Quality Control Chemist Salary at Genzyme Corp BETA

Job Title: Associate Director Crystallization About the Job We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people's lives. We're also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started? Position Overview/Department Description: We are looking for a highly motivated individual with a mindset to lead the implementation of changes. She/He will be recognized as technical expert in the field of crystallization and solid-state chemistry and will have leadership experience. The successful candidate will work in a cutting-edge scientific global crystallization department in Sanofi's R&D CMC Synthetic organization. The job is in Cambridge MA, but close collaboration with colleagues in France is required. Crystallization Scientists work cross functionally to select active pharmaceutic

Here at Entegris, we use advanced science to enable technologies that transform the world, and we are seeking employees who have the drive to continue that mission. The Role: Our site in Billerica, MA is seeking a motivated and talented Analytical Chemist to work in the R&D Metrology Lab in support of our Microcontamination Control (MC) Division. The QA Chemist is responsible for conducting QA testing and will provide analytical support to production of our Micro-contamination control and membrane products, as well as for R&D development. The QA Chemist will prepare and test samples using Ion Chromatography, TOC, FTIR, NVR, Karl Fischer and ICP-MS. Shift: Sunday - Thursday, 10pm - 6:30am. In this role you will: Work in a clean room environment to conduct routine QA product testing of filtration and membrane products from manufacturing. Participate in conversations around non-routine testing and conduct testing once method is established. Follow and document standard operating procedure

Sr Research Associate, Biotherapeutics About the role We are seeking an enthusiastic, and highly motivated scientist to join our team. With a background in conjugation, purification and analytical characterization of antibody drug conjugates (ADCs), and a track record of contributing to multidisciplinary drug discovery teams, this position will play a critical role in driving Treeline's portfolio forward. You will also play a key role in developing the next generation of ADCs using bioconjugation, biochemistry, analytical chemistry techniques and various state-of-the-art scientific approaches. You will closely collaborate with other biochemists, medicinal chemists, biologists, and pharmacologists to enable forward progress of drug discovery programs. Responsibilities Perform, develop and optimize conjugation methods to generate high quality ADCs to support drug discovery campaigns. Conduct routine purification and analytical characterization of ADCs. Evaluate physicochemical properties

Job Description Overview: Position Title: Analyst III Business Title: Analytical Chemist III Entity: Consumer Products Services Division Department: ATL Location: Boston, MA Reports to: ATL Manager FLSA: Non-Exempt Hours Worked: Onsite Monday through Friday, forty-hours per week. Preferred start time between 8:30-9:30am for an 8 hour day. Must be flexible to meet the needs of the department and complete other projects as assigned. Position Summary: The Analytical Chemist III is responsible for bench work, supporting Scientist by running routine assays, preparing instruments and buffers for HPLC related assays and method development. Duties and Responsibilities: * Support research scientists with their experiments based on company protocol, method, and procedures. * Independently run routine HPLC and UHPLC-based analytical assays following already established methods, help with routine data capture, analysis and storage. * Run routine non-LC based assays * Do assay performance check on

Job Description Job Description The Chemist III will create and validate electronic calculations using Empower FR4 Reports within a cGMP environment. Experience with custom calculations is required. Key Responsibilities Include: Creation of Empower reports including custom calculations for HPLC, CE-SDS and icIEF technology. Validation of customized Empower reports. Authoring cGMP documents in support of Empower reports Impact assessment of test methods revisions against Empower reports. Understands, implements and maintains cGMP with respect to laboratory records, procedures and systems in accordance with procedural requirements. Accepts responsibility to complete assigned tasks within required timelines and works with others to accomplish business objectives. Revises procedures as necessary and provides continuous improvement support for the department. Basic: BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree. and 5+ years of related work exper