Quality Supervisor: QC Lead & Compliance Champion

Nissha Medical Technologies; Buffalo (NY); On-site; USD 65,000 - 75,000; Full time

Benefits offered by this job

Medical, dental, and vision coverage

401(k) with company match

Paid time off

Life and disability insurance

Professional development opportunities

Job summary

Nissha Medical Technologies is seeking a Quality Supervisor to lead the Quality Control inspectors and maintain the Quality Management System in Buffalo, NY. The role focuses on ensuring compliance with FDA 21 CFR and ISO 13485, with oversight of CAPAs, audits, and document control.

The ideal candidate will have a Bachelor’s degree, prior quality experience, and supervisory skills. Strong PC abilities and effective communication are essential for success in this role.

Qualifications

• Bachelor’s Degree required.
• Strong PC skills required.
• Experience with FDA 21 CFR and ISO 13485 highly preferred.
• Previous quality experience.
• Supervisory experience preferred.

Responsibilities

• Oversee documentation related to CAPAs, non-conformances, complaints, and internal audits.
• Participate in development of new and sustaining business.
• Review and create standard operating procedures and work instructions as necessary.
• Ensure product specifications and customer requirements are met and compliant.
• Develop and execute departmental training related to quality processes.
• Track, trends, and analyze departmental and organizational metrics.
• Recommend and configure new procedures as necessary.
• Manage assigned projects.
• Provide daily oversight of Quality Control staff.
• Administer performance reviews and payroll for QC staff.

Skills

Bachelor’s Degree

Strong PC skills

FDA 21 CFR & ISO 13485 experience

Quality experience

Supervisory experience

Education

Bachelor’s Degree

Job description

Nissha Medical Technologies is seeking a Quality Supervisor to lead the Quality Control inspectors and maintain the Quality Management System in Buffalo, NY. The role focuses on ensuring compliance with FDA 21 CFR and ISO 13485, with oversight of CAPAs, audits, and document control.

The ideal candidate will have a Bachelor’s degree, prior quality experience, and supervisory skills. Strong PC abilities and effective communication are essential for success in this role.