Quality Engineer I

Lancesoft; Parsippany-Troy Hills (NJ); On-site; USD 55,000 - 75,000; Full time

Job summary

Lancesoft in Parsippany, NJ is seeking a Quality Engineer I to support product conformity through audits, inspections, and testing. This entry-level role collaborates with multiple teams and suppliers to uphold Client quality goals.

You will help formulate procedures, develop corrective actions, and analyze data from gauges and tests. Candidates should have a B.S. in engineering and may hold CQE certification; medical device experience is a plus. Travel up to 20% may be required.

Qualifications

• B.S. in engineering or equivalent with CQE certification.
• CQE certification and medical device industry experience preferred.
• Familiar with QSR/ISO regulations and quality tooling.

Responsibilities

• Formulates procedures, specifications, and standards for products and processes.
• Develops and implements corrective/preventative action plans.
• Collects and analyzes data for gauge and product evaluation.
• Identifies personnel, gauges, procedures and materials for new products.
• Ensures suppliers have information and facilities to deliver quality products.

Skills

Teamwork

Communication

Deadline-driven

Quality mindset

Education

B.S. in Engineering

CQE certification

Tools

MS Office Suite

Blueprint reading

Geometric Dimensioning & Tolerancing

QSR/ISO regulations

FMEA

Optical comparators

CMMs

Job description

Title: Quality Engineer I

Location: Parsippany, NJ 07054

Duration: 12 Months

Job Summary

The Quality Engineer I is an entry level position responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers, and experts outside Client to implement Client Quality goals.

Principal Duties and Responsibilities

• Formulates procedures, specifications, and standards for Client products and processes.
• Develops and implements corrective/preventative action plans.
• Collects and analyzes data for gauge and product evaluation.
• Identifies critical personnel, gauges, procedures, and materials needed for the completion of new products.
• Ensures that suppliers have necessary information and facilities to deliver quality products to Client.
• This is not an exhaustive list of duties or functions and might not necessarily comprise all of the essential functions for purposes of the Americans with Disabilities Act.

Expected Areas of Competence (i.E., knowledge, skills and abilities)

• Ability to work within a team environment and build relationships outside of the department as well as outside the company (suppliers, regulatory agencies, etc.).
• Ability to deliver, meet deadlines and have results orientation.
• Able to communicate both orally and in written form to multiple levels of the company.
• Demonstrates characteristics of high potential for future development opportunities.
• Microsoft Office Suite
• Basic knowledge of blueprint reading and geometric dimensioning and tolerancing, basic understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methods, and are able to use optical comparators and CMMs.

Education/Experience Requirements

• B.S. In engineering or an alternative Bachelor s degree program with certification as a quality engineer (e.G. CQE).
• Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred.

Travel Requirements

• Up to 20%