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Director Quality Control Jobs in Indiana (NOW HIRING)

Moon Fabricating

Safety / Quality Control

Kokomo, IN · On-site

We are seeking a detail-oriented and safety-driven Quality Control / Safety Director to join our team. Key Responsibilities • Inspect fabricated members to ensure compliance with contract ...

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Intellectt INC

QC Analyst

Lebanon, IN · On-site

$23 - $31/hr

Support QC data management, sample/result tracking, and development of Electronic Lab Notebook (ELN ... Direct: 732 204 6550 Desk number: 732 412 6999- Ext: 225

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Evonik

Quality Control Supervisor

Lafayette, IN

The QC Supervisor is responsible for organizing and directing the daily activities of the Quality Control laboratory to ensure safe, compliant, and efficient operations. This role ensures all ...

Clayco

Quality Control Technician

Hobart, IN · On-site

$18.50 - $23.75/hr

The role includes direct oversight and review of the entire documentation and physical inspection ... Provide daily QC reports that reinforce activities that are being constructed in conformance with ...

Clayco

Quality Control Technician

Hobart, IN · On-site

$18.50 - $23.75/hr

The role includes direct oversight and review of the entire documentation and physical inspection ... Provide daily QC reports that reinforce activities that are being constructed in conformance with ...

PinnaclePartners

QC Engineer

Indianapolis, IN

$90K - $100K/yr

Indianapolis, IN Our client is seeking immediate assistance in identifying a candidate for a QC Engineer direct hire in Indianapolis, IN. Responsibilities: Review engineering drawings and ...

Clayco

Quality Control Technician

Hobart, IN

$18.50 - $23.75/hr

The role includes direct oversight and review of the entire documentation and physical inspection ... Provide daily QC reports that reinforce activities that are being constructed in conformance with ...

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Director Quality Control information

How much does a QA director make in the US?

A Quality Assurance (QA) Director in the US typically earns between $100,000 and $160,000 annually, depending on experience, industry, and location. Senior roles with extensive experience and certifications can earn higher salaries, often exceeding $180,000. Compensation may also include bonuses and benefits related to leadership and quality management skills.

Is QC a high paying job?

Quality Control (QC) roles, including positions like Director of Quality Control, tend to offer competitive salaries that increase with experience, industry, and location. Senior QC positions often have higher pay, especially when combined with certifications such as Six Sigma or ISO standards, and may include additional benefits depending on the company.

What does a director of quality control do?

A director of quality control oversees the quality assurance processes within an organization, ensuring products or services meet company standards and regulatory requirements. They develop quality policies, lead testing and inspection activities, analyze data to identify issues, and implement improvements, often managing teams and working with cross-functional departments.

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

To thrive as a Director of Quality Control, you need deep expertise in quality assurance methodologies, regulatory compliance, and management, typically supported by a degree in science or engineering and substantial industry experience. Familiarity with quality management systems (QMS) like ISO 9001, Six Sigma certification, and proficiency in data analysis tools are often required. Strong leadership, problem-solving abilities, and effective communication skills help drive cross-functional collaboration and continuous improvement. These competencies ensure product quality, regulatory adherence, and operational excellence in highly regulated industries.

Which pays more, QA or QC?

For a Director of Quality Control, salaries are generally comparable to those of Quality Assurance directors, but QA roles often have higher pay due to broader responsibilities and strategic planning. Compensation depends on industry, experience, and location, with QA roles sometimes offering higher salaries for leadership positions. Both roles may require certifications like Six Sigma or ISO standards, which can influence pay scales.

What are some common challenges faced by a Director of Quality Control, and how can they be addressed?

Directors of Quality Control often encounter challenges such as maintaining compliance with evolving regulatory standards, managing cross-functional teams, and ensuring consistent product quality across multiple locations. To address these challenges, it's important to stay updated on industry regulations, foster open communication between departments, and implement robust training and quality management systems. Regular audits, data-driven decision making, and strong leadership are also key to overcoming obstacles and ensuring continuous improvement within quality control operations.
What are the most commonly searched types of Quality Control jobs in Indiana? The most popular types of Quality Control jobs in Indiana are:
Director Quality Control jobs near you
Infographic showing various Director Quality Control job openings in Indiana as of June 2026, with employment types broken down into 5% As Needed, 78% Full Time, 11% Part Time, 2% Temporary, 2% Contract, and 2% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution.
Director, Quality Control

Director, Quality Control

Aquestive Therapeutics Inc.

Portage, IN • On-site

Other

This job post has expired 2 days ago. Applications are no longer accepted.

Job description

Job Summary: The Director, Quality Control serves as the commercial CMC analytical owner, accountable for ensuring analytical methods, stability programs, and laboratory operations collectively enable compliant product supply and lifecycle management. This position will be expected to work in a highly collaborative, cross functional team environment, provide expert knowledge to risk identification/mitigation, strategy and execution and is expected to make scientific and business critical decisions. Responsibilities: Analytical Strategy Direct QC support for CMC development, regulatory submissions, and product lifecycle management across all products Ensure alignment of QC activities with regulatory submissions (IND, NDA, MAA) and post-approval commitments Establish robust transfer strategies, protocols, acceptance criteria, and success metrics Commercial Analytical CMC Ownership Accountable for CMC readiness and sustainment post-approval Ensure CMC deliverables are complete, scientifically sound and inspection ready.

Own post-approval analytical CMC lifecycle, including Annual Product Reviews / trending, change controls impacting filings, lifecycle improvements and optimization Stability Program Oversight Own stability as a CMC deliverable linked to shelf life, regulatory and partner commitments and supply Provide scientific assessment of stability trends, OOT results, and potential impact to product quality Partner with Quality, AR&D and Regulatory to support IND/NDA/MAA submissions, post-approval commitments and annual updates Laboratory Operations Direct day-to-day QC lab operations (release, stability, in-process, raw materials) Ensure timely and reliable testing to support manufacturing and release schedules Maintain laboratory compliance with cGMP, data integrity, and ALCOA+ principles Oversee scheduling, capacity planning, and resource management External Laboratories & CDMO Oversight Provide oversight of contract laboratories and CDMOs performing analytical testing Review and approve analytical data, deviations, and investigations from external partners Support Quality Agreements and clearly defined analytical responsibilities Investigations & Problem Solving Lead complex OOS, OOT, and deviation investigations related to analytical results and product performance Drive root cause analysis and scientifically sound CAPAs Partner cross-functionally to resolve issues Compliance & Inspection Readiness Ensure QC systems meet global regulatory expectations (FDA, EMA, ICH) Lead inspection readiness activities and serve as QC lead during inspections Ensure data integrity, documentation practices, and audit responses meet expectations People Leadership Lead, develop, and scale QC laboratory teams (scientists, analysts, managers) Build strong technical and compliance culture with clear accountability Drive capability building in analytical science, problem-solving, and inspection readiness Participate in all third party and customer audits and inspections, and corrective action response. QUALIFICATIONS PhD, MS, or BS in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field 10–15+ years in pharmaceutical/biotech Quality Control or Analytical Sciences Significant experience in: CMC development and commercialization, Analytical method development, validation, and transfer, Managing QC labs in a cGMP environment Strong understanding of regulatory expectations (FDA, EMA, ICH) Experience overseeing CDMOs and contract laboratories Proven leadership in inspections and complex investigations Strong business acumen surrounding pharmaceutical manufacturing. Some travel is required The above statements are intended to describe the general nature and level of the work being performed by colleagues assigned to this position.

This is not intended to be an exhaustive list of all responsibilities, duties, and skills required. Aquestive reserves the right to make changes to the job description whenever necessary. As part of Aquestive’s employment process, final candidate will be required to complete a drug test and background check prior to employment commencing.

Please Note: Aquestive is a drug-free workplace and has a drug free workplace policy in place. Aquestive provides equal employment opportunities to all colleagues and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

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