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Cqa Jobs in Indiana (NOW HIRING)

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Quality Engineer

Avon, IN · On-site

$70K - $90K/yr

ASQ certification such as CQE, CQA, or Six Sigma certification is a plus. * Experience supporting regulatory inspections or third-party certification audits. Ideal Candidate The ideal candidate is a ...

New

Prepare technical reports such as operating plans, CQA reports, and permit applications * Collect air and water monitoring samples * Analyze technical data * Effective communication with colleagues ...

Prepare technical reports such as operating plans, CQA reports, and permit applications * Collect air and water monitoring samples * Analyze technical data * Effective communication with colleagues ...

ASQ Certified Quality Auditor (CQA) certification is preferred. * Experience managing supplier corrective action request (SCAR) programs. * Experience supporting and implementing CAPA programs ...

New

Quality Engineer

Michigan City, IN · On-site

$70K - $90K/yr

ASQ certifications such as CQE, CQA, or CQM, prefered * Hands-on experience with Lean and Six Sigma tools (e.g., Value Stream Mapping, Root Cause Analysis, Cpk/Ppk, GR&R, Kaizen, 5S). * Knowledge of ...

ASQ Certifications (CQA, CQI, CQT) * Manufacturing or machine shop experience General Applicable Company Competencies * Commitment to Watts' values of integrity, accountability, continuous ...

Quality Engineer

Michigan City, IN · On-site

$70K - $90K/yr

ASQ certifications such as CQE, CQA, or CQM, prefered * Hands-on experience with Lean and Six Sigma tools (e.g., Value Stream Mapping, Root Cause Analysis, Cpk/Ppk, GR&R, Kaizen, 5S). * Knowledge of ...

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Cqa information

See Indiana salary details

$14

$35

$65

How much do cqa jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for cqa in Indiana is $35.60, according to ZipRecruiter salary data. Most workers in this role earn between $27.45 and $39.81 per hour, depending on experience, location, and employer.

What are CQA (Certified Quality Auditor) professionals?

CQA professionals, or Certified Quality Auditors, are individuals certified to examine and evaluate the quality systems of organizations. They assess processes, products, and systems to ensure compliance with established standards and identify areas for improvement. CQAs use auditing techniques to verify effectiveness and recommend corrective actions, playing a vital role in maintaining and enhancing quality within a company. Their expertise is recognized across industries, including manufacturing, healthcare, and services.

What is the difference between Cqa vs Quality Assurance Specialist?

AspectCqaQuality Assurance Specialist
CertificationsISO 9001, Six Sigma, CQEISO 9001, Six Sigma, CQE
Work EnvironmentManufacturing, Pharmaceutical, Medical DevicesSoftware, Manufacturing, Healthcare
Employer & Industry UsageManufacturing, Medical Devices, PharmaTech, Manufacturing, Healthcare

Both Cqa (Certified Quality Auditor) and Quality Assurance Specialist roles focus on quality management, with overlapping certifications like ISO 9001 and Six Sigma. Cqas typically work in manufacturing, medical devices, and pharmaceutical industries, conducting audits and ensuring compliance. Quality Assurance Specialists often work across various sectors including software and healthcare, focusing on process improvement and product quality. While their environments differ, both roles aim to uphold quality standards and require similar credentials.

What jobs pay 500,000 a year in the US?

For a CQA (Certified Quality Auditor) or similar quality assurance roles, earning $500,000 annually is uncommon and typically requires executive-level positions, extensive experience, or ownership of a successful business. High salaries in quality assurance are more often found in senior management, consulting, or specialized industries such as pharmaceuticals or aerospace. Achieving such compensation usually involves advanced certifications, leadership skills, and a strong track record of impact.

What does a CQA do?

A CQA (Certified Quality Auditor) is responsible for inspecting and auditing quality systems and processes to ensure compliance with standards and regulations. They analyze data, identify issues, and recommend improvements, often using tools like audit checklists and quality management systems. CQAs typically hold relevant certifications and work in manufacturing, healthcare, or other industries focused on quality assurance.

What are the key skills and qualifications needed to thrive as a Certified Quality Auditor (CQA), and why are they important?

To thrive as a Certified Quality Auditor (CQA), you need a solid understanding of quality management principles, audit processes, and industry regulations, typically supported by a CQA certification from organizations like ASQ. Familiarity with audit management software, data analysis tools, and standards such as ISO 9001 is essential. Strong attention to detail, analytical thinking, and effective communication skills help auditors identify issues and clearly present findings. These capabilities are crucial for ensuring organizational compliance, driving continuous improvement, and maintaining high standards of quality.

What are some common challenges faced by a CQA (Clinical Quality Assurance) professional and how can they be addressed?

A CQA professional often encounters challenges such as staying updated with frequently changing regulatory requirements, managing complex documentation, and ensuring consistent compliance across multiple clinical sites. Addressing these challenges requires continuous professional development, effective communication with cross-functional teams, and strong organizational skills. Building collaborative relationships with clinical operations and regularly participating in training sessions can help CQA professionals navigate evolving standards and maintain high-quality assurance practices.

How to become a CQA?

To become a Certified Quality Auditor (CQA), candidates typically need a combination of education in quality assurance or related fields and relevant work experience, often at least 1-2 years in quality auditing or assurance roles. They must then pass the ASQ Certified Quality Auditor exam, which covers auditing principles, quality systems, and process improvement tools like Six Sigma or ISO standards.

What is the 3 month rule for jobs?

The 3 month rule for jobs, including roles like CQA (Clinical Quality Assurance), often refers to a probation or trial period during which an employee's performance is evaluated. Many companies use this period to determine if the employee is a good fit for the role, and it may impact benefits, job security, or eligibility for permanent employment. In some cases, it also relates to project timelines or training requirements specific to the position.
Infographic showing various Cqa job openings in Indiana as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $74,048 per year, or $35.6 per hour.
Advisor, Data Scientist - CMC Data Products

Advisor, Data Scientist - CMC Data Products

Eli Lilly and Company

Indianapolis, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 5 days ago


Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 62 frontline employees who took The Breakroom Quiz

10th of 74 rated pharmaceutical


Job description

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.

Organizational & Position Overview:

TheBioproductResearch&Development(BR&D) organizationstrivestodelivercreativemedicines topatients by developing and commercializing insulins, monoclonal antibodies, novel therapeutic proteins, peptides, oligonucleotide therapies, and gene therapy systems. This multidisciplinary group works collaboratively with our discovery and manufacturing colleagues.

We are seeking an exceptional Data Scientist with deep data expertise in the pharmaceutical domain to lead the development and delivery of enterprise-scale data products that power AI-driven insights, process optimization, and regulatory compliance. In this role, you'll bridge pharmaceutical sciences with modern data engineering to transform complex CMC, PAT, and analytical data into strategic assets that accelerate drug development and manufacturing excellence.

Responsibilities:

Data Product Development:Define the roadmap and deliver analysis-ready and AI-ready data products that enable AI/ML applications, PAT systems, near-time analytical testing, and process intelligence across CMC workflows.

Data Archetypes & Modern Data Management: Define pharmaceutical-specific data archetypes (process, analytical, quality, CMC submission) and create reusable data models aligned with industry standards (ISA-88, ISA-95, CDISC, eCTD).

Modern Data Management for Regulated Environments: Implement data frameworks that ensure 21 CFR Part 11, ALCOA+, and data integrity compliance, while enabling scientific innovation and self-service access.

AI/ML-ready Data Products: Build training datasets for lab automation, process optimization, and predictive CQA models, and support generative AI applications for knowledge management and regulatory Q&A.

Cross-Functional Leadership:Collaborate with analytical R&D, process development, manufacturing science, quality, and regulatory affairs to standardize data products.

Deliverables include:

  • Scalable data integration platform that automates compilation oftechnical-review-readyandsubmission-readydata packages with demonstrable quality assurance.
  • Unified CMC data repository supporting current process and analytical method development while enabling future AI/ML applications across R&D and manufacturing
  • Data flow frameworks that enable self-service access while maintaining GxP compliance and audit readiness
  • Comprehensive documentation, standards, and training programs that democratize data access and accelerate product development

Basic Requirements:

  • Master's degree in Computer Science, Data Science, Machine Learning, AI, or related technical field
  • 8+ years of product management experiencefocused on data products, data platforms, or scientific data systems and a strong grasp of modern data architecture patterns (data warehouses, data lakes, real-time streaming)
  • Knowledge of modern data stack technologies(Microsoft Fabric, Databricks, Airflow) and cloud platforms (AWS- S3, RDS, Lambda/Glue, Azure)
  • Demonstrated experience designing data products that support AI/ML workflows and advanced analytics in scientific domains
  • Proficiency with SQL, Python, and data visualization tools
  • Experience withanalytical instrumentation and data systems(HPLC/UPLC, spectroscopy, particle characterization, process sensors)
  • Knowledge ofpharmaceutical manufacturing processes,including batch and continuous manufacturing, unit operations, and process control
  • Expertise in data modeling for time-series, spectroscopic, chromatographic, and hierarchical batch/lot data
  • Experience with laboratory data management systems (LIMS, ELN, SDMS, CDS) and their integration patterns

Additional Preferences:

  • Understanding ofDesign of Experiments (DoE), Quality by Design (QbD), and process validation strategies
  • Experience implementing data mesh architectures in scientific organizations
  • Knowledge of MLOps practices and model deployment in validated environments
  • Familiarity withregulatory submissions(eCTD, CTD) and how analytical data supports marketing applications
  • Experience with CI/CD pipelines (GitHub Actions, CloudFormation) for scientific applications

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.


Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is

$126,000 - $244,200

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

#WeAreLilly


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About Eli Lilly

Sourced by ZipRecruiter

Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876