Overview
In-Process Quality Assurance Technician (IPQAT) Jobs in Montgomery, IL at ARM Group
Title: In-Process Quality Assurance Technician (IPQAT)
Company: ARM Group
Location: Montgomery, IL
The ARM Group is seeking detail-oriented In-Process Quality Assurance Technicians (IPQAT) for our manufacturing client located in Montgomery, IL.
The In-Process Quality Assurance Technician will be responsible for performing real-time quality inspections and providing quality oversight throughout the manufacturing process. This individual will ensure products are manufactured, inspected, and documented in compliance with cGMP regulations, customer requirements, internal SOPs, and established quality standards.
Responsibilities
- Conduct regular inspections and quality checks of in-process and finished products to ensure compliance with specifications and quality standards.
- Monitor and verify critical control points throughout the manufacturing process.
- Perform line clearance and cleanliness inspections prior to batch production.
- Ensure production areas are free of previous products, components, materials, and documentation before changeovers.
- Review Batch Manufacturing Records (BMRs) and associated documentation for accuracy, completeness, and compliance with Good Documentation Practices.
- Verify Batch History Records and changeover documentation are completed properly and accurately.
- Verify calibration status of equipment, instruments, and measuring devices used in manufacturing.
- Collect, identify, and label product samples according to established sampling plans for laboratory testing and inspection.
- Ensure compliance with cGMP requirements, SOPs, controlled documents, and quality procedures on the shop floor.
- Identify and document quality issues and issue nonconformance reports as necessary.
- Escalate quality concerns to the QA & QMS Supervisor and Quality leadership.
- Place non-conforming products on quality hold or rejected status and ensure proper segregation from acceptable products.
- Participate in root cause investigations and support Corrective and Preventive Action (CAPA) implementation.
- Monitor product rework activities and ensure all rework is performed and documented according to approved instructions.
- Inspect reworked products to confirm they meet customer and quality requirements.
- Provide day-to-day quality oversight and support to manufacturing and operations teams.
- Perform other duties as assigned.
Qualifications
- College degree in Science or a related field preferred; equivalent experience will be considered.
- Minimum of 2+ years of Quality, Quality Assurance, Operations, or Manufacturing experience in a cGMP-regulated manufacturing environment.
- Strong understanding of cGMP requirements and Good Documentation Practices.
- Experience reviewing manufacturing records and quality documentation.
- Familiarity with nonconformance reporting, root cause analysis, CAPA, product holds, and quality inspections preferred.
- Strong attention to detail with the ability to identify aesthetic defects and quality issues.
- Ability to work independently and collaboratively as part of a team.
- Strong written, verbal, and interpersonal communication skills.
- Proficiency with Microsoft Office and database or computer systems.
Physical Requirements
- Ability to stand and walk for extended periods on the manufacturing floor.
- Ability to sit for extended periods while completing documentation and computer-based tasks.
- Ability to occasionally lift up to 40 lbs.
If you are a quality professional with experience in a cGMP-regulated manufacturing environment and a strong eye for detail, we encourage you to apply!
Disclaimer
ARM GROUP is committed to fostering a diverse and inclusive workplace. We are an Equal Employment Opportunity Employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender identity, sexual orientation, national origin, genetic information, sex, age, disability, veteran status, or any other legally protected basis.
We actively encourage applications from individuals with diverse backgrounds, including people with disabilities. Accommodations are available upon request for applicants participating in all aspects of the selection process.
By applying for this job, you consent to allow representatives of ARM GROUP LLC to contact you regarding your candidacy. This may include communication via email, phone, text, or other means deemed appropriate by ARM GROUP LLC. Rest assured, your information will be handled confidentially and used solely for recruitment purposes.
It’s important to note that ARM Group LLC does not interfere in the decision-making process regarding your selection or rejection. The ultimate decision to hire or reject your candidacy lies solely with the client organization, with whom we have an agreement to source candidates for their consideration.
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. All applicants must submit to background checks and drug screening.
Applicants for this position must be legally authorized to work in the United States. Please be aware that this position does not meet the employment requirements for individuals with F-1 OPT STEM work authorization status.
