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Head Quality Control Jobs in Indiana (NOW HIRING)

Quality Control (QC) Lab Technician

Indianapolis, IN · On-site

$19 - $24/hr

... head count. We realize a job is more than just a job - it's an extension of your life and family ... statistical quality control procedures Reviews and tests incoming raw materials and outside ...

Quality Control (QC) Lab Technician

Lawrence, IN · On-site

$19 - $24/hr

... head count. We realize a job is more than just a job - it's an extension of your life and family ... statistical quality control procedures Reviews and tests incoming raw materials and outside ...

Director of Quality

Greenfield, IN · On-site

$170 - $210/hr

Act as Head of Quality Control, Head of Quality, and Official Correspondent in accordance with US and regional legislation for all government agency authorizations, communications, and registrations.

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Showing results 1-20

Head Quality Control information

See Indiana salary details

$29.5K

$119.5K

$203.2K

How much do head quality control jobs pay per year?

As of Aug 11, 2026, the average yearly pay for head quality control in Indiana is $119,517.00, according to ZipRecruiter salary data. Most workers in this role earn between $86,600.00 and $143,700.00 per year, depending on experience, location, and employer.

What are some common challenges faced by a head quality control, and how can they be addressed?

A Head of Quality Control often navigates challenges such as maintaining consistent quality standards across multiple departments or production lines, managing regulatory compliance, and responding to unexpected quality issues. Effective solutions include implementing standardized procedures, fostering a culture of open communication, and using data-driven analysis to quickly identify and address root causes. Additionally, staying current with industry regulations and investing in ongoing staff training can help mitigate risks and ensure high-quality outcomes.

What is the difference between Head Quality Control vs Quality Control Supervisor?

AspectHead Quality ControlQuality Control Supervisor
ResponsibilitiesOversees entire quality control department, develops policies, and ensures compliance across multiple projects or products.Manages daily quality inspection activities, supervises QC staff, and ensures product standards are met.
Required CredentialsTypically requires a degree in quality management, engineering, or related field; certifications like CQE are common.Often requires a diploma or degree in quality assurance or related field; certifications like CQI or ISO auditor are advantageous.
Work EnvironmentStrategic, managerial setting often involving cross-department coordination.Operational environment focused on on-site inspections and team supervision.

The Head Quality Control role is more strategic and managerial, overseeing the entire quality process, while the Quality Control Supervisor focuses on daily inspection activities and team management. Both roles require relevant certifications and experience, but the head position involves broader responsibilities and higher-level decision-making.

What are the key skills and qualifications needed to thrive as a head quality control, and why are they important?

To thrive as a Head of Quality Control, you need in-depth knowledge of quality assurance processes, regulatory standards, and a relevant degree in science or engineering. Familiarity with quality management systems (such as ISO 9001), statistical analysis tools, and audit procedures is typically required. Strong leadership, attention to detail, and effective communication are essential soft skills for guiding teams and collaborating with stakeholders. These competencies are crucial to ensure product compliance, reduce errors, and maintain high standards throughout production.

What does a head quality control do?

A Head of Quality Control is responsible for overseeing and managing the quality assurance processes within an organization. They develop and implement quality control policies, supervise quality control teams, and ensure that products or services meet established standards and regulatory requirements. This role involves analyzing data, conducting audits, and working closely with other departments to drive continuous improvement in quality. Additionally, the Head of Quality Control often leads training initiatives and addresses any quality-related issues that arise.
What are the most commonly searched types of Quality Control jobs in Indiana? The most popular types of Quality Control jobs in Indiana are:
What cities in Indiana are hiring for Head Quality Control jobs? Cities in Indiana with the most Head Quality Control job openings:
Infographic showing various Head Quality Control 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 $119,517 per year, or $57.5 per hour.

Site QC Head (Associate Director)

Novartis

Indianapolis, IN • On-site

$138K - $257K/yr

Full-time

Medical, Retirement, PTO

Posted 22 days ago


Novartis rating

7.5

Company rating: 7.5 out of 10

Based on 17 frontline employees who took The Breakroom Quiz

64th of 86 rated pharmaceutical


Job description

Job Description Summary

Location: Indianapolis, Indiana
Join Novartis and play a pivotal role in shaping the future of Radioligand Therapy manufacturing. As the Site QC Head, you will lead and inspire a high-performing Quality Control organization at our Indianapolis site, ensuring the highest standards of product quality, patient safety, and regulatory compliance. This is a unique opportunity to influence site strategy, develop exceptional teams, drive inspection readiness, and establish world-class laboratory operations that directly contribute to delivering innovative therapies to patients with serious diseases.


Job Description

Key Responsibilities

  • Build and lead a high-performing Quality Control organization across Chemistry, Microbiology, and Incoming Quality.

  • Ensure compliant testing and release of materials and productsin accordance withregulatory requirements.

  • Establish andoptimizelaboratory processes, workflows, and quality systems to support operational excellence.

  • Oversee laboratory equipment qualification, analytical methods, and testing program effectiveness.

  • Ensureappropriatemanagementof QC related validations, transfers, investigations related activities (deviations, OOS, OOE, OOT, CAPAs, trending), and Change Control systems.

  • Responsible for business planning, budget and resource planning for the Global Quality Control Projects and follow-up on Global TechOps Quality Control metrics monthly and ensure thatrequiredactions taken to achieve the targets and escalate with the action plans to the related stakeholders.

  • Directinspectionreadiness activities and represent Quality Control during regulatory inspections and audits.

  • Foster a culture of qualitywithin the Quality team and across the site ensuring GMP complianceand continuous quality management improvement byfacilitatingand promoting empowerment and accountability.

Essential Requirements

  • Bachelor's degree in Chemistry, Biology, Pharmacy, Engineering, or relatedexperience.

  • 10+ years of experience within the pharmaceutical, biotechnology, or related regulated industryincludingatleast5 years of leadership experience building, developing, and leading high-performing organizations including prior experience leading a QC organization.

  • Strong knowledge of cGMPregulations, Quality Control laboratory operations, and aseptic manufacturing.

  • Demonstrated experience leading regulatory inspections, audits, investigations, and quality system activities.

  • Proven ability to drive organizational performance, develop talent, and foster a culture of quality and continuous improvement.

  • Direct experience with investigations and root cause analysis in pharmaceutical or medical device products.

Desirable Requirements

  • Experience in Radioligand Therapy manufacturing or other advanced therapies.

  • Experience in process improvement approaches (e.g., Lean, Six Sigma, 5s) and leading projects.

The salary for this position is expected to range between $138,600 and $257,400per year.The final salary offered isdeterminedbased on factors like, but not limited to, relevant skills andexperience, and upon joiningNovartiswill be reviewed periodically. Novartis may change the publishedsalary range based on company and market factors.Your compensation will include a performance-based cash incentive and, depending on the level of therole, eligibility to be considered for annual equity awards.US-based eligible employees will receive a comprehensive benefits package that includes health,lifeanddisability benefits, a 401(k) with company contribution and match, and a variety of other benefits. Inaddition, employees are eligible for a generous time off package including vacation, personal days,holidaysand other leaves.

To learn more about the culture, rewards and benefits we offer ourpeopleclickhere.

#LI-Onsite


    EEO Statement:

    The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.


    Accessibility and reasonable accommodations

    The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.


    Salary Range

    $138,600.00 - $257,400.00


    Skills Desired

    Business Acumen, Collaboration, Data Integrity, Leadership, Manufacturing Production, Stakeholder Management

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