Job Title: Associate ScientistJob Description We are seeking an Associate Scientist to perform routine tests of finished products, stability samples, raw materials, and CV samples. This role involves conducting assays, chromatographic purity tests, content uniformity using UV and HPLC, and particle size distribution using various techniques, including water determination by KF. You will evaluate test results, maintain accurate lab notebooks, complete analytical reports, and ensure compliance with SOPs and cGMP regulations. Responsibilities + Perform routine tests of finished products, stability samples, raw materials, and CV samples, including assays, chromatographic purity, content uniformity using UV and HPLC, and particle size distribution using different techniques. + Evaluate test results and decide the acceptability of the samples based on the 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 analytical background , particularly in chemistry. + Experience in a regulated laboratory environment with adherence to FDA and GMP guidelines. + Ability to maintain accurate lab notebooks and complete analytical reports. + Ability to analyze and interpret test results. + Knowledge of SOPs and safety guidelines in a cGMP environment. Additional Skills & Qualifications + Bachelor’s degree in Chemistry or a related scientific field with 1-2 years of related experience in pharmaceutical analysis OR a Master’s degree in Chemistry or a related scientific field with 1 year of related experience in pharmaceutical analysis. + Ability to deal with problems involving several concrete variables in standardized situations. + Proficiency in necessary computations and the ability to draw and interpret graphs. + Working knowledge of instrumentation software used in laboratories. + Experience in writing laboratory reports and summaries. Work Environment This position operates in a lab environment that is FDA and GMP regulated. You will work with various laboratory instruments and software, and adherence to safety and compliance guidelines is essential. The role requires maintaining good housekeeping practices and ensuring proper documentation and review processes are followed. Pay and Benefits The pay range for this position is $28.00 - $32.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision• Critical Illness, Accident, and Hospital• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available• Life Insurance (Voluntary Life & AD&D for the employee and dependents)• Short and long-term disability• Health Spending Account (HSA)• Transportation benefits• Employee Assistance Program• Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Coral Springs,FL. Application Deadline This position is anticipated to close on Feb 17, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.