At ACON labs, we are making a difference in medical care by offering medical devices for diagnosing a variety of conditions. In addition, we are able to streamline and reduce costs for the physician and/or patient directly. Come join us in developing the latest technologies that enhance human life and be a part of our growing, dynamic company.
We are looking for a Process Quality Control Inspector (PQC) onsite at our San Diego location.
The QC Inspector is primarily responsible for performing quality inspections during the production process of products of assigned areas, as well as, reviewing all documentation submitted by the production department and releasing finished or Semi-Finished product or assisting in the release of product.
Some Essential Duties and Responsibilities:
· Perform in-process inspections to ensure that the product is manufactured according to defined specifications.
· Document in-process inspections according to defined inspection and AQL levels.
· Oversee compliance with Good Manufacturing Practices during the production process of ACON products.
· Ensure that all components and raw materials used during the manufacture of products are labeled and properly identified in the manufacturing areas.
· Take sampling randomly according to the applicable procedures, to ensure that all people who are integrated into the manufacturing processes have defined training.
· Verify that the environmental specifications required for the different manufacturing areas are met.
· Ensure the correct start-up of the production lines based on the realization of the line clearances.
· Ensure that all measuring instruments used in the production areas have a valid calibration label.
· Ensure that all equipment used in manufacturing processes have validation in force, as applicable.
· Carefully review each DHR that is submitted by the production department to verify compliance with Good Documentation Practices including corrections, blank spaces, and fields with "N/A".
· Detail review each DHR to ensure that it contains all the production and quality forms required for each process.
· Deliver DHR packets to assigned persons for further review and filing.
· Report and propose solutions to technical errors that arise during the revision of DHR's.
· Release finished product and/or prepare information and data package for quality engineer and/or production quality manager for release of finished product.
Education and /or Experience:
· Associates degree in related field or equivalent combination of education and relevant work experience.
· Minimum 1 year quality assurance experience within a manufacturing or medical environment.
Required Knowledge, Skills and Abilities:
· Must be able to read and understand product requirements. Experience with sampling techniques and safety information preferred.
· Excellent working knowledge of Good Manufacturing Practices Must have strong oral and written communication skills in Spanish.
· Knowledge and proficiency of MS Office.
· Must be well organized, detail-oriented, and able to maintain precise records.
As an ACON Labs team member, you’ll enjoy our competitive benefits and compensation packages as well as working in a supportive team environment. We invite qualified candidates to consider a career with us by submitting your resume.
Job Type: Full-time
Pay: $19.31 - $23.25 per hour
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Employee assistance program
- Flexible spending account
- Health insurance
- Life insurance
- Paid time off
- Vision insurance
Experience level:
Schedule:
Work setting:
- In-person
- Manufacturing facility
Education:
Experience:
- QA within manufacturing or medical environment: 1 year (Required)
- GMP: 1 year (Preferred)
Work Location: In person