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Entry Level Quality Process Engineer Jobs in Florida

Sibex, Inc.

Quality Control Technician 1

Crystal River, FL · On-site

$16 - $19/hr

We are seeking a detail‑oriented and motivated Entry-Level Quality Control Technician to join our ... Collaborate with production, engineering, and QA teams to communicate defects and process issues.

Sibex, Inc.

Quality Control Technician 1

Crystal River, FL · On-site

$16 - $19/hr

We are seeking a detail‑oriented and motivated Entry-Level Quality Control Technician to join our ... Collaborate with production, engineering, and QA teams to communicate defects and process issues.

Leonardo DRS

Quality Engineer II - Optics

Melbourne, FL

$66K - $86K/yr

Consider financial impacts of quality process controls and inspections * Support, communicate ... Prepare quality engineering reports and recommendations * Monitor and mentor junior quality ...

Leonardo DRS

Quality Engineer II - Optics

Melbourne, FL · On-site

$66K - $86K/yr

Consider financial impacts of quality process controls and inspections * Support, communicate ... Prepare quality engineering reports and recommendations * Monitor and mentor junior quality ...

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Entry Level Quality Process Engineer information

What types of projects and responsibilities can an Entry Level Quality Process Engineer expect in their first year?

As an Entry Level Quality Process Engineer, you can expect to be involved in projects focused on process improvement, data analysis, and root cause investigations related to product quality. Typical responsibilities include collaborating with production and engineering teams to identify inefficiencies, assisting with quality audits, creating documentation for standard operating procedures, and using statistical tools to monitor process performance. You'll often work under the guidance of senior engineers and quality managers, gaining exposure to cross-functional teamwork and a variety of manufacturing or operational environments. These experiences provide a strong foundation for advancing into more specialized quality or process engineering roles.

What is the difference between Entry Level Quality Process Engineer vs Quality Assurance Technician?

AspectEntry Level Quality Process EngineerQuality Assurance Technician
Required CredentialsBachelor's in Engineering, Quality Management, or related field; certifications like ASQ CQE beneficialHigh school diploma or associate degree; certifications like ASQ CQTA optional
Work EnvironmentManufacturing plants, production lines, quality departmentsLaboratories, production areas, inspection stations
Employer & Industry UsageManufacturing, automotive, aerospace, consumer goodsFood, pharmaceuticals, electronics, manufacturing

While both roles focus on quality, the Entry Level Quality Process Engineer typically involves developing and improving processes, requiring engineering knowledge and analytical skills. The Quality Assurance Technician mainly conducts inspections and tests to ensure product quality. The engineer often works on process optimization, whereas the technician performs routine quality checks.

What does an Entry Level Quality Process Engineer do?

An Entry Level Quality Process Engineer is responsible for assisting in the development, implementation, and maintenance of quality control processes within a manufacturing or production environment. They work closely with senior engineers to analyze production methods, identify areas for improvement, and ensure products meet company and industry quality standards. Typical tasks include collecting data, performing inspections, supporting root cause analysis, and helping to implement corrective actions. This role is ideal for recent graduates with an engineering background who want to start their career in quality assurance and process improvement.

What are the key skills and qualifications needed to thrive as an Entry Level Quality Process Engineer, and why are they important?

To thrive as an Entry Level Quality Process Engineer, you need a solid background in engineering principles, data analysis, and process improvement, typically supported by a bachelor's degree in engineering or a related field. Familiarity with quality management systems (such as ISO 9001), statistical process control tools, and software like Minitab or Excel is commonly required. Strong attention to detail, problem-solving abilities, and effective teamwork help you excel in identifying and addressing quality issues. These skills ensure efficient process optimization, product consistency, and compliance with industry standards, which are essential for organizational success.
What are the most commonly searched types of Quality Process Engineer jobs in Florida? The most popular types of Quality Process Engineer jobs in Florida are:
What cities in Florida are hiring for Entry Level Quality Process Engineer jobs? Cities in Florida with the most Entry Level Quality Process Engineer job openings:
Entry Level Quality Process Engineer jobs near you
Infographic showing various Entry Level Quality Process Engineer job openings in Florida as of May 2026, with employment types broken down into 79% Full Time, and 21% Contract. Highlights an 95% In-person, and 5% Remote job distribution.
Quality Assurance Associate (Pompano Beach, FL)

Quality Assurance Associate (Pompano Beach, FL)

Cedent

Pompano Beach, FL • On-site

Full-time

Posted yesterday

Job description

Client is seeking an entry-level Quality Assurance / Quality Control Associate to support clinical manufacturing and drug development activities in a GMP-regulated environment. This is a great opportunity for individuals looking to begin their careers in biotech, particularly in quality and regulatory compliance.
Key Responsibilities:
  • Receive and qualify incoming materials and reagents according to GMP requirements
  • Review batch records, laboratory notebooks, and QC testing results for completeness and compliance
  • Assist in deviation investigations and document change control processes
  • Support the organization and maintenance of the electronic document control system
  • Ensure compliance with internal SOPs and applicable cGMP regulations
  • Participate in internal audits and prepare documentation for regulatory inspections
  • Assist with data verification and archiving of quality-related records
  • Contribute to creation and revisions of SOPs, forms, and controlled documents
Qualifications:
  • Associate's or Bachelor's degree in Biomedical Sciences, Life Sciences, or a related field
  • Candidates with degrees in Data Management, Health Information Technology, Technical Writing, Supply Chain Management, or Communications who are looking to enter the biotech industry are also encouraged to apply
  • Strong attention to detail and organizational skills
  • Effective written and verbal communication skills
  • Ability to review and interpret technical documents and records
  • Self-motivated with the ability to work independently and as part of a team
  • Comfortable using digital tools and electronic documentation systems
  • Willingness to work in a GMP-regulated laboratory environment
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About Cedent

Sourced by ZipRecruiter

CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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