HPLC Chemist Salary at Cosway Co BETA

Description Home Search Jobs Job Description Chemist I Contract: Pomona, California, US Salary Range: 23.00 - 25.00 | Per Hour Job Code: 350994 End Date: 2025-04-30 Days Left: 18 days, 3 hours left Apply To discuss more about this job opportunity, please reach out to Chitrank Rastogi (LinkedIn URL - https://www.linkedin.com/in/chitrank-rastogi-55119a102/), email your updated resume at Email - chitrank.rastogi@collabera.com or give me a call at (425) 523-1648. Thank you! Pay Range - $23 to $25/hr. (negotiable) Job Description: Job Roles & Responsibilities: Looking for an experienced chemist/toxicologist to join our Analytical Chemistry group at Pomona. In this role, you will: Perform LCMS test method development for drug testing in oral fluid and urine samples Perform test method characterization (TMC) and validations (TMV) for LCMS product release of calibrators and controls These cals and controls are used in conjunction with urine or oral fluid drugs of abuse assays run on clinical c

Job Title: Production ChemistJob Description We are seeking a dedicated and knowledgeable Production Chemist to join our team. This role offers the opportunity to work in a fast-paced lab environment with high volume and diverse tasks. The ideal candidate will have experience in GMP environments and possess strong skills in HPLC, biochemistry, and purification processes. This position promises great training, upward mobility, and retention within the department. Responsibilities + Ensure compliance with GMP standards. + Perform high-performance liquid chromatography (HPLC) for purification processes. + Conduct biochemistry and purification procedures. + Follow Standard Operating Procedures (SOPs) meticulously. + Utilize gas chromatography (GC) techniques. + Engage in quality control and analytical chemistry tasks. + Support production and pharmaceutical processes. Essential Skills + Bachelor's degree in Biochemistry or Chemistry. + Minimum of 6 months experience in a GMP environment. +

Duties and Responsibilities: Checks reactor system for proper operation in accordance with SOP and/or operation manual. Under general supervision and direction, measures and mixes ingredients according to the BPR (Batch Production Record). Dispensing of raw materials from Pharmastore for Synthesis. During processing, monitors chemical reactions (color and completeness of chemical reactions) and under general direction of supervision and/or senior Production Chemist personnel responds with appropriate actions to ensure proper processing. Using established procedures (safety and process) and under general supervision, performs intermediate chemical processing steps. Prepares solutions for purification and samples. Under general supervision, purifies crude peptide by using HPLC's. Conducts lyophilization process according to established guidelines. Performs drying processes in accordance with established processes and procedures. Reports any problems or issues regarding equipment used in

Piper Companies is seeking a Chemist III to join a leading pharmaceutical manufacturing company located in Lynwood, CA. This role is 100% onsite. The Chemist III will lead advanced analytical testing, method development and training initiatives, keep lab instruments in top shape, and ensure all regulatory standards are met. Responsibilities of the Chemist III include: Conduct advanced analytical testing using HPLC, FTIR, UV, GC, ICP, and wet chemistry techniques. Troubleshoot and maintain critical lab instruments to ensure optimal performance. Perform and document analytical testing for raw materials, in-process, finished products, and stability samples. Ensure compliance with FDA cGMPs, cGLPs, USP, ICH, SOPs, and other recognized standards. Lead the development and validation of analytical and chemical test methods. Train lab analysts in test procedures, equipment usage, and documentation practices. Mentor other chemists and lead laboratory investigations, drafting final reports for m

Job Title: Production Chemist Are you looking to break into the pharmaceutical industry? Now is your chance! Apply NOW for this amazing opportunity with a Market leader in PEPTIDE API Manufacturing services. They are seeking a motivated Production Chemist to join their team. In this key role, you will drive success and improvement by effectively implementing global computerized system procedures. For immediate consideration please email me at hhuffman@ actalentservices.com Pay: $25-30 (based on experience) Job Description: Checks reactor system for proper operation in accordance with SOP and/or operation manual. Under general supervision and direction, measures and mixes ingredients according to the BPR (Batch Production Record). Dispensing of raw materials from Pharmastore for Synthesis. Using established procedures (safety and process) and under general supervision, performs intermediate chemical processing steps. Prepares solutions for purification and samples. Under general supervi

What Nuclear Manufacturing contributes to Cardinal Health Nuclear Manufacturing is responsible for the manufacturing of time sensitive radiopharmaceuticals in an integrity driven, highly regulated environment (i.e. FDA, NRC, DOT) to support patient treatment through disease diagnosis, staging, and monitoring. The Material Science and Technology Transfer Chemist, Nuclear Manufacturing position is part of a growing Technical Operations team within Cardinal Health's Nuclear and Precision Health Solutions organization tasked with the development and technology transfer of radiopharmaceutical products into and among our network of qualified manufacturing facilities. This position will be responsible for the adaptation, setup, transfer, training, and maintenance of drug products with strict adherence to cGMP, GDP, environmental health and safety and related guidelines, and internal policies and procedures. Job Summary Specific duties will at a minimum comprise technical evaluation, process a

Key Responsibilities: Conduct routine and non-routine chemical analysis using HPLC, GC, UV-Vis, FTIR, and other analytical techniques. Perform method development, validation, and transfer following USP, ICH, and FDA guidelines. Analyze raw materials, intermediates, and finished products to ensure compliance with specifications. Prepare and maintain detailed documentation, including test results, validation reports, and lab notebooks, in accordance with cGMP and GLP requirements. Troubleshoot and maintain analytical instruments, ensuring proper calibration and functionality. Assist in investigations of out-of-specification (OOS) results, deviations, and corrective actions. Work collaboratively with Quality Assurance, R&D, and Production teams to support manufacturing and product development. Stay updated with regulatory changes and industry best practices in pharmaceutical and cosmetic analytical testing. Qualifications: Bachelor’s or Master’s degree in Chemistry, Analytical Chemistry,

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Phenomenex, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Phenomenex isn't your typical scientific company. Founded nearly 40 years ago, Phenomenex is a global technology leader committed to developing novel analytical chemistry solutions that solve the separation and purification challenges of researchers, advancing the future of scientific analysis and investigation, ensuring the quality of essentials like your food, water, shampoo, and even cold medication. Be part of our global success and together, we accelerate the discovery, development and delivery of s