What are the responsibilities and job description for the Quality Control Engineer position at Meridian?
COMPANY
Meridian Adhesives Group is a rapidly growing, full service global adhesive solutions provider, specializing in adhesive technologies used in electronics, industrial, and infrastructure applications. Fueled by a series of strategic acquisitions since its formation in 2018, we have established ourselves as an adhesive technology leader for a broad, global, blue-chip customer base comprised of OEMs, distributors, and industrial clients with an expanding global footprint.
Guided by our core values—Safety & Sustainability, Respect, Integrity, Accountability, and Teamwork—we are driven to make a meaningful impact in everything we do. When you join Meridian, you become part of a dynamic team that values diverse perspectives, fosters professional growth, and encourages bold ideas. We’re committed to creating a supportive environment where you can thrive, grow, contribute to groundbreaking projects, and help shape the future of our industry.
JOB SUMMARY
The QC Engineer assists our Quality Department and Production Department with process and system improvements and then documents these improvements in the department’s ISO SOP’s. The QC Engineer is responsible for leading and/or conducting customer complaint investigation through root cause analysis and utilizing the CAPA system to ensure strong corrective actions are implemented ensuring we do not have repeat complaints.
DUTIES & RESPONSIBILITIES
- Document and lead or conduct all root cause investigations from either customer complaints or internal non-conformances.
- Generate reports and interface with customers regarding the results of complaints.
- Implement and track CAPA’s.
- Maintain SOP database and update per company’s ISO processes.
- Collaborate with other Engineers and departments to develop, generate, and implement new SOP’s.
- Collaborate with other Engineers and departments to develop and implement process improvements.
- Work with R&D to complete medical QC documentation for new or improved products.
- Be involved with customer audits/visits.
- Performs other related duties as assigned.
SKILLS & ABILITIES
- Excellent verbal and written communication skills.
- Excellent organizational skills and attention to detail.
- Excellent time management skills with a proven ability to meet deadlines.
- Strong analytical and critical thinking skills.
EDUCATION & EXPERIENCE
- Bachelor’s degree in chemistry or engineering.
- Experience with ISO 9001 Quality System preferred.
- Working knowledge of analytical equipment such as DSC, TGA, TMA, DMA, Brookfield viscometers, and UV/VIS/NIR spectrophotometer desirable
- Proficiency in Microsoft Office including Word, Excel, PowerPoint, and Outlook
*No 3rd Party Recruiters
PHYSICAL REQUIREMENTS
- Prolonged periods of sitting at a desk and working on a computer.
- Must be able to lift up to 15 pounds at times.
The company is an Equal Opportunity Employer, drug free workplace, and complies with ADA regulations as applicable.
