- Provide accurate and timely testing of raw materials, bulk formulations, and finished goods in accordance with established procedures and FDA and GLP standards.
- Ensure inspection and control of incoming raw materials and components as well as finished goods.
- Verify line end-of-shift and end-of-run reconciliation.
- Assemble and verify all batch records.
- Support implementation of Quality Systems to ensure compliance with FDA regulations.
- Coordinate with production lines to identify and document nonconformities and report results as necessary.
- Perform routine verification of instrument calibration and preventive maintenance on laboratory equipment.
- Assist with training of line personnel, batching personnel, and office staff as required.
- Conduct routine environmental microbiological testing.
- Ensure laboratory supplies are current and sufficiently stocked.
- Accurately prepare and document standards, standard solutions, and other reagents.
- Promote quality in both the laboratory and plant environments.
- Maintain an effective and efficient laboratory that processes samples accurately.
- Foster a team environment where individuals feel free to seek support and advice on quality matters.
- Interpret and report analytical data.
- Manage product release or rejection with approval from QC Supervisor/QA Specialist.
Preferred qualifications:
- Quality assurance and control expertise.
- Proficiency in wet chemistry and analytical chemistry.
- Experience with lab equipment such as FTIR, HPLC, GC.
- Understanding of GMP and GLP regulations.
- Strong computer skills and proficiency in Microsoft Office.
- Excellent verbal and written communication skills.
- Ability to work effectively in a team environment.
The position is based in a QC manufacturing lab following GMP/GLP regulations. The work schedule is primarily the first shift, Monday to Thursday from 7 AM to 5 PM, with potential overtime on Fridays and Saturdays.
Pay and Benefits The pay range for this position is $21.00 - $21.00/hr.Eligibility requirements apply to some benefits and may depend on your jobclassification 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 Dayton,OH. Application Deadline This position is anticipated to close on Aug 18, 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.