Actalent is Hiring a Team of Scientists and Analytical Chemists!

Job Description

Perform routine tests of finished product and stability samples, raw materials, and CV samples, including assays, chromatographic purity, content uniformity using UV and HPLC, particle size distribution using different techniques including water determination by KF, and tests according to in-house monographs and USP in a regulated laboratory environment. Evaluate test results and decide 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 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.

Responsibilities

• Perform routine tests of finished product and stability samples, raw materials, and CV samples, including assays, chromatographic purity, content uniformity using UV and HPLC, particle size distribution using different techniques including water determination by KF, and tests according to in-house monographs and USP in a regulated laboratory environment.
• Evaluate test results and decide 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 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 expe in chemistry and pharmaceutical analysis.
• Experience in working in FDA and GMP regulated environments.
• Ability to maintain accurate lab notebooks and documentation in compliance with SOPs.
• Competence in analyzing and interpreting results in both written and oral formats.
• Experience in training new analysts and conducting laboratory investigations.

Additional Skills & Qualifications

• Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis.
• 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.
• Working knowledge of instrumentation software used in the laboratories.

Work Environment

Lab environment; FDA and GMP regulated. Hours are Monday-Friday: 8am-5pm OR 2pm-11pm

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 Fort Lauderdale,FL.

Application Deadline

This position is anticipated to close on Apr 25, 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 for other accommodation options.

Salary : $28 - $32