Qc Associate Scientist Jobs (NOW HIRING)

The Quality Control Associate plays a key role in ensuring that in-process and finished products meet strict customer and regulatory specifications. Working primarily on 3rd shift in a cleanroom environment, this role focuses on precise measurements, visual inspections, and documentation to support high-quality medical and healthcare packaging materials. The position offers training, opportunities for growth into other departments and leadership roles, and exposure to a stable, innovative, and globally recognized manufacturing operation.

Responsibilities

• Inspect in-process and finished products to verify they meet customer specifications and job order requirements.
• Perform strength and tensile testing using measurement tools, including taking highly precise measurements down to 1/64th of an inch.
• Review products for correct color standards and ensure visual appearance meets quality requirements.
• Test seal strength of pouches and other packaging materials to confirm integrity and performance.
• Conduct detailed visual inspections and ruler measurements of pouches, making approximately ten measurements per pouch as part of quality checks and tests.
• Identify pouch quality discrepancies or defects and promptly communicate findings to the machine operator or appropriate personnel so issues can be corrected.
• Complete all required labeling, documentation, and paperwork accurately and in a timely manner in accordance with quality and GMP standards.
• Pack finished products into bundles and prepare them for shipping while maintaining product identification and traceability.
• Follow cleanroom protocols and use required personal protective equipment (PPE) to maintain a controlled and compliant environment.
• Work collaboratively with lab coworkers and production personnel on the production floor to support smooth operations and consistent product quality.
• Adhere to established quality control procedures, Good Manufacturing Practices (GMP), and safety guidelines at all times.
• Maintain an organized work area and manage multiple tasks in a fast-paced production environment.
• Communicate clearly and professionally with team members and occasional visiting clients as needed.

• Experience with quality control or lab testing, which may include experience gained through school or industry (industry experience preferred).
• Familiarity with quality control inspection practices, including visual inspection and measurement-based testing.
• Ability to perform precise measurements with a ruler or similar tools, including measurements down to 1/64th of an inch.
• Strong attention to detail and accuracy in inspections, measurements, and documentation.
• Good organizational skills with the ability to manage repetitive tasks and maintain consistency over long periods of time.
• Comfort working in a fast-paced environment such as production, manufacturing, or food service.
• Ability to follow Good Manufacturing Practices (GMP) and standard operating procedures.
• Comfort with repetitive work and sitting for long periods while performing detailed inspections.
• Strong reliability in terms of transportation and attendance.
• Ability to work effectively as part of a team in both lab and production settings.
• Clear and professional communication skills to report defects and collaborate with colleagues.

• Associate degree, preferably in a scientific or technical field, or non-degreed candidates with relevant quality or lab experience.
• Ideal qualifications include an associate degree in a science-related discipline.
• High school diploma candidates will be considered if they demonstrate reliability, strong attention to detail, and comfort with repetitive work.
• Experience working in a cleanroom or controlled environment is beneficial.
• Familiarity with personal protective equipment (PPE) requirements and safe handling of films, foils, chemicals, and peelable solutions.
• Friendly, cooperative attitude and the ability to work well with a small team of colleagues in the cleanroom.
• Openness to learning and developing within a growing, innovative manufacturing organization.

This is a full-time 3rd shift position, typically working from 11:00 p.m. to 7:00 a.m. Initial training takes place on 1st shift, generally from 7:00 a.m. to 3:00 p.m. for approximately 4 to 6 weeks. The role is based in a cleanroom environment within a manufacturing facility that produces engineered flexible materials for the global healthcare market, including films, foils, chemicals, and peelable solutions. Team members must wear appropriate personal protective equipment (PPE) and steel-toed shoes while in the cleanroom and production areas. The work is team-based, with close collaboration among 4–5 people in the cleanroom and regular interaction with production personnel on the floor. A significant portion of the workday involves sitting and performing detailed measurements and inspections. The facility occasionally hosts visiting clients, so a professional, courteous demeanor is important. Fragrances and phone use in the lab are not allowed to maintain product integrity and a controlled environment. The company culture emphasizes stability, internal promotion, exposure to different departments, and opportunities to grow into leadership roles within a global, innovation-driven business.

Job Type & Location

This is a Contract to Hire position based out of Addison, IL.

The pay range for this position is $18.00 - $18.00/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)

This is a fully onsite position in Addison,IL.

This position is anticipated to close on May 29, 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 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 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.