Job Description
We are seeking a dedicated Manufacturing Quality Engineer to lead quality assurance efforts in our manufacturing environment. This role is crucial in maintaining and enhancing the Quality Management System (QMS) and supporting manufacturing processes.
ResponsibilitiesLead the company's quality assurance efforts in manufacturing.Establish and maintain the Quality Management System (QMS).Maintain certification of the QMS to applicable standards as determined by executive management.Establish and maintain the internal quality audit program.Manage verification (inspection) activities, including quality inspection staff.Develop and write QMS documents such as procedures, work instructions, and forms.Manage document control staff to publish and maintain QMS controlled documents.Resolve non-conformances, perform root cause determination, and develop CAPA plans.Analyze and manage risk using tools like FMEA.Investigate root causes and write reports as required.Perform statistical analysis of processes and product conformance using Minitab and other tools.Manage the resolution of customer complaints.Perform and coordinate internal and external audits.Manage a staff of Quality Inspectors and Quality Administrator.Develop and improve manufacturing processes.Qualify and validate production equipment and processes.Source and/or design equipment, accessories, and/or modifications.Perform equipment, facilities, and utilities qualification.Source, test, and qualify new and alternative sources of materials.Maintain equipment documentation, including engineering drawings, qualification and validation records, and operating manuals.Manage multiple concurrent projects supporting corrective, preventive, and improvement actions.Essential Skills2+ years' experience in a manufacturing environment.2+ years' experience in a Quality Management System environment.Experience with Minitab or equivalent statistical analysis software.Proficiency in performing Process Capability (Cpk and Ppk) measurements and analysis.Experience in writing and managing controlled documents.Experience with CAPA systems and root cause investigation tools.Proficiency in MS Office software, including Excel and Word.Additional Skills & Qualifications2+ years' experience in a regulated environment.Six Sigma Green Belt or Black Belt preferred.Experience communicating with customers and vendors and resolving non-conformances.Experience with medical device manufacturing.Experience with flexible packaging converting, including slitting, web flexography, pouch making, bag making, and die cutting.Experience with flexible packaging films.Bilingual in English/Spanish or English/Gujarati preferred.Bachelor of Science in Engineering or a Technical Field preferred, with emphasis on mechanical, electrical, packaging, biomedical, quality, or manufacturing engineering.Work Environment
This role involves working in a dynamic manufacturing environment, focusing on both quality assurance and manufacturing engineering tasks. The position requires proficiency with various technologies and equipment, including statistical analysis software and 3-D CAD software. Team collaboration is essential, as is the ability to manage multiple projects simultaneously.
Pay and Benefits
The pay range for this position is $40.00 - $40.00/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 Buffalo Grove,IL.
Application Deadline
This position is anticipated to close on Aug 11, 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 actalentaccommodation@actalentservices.com for other accommodation options.