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Quality Control Engineer Intern Jobs in Connecticut

Quality Control Engineer

Monroe, CT · On-site

$75K - $85K/yr

Quality Control Engineer Location: Monroe, CT Position Type: Full-Time Company Overview: Biomerics provides contract manufacturing, laser processing, and finishing services to a wide range of ...

Quality Control Engineer Location: Monroe, CT Position Type: Full-Time Company Overview: Biomerics provides contract manufacturing, laser processing, and finishing services to a wide range of ...

Quality Control Engineer | $85K-$90K + Benefits Join a fast-paced manufacturing team in Milford, CT where you'll own product quality from start to finish and drive continuous improvement. What You'll ...

Quality Control Engineer | $85K-$90K + Benefits Join a fast-paced manufacturing team in Milford, CT where you'll own product quality from start to finish and drive continuous improvement. What You'll ...

Quality Control Engineer | $85K-$90K + Benefits Join a fast-paced manufacturing team in Milford, CT where you'll own product quality from start to finish and drive continuous improvement. What You'll ...

The Quality Engineer develops, assures, and maintains the quality of products and processes ... * 2+ years QA/QC experience including implementing and managing Quality Management Systems

QC Manager

Norwalk, CT

$100K - $130K/yr

Bachelor's degree in Engineering, Construction Management, or related field (or equivalent experience) * 2+ years of experience in a Quality Control role within construction * Strong understanding of ...

QC Inspector

Bridgeport, CT · On-site

$17 - $22/hr

Pay Rate Low: 20 | Pay Rate High: 25 QC Inspector Contract - Bridgeport, CT Pay: $17-22/hour ... Experience interpreting engineering drawings and specifications * Proficiency with inspection tools ...

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Quality Control Engineer Intern information

What types of projects and responsibilities can a Quality Control Engineer Intern expect to handle during their internship?

As a Quality Control Engineer Intern, you can expect to work on a variety of projects such as assisting with product inspections, conducting tests to ensure compliance with quality standards, and compiling reports on findings. Typically, interns support senior engineers by collecting and analyzing data, participating in root cause analysis of defects, and helping to implement corrective actions. You’ll often collaborate with production, engineering, and quality assurance teams, gaining exposure to different stages of the manufacturing process. This hands-on experience provides a solid foundation for understanding industry best practices and can lead to further opportunities within quality assurance or related fields.

What are the key skills and qualifications needed to thrive as a Quality Control Engineer Intern, and why are they important?

To thrive as a Quality Control Engineer Intern, you need foundational knowledge in engineering principles, attention to detail, and an understanding of quality assurance processes, typically supported by coursework in mechanical or industrial engineering. Familiarity with statistical analysis software, quality management systems (QMS), and tools like Six Sigma or ISO standards is often required. Strong problem-solving skills, teamwork, and effective communication help interns excel in collaborative and fast-paced environments. These skills ensure accurate product assessments, efficient issue resolution, and contribute to maintaining high-quality standards within the organization.

What does a Quality Control Engineer Intern do?

A Quality Control Engineer Intern assists in ensuring that products or services meet established quality standards and specifications. They typically help with inspecting materials, conducting tests, analyzing data, and documenting results. Interns may also participate in process improvements, help identify defects, and support the implementation of corrective actions. This role offers hands-on experience in quality assurance and helps interns develop skills in problem-solving, teamwork, and analytical thinking.
What are popular job titles related to Quality Control Engineer Intern jobs in Connecticut? For Quality Control Engineer Intern jobs in Connecticut, the most frequently searched job titles are:
What job categories do people searching Quality Control Engineer Intern jobs in Connecticut look for? The top searched job categories for Quality Control Engineer Intern jobs in Connecticut are:
Quality Control Engineer

Quality Control Engineer

Biomerics

Monroe, CT • On-site

$75K - $85K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 16 days ago


Biomerics rating

5.8

Company rating: 5.8 out of 10

Based on 20 frontline employees who took The Breakroom Quiz


Job description

Job Type
Full-time
Description
Job Title: Quality Control Engineer
Location: Monroe, CT
Position Type: Full-Time
Company Overview:
Biomerics provides contract manufacturing, laser processing, and finishing services to a wide range of industries with a strong commitment to customer service. Biomerics specializes in the most challenging machined and micromachined components, including those used in interventional and medical robotics applications. We pride ourselves in providing a supportive, positive work environment with opportunities for challenge and growth.
Biomerics offers Swiss machining with integrated laser cutting on precision medical tubing. Laser/Swiss machining enables features to be machined and laser cut in the same process. Our core competency lies in smaller medical components, produced with high accuracy and repeatability. Traditional Swiss screw machining capability is also available for rapid prototyping and production.
In addition, Biomerics utilizes 5 axis milling machines capable of producing complex finished components, while holding extremely tight tolerances.
Job Description:
The Quality Control Engineer is responsible for providing Quality Engineering input to support Medical Device Manufacturing, Manufacturing Engineering, Operations, and Distribution activities. The QE will develop, establish and maintain quality engineering methodologies, systems, and practices that meet Biomerics, customer, and regulatory requirements. You will serve as a Quality representative to improve awareness, visibility, communication on quality initiatives to support departmental, functional, site, divisional, and corporate quality goals and priorities. As the Quality Engineer, you will lead Quality Assurance (QA) in support of manufacturing activities in accordance with the requirements of USFDA CFR 820 and ISO 13485.
Responsibilities:
  • Perform Quality Assurance and Quality Control in support of manufacturing activities in accordance with the requirements of USFDA CFR 820 and ISO 13485.
  • Reduces and controls manufacturing process defects (scrap, nonconforming material, customer complaints) leading or participating in efforts and cross-functional teams focused on identifying the primary root causes and implementing corrective and preventative actions
  • Collects and analyzes process defect data for product/process improvement efforts (e.g. scrap, nonconforming product, customer complaints) by systematically gathering quality metric data and performing the appropriate analysis method(s)
  • Owns and drives Nonconforming Event and Correction and Preventive Action investigations
  • Supports continuous improvement activities, NCMRs, CAPA, and Lean initiatives
  • Perform validation activities as established by USFDA CRF 820, ISO 13485, and other regulatory bodies as required.
  • Support engineering efforts by developing, implementing, and maintaining quality requirements and standards throughout the transfer and manufacturing of products.
  • Responsible for creating control plans and risk analyses (PFMEAs)

Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues
Requirements
Requirements
  • Bachelor's Degree in Engineering, Biomedical Engineering, or related science discipline
  • Minimum of 3 years' experience in Quality Engineering within a Medical Device Manufacturing environment for a company in a regulated industry (IVD, pharmaceuticals, medical device, biologics, etc.)
  • ASQ CQE certification is a plus
  • Six Sigma Certified Green or Black Belt is a plus
  • Working knowledge of FDA QSR (21 CFR Part 820), ISO 13485, MDD/AIMDD, CMDR; Ability to understand other medical device regulations and standards
  • Experience in nonconforming material and CAPA methodologies/systems preferred
  • Strong communication, presentation, facilitation, and project management skills
  • Experience working in cross-functional teams and driving projects to completion
  • Familiar with Microsoft Office Suite, and Minitab Statistical Analysis software (or equivalent)
  • High sense of urgency and commitment to execution
  • Applies continuous improvement principles in the development of the quality system
  • Driven, energetic, self-assured professional with high personal integrity
  • Knowledge of analytical techniques and statistical analysis
  • Ability to develop effective, positive interpersonal relationship

"Equal Opportunity Employer: Minority, Female, Protected Veteran, Individual with Disabilities are encouraged to apply."
Benefits: Medical/Dental/Vision Insurance, Short-Term Disability, Long-Term Disability, Life Insurance, Paid Vacation Days, Paid Holidays, 401k
Please, No Recruitment Agency calls or emails (we are not using recruitment services for this, or any other role posted).
Biomerics does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on Biomerics approved agency list. Unsolicited resumes or candidate information submitted to Biomerics by search/recruiting agencies not already on Biomerics approved agency list shall become the property of Biomerics and if Biomerics subsequently hire the candidate, Biomerics shall not owe any fee to the submitting agency.
The salary estimates are estimates from this job board and not a guarantee from Biomerics salary range.
Salary Description
$75k - $85k

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