Quality Engineer - Medical Devices

Planet Pharma; North Haven (CT); On-site; USD 60,000 - 85,000; Full time

Job summary

A leading Medical Device company is seeking a Junior Quality Engineer to ensure product quality standards while collaborating with engineering and manufacturing teams. Responsibilities include developing quality protocols, conducting inspections, and performing statistical analyses. The ideal candidate holds a Bachelor's degree in Engineering and has two years of experience in the Medical Device industry. This role offers the opportunity to contribute to product quality and reliability within a growing team.

Qualifications

• Bachelor's Degree within an Engineering realm.
• 2 years of experience within Medical Device.

Responsibilities

• Develops and maintains quality standards for finished products.
• Collaborates with engineering and manufacturing to ensure quality.
• Implements inspection and testing methods for products.
• Conducts quality assurance tests and performs statistical analysis.
• Ensures corrective measures meet reliability standards.
• Specializes in areas such as incoming material, production quality, or product evaluation as needed.

Skills

Technical Writing

Data Analysis

Project Management

Education

Bachelor's Degree in Engineering

Job description

Our client, a leading Medical Device company, is seeking an experienced Junior Quality Engineer to join its growing team. See below for other details!

Top 3 technical skills that required for the role:

• Technical Writing
• Data Analysis
• Project Management

Responsibilities:

• Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product.
• Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
• Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
• Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests.
• Performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
• Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
• May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.

Requirements:

Bachelor's Degree within an Engineering realm and 2 years of experience within Medical Device