- Operate GC/HPLC instruments under GxP requirements with at least 1 year of hands-on experience.
- Perform analytical testing in accordance with method SOPs under GMP conditions.
- Inspect production and packaging activities; ensure completeness and accuracy of manufacturing records.
- Lead method validation efforts per USP and other applicable regulatory standards.
- Revise and maintain method SOPs to ensure compliance with current regulations.
- Coordinate calibration and maintenance of laboratory instruments and equipment.
- Manage vendor qualification programs and coordinate testing with external laboratories.
- Review laboratory results, notebooks, and related documentation for accuracy and compliance.
- Receive, inspect, and release or reject raw materials and packaging components; update inventory systems.
- Maintain and manage the stability program, including drafting protocols, reviewing results, and performing trend analysis.
- Control and maintain master labels and retain sample programs.
- Conduct environmental monitoring and maintain temperature and water system records.
- Perform regular sampling and sanitization of the water system.
- Manage laboratory standards, reagents, and chemicals; ensure timely disposal of expired materials.
- Bachelors degree in Chemistry, Pharmaceutical Sciences, or a related field.
- Minimum 1 year of experience operating GC/HPLC under GxP/GMP conditions.
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 Chicago,IL. Application Deadline This position is anticipated to close on Jun 13, 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.