Quality Control Engineer

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Location: Charleston, South Carolina, US

SHL Medical is a world‑leading provider in the design, development, and manufacturing of advanced self‑injection devices. With 6,000 employees worldwide, we partner with leading pharmaceutical and biotech companies to deliver innovative autoinjectors, pen injectors, and other drug delivery systems that ensure effective treatment for patients. Headquartered in Switzerland since 2018, we also operate key sites in Sweden, Taiwan, and the US.

We are committed to innovation, impact, and growth, and we empower our people to develop solutions that make a meaningful difference in patients’ lives while fostering a supportive, inclusive, and dynamic workplace.

This role is embedded in the Manufacturing Engineering group within our Global Operations Engineering team at our new state‑of‑the‑art device manufacturing facility in North Charleston, South Carolina. Together with the rest of the team, you will drive and support manufacturing automation, with a particular focus on our automated assembly equipment used for final production.

• Develop documentation (work instruction, training material, etc.) for the QC Lab
• Train QC Inspectors to new test methods / equipment
• Serve as liaison and receive test method / system updates from Metrology, Testing, and transfer team
• Review planned equipment for QC lab, ensure it meets local SHL expectations, and will work in the QC Lab
• Attend planning meetings for New Products to understand New Measuring Methods and plans for QC Testing
• Coordinate local support (calibration / preventive maintenance) for new QC Lab equipment
• Act as point of contact for QC Lab for any upcoming changes or needs
• Identify problem statements and build relationships with external SHL support teams for issues related to internal systems (SAP, EiQMI, and MES)
• Manage all QC equipment and tool/fixtures to ensure QC Lab testing for production and validation activities
• Perform other related duties as assigned

• Bachelor’s degree in Engineering or Life Science discipline
• 2+ years of experience in the medical device, pharmaceutical or biotechnology industry
• Clear / logical thinking with strong organization and communication skills
• Ability to prioritize and thrive in a cross‑functional, inter‑company and international environment
• Team player and self‑starter, able to perform with low supervision
• A solution‑oriented growth mindset coupled with decision‑making skills
• Experience writing work instructions, training material, and validation documentation

• Knowledge of regulatory compliance: GMP (good manufacturing practice), QSR (quality system regulations), and ISO 13485
• SAP (Enterprise Resource Planning quality module) will be an advantage

• 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

Please note that SHL is a drug‑free employer. This offer of employment is contingent upon your successful completion of various pre‑employment screenings, including, but not limited to, a drug test, employment verification, reference checks, and a criminal background check.

For more information on SHL Medical, please visit: shl‑

Associate

Full‑time

Quality Assurance

Medical Device