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Quality Associate Jobs in Orlando, FL (NOW HIRING)

K2 is seeking a Quality Control Associate to support our clinics out of either Maitland or Winter Garden , FL . This position is hybrid with support needed one to two days out of the week at the ...

K2 is seeking a Quality Control Associate to support our clinics out of either Maitland or Winter Garden , FL . This position is hybrid with support needed one to two days out of the week at the ...

Life Insurance at no cost to the associate. * Short/Long-Term disability at no cost to the ... Quality Manager Job Type: Full Time Job Location: Orlando, FL Department: Operations

Quality Inspector Company Overview At Mitsubishi Power, we're not just building better clean energy ... Associate's degree from a two-year college or technical school, or a minimum of 3 years of related ...

Quality Inspector Company Overview At Mitsubishi Power, we're not just building better clean energy ... Requirements • Associate's degree from a two-year college or technical school, or one (1) to ...

Lead a team of production associates and partner with the Inspection Center General Manager to repair or reject inventory based on estimated cost of repairs and/or the overall quality of the vehicle.

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Quality Associate information

See Orlando, FL salary details

$10

$25

$47

How much do quality associate jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for quality associate in Orlando, FL is $25.12, according to ZipRecruiter salary data. Most workers in this role earn between $17.02 and $29.38 per hour, depending on experience, location, and employer.

What is a quality associate?

Quality Associates are professionals responsible for ensuring that products or services meet established quality standards before reaching customers. They assist in monitoring production processes, performing inspections, and documenting quality issues or defects. Quality Associates also help implement quality control procedures and work closely with other departments to resolve any quality-related problems. Their role is essential in maintaining compliance with regulatory requirements and ensuring customer satisfaction.

What does a quality associate do?

A quality associate works as part of a team, typically in the manufacturing industry, to inspect and audit a factory to ensure that production follows the necessary protocols and delivers the expected results. In this role, your responsibilities involve all aspects of quality control. You test procedures and make adjustments as required to meet goals and deadlines. As part of your duties, you log your findings and implement a plan for the smooth operation of the line for the long-term. Some people in this career specialize in a particular facet of the manufacturing process.

What are the key skills and qualifications needed to thrive as a quality associate, and why are they important?

To thrive as a Quality Associate, you need attention to detail, knowledge of quality control principles, and often a degree in science, engineering, or a related field. Familiarity with quality management systems (such as ISO 9001), statistical analysis tools, and documentation software is typically required. Strong analytical thinking, communication skills, and problem-solving abilities help you collaborate across teams and address process issues effectively. These skills and qualities ensure that products and processes consistently meet standards, minimizing errors and maintaining compliance.

What are some common challenges quality associates face when working on cross-functional teams?

Quality Associates often collaborate with departments like manufacturing, engineering, and regulatory affairs to ensure product quality standards are met. One common challenge is balancing differing priorities—while production teams may be focused on output and speed, Quality Associates must prioritize compliance and thorough documentation. Navigating these competing interests requires strong communication skills and a proactive approach to problem-solving. Building positive relationships across teams and fostering a culture of quality can help overcome these challenges and ensure successful outcomes.

What is the difference between Quality Associate vs Quality Technician?

AspectQuality AssociateQuality Technician
Required CredentialsHigh school diploma or equivalent; some roles may prefer certifications like ASQ CQPAHigh school diploma; certifications like CQTA are common but not always required
Work EnvironmentOffice settings, manufacturing floors, labsManufacturing plants, labs, production lines
Employer & Industry UsageManufacturing, healthcare, aerospace, automotiveManufacturing, electronics, pharmaceuticals
Common Search & ComparisonOften compared for entry-level quality rolesSimilar roles but more technical focus

While both roles focus on quality assurance, a Quality Associate typically handles documentation, audits, and process improvements, often in office or administrative settings. A Quality Technician usually performs hands-on inspections, testing, and data collection directly on the production floor. Both roles are essential in maintaining product quality but differ in their daily tasks and work environments.

What are the most commonly searched types of Quality jobs in Orlando, FL?

The most popular types of Quality jobs in Orlando, FL are:

What cities near Orlando, FL are hiring for Quality Associate jobs?

Cities near Orlando, FL with the most Quality Associate job openings:

Infographic showing various Quality Associate job openings in Orlando, FL as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $52,294 per year, or $25.1 per hour.

Quality Control Associate

K2 Staffing LLC

Maitland, FL • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 11 days ago


Job description

At K2 Medical Research, we are transforming healthcare by delivering tomorrow’s treatments today. As a rapidly growing clinical research organization across Florida, Tennessee, and Rhode Island, we lead multiphasic trials in therapeutic areas ranging from neurodegenerative to cardiometabolic medicine. Our culture is grounded in clinical excellence and a patient-first mission. We are seeking mission-driven individuals ready to play a meaningful role in bringing life-changing treatments to the patients who need them most.

K2 is seeking a Quality Control Associate to support our clinics out of either Maitland or Winter Garden, FL

This position is hybrid with support needed one to two days out of the week at the designated clinics, and remaining days remote. The Quality Control (QC) Associate monitors and performs routine compliance checks on all source data in alignment with protocol requirements and in compliance with ICH-GCP, FDA Regulations, and K2 Medical Research SOPs.

Primary Responsibilities:

  • Serving as a point of contact for K2 site(s) regarding quality related questions.
  • Working closely with Quality Management to discuss quality concerns and collaborate resolutions for sites
  • Review of source documents to verify subjects meet Inclusion/Exclusion criteria per protocol requirements to verify eligibility prior to randomization.
  • Review of source documents to confirm adherence to organization policies, procedures and best practices.
  • Create queries for the Project Managers to address missing or incomplete source records or to clarify requirements in the source records.
  • Review of Investigator Site Files to ensure complete, accurate and meeting applicable regulatory requirements.
  • Communicates compliance trends and reports significant quality issues to Quality Management in a timely manner.
  • Assists in ensuring the site(s) are maintaining proper training documents required for GCP and SOP compliance and verifying via eReg.
  • Assists in the tracking and reporting of compliance trends and metrics.
  • Provides training to clinical research staff as needed on quality related procedures and best practices, at the discretion of Quality Management.
  • Perform ad-hoc projects or other assigned duties on as needed basis.
  • Able to commute to assigned location(s) a minimum of once per week, or more, at the discretion of Quality Management.
  • Meet monthly performance goals established for the QC Associate role.

Knowledge, Skills, Abilities:

  • Strong judgment, planning, and organizational skills
  • Ability to manage multiple tasks/projects simultaneously
  • Ability to work independently
  • In depth knowledge of applicable laws, regulations, and policies
  • Strong patient care background; familiar with medical terminology
  • Proficient with Microsoft Office
  • Learn and support the mission and goals of K2 Medical Research's program
  • Ability to communicate clearly/effectively (written and oral)
  • Excellent interpersonal and customer services skills

Qualifications:

  • Bachelor’s Degree required; CCRC and/or CCRP preferred.
  • Minimum 5 years of clinical research experience with at least 3 years of patient care experience.
  • Applicants that don't meet 100% of the above qualifications but who have a combination of related education, applicable experience, demonstrated capability, and a genuine passion for success in this position may also be considered.

Your growth and well-being are our priority. Our comprehensive benefits package for full-time employees includes medical, dental, and vision options, supplemental insurance plans, 401(k) with immediate employer match, generous paid time off, and paid holidays. Most notably, we support a healthy work-life balance through a four-day work week, consisting of 10-hour shifts from Monday through Thursday. Fridays are reserved only for critical business needs or administrative tasks; otherwise, they are your chance to kick-start your weekend.

Join the K2 Family: Where Compassion and Connection Lead the Way! At K2 Medical Research, people come first and we're seeking warm, wonderful humans who effortlessly click with everyone, from our incredible patients to brilliant physicians and dedicated research staff.

We are an equal opportunity employer. We celebrate what makes you uniquely you and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital, or veteran statuses.

We value the differences among our team members and are committed to providing reasonable accommodations for qualified individuals with disabilities. If you require a reasonable accommodation to participate in the job application or interview process, please contact Talent@k2med.com. We are here to ensure you have the support and tools you need to shine.