- Conduct in-process quality testing and ensure products meet FDA regulations.
- Verify the accuracy of labels, including fill weight, lot codes, expiration dates, leakers, label placement, foreign material, and shipping labels.
- Submit samples to QC Chemistry and QC Microbiology labs for testing hourly, following the lab schedule.
- Manage and close paperwork, submit reports including weight averages, and review batch records.
- Monitor for QC issues and non-conforming products, with the authority to stop production if products do not pass quality testing.
- Assist the team with root cause analysis and investigations.
- Strong math skills with the ability to perform calculations and percentages.
- Attention to detail and the ability to identify mistakes and non-conformances.
- Ability to work independently and make judgment calls/decisions.
- Ability to work well within a team, especially in handling non-conformances.
- Knowledge of Quality Control, GMP, and FDA regulations is preferred.
- Minimum High School diploma required. Preferred: Bachelors degree in Biology, Chemistry, or a related field.
- Opportunity for advancement, especially with a BS in Chemistry, Microbiology, Biology, or related field.
- Career path includes positions such as QC I, QC II, Lab Tech I, Lab Tech II, Chemist, Microbiologist, or Regulatory roles.
Pay and Benefits The pay range for this position is $19.00 - $19.00/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 Streamwood,IL. Application Deadline This position is anticipated to close on Jul 15, 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.