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Associate Qa Engineer Jobs in Alachua, FL (NOW HIRING)

Advita Ortho

Quality Assurance Intern

Gainesville, FL · On-site

Gainesville, FL Reporting To: Sr. Manager, Supplier Quality Description The primary scope of this internship is to assist the QA Engineering team with various projects, pushing forward a lean and ...

Exactech

Quality Assurance Intern

Gainesville, FL

The primary scope of this internship is to assist the QA Engineering team with various projects, pushing forward a lean and efficient Quality program. * Provide support for post-market complaint ...

Palco

QUALITY ASSURANCE TESTER II

Gainesville, FL · On-site

Collaborate with developers, product managers, and business analysts to clarify requirements and ... Associate's or Bachelor's degree in an IT-related discipline, or equivalent work experience. * 5+ ...

Sandvik

Quality Assurance Inspector

Alachua, FL · On-site

About Sandvik Sandvik is a global engineering leader with over 41,000 employees worldwide. We're ... Organize, develop and perform QA audits and inspections for all operations. * Use data to improve ...

Exactech

QA PM Specialist

Gainesville, FL · On-site

Education: * Associate's Degree from an accredited institution required; Bachelor's Degree ... Degree in Allied Health, Statistics, Epidemiology, Life Sciences or Biomedical Engineering, highly ...

SMC Region USC

Quality Assurance Inspector

Alachua, FL · On-site

About Sandvik Sandvik is a global engineering leader with over41,000 employeesworldwide.We'reproud ... Organize,developand perform QA audits and inspections for all operations. * Use data to improve ...

Advita Ortho

QA PM Specialist

Gainesville, FL · On-site

$65 - $95/hr

Associate's Degree from an accredited institution required; Bachelor's Degree preferred. Experience ... Degree in Allied Health, Statistics, Epidemiology, Life Sciences or Biomedical Engineering, highly ...

Advita Ortho

Manager, Quality Engineering

Gainesville, FL · On-site

$90 - $120/hr

Overall responsibility for managing Quality Engineering, Specialist support, managing key projects, and QA related aspects of the Quality Program. Apply appropriate resources and ensure project ...

Evergen

Sr. Quality Engineer

Alachua, FL · On-site

$90K - $115K/yr

Supervises the Quality Assurance Engineering team including performance management, corrective action, hiring and selection, and allocation of engineering support as it relates to quality assurance ...

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All JobsAssociate Qa Engineer JobsAssociate Qa Engineer Jobs in Alachua, FL

Associate Qa Engineer information

See Alachua, FL salary details

$15

$29

$43

How much do associate qa engineer jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for associate qa engineer in Alachua, FL is $29.31, according to ZipRecruiter salary data. Most workers in this role earn between $23.37 and $33.75 per hour, depending on experience, location, and employer.

What is an associate QA engineer?

Associate QA Engineers are entry-level professionals responsible for testing software to ensure it meets quality standards before release. They create and execute test cases, report bugs, and work closely with developers to resolve issues. Their role is crucial in identifying problems early in the development process to improve product reliability and user satisfaction. Associate QA Engineers typically use various testing tools and may be involved in both manual and automated testing.

What are the key skills and qualifications needed to thrive as an associate QA engineer?

To thrive as an Associate QA Engineer, you need a strong understanding of software testing principles, attention to detail, and a foundational knowledge of programming or scripting languages, often supported by a degree in computer science or a related field. Familiarity with testing tools such as Selenium, Jira, or TestRail, and knowledge of automated testing frameworks or ISTQB certification are typically required. Effective communication, problem-solving abilities, and a collaborative mindset help you excel in cross-functional teams and adapt to changing project needs. These skills ensure the delivery of high-quality software products by identifying and resolving issues efficiently throughout the development lifecycle.

What are some common challenges faced by associate QA engineers when working with cross-functional teams?

Associate QA Engineers often collaborate with developers, product managers, and designers to ensure software quality. A common challenge is clearly communicating defects or requirements, especially when different teams use technical jargon or have different priorities. Balancing tight project deadlines with thorough testing can also be demanding. Being proactive in asking questions and fostering open communication helps Associate QA Engineers navigate these challenges and contribute effectively to the team's success.

What is the difference between Associate Qa Engineer vs QA Tester?

AspectAssociate Qa EngineerQA Tester
Required CredentialsTypically a bachelor's degree in Computer Science or related field; some certifications like ISTQB are commonHigh school diploma or equivalent; certifications like ISTQB are also common but less frequently required
Work EnvironmentCollaborates with development teams, involved in test planning, automation, and process improvementPrimarily executes test cases, reports bugs, and verifies fixes
Employer & Industry UsageUsed across software development companies, especially in roles involving quality assurance and testingCommon in software companies, often as entry-level testing roles

The Associate Qa Engineer typically has a broader role involving test planning and automation, requiring more technical skills and collaboration. In contrast, a QA Tester mainly focuses on executing tests and reporting issues. Both roles are essential in software quality assurance but differ in scope and responsibilities.

Is associate QA engineer still in demand?

Associate QA engineers are still in demand as companies continue to prioritize software quality assurance, especially with the growth of agile development and automation tools like Selenium and JIRA. Entry-level QA roles often require knowledge of testing methodologies, scripting, and familiarity with testing frameworks, making them valuable for organizations seeking to improve product reliability.

What cities near Alachua, FL are hiring for Associate Qa Engineer jobs?

Cities near Alachua, FL with the most Associate Qa Engineer job openings:

Associate Qa Engineer jobs near you
Infographic showing various Associate Qa Engineer job openings in Alachua, FL as of August 2026, with employment types broken down into 1% As Needed, 65% Full Time, 31% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $60,959 per year, or $29.3 per hour.

Senior Associate, Quality Assurance - Temporary Contract

Kincell Bio, LLC

Gainesville, FL • On-site

Temporary

Posted 9 days ago

Job description

Kincell Bio engineers cells into therapies. With manufacturing facilities located in Research Triangle Park, NC and Gainesville, FL, Kincell Bio is a contract development and manufacturing organization (CDMO) with the mission to streamline CMC development, apply expertise in analytical and process development and GMP manufacturing, testing and release from early clinical to pivotal studies and product launch. Kincell Bio is focused on supporting innovative companies developing immune cell therapies, including autologous and allogeneic CAR-T, TCR, TILs, Tregs and CAR-NK technologies. We offer challenging career opportunities, competitive benefits, and an environment that recognizes and rewards performance.
For more information, please visit our website at www.kincellbio.com.
The Senior Quality Assurance Associate supports the day-to-day early phase cell and gene therapy clinical GMP manufacturing operations via execution of all operational elements of the Quality Management System (QMS), including but not limited to the EDMS (electronic document management system) and training management system in support of gene and cell therapy manufacturing production. They will collaborate cross-functionally with Manufacturing, Supply Chain, Facilities, and the Laboratories to ensure cGMP compliance and establish a quality culture. This is a unique opportunity to help build and grow the Quality Assurance organization in a dynamic new environment. Experience with administrative access using Veeva as a document control and training management system preferred.
Essential Duties and Responsibilities
Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions of this position.This list contains the major duties and requirements of the job and is not all-inclusive. Incumbent(s) may be expected to perform role-related duties other than those contained in this document.
Essential Duties and Responsibilities
  • Assist in executing QA responsibilities to support material and product release.
  • Work with Quality team members to develop, implement, and maintain a phase appropriate Quality Management System (QMS) through the creation, review, and approval of documentation including policies and standard operating procedures (SOPs). Primary focus will be on cGXP operations.
  • Partner with Manufacturing and Quality Control to review/edit documentation such as batch records, methods, validation protocols and reports, and testing data.
  • Support the continuous improvement and oversight of Quality Management System procedures.
  • Assist with company-wide understanding and adopting GMP / GDP practices in alignment with established procedures.
  • Actively participates in fostering a positive, collaborative work culture.
  • Support other QA functions with other projects and tasks, where applicable.
  • Other duties as assigned.

Qualifications
The requirements listed below are representative of the knowledge, skill, and/or ability required to perform this job successfully.
  • BS or equivalent in life science or related field and 5+ years industry experience in manufacturing/testing (GMP) and/or clinical (GCP) Quality Assurance; or equivalent combination of education and experience.
  • Knowledge of FDA regulations and standards, especially those pertaining to cell therapy, gene therapy, bioanalytical testing, and clinical research.
  • Experience authoring, reviewing, and/or approving procedures, policies, work instructions, and any other related controlled documentation needed to support site requirements.
  • Experience authoring, reviewing, and/or approving quality events such as deviations and laboratory investigations/OOS/OOT.
  • Exceptional communication and interpersonal skills including the ability to influence behaviors and negotiate and resolve challenges.
  • Exceptional oral and written communication skills to all organization levels as well as clients and vendors.
  • Strong organizational skills; able to prioritize and manage through complex processes/projects.
  • Ability to be hands-on and detail orientated.
  • Proficient in MS Office application suite as well GMP electronic applications such as QMS / LIMS
  • Veeva document management and vault training manager experience preferred.
  • Effectively manages cross-functional communication.
  • Strong organizational skills; able to prioritize and manage through complex processes/projects.
  • Ability to define problems, collect data, establish facts, and draw valid conclusions.
  • Ability to work independently and stay on task in a fast-paced environment.

Physical Demands
  • Adjusting or moving objects weighing up to 25lbs
  • Must be able to become gown-qualified with participation within an ISO 7 cleanroom environment

Travel Requirements
  • N/A

Location
  • This is a site-based temporary position located in Gainesville, FL, and will require some non-standard working hours, including early morning or late evening.

Schedule
  • Monday through Friday
  • 1st Shift with occasional 2nd shift support as needed
  • Occasional Weekends and Overtime Required

#LI-Onsite
Kincell Bio provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable, federal, state, and local laws. Kincell Bio complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
NOTE TO EMPLOYMENT AGENCIES: Kincell Bio values our relationships with our Recruitment Partners. We will only accept resumes from those partners who have been contracted by a member of our Human Resources team to collaborate with us. We are not responsible for any fees related to resumes that are unsolicited or are received without contract.

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