Senior Scientist Salary at Oncoone BETA

Overview At the heart of QIAGEN's business is a vision to make improvements in life possible. We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many initiatives and to our presence across the globe. Our most valuable asset are our employees - around 6000 in over 35 locations around the world. Our ambition is to ensure we have outstanding and passionate people working in the best teams and we are constantly looking for new talent to join us. There are few players who have shaped the world of modern science and healthcare as much as QIAGEN, and we have only just started. If you are looking to advance your career, are seeking new challenges and opportunities, enjoy working in dynamic and international, diverse teams and want to make a real impact on people's lives, then QIAGEN is where you need to be. Join us. At QIAGEN, you make a

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

Job Details Level Experienced Job Location Rockville MD - Rockville, MD Position Type Full Time Education Level PhD Salary Range $80000.00 - $100000.00 Salary Travel Percentage Up to 25% Job Shift Day Job Category Research Description POSITION TITLE:Senior Scientist, Radiopharmacology REPORTING LOCATION:Rockville, MD PRIMARY OBJECTIVES:The Sr. Scientist will oversee the program including study design and study conduct. Join our team to advance radiochemistry and cancer research, supporting the launch of our in vivo radio conjugate program. Support the operations and commercial teams for in vivo study planning and execution utilizing radio conjugates for testing in Champions extensive PDX Tumorbank in preclinical mouse pharmacology studies. DUTIES, RESPONSIBILITIES AND PRODUCTIVITY EXPECTATIONS: Collaborate with stakeholders, leveraging expertise in radiochemistry and radiobiology for in vivo radio conjugate studies. Plan and execute high-quality in vivo studies using radiopharmaceutica

Senior Scientist / NRDA Lead - ( 2500002Y ) Description Grounded in safety, quality, and ethics, our experts lead their fields and guide our work with rigor, a creative spirit, and vision for growth. We draw from more than 20 technical specialties around the globe and are committed to fostering an inclusive community of diverse talents, backgrounds, and expertise. We're a place to apply your passion and collaborate with top environmental talents on work that's critical to our clients and the communities they support. Join a team that has the environment down to a science. Remote/Flexible Location: Position can be based anywhere in the US Your Opportunity Stantec's Environmental Services practice seeks a Senior Consultant to help manage our NRDA Program. This position requires an individual with extensive experience in leading NRDA projects. The successful professional will have a strong academic background and at least 10 years of scientific experience in a discipline and has been focu

Title: Molecular Biology Senior Scientist Location: On site, Frederick, MD Status: Full Time Travel: Negligible Safety Sensitive: No Position Summary: USAMRIID, located at Fort Detrick, Maryland, works closely with other U.S. Army Medical Research and Development Command (USAMRDC) organizations, D...

**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

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

Job Description General Responsibilities: Investigate sites to identify any physical and/or environmental risks. Perform and/or manage field studies including indoor air quality, asbestos/lead paint/mold surveys, pre-demolition and hazardous materials surveys, and Phase I environmental site assessments. Assist with management and quality review of site investigations including soil, groundwater, and soil gas sampling, voluntary cleanup work, and remediation oversight. Develop sampling strategies and outline required analysis. Research regulatory standards and hazardous materials data. Evaluate sampling results. Manage and mentor staff on completing various reports including risk assessments and develop recommendations to correct and improve the environment. Present and communicate findings and report recommendations to clients. Identify areas of potential growth and target clients to help stabilize our asbestos and industrial hygiene services. Obtain state licensures to help with this