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Qc Laboratory Manager Jobs in Indiana (NOW HIRING)

Quality Control Chemist Summary: INCOG is seeking a Quality Control (QC) Chemist with a passion for ... laboratory waste management * Assist in the control and management of laboratory waste in ...

Laboratory Manager

Greenfield, IN

$30/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Laboratory Manager - Up to $30/hr DOE! This position is a direct hire opportunity! Integrity Trade ... Conduct routine quality control checks and assist with audits, proficiency testing, and corrective ...

Laboratory Manager

Greenfield, IN · On-site

$62K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Laboratory Manager - Up to $30/hr DOE! This position is a direct hire opportunity! Integrity Trade ... Conduct routine quality control checks and assist with audits, proficiency testing, and corrective ...

Senior Chemist QC

Lafayette, IN · Hybrid

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Chemist serves as a technical resource to QC personnel, collaborates with cross ... Demonstrated ability to independently manage laboratory investigations and technical projects.

Senior Chemist QC

Lafayette, IN · Hybrid

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Chemist serves as a technical resource to QC personnel, collaborates with cross ... Demonstrated ability to independently manage laboratory investigations and technical projects.

Senior Chemist QC

Lafayette, IN · On-site

$85 - $120/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Chemist serves as a technical resource to QC personnel, collaborates with cross ... Demonstrated ability to independently manage laboratory investigations and technical projects.

Senior Chemist QC

Lafayette, IN · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Chemist serves as a technical resource to QC personnel, collaborates with cross ... Demonstrated ability to independently manage laboratory investigations and technical projects.

Senior Chemist QC

Lafayette, IN · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Chemist serves as a technical resource to QC personnel, collaborates with cross ... Demonstrated ability to independently manage laboratory investigations and technical projects.

In this people management role, the QC Chemistry Supervisor works with the Quality Control team in ... Supervision of laboratory personnel. * Provide oversight for personnel work schedules as well as ...

Quality Control Technician

Greenwood, IN · On-site

$17.75 - $22.75/hr

All laboratory activities are to be conducted according to good laboratory practices (GLP) and ... Most possess good time management skills and be able to plan and execute daily functions with ...

Quality Control Technician

Greenwood, IN

$17.75 - $22.75/hr

All laboratory activities are to be conducted according to good laboratory practices (GLP) and ... Most possess good time management skills and be able to plan and execute daily functions with ...

Quality Control Technician

Greenwood, IN

$17.75 - $22.75/hr

All laboratory activities are to be conducted according to good laboratory practices (GLP) and ... Most possess good time management skills and be able to plan and execute daily functions with ...

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Chemist serves as a technical resource to QC personnel, collaborates with cross ... Demonstrated ability to independently manage laboratory investigations and technical projects.

QC Sample Management Technician, 2nd Shift

Fishers, IN · On-site

$17.50 - $22.50/hr

The QC Sample Management Technician plays a critical role in maintaining data integrity, inspection readiness, and efficient laboratory operations by ensuring samples are handled in accordance with ...

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Chemist serves as a technical resource to QC personnel, collaborates with cross ... Demonstrated ability to independently manage laboratory investigations and technical projects.

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Showing results 1-20

Qc Laboratory Manager information

What is a QC Laboratory Manager?

A QC (Quality Control) Laboratory Manager oversees the daily operations of a quality control laboratory, ensuring that all testing procedures and results meet regulatory and company standards. They are responsible for supervising laboratory staff, developing and implementing quality control protocols, and maintaining compliance with health and safety regulations. QC Laboratory Managers also analyze test data, troubleshoot issues with equipment or procedures, and communicate findings with other departments to ensure product quality. Their role is crucial in industries like pharmaceuticals, food and beverage, and manufacturing, where product safety and quality are paramount.

What are the key skills and qualifications needed to thrive as a QC Laboratory Manager?

To thrive as a QC Laboratory Manager, you need a strong background in chemistry or biology, experience in laboratory operations, and a relevant degree, often supported by prior supervisory experience. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP), and industry-specific quality standards such as ISO 17025 is essential. Leadership, attention to detail, and effective communication are key soft skills that help manage teams and ensure regulatory compliance. These skills are crucial for maintaining high-quality standards, ensuring accurate test results, and leading laboratory teams efficiently.

What is the difference between Qc Laboratory Manager vs Qc Analyst?

AspectQc Laboratory ManagerQc Analyst
CredentialsBachelor's or higher in Chemistry, Biology, or related; often requires management experienceBachelor's in Chemistry, Biology, or related; certifications like ASQ are common
Work EnvironmentOversees laboratory operations, manages staff, ensures compliancePerforms testing, analyzes data, reports results
Industry UsageUsed in pharmaceutical, biotech, food, and manufacturing industriesCommonly employed in similar industries for quality testing

The Qc Laboratory Manager focuses on overseeing laboratory operations, managing staff, and ensuring compliance with regulations. In contrast, the Qc Analyst primarily conducts testing and analyzes quality data. Both roles require relevant scientific credentials and are integral to quality assurance in manufacturing and biotech sectors.

What are the main challenges a QC Laboratory Manager faces when leading a team in a fast-paced manufacturing environment?

A QC Laboratory Manager often navigates the challenge of balancing strict regulatory compliance with the need for efficient turnaround times. Managing a diverse team requires strong communication and training to ensure consistent testing and data integrity. Additionally, adapting to rapid changes in production schedules and troubleshooting equipment or process issues are frequent demands. Success in this role involves proactive planning, fostering a culture of continuous improvement, and effective cross-department collaboration.
Infographic showing various Qc Laboratory Manager job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution.

QC Chemist, 3rd Shift

INCOG

Fishers, IN • On-site

Full-time

Re-posted 16 days ago


Job description

Quality Control Chemist Summary:

INCOG is seeking a Quality Control (QC) Chemist with a passion for working within a team, a desire to drive Quality processes in a regulated setting, and a commitment to upholding the integrity of data generated for clients.

The QC Chemist will work closely with the QC Chemistry Manager and Quality Control Method Transfer Scientists, as well as Project Management and Supply Chain teams, to support development, readiness, and routine testing activities for the Quality Control Chemistry laboratory.

This role is crucial in generating ALCOA+ data and upholding our Quality Mindset through attention to detail, on-time delivery, and commitment to Quality excellence. Strict adherence to Good Documentation Practices (GDP) is required as Good Manufacturing Practice (GMP) testing is performed.

Excellent written and oral communication skills with the ability to clearly and concisely articulate complex issues to a range of target audiences is critical in this role. The QC Chemist will exemplify excellent interpersonal skills and be capable of developing productive, customer-centric working relationships with colleagues, clients, suppliers, and partners. The QC Chemist will thrive in a team environment but can also work autonomously with strong self-management and organizational skills.


Essential Job Functions:

  • Perform routine and batch-related testing on incoming components, raw materials, in-process samples, finished product, and stability samples according to validated methods as well as special testing deemed necessary by protocols
  • Assist in sampling and testing of incoming materials requiring QC testing as needed
  • Create/revise SOPs and other relevant documents related to laboratory equipment and/or processes
  • Participate in the completion of laboratory investigations/deviations and provide SME support where needed
  • Perform basic troubleshooting activities with respect to methods/assays, equipment malfunctions, and investigations (Deviations and OOS)
  • Execute routine laboratory work orders for maintenance and non-critical calibrations
  • Perform minor preventative maintenance on QC laboratory instrumentation as needed using written SOPs or assist vendors with access to systems/materials when vendor performs maintenance
  • Execute day-to-day tasks within the laboratory including sample inventory disposition/disposal, consumables ordering/inventory, preparing instruments for testing, and laboratory waste management
  • Assist in the control and management of laboratory waste in cooperation with relevant EH&S standards
  • Assist in the development and execution of protocols for method transfers, method validations, stability studies, cleaning validations, and any other special testing required from the Quality Control Chemistry laboratory
  • Support internal and external customers to ensure proper and timely execution of all aspects of the clinical/commercial analytical method life cycle across clients
  • Conduct periodic reviews of analytical test procedures and SOPs as required
  • Review and approve analytical testing procedures and protocols as needed
  • Assist in training fellow QC and Development personnel on instruments and assays when cross-training is needed
  • Assist in the professional support and development of QC Chemistry Technician staff within the QC laboratory
  • Be team-oriented and willing to act as both a facilitator of special projects and a contributor to special projects when needed
  • Set deadlines and prioritize work for self, group members, and support groups involved
  • Review/approve work performed by coworkers for accuracy and alignment with procedures
  • Collaborate with internal departments and teams to resolve quality issues regarding facility, products manufactured, and released
  • Identify, evaluate, and implement continuous business process improvements

Special Job Requirements:

  • This position will support primarily third shift (11:00pm-7:30am)
  • Bachelor's Degree in Science (Chemistry or Biochemistry)
  • Minimum of 3+ years of biopharma industry experience, with at least 2 years of hands-on experience in a GMP environment/Quality Control testing in a regulated environment or other related experience
  • High proficiency level in operating UHPLC/HPLC, GC, SoloVPE, UV-VIS, TOC, particulate matter analyses, method validation/transfer, and relevant laboratory computer systems with associated data integrity requirements
  • Excellent working knowledge, understanding, and experience with practical implementation of FDA, EMA, and other regulatory authority expectations for Quality Control
  • Exceptional computer skills evidenced by hands-on work with automated data management and/or data analysis systems (LIMS, JMP, Minitab, etc.)

Additional Preferences:

  • Experience with Continuous Improvement, Six Sigma, and/or Lean principles
  • Experience with building processes and procedures
  • Experience in performing testing and/or characterization of biologic (monoclonal antibody, enzyme) and small molecule (peptide, mRNA) products
  • Experience performing container closure integrity testing (CCIT)


Additional info about INCOG BioPharma Services:

At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.


If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.


INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.


By submitting your resume and details, you are declaring that the information is correct and accurate.

Employment Type: Full-Time

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About INCOG

Sourced by ZipRecruiter

Industry

Public administration

Company size

51 - 200 Employees

Headquarters location

Tulsa, OK, US

Year founded

1967