Scientist I Salary at Adesis Inc BETA

Solenis is a leading global producer of specialty chemicals focused on delivering sustainable solutions for water-intensive industries, including consumer, industrial, institutional, food and beverage, and pool and spa water markets. Owned by Platinum Equity, the company's product portfolio includes a broad array of water treatment chemistries, process aids, functional additives, and cleaners and disinfectants, as well as state-of-the-art monitoring and control systems. These technologies are used by customers to improve operational efficiencies, enhance product quality, protect plant assets, minimize environmental impact, and create cleaner and safer environments. Headquartered in Wilmington, Delaware, the company has 69 manufacturing facilities strategically located around the globe and employs a team of over 16,100 professionals in 130 countries across six continents. Solenis is a 2024 US Best Managed Company, recognized fouryears in a row. For more information about Solenis, please

Job Description The Department of Neurology at Nemours Children's Health-Delaware seeks a motivated Research Scientist (tenure-track Assistant Professor equivalent) to be part of the highly collaborative and growing Neuroscience Center at Nemours. The Research Scientist will be responsible for the planning and execution of a wide range of research projects to develop and oversee an independent research program. Research activities include designing and fostering collaborative and independent research projects related to neuroscience and neurologic disease, supervision of postdoctoral associates, technicians and students, obtaining and coordinating external funding, and disseminating research in the form of manuscripts and conference presentations. Must hold academic rank (Assistant Professor) at one of Nemours' partner academic institutions at the time of accepting the position or immediately thereafter. The position includes a highly competitive salary, high-quality laboratory space,

Company Overview: SKPT pharmteco (SKPT, the Corporation) is a U.S.-based global Contract Development and Manufacturing Organization (CDMO) that consolidates the operations of sites worldwide - Korea, France, Ireland, and the United States (CA and PA). Built on over 75 years of experience, SK pharmteco is a trusted partner specializing in the manufacture of small molecule APIs and intermediates, viral vectors for gene therapies, cell therapies, registered starting materials and analytical services for the pharmaceutical industry worldwide. Position Summary: SK pharmteco, Cell and Gene US, is looking for a highly skilled Associate Scientist/Senior Associate Scientist to join the Bioanalytical and Biophysical Analytical Development team. The Associate Scientist/Senior Associate Scientist will primarily engage in analytical development, assay qualification/validation, and analytical testing for cell and gene therapy products. Primary Responsibilities: Collaborate effectively with a dynamic

Description Completing daily manufacturing tasks per standard operating procedures and batch document instructions. Documenting all manufacturing activities clearly and accurately. Ensures all production activities are completed in a safe and compliant manor. Maintain and prepare high quality documentation. Dispense large and small amounts of raw materials Perform CIP and SIP of product tanks Work with hazardous materials under the appropriate safety procedures Performs other functions as necessary or as assigned. Qualifications Bachelor of Science degree in Chemical Engineering, Biology, Chemistry, or other engineering or scientific field. 1+ years of cGMP experience Familiarity with Good Manufacturing Practices (GMP) regulations. Knowledge of cGMP guidelines and standards. Knowledgeable of: upstream equipment (aka unit operations) and process overview (media prep, small scale, large scale), Analytical equipment (VI-Cell, NOVA, Centrifuge, tubing welder), PLC / DCS / HMI Proficiency i

Overview: Building our Future Together. FXI is a leading manufacturer of polyurethane foam, which provides an array of comfort solutions to the Bedding, Furniture and Transportation markets. We have made it our mission to provide tailored solutions that delight our customers and consumers. We are an industry leader in the rapidly growing Mattress in a Box segment of the bedding market. We have created a molecules to doorstep business model that leverages our leading innovation, scale, and footprint to deliver our own brands as well as other leading brands to the market and to consumers doorsteps. With our corporate headquarters, high-tech research and development facility, and multiple manufacturing locations in North America, FXI has built a culture of innovation and achievement that is recognized by customers, suppliers and peers. We provide one of the broadest sets of comfort solutions to the broadest set of industry players, through the broadest manufacturing platform in the indust

Description Job Description: Accession of forensic evidence in the Laboratory Information System Analysis (LISA), maintain accurate and complete chain of custody for evidence, responsible for data entry into LISA and the Armed Forces Medical Examiners Tracking System (AFMETS), preparation of correspondence/documents ensuring proper format, mathematical correctness, grammar, punctuation, and spelling, and preparation & editing of recurring reports regarding case status and case tracking. Prepare reagents and maintain documentation of reagent prep and Quality Control testing in accordance with SOPs. Perform laboratory house-keeping activities such as preparing common laboratory reagents, maintaining appropriate stock levels of expendable supplies, and maintaining a clean environment within laboratory work areas. Perform service casework involving nucDNA and mtDNA typing and profiling procedures. Support validation projects focusing on systems with increased sensitivity and discrimination

Job Description Develop new or optimize existing analytical release or characterization methods (CE or HPLC based) based on knowledge of biological and biochemical analytical techniques to support rAAV process development and product release/characterization. Write and edit internal technical reports, quality documents and external presentations. Troubleshoot technical issues and resolve the issues timely. Conduct analytical experiments to support process and technology development, and to deliver a reliable high-quality experimental data and prepare experimental reports in a timely manner. Manage critical samples and prepare critical assay reagents as needed. Maintain GXP compliant good documentation with high level of detail. Requirements Working in the labs to perform experiments described above in the job primary duties Design experiments, organize, discuss and record experimental data. Prepare presenting materials, literature search and so on. Trainings, lab meetings and administr

Job Summary: Product Development Science and Technology (PDS&T) is seeking a motivated Scientist to support parenteral drug product process development, scale-up, and technology transfer to commercial manufacturing sites. This role will focus on the development of robust manufacturing processes for clinical and commercial-phase products, with an emphasis on antibody-drug conjugates (ADCs). The Scientist will independently design and execute laboratory studies, generate and analyze precise and reproducible data, and contribute to cross-functional product development and Chemistry, Manufacturing, and Controls (CMC) teams. Responsibilities: Design and execute studies to develop and optimize manufacturing processes for parenteral drug products. Conduct stability assessments of biologics by evaluating their chemical and physical properties under various conditions, including pH, ionic strength, temperature, light, and moisture exposure. Assess the impact of manufacturing process stresses (e