuticals (Boston, MA)
- …Improvement in our Cambridge office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led ... processes. + Design systems that facilitate the automation of repetitive tasks and data analysis to free up valuable scientific resources for critical thinking and… more
- ThermoFisher Scientific (Greenville, NC)
- …sterile injectables and work on problems of moderate scope where analysis of situations or data requires a review of a variety of factors. This colleague follows ... when performing the following duties. A Day in the Life: + Ensure pharmaceutical products are manufactured in accordance with area SOPs and current cGMP +… more