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Senior Qa Associate Jobs in Florida (NOW HIRING)

Sr QA Engineer

Orlando, FL · On-site

$111K - $150K/yr

Job Posting Title: Sr QA Engineer Req ID: 10155838 "We Power the Magic!" That's our motto at Disney Experiences (DX). Our team creates world-class immersive digital experiences for the Company ...

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Senior Qa Associate information

See Florida salary details

$21.7K

$55.4K

$99.4K

How much do senior qa associate jobs pay per year?

As of Aug 12, 2026, the average yearly pay for senior qa associate in Florida is $55,448.00, according to ZipRecruiter salary data. Most workers in this role earn between $33,300.00 and $71,000.00 per year, depending on experience, location, and employer.

What does a Senior QA Associate do?

A Senior QA (Quality Assurance) Associate is responsible for overseeing and executing quality control processes to ensure that products or services meet established standards and regulatory requirements. They design and implement test plans, conduct inspections, analyze data, and collaborate with cross-functional teams to identify and resolve quality issues. Additionally, Senior QA Associates often mentor junior team members and help improve overall quality systems and procedures within an organization.

What are some typical challenges faced by Senior QA Associates when managing multiple testing projects simultaneously?

Senior QA Associates often juggle several testing projects at once, which requires excellent organizational and prioritization skills. Common challenges include balancing tight deadlines, ensuring thorough test coverage, and coordinating with cross-functional teams such as development, product management, and regulatory affairs. Proactively communicating and setting clear expectations with stakeholders is key to managing these challenges. Additionally, Senior QA Associates often mentor junior team members, adding another layer of responsibility to their role.

What are the key skills and qualifications needed to thrive as a Senior QA Associate?

To thrive as a Senior QA Associate, you need a solid background in quality assurance methodologies, process validation, and regulatory compliance, typically supported by a relevant degree and several years of industry experience. Familiarity with quality management systems (QMS), electronic documentation tools, and regulatory standards like GMP or ISO is essential. Strong analytical thinking, attention to detail, and effective communication skills help you identify issues and collaborate across teams. These competencies are crucial to ensure product quality, regulatory adherence, and continuous process improvement in highly regulated environments.

What is the difference between Senior Qa Associate vs Quality Assurance Tester?

AspectSenior Qa AssociateQuality Assurance Tester
Required CredentialsBachelor's degree in Computer Science or related field; experience in QAHigh school diploma or equivalent; some technical training or certifications preferred
Work EnvironmentCollaborates with cross-functional teams; involved in planning and oversightPrimarily executes test cases; reports bugs and issues
Employer & Industry UsageUsed in software development, technology companies, and IT servicesCommon in software firms, startups, and quality-focused organizations
Search & Comparison IntentOften compared for experience level and responsibilitiesCompared for entry-level or mid-level QA roles

The Senior Qa Associate typically has more experience, responsibilities in planning, and oversight in quality assurance processes, whereas a Quality Assurance Tester focuses on executing tests and identifying bugs. The senior role often involves collaboration with development teams and strategic planning, making it suitable for professionals with more experience in QA.

What are the most commonly searched types of Senior Qa jobs in Florida? The most popular types of Senior Qa jobs in Florida are:
Infographic showing various Senior Qa Associate job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 72% Full Time, 25% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $55,448 per year, or $26.7 per hour.

Quality Assurance Associate

Catalent Pharma Solutions

Saint Petersburg, FL • On-site

Full-time

Medical, Dental, Vision, PTO

Posted 29 days ago


Catalent rating

7.6

Company rating: 7.6 out of 10

Based on 55 frontline employees who took The Breakroom Quiz

59th of 86 rated pharmaceutical


Job description

About Site

Join Catalent's flagship Softgel development and manufacturing facility in North America, located in St. Petersburg, FL, with a capacity of 18 billion capsules per year. This role offers competitive pay, day-one benefits, and career growth in a state-of-the-art, turn-key facility.

This role will provide hands-on quality support on the manufacturing floor by assisting with documentation review, investigation activities, ensure compliance with GMPs, and Standard operating Procedures.

Position Summary

The Quality Assurance Associate is an entry-level role designed to support Quality Assurance activities in a GMP pharmaceutical manufacturing environment.

Shift: Monday - Friday 8 am - 5 pm

Location: St. Petersburg

100% Onsite

The Role

  • Provide routine QA support to manufacturing operations by monitoring activities on the manufacturing floor and ensuring compliance with cGMPs and approved SOPs.
  • Assist in the documentation, review, and follow-up of manufacturing events, deviations, and discrepancies under guidance from senior QA staff or QA management.
  • Support investigation activities by gathering documentation, assisting with fact-finding, and helping draft investigation reports related to process, equipment, or documentation events.
  • Perform work order evaluations and quality impact assessments related to equipment breakdowns, maintenance activities, and equipment-related events, in accordance with site procedures.
  • Support batch record review activities to ensure documentation accuracy, completeness, and compliance with Good Documentation Practices (GDP).
  • Provide real-time guidance to Operations during production events as defined by SOPs and escalate issues appropriately to senior QA or QA management.
  • Perform other duties as required to support high performance at Catalent Pharma Solutions.

The Candidate

Minimum Requirements

  • Bachelor's degree in Science or a related field (e.g., Biology, Chemistry, Microbiology) with little or no prior GMP manufacturing experience, OR High school diploma or equivalent with at least three years of experience in pharmaceutical, medical device, or other regulated manufacturing environments.
  • Ability to work effectively under pressure to meet deadlines. Individual may be required to sit, stand, walk regularly and occasionally lift to 15 pounds; no lifting greater than 44.09 pounds without assistance. Be accessible to manufacturing floor and office staff and to use required office equipment. Specific vision requirements include reading of written documents and frequent use of computer monitor.

Preferred Skills & Background

  • Basic understanding of cGMP principles or willingness to learn.
  • Ability to follow procedures and work effectively in a regulated environment.
  • Good written and verbal communication skills (ESL-friendly environment). Strong organizational skills and ability to manage multiple tasks under supervision.
  • Proficient in Microsoft Office applications (Word, Excel, PowerPoint).
  • Team-oriented mindset with the ability to collaborate with Operations, QC, Engineering, and QA personnel.

Why You Should Join Catalent

  • Positive and fast-paced working environment focused on continuous improvement and innovation
  • Competitive Paid Time Off plus 8 paid holidays
  • Medical, dental, and vision benefits effective from day one
  • Tuition reimbursement to support your educational goals
  • Engaging site-based activities such as NCAA Basketball Brackets, Golf Scrambles, and Onsite Pet Adoption Events
  • Employee Resource Groups promoting diversity and inclusion
  • Community engagement initiatives including Adopt-a-Highway clean-up
  • Defined career path with annual performance reviews and growth opportunities
  • WellHub program for physical and mental wellness
  • Exclusive discounts through Perkspot from over 900 merchants

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.


What Catalent employees say

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About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

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