Quality Control Inspector
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Apply Now Application ends in 22d 12h 33min
Job Detail
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Offered Salary 0
Job Description
Changing lives. Building Careers.
Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.
The Quality Inspector is responsible for product and material inspections, verifications, and checks. The Quality Inspector shall ensure documentation is complete and accurate, release material physically and electronically, and maintain quarantine areas.
Responsibilities:
- Performs all incoming inspections and testing of materials and components, for in-process functional testing and verifications, and for quality control of instruments as applicable
- Performs QC testing/ inspections/verifications on manufacturing supplies, in-process materials, and finished products as necessary
- Performs label inspection and verification, as applicable
- Enters inspection results into appropriate software database
- Reviews incoming inspection records on components to ensure compliance to product specifications
- Maintains strict control of quarantine areas in an organized manner
- Participates in RMA (Return Material Authorization) inspection activities, as applicable
- Coordinates supply orders for inspection activities with QC Management
- Report non-conforming product to QC Management
- Works in a Team environment to coordinate job duties
- Performs environmental monitoring in controlled areas
- Performs weekly water sampling
- Performs product discard and destruction activities, as needed
- Maintains product retains, as applicable
- Perform other related duties as assigned and delegated by Quality Control Management
The employee must be able to work in a cleanroom environment.
Qualifications:
- High School Diploma or equivalent
- Experience in medical devices, pharmaceuticals, or other regulated industry preferred.
- Ability to assess results against acceptance criteria.
- Ability to follow instructions precisely, recognize deviations, and recommend corrective action.
- Working knowledge of current Good Manufacturing Practices.
- Familiarity with application of FDA and ISO quality standards in a government regulated industry.
- Proficient computer skills, including experience with database applications and Microsoft Office.
- Working knowledge of standard laboratory practices and safety.
- Detail-oriented.
- Excellent organizational and time management skills.
Apply Now
Application ends in 22d 12h 33min