Quality Control Chemist Salary in the United States

Biote Medical is the world leader in hormone optimization and we are adding to our team! We partner with providers to take a complete approach to healthier aging through patient-specific bioidentical hormone replacement therapy and the only nutraceutical line created specifically to support hormone health. We are currently looking for a Quality Control Chemist to join our team based in Birmingham, AL. This person must be based on-site in Birmingham. Overview of Position The QC Chemist is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance pos

Job Description: Title - QC Scientist I Location - St. Louis, MO Duration - 6 months assignment How will you make an impact? Perform HPLC/UPLC testing on In-Process, DS release, DP release, DS stability, DP Stability, process validation, analytical method validation/transfer, method establishment/qualification, and various other non-routine samples. What will you do? Demonstrate proper laboratory safety and housekeeping practices through weekly 5S Lab audits and monthly laboratory inspections. Assure all activities meet EHS requirements. Conduct GMP testing in an analytical laboratory environment using HPLC and UPLC test methods (i.e.,Reverse Phase, SEC, Titer concentration, CEX, etc.). Accurately record and report analysis results in accordance with lab procedures and quality systems. Recognize and report out-of-specification/ out-of-trend results to laboratory management; recommend solutions. Maintain and troubleshoot analytical instrumentation and workspace as needed. Perform method

We are currently seeking qualified professionals for various contract positions with our established corporate clients in the Katy, TX area. While these roles are temporary, they offer a valuable opportunity to gain experience and potentially transition into a permanent position within these reputable organizations. Kelly Services proudly provides comprehensive health benefits to all contract employees, allowing you to focus on your performance and career development during the engagement. After the contract concludes, you will have the option to reassess your career goals and explore potential internal opportunities. If you are interested in learning more about these exciting opportunities and how Kelly Services can support your career aspirations, please don't hesitate to contact me to schedule a brief informational call at your convenience. Thank you for your time and consideration. TITLE: QC Chemist PAY: $31.25-35/hour W2 DURATION: 18 months - possibility to extend LOCATION: Onsite

Job Description Job Description SUMMARY The Quality Control Chemist is responsible for daily lab testing with the purpose of accepting or rejecting test samples based on pre-determined specifications. The successful candidate will be able to work quickly and safely and will assist the Quality Control Manager with other tasks, as needed. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. • Performs laboratory tests including pH, fluoride, viscosity, specific gravity, color, and appearance. • Tests raw materials, bulk intermediates, finished products and stability samples for specific quality attributes. • Uses and maintains HPLC, GC, FTIR, and other instruments. • Assists in performing method validations. • Performs a variety of wet lab techniques including but not limited to: titrations, pH, ISE, etc. • Writes and revises SOPs and tests methods as needed. • Follows documented procedures: SOPs, test methods, transfer protocols. • Prepares reports

Quality Control Chemist 5 days on-site Support a well-established CDMO in Irvine, CA, while expanding on your analytical experience in a cGMP environment. Day to day: Analytical testing of raw materials, in-process samples, and final products Predominately utilize HPLC, as well as other analytical instrumentation Adhere to all SOPs and cGMP regulations Provide peer review for other technician's data Maintain and troubleshoot HPLC and other analytical instrumentation Support equipment calibrations Additional relevant tasks as needed Experience: Bachelor of Science in Chemistry or related field Experience in pharmaceutical/biotech environment Exposure to working with small molecules Experience working with HPLC

Biote Medical is the world leader in hormone optimization and we are adding to our team! We partner with providers to take a complete approach to healthier aging through patient-specific bioidentical hormone replacement therapy and the only nutraceutical line created specifically to support hormone health. We are currently looking for a Quality Control Chemist to join our team based in Birmingham, AL. This person must be based on-site in Birmingham. Overview of Position The QC Chemist is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance pos