Quality Assurance Inspector

Actalent; Downers Grove (IL); On-site; USD 28,000 - 32,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Paid time off

Job summary

Actalent is seeking a Quality Assurance Inspector for a contract role based in Downers Grove, IL. You will focus on receipt and production inspections, sampling, testing, documentation, and collaboration with Production and Quality teams to ensure all batches meet established specifications.

Responsibilities include line clearance monitoring, labeling checks, sample retention, and QA liaison activities. The role emphasizes accuracy, compliance, and detailed record-keeping in aHealthcare/Pharma

Qualifications

• Minimum 1 year of QA experience in cosmetics or pharmaceutical environments.
• Demonstrated QA experience including document review and quality documentation practices.
• Working knowledge of GMP and its application in production settings.
• Strong computer literacy and familiarity with quality/document systems.
• Ability to interpret vendor documentation for shelf-life and specs.
• Ability to perform basic arithmetic and two-dimensional measurements with tools.

Responsibilities

• Sample and inspect incoming packaging and raw materials to verify conformance with PO requirements and internal standards.
• Verify container integrity and labeling before acceptance.
• Perform sampling using a defined plan and inspect items with scales, calipers, micrometers, etc.
• Document inspection activities clearly with traceable records.
• Maintain organized files of inspection reports and supplier performance.

Skills

QA experience

GMP knowledge

Documentation

Computer literacy

Measurement tools

Regulatory compliance

Tools

QMS software

Calipers

Micrometers

Rulers

Scales

Job description

Job Description

The Quality Assurance Inspector plays a key role in ensuring that incoming packaging and chemical raw materials, as well as in-process and finished products, meet all regulatory and internal quality standards. This position focuses on both receipt inspection and production inspection, including sampling, testing, documentation, and coordination with Production and Quality teams to ensure that every batch is produced and packaged in full compliance with established procedures and specifications.

Job Title: Quality Assurance Inspector

Job Description

The Quality Assurance Inspector plays a key role in ensuring that incoming packaging and chemical raw materials, as well as in-process and finished products, meet all regulatory and internal quality standards. This position focuses on both receipt inspection and production inspection, including sampling, testing, documentation, and coordination with Production and Quality teams to ensure that every batch is produced and packaged in full compliance with established procedures and specifications.

Responsibilities

• Sample and inspect incoming packaging and chemical raw materials to verify conformance with purchase order requirements, regulatory expectations, and internal quality standards.
• Verify the integrity of shipping containers and confirm that each container is properly labeled before acceptance.
• Perform sampling of receipts using a defined statistical sampling plan and inspect sampled items using visual checks and measurement devices such as scales, rulers, micrometers, and calipers.
• Document all inspection activities clearly and accurately, maintaining complete and traceable records.
• Maintain organized files of receipt inspection reports and vendor performance reports to support ongoing supplier evaluation.
• Perform computer transactions in accordance with the Quality Systems receipt inspection process, ensuring data accuracy and completeness.
• Assist in the development and maintenance of item specifications and master files to support consistent quality standards.
• Coordinate with the Purchasing Department to establish and maintain quality standards with suppliers.
• Read, review, and compare documents, including specifications and batch records, and consistently follow established procedures.
• Monitor line clearance functions to ensure that production lines are properly cleared and set up before operations begin.
• Issue production paperwork and labels required for manufacturing and packaging operations.
• Draw samples from production lines for testing, retention, stability, and other purposes, and maintain accurate records of all samples.
• Act as a liaison between the Production and Quality departments to support effective communication and issue resolution.
• Perform yearly monitoring and review of retain samples to ensure ongoing product quality and stability.
• Examine filling and packaging labeling prior to the start of filling operations to confirm accuracy and compliance with specifications.
• Develop a solid understanding of batch documentation requirements and all associated production and compliance steps.
• Review and verify all compliance steps associated with the production of regulated products, including line clearances, filling and packaging labeling, and production sampling requirements.
• Quarantine filling and packaging materials brought to production lines if they do not conform to standard specifications, artwork, or if they are found defective.
• Quarantine finished products that are found defective due to labeling issues, weight deficiencies, coding errors, or other nonconformances.
• Prepare and apply REJECT stickers for nonconforming filling and packaging materials from production lines, as needed.
• Assist Quality Assurance leadership with the internal Auditing Program by supporting audits and related activities.
• Assist with Annual Product Review (APR) activities by providing documentation and data as required.
• Organize and maintain samples within the retain room to ensure proper storage, traceability, and accessibility.
• Support projects as assigned by Quality Assurance leadership, contributing quality expertise and documentation.
• Prepare detailed and accurate documentation and proficiently search, retrieve, and issue documents via the organizations Quality Management System (QMS).
• Perform additional duties and responsibilities as required by Quality Assurance leadership to support overall quality objectives.

Essential Skills

• Minimum of 1 year of experience in a Quality Assurance environment, preferably within the cosmetics or pharmaceutical industry.
• Demonstrated quality assurance experience, including document review and quality documentation practices.
• Working knowledge of Good Manufacturing Practices (GMP) and their application in a production environment.
• Strong computer literacy and experience using computer-based quality and documentation systems.
• Ability to understand and interpret vendor documentation for component shelf-life and related specifications.
• Capability to perform basic arithmetic and complete 2-dimensional measurements using appropriate tools.
• Ability to understand and review all compliance steps associated with the production of regulated products, including line clearances, filling and packaging labeling, and production sampling requirements.

Additional Skills & Qualifications

• Experience in the cosmetics or pharmaceutical industry is highly desirable.
• Experience supporting or participating in internal auditing programs is an asset.
• Experience assisting with Annual Product Reviews (APR) is beneficial.
• Ability to support assigned projects and adapt to changing priorities.
• Demonstrated ability to actively listen and readily assume responsibility for actions.
• Proficiency with Quality Management Systems (QMS) for searching, issuing, and managing documents.
• Interest in gaining experience in the cosmetic and pharmaceutical industries and developing a long-term career in quality.
• Openness to internal mobility, with the opportunity to apply for other roles within the organization after six months.

Work Environment

The role is primarily based in a quality office environment, with approximately 8090% of the time spent in the office and 1020% of the time spent on the production floor. The standard schedule for this position is a second-shift assignment, working Monday through Friday from 2:00 p.m. to 10:30 p.m. New hires receive initial training on the first shift, typically from 6:00 a.m. to 2:30 p.m. for about two weeks at the start of employment. The position involves regular interaction with production lines, packaging areas, and quality offices, using measurement tools such as scales, rulers, micrometers, and calipers, as well as computer-based quality and documentation systems. The environment supports steady hours with very minimal overtime and offers exposure to both cosmetic and pharmaceutical manufacturing settings.

Job Type & Location

This is a Contract position based out of Downers Grove, IL.

Pay And Benefits

The pay range for this position is $20.00 - $23.00/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)

Job Type & Location

This is a Contract position based out of Downers Grove, IL.

Application Deadline

This position is anticipated to close on Nov 9, 2026.

Workplace Type

This is a fully onsite position in Downers Grove,IL.

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 [e-mail] 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.