Position Summary

Quality Control Technician will ensure the quality and reliability of the processes and products by inspecting the production area, ensuring the finished products are up to the quality that the company expects them to be, making recommendations to management for improvement of systems, processes, and policies, and performing hands-on quality control work. Hours are: Monday through Friday 2:30pm-11:00pm.

Job Type
Full Time
401K, Vision, Dental, PTO

• Conduct testing of raw materials, in process and finish good samples in accordance to local, corporate procedures and cGMP guidelines.

• Follow SOPs, test methods and approved written procedures in the laboratory.

• Collaborate with internal and cross functional colleagues to assure testing and releases are completed on time.

• Manage material flow in conjunction with Planning and Scheduling.

• You will perform inspections by using processes and procedures set in place for determining whether incoming and finished products are of a specified quality and report results to management.

• Investigate and report all non-conformance findings to Management; Trace a quality issue through internal company processes to identify the root cause and possible solutions.

• Act as a technical resource to the Quality Manager.

• Ensure proper documentation of processes, product quality, and test results.

• Recommend and implement methods to minimize the amount of scrap, or leftover material, which is thrown away after a product has been manufactured.

• Maintain, file, and archive all quality and process related documents, both in hard copy and electronic.

• Communicating quality issues and concerns immediately with all relevant personnel to achieve timely and effective results.

• Adhere to testing and project deadlines as assigned by quality lab management.

• Act as back-up to the Quality Control Manager in his/her absence.


• Associate or technical degree or equivalent years of experience in Quality-related disciplines.

• BS degree in Chemistry, Biology or related field preferred.

• Two or more years of experience in a manufacturing and/or Quality Control area

• Must be able to work under minimum supervision.

• Acute attention to detail. • Ability to handle multiple tasks/projects simultaneously.

• Effective organizational, problem solving, prioritizing and follow up skills.

• Working knowledge of FDA 21 CFR part 210 and 211 requirements.

• Excellent interpersonal and communications (both verbal and written) skills.

• Proficiency with MS Word, Excel and PowerPoint.

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