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Qc Laboratory Manager Jobs in Indiana (NOW HIRING)

H.B Fuller

Quality Control Manager

South Bend, IN

The QC Manager plans and coordinates activities of the QC lab and is accountable for timely and accurate test reports and product disposition. The QC Manager coordinates and leads all quality control ...

Kent Corporation

QUALITY CONTROL ANALYST

Washington, IN · On-site

$20.50 - $27.75/hr

The Quality Control Analyst will perform testing on defined routine samples of products produced by ... Properly use Laboratory Information Management System (LIMS), the system used to store all lab data.

Actalent

Lab Technician

Kokomo, IN

$16.75 - $22.50/hr

Quality Control Laboratory Technician (3rd Shift) The Quality Control Laboratory Technician ... Familiarity with ISO 9001, IATF, or other regulated quality management systems. * Experience ...

New

Kent Corporation

QUALITY CONTROL ANALYST

Washington, IN · On-site

$20.50 - $27.75/hr

The Quality Control Analyst will perform testing on defined routine samples of products produced by ... Properly use Laboratory Information Management System (LIMS), the system used to store all lab data.

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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.

What are popular job titles related to Qc Laboratory Manager jobs in Indiana?

For Qc Laboratory Manager jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Qc Laboratory Manager jobs in Indiana look for?

The top searched job categories for Qc Laboratory Manager jobs in Indiana are:

Qc Laboratory Manager jobs near you
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 Metrology Supervisor

Simtra BioPharma Solutions

Bloomington, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer a wide range of delivery systems including pre-filled syringes, liquid/lyophilized vials, diluents for reconstitution, powder-filled vials and sterile crystallization.
Our product types include biologics and small molecules, cytotoxics, highly potent compounds, diluents for reconstitution and vaccines - which are all directly injected into patients worldwide. As such, there is a strong emphasis on quality and continuous improvement at Simtra. We hold ourselves to the highest quality and regulatory standards.
While our primary focus is cGMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packaging. Our teams are driven to help clients scale, innovate and bring life-changing medicines to patients worldwide.
Why join Team Simtra?Because we:
Make it HAPPEN - We bring a growth mindset to every opportunity, developing new skillsets and exceeding our expectations and those of our customers.
Make it TOGETHER - We work as one, respecting each voice and tapping into our unique strengths across teams-so we can solve problems in new ways.
Make it RIGHT - We hold ourselves to a high standard of excellence, fulfilling our commitments to the customer, their patients, and our team members.
Make it COUNT - We take pride in our day-to-day work, knowing the impact we make - taking on challenges big and small to improve patient health.
The role:
The Quality Control Metrology Supervisor manages the activities in the QC Metrology department and the analysts that perform instrument maintenance and instrument projects in support of the company's quality program. This role works as part of the quality control function, training, and leading others within the laboratory. This position reports to Quality Control Chemistry Manager.
The responsibilities:
  • Manages the daily activities of the QC Metrology department.
  • Ensure timely Metrology support to Production, QC Chemistry, QC Microbiology, QC Critical, Incoming Quality Control and other current Good Manufacturing Practices (cGMP) production areas where analytical instruments are deployed.
  • Manage new instrument projects to ensure timely and compliant installation and qualification.
  • Calibrate analytical instruments for conformance to established government, commercial, and specification standards.
  • Develop and execute validation protocols (Installation Qualification/Operational Qualification/Performance Qualification) for analytical instruments.
  • Manage standard operating procedures (SOPs) on new and existing instruments.
  • Responsible for instrument re-certification with outside standard laboratories, which includes performing incoming inspections and documentation reviews on these instruments.
  • Write, revise and review SOPs.
  • Participate in continuous improvement functions (Lean initiatives) teams, which increase efficiency, solve problems, generate cost savings, improve customer service activities, and improve quality.
  • Perform/assist in internal assessments/investigations by collecting and analyzing accurate, objective evidence regarding risks and their magnitude.
  • Serve as a technical resource for process and/or product development activities.
  • Participate in client and regulatory audits and responds to audit observations.
  • Serve as project Subject Matter Expert (SME) on lab instruments and processes.
  • Understands advanced biological and chemical assays requiring precise analytical skills and understanding of biology and chemistry principles.
  • Can operate advanced laboratory equipment (HPLC, UV, Karl Fischer, pH meter, etc.).
  • Has a thorough knowledge of the US and EU pharmacopeias and a working knowledge of JP pharmacopeia.
  • Ensure that data integrity requirements are maintained.
  • Initiates and authors Laboratory Investigation Reports.
  • Performs general laboratory/personal area clean-up.
  • Identifies and leads special projects that involve new methods, instrumentation, and technologies.

The requirements:
  • Bachelor's degree required, preferably in a physical science related field
  • Minimum of 5 years of experience with QC instruments
  • Previous leadership experience preferred.
  • Computer proficiency in Microsoft Word, Excel, and Outlook and the ability to use enterprise software.
  • Knowledge of instrument/software/documentation repair and calibration systems required.
  • Knowledge and navigation skills of QC documentation required.

Physical / Safety Requirements:
  • Must be able to wear personal protective equipment.
  • Duties may require overtime work, including nights and weekends.
  • Use of hands and fingers to manipulate office equipment is required.
  • Position may require sitting or standing for long periods of time.
  • This position requires handling of laboratory chemicals.
  • Must be able to qualify for 20/40 corrected vision.

In return, you'll be eligible for[1]:
  • Day One Benefits
    • Medical & Dental Coverage
    • Flexible Spending Accounts
    • Life and AD&D Insurance
    • Supplemental Life Insurance
      • Spouse Life Insurance
      • Child Life Insurance
    • 401(k) Retirement Savings Plan with Company Match
    • Time Off Program
      • Paid Holidays
      • Paid Time Off
      • Paid Parental Leave and more
    • Adoption Reimbursement Program
    • Education Assistance Program
    • Employee Assistance Program
    • Community and Volunteer Service Program
    • Employee Ownership Plan
  • Additional Benefits
    • Short and Long-Term Disability Insurance
    • Voluntary Insurance Benefits
      • Vision Coverage
      • Accident
      • Critical Illness
      • Hospital Indemnity Insurance
      • Identity Theft Protection
      • Legal and more
    • Onsite Campus Amenities
      • Workout Facility
      • Cafeteria
      • Credit Union

[1] Current benefit offerings are in effect through 12/31/26
Disclaimer
This job description is intended to provide the minimum knowledge, skills and abilities necessary to perform the job. It may not be inclusive of all the duties and responsibilities of the job. Simtra reserves the right to make modifications based on business requirements.
Equal Employment Opportunity
Simtra is proud to be an equal opportunity employer. Simtra evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
Data Privacy
To learn more about Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy: https://simtra.com/privacy-policy/

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