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Quality Control Associate Jobs in Avon, IN (NOW HIRING)

Langham Logistics

Quality Supervisor

Whitestown, IN

This role oversees a team of Quality Associates engaged in receiving, inspecting, sampling, and ... Material Quality Control Oversee quality checks for incoming raw materials and sampling processes ...

Langham Logistics

Quality Supervisor

Whitestown, IN · On-site

This role oversees a team of Quality Associates engaged in receiving, inspecting, sampling, and ... Material Quality Control Oversee quality checks for incoming raw materials and sampling processes ...

Langham Logistics Inc.

Quality Supervisor

Whitestown, IN · On-site

$70 - $90/hr

This role oversees a team of Quality Associates engaged in receiving, inspecting, sampling, and ... Material Quality Control Oversee quality checks for incoming raw materials and sampling processes ...

Langham Logistics Inc

Quality Supervisor

Whitestown, IN · On-site

This role oversees a team of Quality Associates engaged in receiving, inspecting, sampling, and ... Material Quality Control Oversee quality checks for incoming raw materials and sampling processes ...

Novartis

QA Operations Specialist

Indianapolis, IN · On-site

$88K - $132K/yr

We are looking for experienced Quality Control professionals to help us reach our ambitious goals ... associates. * Ensure compliance of site personnel and application of aseptic techniques and full ...

DHL

Inventory Control Clerk

Indianapolis, IN · On-site

$20.50/hr

Cycle Count, Inventory, Warehouse, General Labor, Line Operator, Forklift, Quality Control ... associates, including paid holidays and vacation - 401(k) with generous company match - Tuition ...

DPDHL

Inventory Control Clerk

Indianapolis, IN · On-site

$20.50/hr

Cycle Count, Inventory, Warehouse, General Labor, Line Operator, Forklift, Quality Control ... associates, including paid holidays and vacation - 401(k) with generous company match - Tuition ...

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Quality Control Associate information

See Avon, IN salary details

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How much do quality control associate jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for quality control associate in Avon, IN is $24.42, according to ZipRecruiter salary data. Most workers in this role earn between $17.74 and $29.76 per hour, depending on experience, location, and employer.

What does a quality control associate do?

A Quality Control Associate is responsible for ensuring that products meet established standards of quality, including reliability, usability, and performance. They conduct inspections, perform tests, and document their findings to identify defects or deviations from specifications. Quality Control Associates often work closely with production teams to address issues and help maintain compliance with industry regulations. Their role is critical in maintaining customer satisfaction and upholding the reputation of their company. They may work in a variety of industries, including pharmaceuticals, manufacturing, and food production.

What are the key skills and qualifications needed to thrive as a quality control associate?

To thrive as a Quality Control Associate, you need a solid understanding of quality assurance principles, attention to detail, and often a background in science or manufacturing. Familiarity with inspection tools, laboratory equipment, and quality management systems (such as ISO standards) is typically required, and certifications like Six Sigma or ASQ may be advantageous. Strong analytical thinking, problem-solving abilities, and effective communication skills set exceptional candidates apart. These skills ensure that products consistently meet standards, reduce errors, and support overall operational excellence.

What are some common challenges quality control associates face when ensuring product consistency across different production batches?

Quality Control Associates often encounter challenges such as variations in raw material quality, changes in manufacturing processes, and tight production schedules that can lead to inconsistencies between batches. Addressing these issues requires keen attention to detail, effective communication with production teams, and a strong understanding of standard operating procedures. Staying proactive in identifying potential sources of variation and collaborating closely with other departments helps maintain high product standards and minimizes the risk of defects.

What is the difference between Quality Control Associate vs Quality Assurance Technician?

AspectQuality Control AssociateQuality Assurance Technician
CertificationsOften requires GMP, ISO, or industry-specific quality certificationsSimilar certifications, with focus on quality standards and compliance
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or quality compliance environments
Primary FocusInspecting products, testing samples, identifying defectsDeveloping and implementing quality systems, audits, and process improvements
Employer & Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, pharmaceuticals, food industry

While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.

What cities near Avon, IN are hiring for Quality Control Associate jobs?

Cities near Avon, IN with the most Quality Control Associate job openings:

Quality Control Associate jobs near you
Infographic showing various Quality Control Associate job openings in Avon, IN as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $50,793 per year, or $24.4 per hour.

Associate, Quality Operations

Genezen

Indianapolis, IN

Full-time

Re-posted 29 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.

PURPOSE

Be an integral part of the quality assurance and quality systems team by providing quality oversight and expertise to operations, manufacturing, and quality control activities. Address terms of product quality and conformance to regulations and Genezen quality policies/procedures. Help in the development of QA people and teams.

ESSENTIAL JOB FUNCTIONS / DUTIES

  • Responsible for Quality Oversight of Manufacturing, Quality Control, and other areas as appropriate, through on the floor presence. Perform assessments during operations activities to ensure all work is performed in compliance with GMP, SOP and regulatory requirements
  • Provide guidance to production employees with the intent to foster understanding and compliance with SOPs, GMPs and process improvements.
  • Review cleanroom and supporting area documentation for accuracy and contemporaneous completion in batch records and logbooks
  • Responsible for ensuring the Genezen documentation is compliant with cGMPs, GDPs, and consistent with other Genezen policies and procedures.
  • Develop and optimize SOPs and other controlled documents for the Quality Assurance department.
  • Review and approve SOPs and other controlled documents for the functional areas as the Quality representative.
  • Review, approve and release critical raw materials for use in production and the quality control laboratories according to established specifications.
  • Review, assess, and release quality control tests and Certificates of Analysis
  • Review and approve executed batch records. Provide guidance and support to departments on errors to ensure error reduction.
  • Assist in the final disposition of master cell banks and viral vector products.
  • Review and approve qualification/validation protocols and reports and technology transfer reports.
  • Provides site GMP and GDP training (annually, for new-hires, and as needed).
  • Initiate and perform Root Cause Analysis for Quality Events such as Deviations and Environmental Excursions. This includes gathering data from various sources across the site (ex. Quality oversight, trend data, and training records), as well as performing interviews of personnel related to the Quality Events.
  • Working cross-functionally with all departments to ensure Quality Events are thorough and accurate.
  • Drive Quality Events to closure within on-time closure deadlines.
  • Review and approve, and implement (as applicable) specifications for labels for media fills, master cell banks and viral vector products,
  • Review and approve Master Batch Records.
  • Review and approve Media Fill Protocols and Reports, as well as participate as a Quality observer as needed.
  • Review and approve Stability Protocols.
  • Initiate, review, and approve Corrective and Preventative Actions (CAPAs) and monitor CAPA effectiveness with collaboration from Operational areas
  • Initiate, review, approve and monitor Change Management activities
  • Work with the other functional areas to give guidance on use of quality systems.
  • Assist the Lead Auditors to perform site internal audits.
  • Lead and/or support customer audits and regulatory inspections by participating in either front or back room.
  • Collaborate cross-functionally (e.g., Operations, Manufacturing, Regulatory, QC, other QA areas) to ensure product is manufactured according to approved procedures and complies with applicable regulations

SPECIAL JOB REQUIREMENTS

  • Adaptability required as work schedule may change based on business needs
  • Criminal background check and drug screen required
  • Other duties as assigned

KNOWLEDGE, SKILLS & EXPERIENCE

EDUCATION / CERTIFICATIONS / LICENSES

Essential/Desired

Bachelor's degree in science or related field

Essential

Experience in industries regulated in-part by, 21 CFR Part 11, 21 CFR 210, 21 CFR 211, 21 CFR 600, 21 CFR 610, Eudralex Volume 4, ICH Quality Guidelines, and Guidance to Industry dockets, as applicable for early phase clinical trials

Essential

Familiarity of eQMS systems such as Veeva

Desired

Knowledge of cGxPs, clean room controls, aseptic processing, and EMA and ISO standards for cleanrooms

Desired

ON-THE-JOB EXPERIENCE

3-5 years of working experience in a Pharmaceutical or Biologics industry in a Quality Assurance role

Essential

Experience working in with early phase clinical trial production and testing

Desired

Previous experience with a startup CDMO and/or in the field of Gene Therapy

Desired

SKILLS / ABILITIES

Manage multiple projects, set priorities, and work in fast-paced environment

Essential

Communicate confidently and effectively with management, peers and key stakeholders

Essential

Demonstrate effectiveness in task completion, decision-making, empowerment of others, deviation/nonconformance management, training, and problem solving

Essential

Work independently and be self-motivated

Essential

Proven ability to work cross-functionally to achieve business outcomes

Essential

PHYSICAL DEMANDS
While performing the duties of this job, the employee is required to meet the following physical demands:
Work Environment

  • Occasionally exposed to loud noise levels
  • Regularly sit for long periods of time

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

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
  • 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.