Job Title: Associate ScientistJob DescriptionWe are seeking a dedicated and detail-oriented Associate Scientist to perform routine tests of finished products, stability samples, raw materials, and CV samples in a regulated laboratory environment. The ideal candidate will have experience with assays, chromatographic purity, content uniformity, particle size distribution, water determination, and other tests in compliance with in-house monographs and USP standards.Responsibilities
Perform routine tests of finished products, stability samples, raw materials, and CV samples, including assays, chromatographic purity, content uniformity using UV and HPLC, particle size distribution using various techniques, and water determination by KF.
Evaluate test results and decide on 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 both written and oral formats.
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 chemistry experience.
Experience in a regulated laboratory environment.
Familiarity with FDA and GMP standards.
Ability to maintain accurate lab notebooks and documentation.
Experience in analyzing and interpreting test results.
Knowledge of instrumentation software used in laboratories.
Additional Skills & Qualifications
Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis OR 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.
Work EnvironmentThis role is based in a lab environment regulated by FDA and GMP standards. The laboratory is equipped with advanced analytical instrumentation and follows strict compliance with safety guidelines and good housekeeping practices.Pay and BenefitsThe 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 TypeThis is a fully onsite position in Coral Springs,FL.Application DeadlineThis position is anticipated to close on Mar 15, 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 [email protected] (%[email protected]) for other accommodation options.