IC Biomedical, LLC manufactures cryogenic storage and transport equipment for life sciences, healthcare, and animal husbandry markets.

Job Summary

Quality Assurance Specialists are responsible for monitoring, inspecting, and proposing measures to correct or improve a company's final products and processes to meet established quality standards. Also is responsible for quality assurance audits and ensures the product integrity and standards are being met. The QA specialist will know how to troubleshoot systems to ensure reliability, usability, and performance. The specialist will monitor the quality of a company's product and create testing parameters for products and services, develop quality control procedures, perform audits, and oversee quality control teams.

Essential Duties & Responsibilities to Include:

The Quality Assurance Specialist's responsibilities include developing and implementing quality assurance policies, conducting tests and inspections, identifying production, process, or product issues, and presenting solutions. To be successful as a Quality Assurance Specialist you should be incredibly thorough and able to help our company maintain the highest quality standards.

Duties include, but are not limited to:

• Preparing and implementing quality assurance policies and procedures.
• Performing routine inspections and quality tests.
• Identifying and resolving workflow and production issues.
• Ensuring that standards and safety regulations are observed.
• Addressing and discussing issues and proposed solutions with superiors.
• Documenting quality assurance activities and creating audit reports.
• Making recommendations for improvement.
• Creating training materials and procedures.
• Support to issue and solve internal corrective action report.
• Ensure current product quality specification fulfill client’s requirements.
• Support quality management systems operation within organization.
• Provide support for design, execution, and maintenance of quality system processes at respective departments.
• Help departments to coordinate training to operating procedure changes or new system implementation.
• Develop and conduct a variety of tests on inbound materials from vendors and outbound products for shipping.

Education

High School diploma / GED

Qualifications

• Minimum of 3 plus years of previous experience in quality assurance.
• Solid knowledge of relevant regulatory standards, (ISO 13485 - 2016)
• Good communication skills, both written and verbal
• Excellent data collection and analysis skills.
• Strong attention to detail
• Proficient in computer technology and systems.
• Certification by the American society for Quality (ASQ) a plus

IC Biomedical is an equal employment opportunity employer.

Job Type: Full-time

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Vision insurance

Experience level:

• 3 years

Schedule:

• 8 hour shift
• Day shift

Work setting:

• In-person
• Manufacturing facility

Experience:

• Manufacturing: 2 years (Preferred)

Shift availability:

• Day Shift (Preferred)

Ability to Commute:

• Cartersville, GA 30121 (Required)

Work Location: In person