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St. Charles, IL 60174
Job Posting External
Position Quality Engineer Reports to Chief Executive Officer (CEO)
Type Full Time Department Executive (005)
Position Description: The Quality Engineer will be responsible for all aspects of quality throughout the company; including the development, implementations, and auditing of policies, procedures, supporting documents, and training requirements to support the Quality Management System (QMS).
Areas of Responsibility include:
Develop inspection methods to analyze product quality.
Improve product quality by making recommendations for change.
Work together with relevant teams and departments to improve products.
Ensure products adhere to company and industry quality standards.
Brainstorm ideas to create solutions for identified problems.
Formulate a strategic plan to increase productivity in the business.
Document results and findings after inspections are carried out.
Implement a working system to ensure conformity and accuracy in the production process.
Specific Responsibilities include:
Ensure compliance to daily inspections, tests, and cleaning requirements as required by the QMS.
Ensure accurate records are collected as required to support QMS activities.
- Conduct root cause analysis for all situations which do not conform to QMS requirements.
- Ensure management review is conducted as required by QMS system policies.
Ensure Corrective Action/Preventative Action (CAPA) activities are performed as required by the QMS.
Ensure personnel are following all cleaning, handling, and containment procedures by properly measuring disinfecting agents and applying products as directed by product usage labels or other documentation as required by the QMS.
Ensure all personnel are following all Hazardous Material (HAZMAT) procedures and policies established by the company.
Ensure all personnel are complying with all rules, procedures, and policies concerning the safe operation of equipment including but not limited to fillers, mixers, sealers, lifts, pumps, compressors, and forklifts.
- Report any safety, quality, or regulatory concerns to management or HR immediately.
- Continually review work process and provide recommendations for improvements to management.
Quality Engineering 1 to 3 years experience working in related field.
Experience in 21 CFR 211 and other relevant FDA regulations.
- Demonstrated abilities capable of following complex instructions to complete job requirements.
Physical Demands: The Quality Engineer will be required to stand 2-4 hours daily and will also be required to lift 50lbs occasionally.
Work Environment: The position will work in office spaces and a high bay warehouse with normal noise and lighting for that environment.
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.
United Laboratories allows ESDS to provide us with priority referrals of protected veterans.
United Laboratories, Inc. is a VEVRAA Federal Contractor.