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Quality Control In Jobs in Lebanon, IN (NOW HIRING)

WORKING AT GENEZEN Many people have worked in environments where you feel like just another ... Represent QC Analytical and Microbiological in client meetings and programs * Establish and ...

Lab QC Inspector

Indianapolis, IN · On-site

$46.20K - $96.20K/yr

In this role, you will apply quality control expertise to evaluate, monitor, and recommend corrective actions for company procedures and processes, ensuring compliance and continuous improvement. We ...

In this role, you will apply quality control expertise to evaluate, monitor, and recommend corrective actions for company procedures and processes, ensuring compliance and continuous improvement. We ...

Perform in-depth technical data review of all analytical and microbiological testing performed on finished products - in-process samples, stability samples, raw material samples, and environmental ...

In this people management role, the QC Chemistry Supervisor works with the Quality Control team in supporting our efforts of RLT therapy. This role is responsible for the day-to-day oversight of the ...

In this role, you will apply quality control expertise to evaluate, monitor, and recommend corrective actions for company procedures and processes, ensuring compliance and continuous improvement. We ...

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... RESIDE IN THE UNITED STATES Position Overview: We are seeking an experienced Quality Control ... Manager to lead the project-wide QA/QC program for a large greenfield semiconductor facility. This ...

The job of a Qualified Technician is to test concrete and materials used for producing concrete in ... Perform testing procedures and report those results to the QC Manager * Demonstrate a commitment to ...

We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the ... The QC Senior Director provides administrative and technical leadership in the development ...

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Showing results 1-20

Quality Control In information

See Lebanon, IN salary details

$29.2K

$77.9K

$124.1K

How much do quality control in jobs pay per year?

As of May 30, 2026, the average yearly pay for quality control in in Lebanon, IN is $77,902.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,000.00 and $95,800.00 per year, depending on experience, location, and employer.

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

To thrive as a Quality Control Inspector, you need a solid understanding of quality assurance principles, attention to detail, and familiarity with industry standards, often supported by a high school diploma or technical certification. Experience with measurement tools (such as calipers and micrometers), inspection software, and knowledge of ISO standards are typically required. Strong analytical thinking, effective communication, and problem-solving skills set top performers apart in this role. These abilities are crucial for ensuring product consistency, meeting regulatory requirements, and maintaining customer satisfaction.

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

Quality Control Inspectors often encounter challenges such as identifying subtle defects, maintaining consistency across large batches, and managing tight deadlines. Effective communication with production teams and a thorough understanding of product specifications are crucial for addressing these challenges. Leveraging checklists, standardized procedures, and ongoing training can help inspectors stay accurate and efficient. Additionally, embracing new quality management technologies can improve inspection processes and facilitate collaboration with other departments.

What are Quality Control Inspectors?

Quality Control Inspectors are professionals responsible for examining and testing products or materials to ensure they meet established quality standards and specifications. They work in various industries, including manufacturing, food production, and pharmaceuticals, using specialized tools and techniques to detect defects or deviations. Their role is vital in maintaining product safety, compliance, and customer satisfaction by identifying issues early in the production process. Inspectors document their findings, recommend improvements, and sometimes help implement corrective actions. Their work helps organizations maintain high-quality standards and avoid costly recalls or customer complaints.

What is the difference between Quality Control In vs Quality Control Inspector?

AspectQuality Control InQuality Control Inspector
Primary RoleOversees quality assurance processes within production or manufacturing teams, ensuring compliance with standards.Performs inspections and tests on products or materials to identify defects or deviations from specifications.
CredentialsOften requires certifications like ISO or Six Sigma, with experience in quality management systems.Typically requires technical training or certifications such as ASQ Certified Quality Inspector.
Work EnvironmentWorks mainly in manufacturing or production settings, collaborating with quality teams and production staff.Works on the production floor or in labs, inspecting products directly.

While both roles focus on quality, Quality Control In involves managing quality processes and systems, whereas Quality Control Inspectors perform hands-on product inspections. Both roles are essential for maintaining product standards but differ in scope and responsibilities.

What cities near Lebanon, IN are hiring for Quality Control In jobs? Cities near Lebanon, IN with the most Quality Control In job openings:
Infographic showing various Quality Control In job openings in Lebanon, IN as of May 2026, with employment types broken down into 64% Full Time, 19% Part Time, 2% Temporary, and 15% Contract. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $77,902 per year, or $37.5 per hour.
Director, Quality Control

Director, Quality Control

Genezen

Indianapolis, IN

Other

Posted 22 days ago


Job description

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