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Associate Quality Assurance Analyst Jobs in Indiana

INCOG

QA Associate, 2nd Shift

Fishers, IN · On-site

The QA Associate will need to provide support with identifying operational and quality gaps. The ... Use technical skills and applied statistics to analyze and track deviations and to identify sources ...

INCOG

QA Associate, 3rd Shift

Fishers, IN · On-site

The QA Associate will need to provide support with identifying operational and quality gaps. The ... Use technical skills and applied statistics to analyze and track deviations and to identify sources ...

DPDHL

Quality Assurance Supervisor

Whiteland, IN · On-site

$55K - $90K/yr

Position is direct supervisor of hourly associates supporting quality activities. Responsibilities ... Data analysis experience * Training and facilitation skills * Self management DHL Supply Chain ...

DHL

Quality Assurance Supervisor

Whiteland, IN · On-site

$55K - $90K/yr

Position is direct supervisor of hourly associates supporting quality activities. Responsibilities ... Data analysis experience * Training and facilitation skills * Self management DHL Supply Chain ...

ENTEK

Quality Assurance Manager

Terre Haute, IN · On-site

$120K - $135K/yr

... analytical skills, and the ability to lead high-performing teams in a dynamic production ... Associate's degree (minimum two-year degree) and at least five (5) years of quality experience in ...

Genezen

Associate, Quality Operations

Indianapolis, IN · On-site

PURPOSE Be an integral part of the quality assurance and quality systems team by providing quality ... Initiate and perform Root Cause Analysis for Quality Events such as Deviations and Environmental ...

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Associate Quality Assurance Analyst information

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How much do associate quality assurance analyst jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for associate quality assurance analyst in Indiana is $38.10, according to ZipRecruiter salary data. Most workers in this role earn between $27.21 and $47.12 per hour, depending on experience, location, and employer.

What does an associate quality assurance analyst do?

An Associate Quality Assurance Analyst is responsible for testing software applications to ensure they meet quality standards and function as intended. They create and execute test cases, identify bugs or issues, and work closely with developers to resolve problems. This role is typically entry-level and provides support to more senior QA team members, helping to document test results and maintain testing processes. The position is crucial for delivering reliable software products and improving user satisfaction.

Is a quality assurance analyst an entry-level job?

A quality assurance analyst can be an entry-level position, especially for those with basic knowledge of testing processes, attention to detail, and familiarity with testing tools. Many companies offer entry-level QA roles that provide on-the-job training and opportunities to develop skills in software testing, documentation, and quality standards.

What is the difference between Associate Quality Assurance Analyst vs Quality Assurance Tester?

AspectAssociate Quality Assurance AnalystQuality Assurance Tester
Required CredentialsTypically an associate degree or relevant certificationsHigh school diploma or equivalent; certifications are a plus
Work EnvironmentCollaborative teams in software or product developmentTesting environments, often under supervision
Employer & Industry UsageUsed across IT, software, and manufacturing industriesCommon in software development and tech companies
Common Search & ComparisonOften compared for entry-level roles and responsibilitiesCompared for hands-on testing tasks and skills

The Associate Quality Assurance Analyst typically has broader responsibilities, including analysis and documentation, while a Quality Assurance Tester mainly focuses on executing test cases. Both roles are essential in quality assurance processes, with the analyst often involved in planning and the tester in execution.

What are some typical challenges faced by an associate quality assurance analyst, and how can they be effectively managed?

Associate Quality Assurance Analysts often encounter challenges such as understanding complex software requirements, managing tight testing deadlines, and keeping up with evolving testing tools and methodologies. To effectively manage these challenges, it is helpful to maintain clear communication with development teams, prioritize tasks based on project needs, and proactively seek out learning opportunities to stay updated on best practices. Collaborating closely with more experienced QA team members can also provide valuable support and guidance when facing new or difficult testing scenarios.

What are the key skills and qualifications needed to thrive as an associate quality assurance analyst?

To thrive as an Associate Quality Assurance Analyst, you generally need a solid understanding of software testing methodologies, analytical thinking, and a relevant degree in computer science or a related field. Familiarity with test management tools (such as JIRA or TestRail), defect tracking systems, and basic scripting or automation tools is often required. Attention to detail, effective communication, and problem-solving skills help you identify issues and collaborate with development teams. These skills ensure the delivery of high-quality software products and efficient resolution of defects in the development process.
What are the most commonly searched types of Quality Assurance Analyst jobs in Indiana? The most popular types of Quality Assurance Analyst jobs in Indiana are:
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What job categories do people searching Associate Quality Assurance Analyst jobs in Indiana look for? The top searched job categories for Associate Quality Assurance Analyst jobs in Indiana are:
What cities in Indiana are hiring for Associate Quality Assurance Analyst jobs? Cities in Indiana with the most Associate Quality Assurance Analyst job openings:
Associate Quality Assurance Analyst jobs near you
Infographic showing various Associate Quality Assurance Analyst job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $79,242 per year, or $38.1 per hour.

QA Associate, 2nd Shift

INCOG BioPharma Services

Fishers, IN • On-site

Full-time

Re-posted 5 days ago

Job description

Description
Working closely with the QA Supervisor, the QA Associate will be instrumental in ensuring site compliance with Regulations, ISO Standards, organizations SOPs as well as support in championing and developing organization's Quality Mindset, as well as a culture of efficiency, attention to detail, and on time delivery. The QA Associate will need to provide support with identifying operational and quality gaps.
The Quality Assurance Associate will exemplify excellent interpersonal skills and be capable of developing productive, customer-centric working relationships with colleagues, internal customers, and partners. The QA Associate will demonstrate excellent written and oral communication skills with the ability to clearly and concisely articulate complex issues to a range of target audiences. The QA Associate will thrive in a team environment but will also work autonomously utilizing strong self-management and organizational skills. The QA Associate will value process owners and subject matter experts and will possess a demonstrated ability in influencing positive outcomes without direct reporting authority.
Essential Job Functions:
  • Maintain a Quality Assurance presence and provide process confirmation on the manufacturing floor.
  • Review and approve documentation for Quality approval, including but not limited to on-floor batch record review, logbooks, work orders, procedures, etc.
  • Collaborate with Manufacturing/Operations team and lead or provide support with investigations to resolve equipment and process related deviations.
  • Support other QA personnel with batch record reviews, material release, etc.
  • Prioritize and coordinate his/her time in balancing production timelines with product quality assurances.
  • Exercise rapid decision-making in the preliminary evaluation of the scope and impact of deviating events, requirements for product segregation, and the implementation of initial corrective actions or escalate the issue to Manager for resolution.
  • Provide support as needed in a cross-functional capacity on deviation investigative processes using root cause analysis tools, report writing, and mitigation development using risk analysis tools.
  • Exemplify and take proactive approaches in terms of safety expectations, practice positive intervention, and enforce best practices that align to SOPs, compliance requirements, quality guidelines, and site goals.
  • Utilize various paper and automated systems (Veeva, SCADA, BMS, CMMS, LIMS, lab instrument software, etc.) to ensure data integrity for site policies, procedures, and batch records.
  • Use technical skills and applied statistics to analyze and track deviations and to identify sources of variability and error site processes.
  • Ability to manage multiple projects in a fast-paced environment.

Special Job Requirements:
  • This position will support primarily second shift (3 pm to 11:30 pm) with occasional weekend support, dependent on operations' needs.
  • Bachelor's Degree required or equivalent; degree preferred to be in Science (Chemistry, Biology, Biochemistry, Microbiology etc.).
  • Must demonstrate visual acuity of 20/20 or better, with or without corrective lenses.
  • Minimum of 2 years with experience working as Quality in a GMP Manufacturing environment, and/or as an Operator within a Pharmaceutical Manufacturing environment.
  • Moderate knowledge of regulations and quality systems such as deviations, Non-Conformance, CAPA, etc..
  • Understanding of Good Documentation Practices (GDPs) and its criticality.
  • Excellent written and verbal communication skills.
  • General computer skills evidenced by hands-on work with computerized Operations equipment (SCADA); and reporting and data analysis software (Word, Excel, Visio, JMP, Minitab, etc.).

Additional Preferences:
  • Hands-on experience with aseptic manufacturing, inspecting finished products, and Acceptable Quality Limits (AQLs).
  • Experience with Continuous improvement, Six Sigma, and/or Lean principles.

Additional info about INCOG BioPharma Services:
At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.
If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.
INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.
Qualified applicants must be authorized to work in the United States on a full-time basis. INCOG will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.
By submitting your resume and details, you are declaring that the information is correct and accurate.

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