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Quality Analyst I - Evenings (2:30pm - 11:00pm) M-F

LSI Solutions Inc

Victor, NYOnsitePosted 15 days ago$21.00 - $27.00/hour
Full TimeEntry LevelQuality (QA / QC)Medical Device
Original posting ↗

Summary

Quality Control Inspection, Line Audit and Documentation Review preferred

Job description

Essential Functions

Quality Control Inspection, Line Audit and Documentation Review preferred

Level I

  • Process paperwork accurately and neatly.
  • Work in Cleanroom Environment.
  • Maintain consistent quality and workmanship.
  • Conduct detailed records review.
  • Search and locate documents in Grand Avenue Software (GAS).
  • Perform all process steps within 2 product families.
  • Properly transact materials in ERP system.
  • Conduct inspection and in-process audit of material status throughout product realization.
  • Ensure enforcement of good documentation practices within Device History Records.
  • Originate Nonconformance reports.
  • Segregate and control non-conforming product.

Level II

  • Perform Level I functions efficiently and effectively without continuous supervision.
  • Understand and support Cleanroom and Quality System processes.
  • Participate in the creation of metrics reports with Quality Engineers.
  • Maintain databases to support metrics reporting.
  • Participate in developing standard work instructions.
  • Assist in internal audits, as necessary.
  • Suggest process and system continuous improvements.
  • Participate in Continuous Improvement Teams.
  • Support Quality Engineers in project completion.
  • Perform PM activities (i.e. bioburden, environmental monitoring).

Level III

  • Coordinate Nonconformance reports.
  • Assist in supervision of staff and monitoring productivity.
  • Assist in training of new employees and coaching existing employees.
  • Assist team members.
  • Be helpful and encouraging.

Knowledge, Skills & Abilities

Level I: Excellent verbal and written communication skills with various levels of management and coworkers. Demonstrated ability to follow instructions, both written and verbal. Able to communicate effectively with cross-functional teams in a manner that supports internal and external customers alike. Ability to exercise independent judgement as well as work alongside team members. Demonstrated proficiency using Microsoft Office applications including Excel. Working knowledge of ERP systems and other electronic databases. Maintain good and cooperative relationships with colleagues involved in other aspects of the process or operations in order to promote strong teamwork. Attention to detail, technical aptitude, and process-oriented troubleshooting skills necessary.

Level II: Able to create metrics, maintain databases, analyze and recognize trends and inconsistencies. Experience with continuous improvement efforts of systems and processes. Familiarity assisting with quality audits.

Level III: Demonstrated ability to assist in the supervision, training, and coaching of others.

Education & Experience

Associate degree in a technical discipline preferred. High School Diploma or equivalent and 2 years of demonstrated success in a highly regulated manufacturing environment acceptable in lieu of Associate degree. ASQ CQPA or CQA Certification preferred. Familiarity with GMPs, Quality Standards, and Regulatory Compliance is highly desired. Quality Control Inspection, Line Audit and Documentation Review preferred.

Requirements

  • Associate degree in a technical discipline preferred
  • High School Diploma or equivalent and 2 years of demonstrated success in a highly regulated manufacturing environment acceptable in lieu of Associate degree
  • ASQ CQPA or CQA Certification preferred
  • Familiarity with GMPs, Quality Standards, and Regulatory Compliance is highly desired
  • Quality Control Inspection, Line Audit and Documentation Review preferred
  • Excellent verbal and written communication skills
  • Demonstrated ability to follow instructions, both written and verbal
  • Able to communicate effectively with cross-functional teams
  • Ability to exercise independent judgement
  • Demonstrated proficiency using Microsoft Office applications including Excel
  • Working knowledge of ERP systems and other electronic databases
  • Attention to detail, technical aptitude, and process-oriented troubleshooting skills

Benefits

  • Bonus Plan
  • 401(k) Matching
  • Tuition Assistance
  • Employee Assistance Program
  • Product Discounts
  • 15 Paid Holidays
  • Paid Time Off
  • Sick Time
  • Medical, Vision & Dental

Company overview

LSI Solutions Inc, founded in 1986 by Dr. Jude S. Sauer, is a leading medical device company headquartered in Victor, New York, specializing in the development, manufacturing, and marketing of minimally invasive surgical devices. The company operates as a vertically integrated manufacturer, maintaining complete control over its production processes from research and design through in-house manufacturing. LSI Solutions focuses on creating innovative surgical technologies that enable surgeons to perform procedures with enhanced safety, precision, and efficiency across multiple surgical specialties including cardiac, general, bariatric, gynecologic, and urologic surgery. With approximately 500-1,000 employees, the company has established itself as a global leader in surgical innovation, delivering products that improve patient outcomes and recovery times worldwide. Their commitment to precision manufacturing and deep surgical collaboration has positioned them as a trusted partner for surgical teams seeking advanced solutions for minimally invasive procedures.

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