What are the responsibilities and job description for the QC Inspector (Nights) position at SHL Medical?
Quality Control Inspector (Nights)
Location: North Charleston, SC
Reporting Into: Quality Control Manager
SHL Medical is the world-leading solution provider in the design, development, and manufacturing of advanced drug delivery systems with more than 5000 employees worldwide. Our customers include top pharmaceutical and biotech companies from around the globe that require innovative devices such as auto-injectors or pen injectors to effectively deliver their drugs. Headquartered in Switzerland since late 2018, with sites in Sweden, Taiwan, and the United States.
Job Overview
The primary duty of the Quality Control Inspector is to provide support to commercial manufacturing lines ensuring delivery of the highest quality product to the customer while supporting continuous improvement projects and quality initiatives. This is a dynamic support role requiring cross-functional collaboration with production, manufacturing, and quality team members. This role includes responsibility for providing day-to-day quality support for manufacturing, including the processing of non-conforming product (identification, documentation, segregation evaluation and disposition) and responding to quality signals.
Main Responsibilities
- Perform routine Incoming Quality Control (IQC), In -Process Quality Control (IPQC), and Final Quality Control (FQC) testing / inspection and recording of test results.
- Update databases and spreadsheets used to track, monitor, and report department activities.
- Use the inventory and traceability management systems to transact material.
- Review and update of QA Documentation.
- Compliance to all QC and relevant plant wide procedures and practices.
- Collect and compile statistical quality data.
- Provide excellent service to all internal and external customers of the QC Laboratory / QC department.
- Communicate concerns about work process regarding environmental impact, health, or safety issues to their supervisor.
- Excellent attention to detail.
Skills and Qualifications
- Associate degree in technical discipline (or equivalent)
- 2 years of quality or manufacturing experience in the medical device industry
- Good interpersonal skills and organizational skills
- Able to read, understand, and communicate procedural requirements
- Highly Proficiency with Microsoft desktop environment: Windows and Office 365
- Familiarity with product/component inspection and testing and Manufacturing Execution System (MES)
- Fluent in English language, written and spoken
We Offer
- Competitive compensation package
- Modern working environment with state-of-the-art facilities and technologies
- Challenging assignments in a fast-growing and innovative industry
- Position in a dynamic, international team of highly skilled professionals
- Various opportunities for personal and professional development within a global organization
