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Scientist II, Mass Spectrometry | Scientist in Science & Pharmaceutical Job in Wayne PA | 72561

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Scientist II, Mass Spectrometry

Location:
Wayne, PA
Description:

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well:being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about. Job Summary Charles River Labs and our Biologics Testing team located in Wayne, PA/Erkarth, Germany are seeking a Scientist II, Mass Spectrometry. Our Scientist II role will be responsible for the development and execution of moderately complex testing and characterization of biotherapeutics using analytical instrumentation and methodologies. This role will be responsible for methodologies under both R and D and cGMP environments which will include managing projects and client interactions. Duties and Responsibilities - Implement and qualify mass spectrometry equipment at Charles River sites in Germany and US.- Develop, perform, and troubleshoot laboratory experiments, tests, and procedures within accepted regulatory compliance for the characterization and analysis of biotherapeutics through use of mass spectrometry instrumentation and methodologies using associated software. - Generate high quality method and study protocols for sponsor and internal characterization and sample testing programs.- Function as contact for the planning and execution of Sponsor interaction related to proposal management, research and method development, and for the design, scheduling, conduct and reporting of studies.- Assist in oversight of laboratory and mentor technical staff in the development and execution of studies to generate high quality scientific data within accepted regulatory compliance.- Implement techniques to improve productivity, increase efficiencies and maintain laboratory state:of:the:art practices.- Use of Agilent and Thermo MS Platforms/evaluating Mass Spectrometry software.- Review, interpret, analyze, evaluate, and present data on assigned studies, with minimal assistance from senior scientific staff. - Prepare high quality final reports appropriate for assigned study, including integration of supporting subcontractor(s)'s reports into final reports as required, with minimal assistance- Interact with clients regarding project design, scheduling and conduct as requested.- Collaborate with appropriate departments to coordinate performance of projects, discuss issues and prepare reports.- Provide scientific and technical guidance within Biologics to resolve analytical challenges in a timely fashion, including research and development of new methodologies in study conduct.- Manage or assist with improvement projects (e.g. redesign of SOP's, research procedures or report formats).- Independently compose quality documentation including deviation reports and change control documentation with no/minimal guidance.- Create, review and edit SOPs, protocols and other data Forms and testing documentation.- Follow all SOPs, CTMs and cGMP as they relate to specific tasks.- Perform other related duties as required. Job Qualifications - Education: Bachelor's degree (B.A. /B.S.) or equivalent in Chemistry/ Biochemistry or related scientific discipline. M.S. or Ph.D. preferred.- Experience: Minimum 5 year's relevant experience within a contract research, academic or pharmaceutical industry, including experience in the core competencies of characterization and analysis of biotherapeutics. cGMP experience is highly preferred.- An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.- Other : Demonstrated knowledge of cGMPs o
Posted:
May 1 on Tip Top Job
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