Evenings Quality Analyst I - Medical Devices

LSI Solutions; New York (NY); On-site; USD 29,000 - 37,000; Full time

Benefits offered by this job

Bonus Plan

401(k) match

Tuition Assistance

Employee Assistance Program (EAP)

Product Discounts

15 Paid Holidays

PTO and Sick Time

Medical, Vision, Dental

Job summary

LSI SOLUTIONS® in Victor, NY seeks a Quality Analyst I for evening shifts (2:30 pm–11:00 pm, M-F). The role involves quality control inspections, line audits, and documentation reviews in a GMP environment.

Onsite work in a growing medical device company with opportunities to advance through Levels I-III and participate in continuous improvement initiatives. Requirements include an associate degree in a technical field or HS diploma with manufacturing experience; familiarity with GMPs and ERP

Qualifications

• Associate degree in a technical discipline preferred.
• HS Diploma or equivalent with 2 years of regulated manufacturing experience acceptable in lieu of Associate.
• ASQ CQPA or CQACertification preferred.
• Familiarity with GMPs, Quality Standards, and Regulatory Compliance is highly desired.
• Quality Control Inspection, Line Audit and Documentation Review preferred.

Responsibilities

• Coordinate Level I, II, and III quality control tasks.
• Perform quality inspections and line audits; document review.
• Maintain records and ensure good documentation practices in Device History Records.
• Originate Nonconformance reports and segregate non-conforming product.
• Support continuous improvement initiatives and metrics reporting.
• Participate in internal audits and training of new staff.

Skills

Verbal communication

Written communication

Excel proficiency

ERP systems familiarity

Education

Associate degree in technical discipline

HS diploma with 2 years regulated manufacturing experience

ASQ CQPA or CQACertification

Tools

Grand Avenue Software (GAS)

ERP system

Microsoft Office

Job description

LSI SOLUTIONS® in Victor, NY seeks a Quality Analyst I for evening shifts (2:30 pm–11:00 pm, M-F). The role involves quality control inspections, line audits, and documentation reviews in a GMP environment.

Onsite work in a growing medical device company with opportunities to advance through Levels I-III and participate in continuous improvement initiatives. Requirements include an associate degree in a technical field or HS diploma with manufacturing experience; familiarity with GMPs and ERP