Quality Control Lead - 2nd Shift
Description
The Quality Control (QC) Lead is a highly skilled individual that contributes to the development of concepts and techniques. Completes complex tasks in creative and effective ways. Consistently works on complex assignments requiring independent action and a high degree of initiative to resolve issues. Makes recommendations for new procedures.
QC Lead helps assign QC tasks among incoming, in-process, and finished product inspection; product validation testing and Administrative Return Merchandise Authorization (RMA-A) to ensure all business needs and department goals are fulfilled. The lead has an active role in training and developing QC personnel.
Responsibilities
- Coordinate with local leadership as well as leadership of Production, Warehouse, and
- Engineering to perform raw material, in-process, and finished products, returned products, and other quality related inspections.
- Review receiving inspection records, develop and support procedures via support redline initiation.
- Utilize Visual Inspection Systems and other inspection tools (tensile strength machines/calipers/pin gauges/etc.) per inspection requirements.
- Coordinate and delegate daily priorities to ensure accurate and timely completion.
- Maintain accurate records for compliance with regulations.
- Review documentation for accuracy, completion, legibility in alignment with Good Documentation Practices (GDP).
- Ensure adherence to regulations and internal quality procedures.
- Assist in department inventory control activities and organizational initiatives.
- Assist in the evaluation and setting up of new inspection equipment.
- Train new employees in inspections and procedures.
- Provide guidance and continuous support to QC Inspectors.
- Review out-of-specification results with engineering and initiates NCRs as required.
- Review Lot specifications for QC Digital Data Sheets.
- Assist with Receiving Inspection Records per Management direction.
- Process non-conforming materials/products according to NCR disposition.
- Provide cross-functional support to peripheral projects and assignments as needed.
- Ensure necessary supplies, instruments, and equipment are available.
- Perform other activities as required.
Qualifications
- High school diploma or equivalent preferred.
- Minimum 5 years of QA/QC experience with medical device manufacturer.
- Prior experience in regulated environment (e.g. FDA QSR, ISO 13485, etc.)
- Good attention to detail.
- Able to work independently with minimal supervision.
- Able to prioritize and efficiently complete tasks with consistency and accuracy.
- Able to lead, provide clear direction, delegate tasks, and train team members.
- Able to interpret blueprints.
- Computer skills including Word, Excel, and Internet experience.
Preferred
- Cleanroom experience preferred.
Inari Medical offers competitive health and wealth benefits for our employees. The base pay range for this position is $29.00- $36.00. A range of factors, including location, skills, and experience, will be considered. Actual compensation may vary.
Schedule 3:30 - 12:00 PM
Inari Medical, Inc. advises applicants that employment is subject to completion of a successful background check.