Job Title:

Stability CoordinatorJob Description The Stability Coordinator is a key member of the Quality Control Team with the primary responsibility of ensuring the stability program is in compliance with current good manufacturing practices (cGMP). This role serves as an essential link between research and development, regulatory affairs, quality systems, and site operations to maintain an inspection-ready stability program for our liquid pharmaceutical and topical antiseptic product lines. Responsibilities Maintain stability standard operating procedures (SOP), protocols, reports, and equipment in a current state. Ensure inspection readiness by keeping protocols, samples, equipment, and reports in compliance with SOPs. Notify management of investigations, determine root causes, and write investigation reports. Collaborate with Quality Control, Quality Operations, and Quality System for comprehensive report completion. Provide routine metric reports and status updates on the stability program to the Quality Council. Deliver stability reports for annual product reviews and metric reports on a routine basis. Manage stability chambers, maintain sample inventory, oversee calibration status, and act as the point of contact for out-of-limits notifications. Work with maintenance and engineering to resolve any issues. Coordinate annual stability sample management from manufacturing batches, pull samples for Quality Control testing, and manage any outsourced testing. Essential Skills Proficiency in quality control, GMP, and laboratory procedures. Experience in stability testing, HPLC/GC, wet chemistry, SOP, and data entry. Familiarity with LIMS, SLIMS, data integrity, root cause analysis, and investigations. Bachelor's degree in science, engineering, or a related pharmaceutical technical discipline. 3-5+ years of industry experience in pharmaceutical quality operations, particularly with liquid dosage forms or topical lines. Working knowledge of cGMP regulations and stability regulations. Additional Skills & Qualifications Familiarity with stability software programs (SLIMS) and Microsoft Office. Ability to organize and coordinate using standard processes. Work Environment This is an office-based role with frequent interaction in a GMP QC laboratory. The position focuses on coordination, tracking, and communication rather than testing. The facility is a fully FDA-approved site with over 106,000 square feet of space, equipped with state-of-the-art technology, including high-performance liquid chromatography and gas chromatography instrumentation. The work environment promotes a unique, all-in-one pharmaceutical manufacturing and operations process under one roof, ensuring unprecedented quality control. Job Type & Location This is a Contract to Hire position based out of Mount Prospect, IL. Pay and Benefits The pay range for this position is $32.00 - $36.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. 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 Mount Prospect,IL.

Application Deadline This position is anticipated to close on Sep 2, 2026. 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. 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.

San Francisco Fair Chance Ordinance:

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.