Associate Scientist Position Available In Broward, Florida

Actalent is Hiring a Team of Scientists and Analytical Chemists! Job Description Perform routine tests of finished product and stability samples, raw materials, and CV samples, including assays, chromatographic purity, content uniformity using UV and HPLC, particle size distribution using different techniques including water determination by KF, and tests according to in-house monographs and USP in a regulated laboratory environment. Evaluate test results and decide the acceptability of the samples based on the test results. Maintain accurate lab notebooks and complete all related analytical reports, write summaries, and keep proper documentation in compliance with SOPs. Maintain the laboratories with good housekeeping practices and in compliance with cGMP. Ensure notebooks are reviewed promptly, in accordance with SOPs. Analyze and interpret results in written and oral format. Assist in the training of new analysts. Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed. Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment. Responsibilities Perform routine tests of finished product and stability samples, raw materials, and CV samples, including assays, chromatographic purity, content uniformity using UV and HPLC, particle size distribution using different techniques including water determination by KF, and tests according to in-house monographs and USP in a regulated laboratory environment. Evaluate test results and decide the acceptability of the samples based on the test results. Maintain accurate lab notebooks and complete all related analytical reports, write summaries, and keep proper documentation in compliance with SOPs. Maintain the laboratories with good housekeeping practices and in compliance with cGMP. Ensure notebooks are reviewed promptly, in accordance with SOPs. Analyze and interpret results in written and oral format. Assist in the training of new analysts. Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed. Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment. Essential Skills Proficiency in HPLC, UPLC, UV-Vis, and other analytical techniques. Strong expe in chemistry and pharmaceutical analysis. Experience in working in FDA and GMP regulated environments. Ability to maintain accurate lab notebooks and documentation in compliance with SOPs. Competence in analyzing and interpreting results in both written and oral formats. Experience in training new analysts and conducting laboratory investigations. Additional Skills & Qualifications Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis. Master’s degree in Chemistry or related scientific field with 1 year of related experience in pharmaceutical analysis. Ability to deal with problems involving several concrete variables in standardized situations. Ability to carry out necessary computations and to draw and interpret graphs. Working knowledge of instrumentation software used in the laboratories. Work Environment Lab environment; FDA and GMP regulated. Hours are

Monday-Friday:

8am-5pm OR 2pm-11pm