Job Details: Job Location: Miramar Aveva - Miramar, FL, Salary Range: $70000.00 - $75000.00Salary/year, Job Summary: Laboratory position which involves development and validation of analytical methodology in support of the research projects involving testing of pharmaceutical components and/or drug products. Under general supervision, the position may require proficiency in support formulation, development method improvement and validation, testing per compendial pharmacopeia, etc. Job Responsibilities Proficiency in multiple instrumentation techniques such as HPLC, GC, UV-VIS, dissolution equipment, pH measurement, titration, etc. General knowledge of cGMP and FDA requirements. Perform stability testing for GMP and R&D finished products Conduct analytical testing of API, excipients and components  following compedial and validated methods Perform analytical method validation and method transfer with a minimum supervision. Follow company’s SOPs, STPS and comply with safety regulations. Maintain detailed record of experiments in the laboratory notebook. Timely communicate to supervisor(s) the obtained data and any issues aroused during testing Ability to analyze and interpret the analytical data under minimum supervision. Interpret specifications, standard operating procedures, and standard testing procedures. Writes/reviews protocols, reports, SOPs and STPs applicable to analytical laboratory under the supervision. Works as a member of a team to achieve all outcomes Operates in accordance with our Code of Conduct and Business Ethics, and all established regulatory, compliance and safety requirements. Performs all work in support of our Values: Collaboration, Courage, Perseverance, and Passion All other relevant duties as assigned   Qualifications: Job Requirements   Education Bachelor’s degree (B.S.) in chemistry or related field Master’s degree (M.S.)   Knowledge, Skills and Abilities General statistical applications such as normal ant T-test distribution, regression analysis, determination of test reliability and validity, analysis of variance, correlation techniques Analytical chemistry and common instrumentation General understanding of HPLC, GC, Drug Release, UV, IR, Titration. Using common computer software and analytical applications programs. Writing and interaction in English   Experience At least two (2) to five (5) years experience in pharmaceutical laboratory (B.S) At least zero (0) to three (3) years experience (M.S.)