Chemist

We are seeking a dedicated Associate Scientist to perform routine tests of finished products, stability samples, raw materials, and CV samples. The role involves assays, chromatographic purity, and content uniformity analysis using UV and HPLC, and particle size distribution using various techniques. This position requires working in a regulated laboratory environment, adhering to in-house monographs and USP standards.

Responsibilities

• Perform routine tests on finished products, stability samples, raw materials, and CV samples using UV and HPLC.
• Evaluate test results and decide on the acceptability of samples.
• Maintain accurate lab notebooks and complete analytical reports, summaries, and proper documentation in compliance with SOPs.
• Ensure laboratories are maintained with good housekeeping practices and are in compliance with cGMP.
• Ensure notebooks are reviewed promptly according to SOPs.
• Analyze and interpret results in 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.

• Proficiency in HPLC, UPLC, and UV-Vis.
• Strong background in chemistry and analytical techniques.
• Experience with SOPs and GMP compliance.
• Ability to analyze and interpret data accurately.

• Bachelor's degree in Chemistry or related scientific field with 1-2 years of pharmaceutical analysis experience, or Master's degree with 1 year of experience.
• Ability to manage problems involving several concrete variables in standardized situations.
• Competence in performing necessary computations and interpreting graphs.
• Working knowledge of instrumentation software used in laboratories.

This position is based in a lab environment regulated by FDA and GMP standards. Work schedule is 1st shift 8am-5pm OR 2nd shift 2pm-11pm, with all training taking place during the first shift.

The pay range for this position is $29.00 - $35.00/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 Fort Lauderdale,FL.

Application Deadline

This position is anticipated to close on Sep 5, 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.

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 due to a disability, please email ... for other accommodation options.