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Quality Control Analyst Jobs in Indiana (NOW HIRING)

Genezen

Director, Quality Control

Indianapolis, IN · On-site

JOB SUMMARY Responsible for driving all aspects of the Analytical and Microbiological Quality Control (QC) laboratories at Genezen. This individual provides leadership, scientific and technical ...

Genezen

Director, Quality Control

Indianapolis, IN

JOB SUMMARY Responsible for driving all aspects of the Analytical and Microbiological Quality Control (QC) laboratories at Genezen. This individual provides leadership, scientific and technical ...

Genezen

Director, Quality Control

Indianapolis, IN

JOB SUMMARY Responsible for driving all aspects of the Analytical and Microbiological Quality Control (QC) laboratories at Genezen. This individual provides leadership, scientific and technical ...

Ozinga

Quality Control Technician

Crown Point, IN

$51.35K - $64K/yr

Quality Control Analysis: • Conduct tests and inspect concrete to evaluate quality or conformance to specifications • Sample and evaluate quality of materials related to concrete • Monitor ...

BW Fusion

QC Microbiologist

Fort Wayne, IN

$50K - $75K/yr

Sample management and QC testing * Documentation completion and review in compliance with GMP ... Prior experience working in an analytical or biological lab or managing third-party lab testing.

SRM360

Quality Control Technician

Indianapolis, IN · On-site

$18 - $23/hr

You will be responsible for conducting tests, analyzing data, and developing solutions to improve ... of quality control training programs for production staff. * Maintain accurate and organized ...

MetroNet

Fielding & IPE QC Supervisor

Evansville, IN · On-site

Lead the team on conducting full QC analysis on pole applications and provide training/updates on associate feedback * Review and annotate Map site files submitted by pole engineering team and ...

Hilltop Companies

Quality Control Technician

Patriot, IN · On-site

$17 - $21.75/hr

Perform routine QC testing (e.g., gradation/sieve analysis, moisture, specific gravity/absorption, unit weight, cleanliness, and other aggregate-related tests as assigned) per applicable procedures ...

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How much do quality control analyst jobs pay per hour?

As of May 30, 2026, the average hourly pay for quality control analyst in Indiana is $26.56, according to ZipRecruiter salary data. Most workers in this role earn between $21.97 and $29.52 per hour, depending on experience, location, and employer.

What Is a Quality Control Analyst?

A quality control (QC) analyst or quality assurance analyst tests computer programs to ensure that software applications function properly before being deployed in production or going to market. As a quality control analyst, your job is to identify and fix bugs in software applications and computer systems and make recommendations to management about how to improve a software application’s functionality, user experience (UX), and user interface (UI). Your QC process typically involves a significant amount of collaboration with other analysts and software developers.

What are the key skills and qualifications needed to thrive as a Quality Control Analyst, and why are they important?

To thrive as a Quality Control Analyst, you need a solid understanding of quality assurance principles, data analysis, and laboratory or manufacturing processes, often supported by a degree in a related scientific or technical field. Familiarity with tools such as LIMS (Laboratory Information Management Systems), statistical software, and regulatory standards (like GMP or ISO) is typically required. Attention to detail, problem-solving abilities, and strong communication skills help analysts identify issues and collaborate effectively with team members. These skills ensure products or processes consistently meet quality standards, safeguarding consumer safety and organizational reputation.

What are some common challenges faced by Quality Control Analysts, and how can they be effectively managed?

Quality Control Analysts often encounter challenges such as tight production deadlines, variability in sample quality, and adapting to frequent changes in testing protocols or regulatory standards. Managing these challenges involves strong organizational skills, proactive communication with production and laboratory teams, and staying current with industry regulations. Developing efficient documentation practices and using digital tools for data management can also help maintain accuracy and streamline workflow, ultimately supporting consistent product quality.

What does a Quality Control Analyst do?

A Quality Control Analyst is responsible for testing and inspecting products or processes to ensure they meet established quality standards. They analyze samples, identify defects or inconsistencies, and document their findings to help maintain product quality and safety. Their work helps organizations comply with regulations and deliver reliable products to customers. Quality Control Analysts often work in industries such as pharmaceuticals, manufacturing, and food production.

What is the difference between Quality Control Analyst vs Quality Assurance Specialist?

AspectQuality Control AnalystQuality Assurance Specialist
CertificationsOften requires certifications like ASQ CQE or ISO auditorSimilar certifications, with focus on process audits
Work EnvironmentLaboratory, manufacturing, or production settingsOffice-based, process review, and compliance environments
Primary FocusTesting products, identifying defects, ensuring quality standardsDeveloping and maintaining quality systems, preventing defects
Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, software, healthcare industries

While both roles aim to ensure product quality, the Quality Control Analyst primarily tests and inspects products to identify defects, whereas the Quality Assurance Specialist focuses on creating and improving processes to prevent defects. Both roles often require similar certifications and work in related environments, but their core responsibilities differ in focus and approach.

More about Quality Control Analyst jobs
What are the most commonly searched types of Quality Control Analyst jobs in Indiana? The most popular types of Quality Control Analyst jobs in Indiana are:
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What job categories do people searching Quality Control Analyst jobs in Indiana look for? The top searched job categories for Quality Control Analyst jobs in Indiana are:
What cities in Indiana are hiring for Quality Control Analyst jobs? Cities in Indiana with the most Quality Control Analyst job openings:
What are popular job titles related to Quality Control Analyst jobs in IN? For Quality Control Analyst jobs in IN, the most frequently searched job titles are:
Quality Control Analyst jobs near you
Infographic showing various Quality Control Analyst job openings in Indiana as of May 2026, with employment types broken down into 66% Full Time, 31% Part Time, 1% Temporary, and 2% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $55,253 per year, or $26.6 per hour.
Director, Quality Control

Director, Quality Control

Genezen

Indianapolis, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 22 days ago

Job description

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures.
WORKING AT GENEZEN
Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team.
JOB SUMMARY
Responsible for driving all aspects of the Analytical and Microbiological Quality Control (QC) laboratories at Genezen. This individual provides leadership, scientific and technical expertise for all QC activities, as well as support to Analytical Development for all method qualification/validation activities. This person is also the facility aseptic subject matter expert, including responsibilities for the environmental monitoring program. The ideal candidate must have in-depth knowledge and experience in a cGMP/ GLP testing lab.
ESSENTIAL JOB FUNCTIONS
  • Ensure timely in-process and release testing of early clinical grade biopharmaceuticals
  • Maintain familiarity with current analytical and bioassay methods used for characterizing viral vectors (Assays include genome titer by Flow, ELISA, qPCR, ddPCR, genome integrity assay, empty/full particle ratio assay, and cell-based assays)
  • Monitor, maintain and continuously improve the environmental monitoring program, including conducting Environmental Monitoring Performance Qualifications as needed
  • Develop, implement and maintain EM trending program and metrics, including Annual Reports and evaluation of alert levels
  • Develop, implement and maintain an in-house isolates program
  • Responsible for Disinfectant Efficacy Program
  • Responsible for the Analytical laboratory equipment systems and software (e.g., ddPCR, Flow, etc.) including purchase, calibration, IOPQ activities, etc. to meet the compliance (data integrity) requirements and project timelines.
  • Support the Analytical Development team in qualification/validation of analytical methods to support the cGMP manufacturing of viral vectors
  • Support the tech transfer of bioassays from clients to cGMP QC testing lab
  • Represent QC Analytical and Microbiological in client meetings and programs
  • Establish and maintain the stability program
  • Oversee LIMS development, implementation, operation, troubleshooting and maintenance
  • Responsible for all laboratory logistics activities including, but not limited to sample management, test/release schedule, cycle time matrix, capacity management, etc.
  • Manage outside contract laboratory relationships, including method qualification/validations, investigations, audits, cost and invoices to meet project timelines and business requirements
  • Support OOSs/OOTs and other lab investigations, deviations, CAPAs, change controls, audits, and training
  • Analyze regulatory authorities' programs, guidance documents, and activities in areas relevant to testing of cell and gene products
  • Develop, implement and present metrics for monitoring of lab operations and stability program
  • Participation in client audits and regulatory inspections as SME and development of responses to observations
  • Responsible for hiring and development of team members, conduct performance review and disciplinary actions.
  • Ensure safe working environment and compliance with OSHA, EHS, Quality, and cGMP procedures and policies within the QC functional area

KNOWLEDGE, SKILLS, AND EXPERIENCE
EDUCATION / CERTIFICATIONS / LICENSES
Essential/Desired
BS in a scientific/technical discipline
Essential
MS in a scientific/technical discipline
Preferred
ON-THE-JOB EXPERIENCE
7+ years of experience in a QC leadership position within the biological industry
Essential
Proven technical leadership and experience in bioanalytical methods (method development, validation and transfer). Methods include but not limited to: ELISA, PCR, qPCR, ddPCR, cell-based assays, and flow cytometry-based assays.
Essential
Familiarity with viral vector release assays
Preferred
Proven lab operations management experience
Preferred
3+ years of cGXP experience
Preferred
SKILLS / ABILITIES
Ability to maintain multiple projects and timelines
Essential
Strong people leadership skills
Essential
PHYSICAL DEMANDS
While performing the duties of this job, the employee is required to meet the following physical demands:
Work Environment
  • Frequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowning
  • Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities
  • Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock
  • Occasionally exposed to extremely loud noise levels
  • Spending time on the floor during activity execution (maintenance, construction, commissioning and qualification) is required

Movement
  • Frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms
  • Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl

Lifting
  • Frequently lift and/or move up to 10 pounds
  • Occasionally lift and/or move up to 25 pounds

Vision
  • Frequently utilize close vision and the ability to adjust focus

Communication
  • Frequently required to communicate by talking, hearing, using telephone and e-mail

GENEZEN'S CURES VALUE-BASED COMPETENCIES
Committed to Science
We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare.
Urgency in action for the patients
We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs.
Resilience & Grit in operations
We are committed to overcoming challenges, learning from failures, and persistently striving for success.
Execute with Excellence & Integrity
We are dedicated to delivering quality results and upholding ethical principals.
Solutions driven for our partners
We are committed to being a proactive, collaborative, creative and open-minded partner.
GENEZEN'S BENEFITS
  • Paid vacation days, amount based on tenure
  • Paid sick time
  • 10 observed holidays + 2 floating holiday + 1 volunteer day
  • 401(k) plan with company match up to 6% of salary, vested immediately
  • Share Appreciation Rights
  • Choice of several healthcare plans
  • FSA and HSA programs
  • Dental & vision care
  • Employer-paid basic term life/personal accident insurance
  • Voluntary disability, universal life/personal accident insurance
  • Accidental Death & Dismemberment (AD&D) Insurance

ADDITIONAL DETAILS
  • Nothing in the job description for this role restricts management's right to assign or reassign duties and responsibilities to this job at any time.
  • This position requires a criminal background check.
  • Genezen is an Equal Opportunity Employer.
  • Genezen participates in EVerify.
  • Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.

Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts.
Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world's largest children's museum--to name just a few reasons why this area is a great place to live.
Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.

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