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Associate Scientist

Actalent

Posted Tuesday, August 26, 2025

Posting ID: JP-005503186

Coral Springs, FL
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Actalent is Hiring a Team of Analytical Scientists // First and Second Shift!

Job Description

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.

Essential Skills

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

Additional Skills & Qualifications

  • 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.

Work Environment

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.

Compensation:$35

Contact Information

Email: jsaintizaire@actalentservices.com

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
On-Site
Housekeeping
Pharmaceuticals
Change Control
Investigation
Chemistry
Corrective And Preventive Action (CAPA)
Biochemical Assays
Good Manufacturing Practices
High-Performance Liquid Chromatography
Chromatography
Lab Notebooks
Particle-Size Distribution

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