Associate Scientist I-II (Contract)

Associate Scientist I-II Kelly Science has immediate needs for multiple Associate Scientist I-IIs to join a growing client located in the Miami/Fort Lauderdale FL area. Location: Fort Lauderdale/Miami, FL Shift: Monday-Friday 4pm-12am Salary Range: $30-$40/hour 12 month contract opening Essential Duties and Responsibilities: Conduct laboratory activities with limited supervision, including analyzing raw materials, in-process materials, and finished pharmaceutical products for quality, safety, purity, strength, and identity, following applicable methods and relevant guidelines (cGMP, EH&S, FDA, and other governing bodies). Independently set up and operate lab equipment, prepare reagents, solvents, and solutions for analytical and formulation activities. Maintain accurate records in lab notebooks for all testing performed. Process analytical data using lab equipment such as HPLC/UPLC and enter data into spreadsheets; conduct routine calculations. Support the manufacture of inhalation drug products and prepare samples for blend uniformity. Perform equipment qualification and calibrations as directed. Execute approved method transfer protocols. Assist in training other scientists and team members. Perform additional tasks as assigned. Participate in project activities, support project timelines, and proactively contribute to meeting team objectives. Communicate effectively with team members and maintain effective relationships. Conduct lab work in accordance with SOPs and STPs and follow corporate safety rules and procedures. Comply with all corporate guidelines and policies. Qualification Requirements: Associate Scientist II: BSc in Chemistry, Pharmacy, or related fields with at least 3 years of experience in Pharmaceutical R&D, or MSc in Chemistry, Pharmacy, or related fields with 0-2 years of experience in Pharmaceutical R&D. 2 years minimum industry experience with HPLC method development and Empower software Proven ability and/or experience with compendial test methods or pharmaceutical manufacturing equipment. Understanding of pharmaceutical equipment and computerized systems for operation and troubleshooting, including experience with analytical and/or process equipment such as HPLC, IR/FTIR, UV-Vis, AA, powder blenders, etc. Knowledge and understanding of FDA cGMP requirements as it applies to the pharmaceutical industry. Strong written and oral communication skills in English, with the ability to write short technical documents such as memos, laboratory investigations, protocols, and reports. #p1 9748438