Actalent
Associate Scientist/Chemist
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Associate Scientist/Chemist
role at
Actalent .
Job Description We are seeking a team of Analytical Chemists to join our team, performing routine tests on various samples, including finished products, stability samples, and raw materials. This role involves using techniques such as UV and HPLC in a regulated laboratory environment, evaluating test results, maintaining accurate documentation, and ensuring compliance with SOPs and cGMP standards.
Responsibilities
Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution.
Evaluate test results and determine the acceptability of samples based on the results.
Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs.
Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards.
Review notebooks promptly and ensure compliance with SOPs.
Analyze and interpret results in both written and oral formats.
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.
Skills & Qualifications
Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master’s degree with 1 year of experience.
Proficiency in HPLC, UPLC, and UV-Vis techniques.
Familiarity with FDA and GMP regulations.
Ability to analyze and interpret complex data.
Working knowledge of instrumentation software used in laboratories.
Require Bachelors in Chemistry, No Ph.D.
Work Environment This position is based in a lab environment regulated by FDA and GMP standards. The work schedule offers flexibility with a 1st shift from 8am‑5pm or a 2nd shift from 2pm‑11pm. All training will take place during the first shift.
Pay and Benefits 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 include:
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&DD 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)
Location Coral Springs, FL (Fully onsite)
Application Deadline This position is anticipated to close on Oct 25, 2025.
Equal Opportunity Employer Actalent 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.
Accommodations 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
actalentaccommodation@actalentservices.com
for other accommodation options.
Seniority Level Entry level
Employment Type Full‑time
Job Function Research, Analyst, and Information Technology
Industries Business Consulting and Services
#J-18808-Ljbffr
Associate Scientist/Chemist
role at
Actalent .
Job Description We are seeking a team of Analytical Chemists to join our team, performing routine tests on various samples, including finished products, stability samples, and raw materials. This role involves using techniques such as UV and HPLC in a regulated laboratory environment, evaluating test results, maintaining accurate documentation, and ensuring compliance with SOPs and cGMP standards.
Responsibilities
Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution.
Evaluate test results and determine the acceptability of samples based on the results.
Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs.
Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards.
Review notebooks promptly and ensure compliance with SOPs.
Analyze and interpret results in both written and oral formats.
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.
Skills & Qualifications
Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master’s degree with 1 year of experience.
Proficiency in HPLC, UPLC, and UV-Vis techniques.
Familiarity with FDA and GMP regulations.
Ability to analyze and interpret complex data.
Working knowledge of instrumentation software used in laboratories.
Require Bachelors in Chemistry, No Ph.D.
Work Environment This position is based in a lab environment regulated by FDA and GMP standards. The work schedule offers flexibility with a 1st shift from 8am‑5pm or a 2nd shift from 2pm‑11pm. All training will take place during the first shift.
Pay and Benefits 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 include:
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&DD 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)
Location Coral Springs, FL (Fully onsite)
Application Deadline This position is anticipated to close on Oct 25, 2025.
Equal Opportunity Employer Actalent 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.
Accommodations 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
actalentaccommodation@actalentservices.com
for other accommodation options.
Seniority Level Entry level
Employment Type Full‑time
Job Function Research, Analyst, and Information Technology
Industries Business Consulting and Services
#J-18808-Ljbffr