Senior Scientist II Salary at Imre Ltd BETA

Description. Chimera Enterprises International is seeking a Senior Scientist to support the Joint Program Executive Office for Chemical, Biological, Radiological and Nuclear Defense (JPEO- CBRND) JPEO-CBRND Headquarters (HQ). The JPEO-CBRND manages our nations investments in chemical, biological, radiological, and nuclear defense equipment, and medical countermeasures. battlespace worldwide. This position requires a Secret clearance. Job Duties: + Provide Senior Scientist support services to the Joint Program Executive Office CBRND HQs to support both the mission of the CTO (75-80% of the time) and the Wearables Pilot Program (20-25% of the time). + Research the latest scientific technology innovations and tools and evaluate how these can be transitioned into the JPEO-CBRNDs portfolio of technology demonstrations and acquisition programs. + Remain informed of the latest scientific innovations associated with CBRND wearable sensor and information technology developments that can be used

POSITION SUMMARY A Senior Quality Scientist is responsible for independently managing testing priorities, design of experiments for troubleshooting and trending product performance, technical transfer, mentoring and training analysts and associate scientists on trouble shooting techniques and experimental design, advanced troubleshooting of protein-based immunoassays, and approving disposition status for materials under investigation. This may include responsibilities for product release. The incumbent is expected to display a wide-degree of latitude, creativity, and self-management and to be able to independently manage multiple projects in addition to providing oversight and guidance to other team members as needed. DUTIES AND RESPONSIBILITIES: Manage the process of troubleshooting non-conforming products and/or independently manage multiple high-impact projects to improve product and process quality. Direct testing, analyze data, review and approve results and conclusions of others

Senior Scientist Vector and Cell-line development Summary: Catalent Cell and Gene Therapy is looking to recruit a Senior Scientist Vector and Cell-line development to join our growing team in Baltimore, MD. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life

Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide. At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, the partnerships we build, and the conversations we foster, we affirm the value of Diversity, Equity, Inclusion, and Belonging in building a world where everyone can be confident of quality in health and healthcare. USP is proud to be an equal employmen

This position is responsible for developing, planning, and executing research and product development projects for various disciplines within the clinical and life sciences fields. The incumbent will be responsible for designing and executing experim Scientist, Product Development, Senior, Research, Manufacturing, Technology, Skills

The **Sr. QC Scientist - Compliance** role is critical to our patients. This role is responsible for supporting compliance in the Quality Control Laboratory, including authoring, management and/or tracking of investigations/events/deviations, Corrective Action / Preventive Action (CAPA), change control, and other Quality records. This position will facilitate the compiling, trending, completing, and reporting of key quality metrics for management accountability, and other quality control functions, as needed. Continuously monitor systems, logbook management, and testing procedures to ensure compliance with applicable regulatory and industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mis

Overview: Are you looking for a Great place to work? Our team at Maryland Oncology Hematology is looking for "star" talent. If you believe you have what it takes to create a rewarding experience for our Physicians, patients, and team members, wed enjoy the opportunity to speak with you! Maryland Oncology Hematology is dedicated to providing the most advanced cancer care available anywhere in an atmosphere of caring compassion. We have over 16 convenient locations throughout Maryland and in DC. SCOPE: Moderate and High Complexity Laboratory Testing Is responsible for accurately performing specimen analysis, instrument maintenance, and quality control procedures including moderate and high complexity laboratory tests. Initiates and follows quality assurance and safety policies and procedures. Performs specimen collection and assists with patient flow as needed. Trains employees in laboratory procedures. May act as primary operator for at least one laboratory instrument. Acts as a resourc

**Join Amgens Mission of Serving Patients** At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do. Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Process Development Senior Scientist **What you will do** Lets do this