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Quality Control Laboratory Manager Jobs (NOW HIRING)

The QC Laboratory Coordinator supports daily operations in QC Chemistry and Microbiology labs by managing sample logistics, documentation, and laboratory supplies within a GMP environment. The role ...

Lead and manage the Quality Control laboratory and incoming sampling activities to support manufacturing operations and customer requirements. * Provide day-to-day leadership for analytical, raw ...

Lead and manage the Quality Control laboratory and incoming sampling activities to support manufacturing operations and customer requirements. * Provide day-to-day leadership for analytical, raw ...

QC Supervisor

Morton Grove, IL · On-site

$34 - $40.86/hr

Manage the QC laboratory during the 3rd shift and serve as the primary point of contact for all quality control activities. * Oversee the maintenance and calibration of laboratory equipment to ensure ...

The Quality Control Data Associate plays a critical role in ensuring the accuracy, integrity, and ... Develop and maintain proficiency with the Laboratory Information Management System (LIMS), product ...

Quality Control Data Associate Department: Lab Employment Type: Full Time Location: Summerville, SC ... Develop and maintain proficiency with the Laboratory Information Management System (LIMS), product ...

Showing results 41-60

Quality Control Laboratory Manager information

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$30.5K

$81.3K

$129.5K

How much do quality control laboratory manager jobs pay per year?

As of Sep 10, 2026, the average yearly pay for quality control laboratory manager in the United States is $81,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $100,000.00 per year, depending on experience, location, and employer.

What does a quality control laboratory manager do?

A Quality Control Laboratory Manager oversees the operations of a laboratory that tests products for quality and compliance with industry standards. They manage laboratory staff, ensure testing procedures are followed accurately, and maintain equipment. The manager is responsible for implementing quality assurance protocols, analyzing test results, and reporting findings to upper management. Their work helps ensure that products meet safety and quality requirements before reaching consumers.

What are the key skills and qualifications needed to thrive as a quality control laboratory manager?

To thrive as a Quality Control Laboratory Manager, you need a strong background in laboratory science, quality assurance, and regulatory compliance, typically supported by a relevant degree and industry experience. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP), and certifications such as ASQ Certified Quality Auditor are often required. Excellent leadership, problem-solving, and communication skills help manage teams and ensure smooth operations. These competencies are crucial for maintaining high standards, ensuring product safety, and meeting regulatory requirements in laboratory environments.

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

Quality Control Laboratory Managers often face challenges such as maintaining compliance with strict regulatory standards, managing a diverse team, and ensuring timely turnaround of test results. To address these, effective managers implement robust training programs, foster clear communication across teams, and establish standardized operating procedures. Proactive planning and continuous process improvement are key to staying ahead of regulatory updates and ensuring consistent data quality, which ultimately supports both operational efficiency and product safety.

What is the difference between Quality Control Laboratory Manager vs Quality Control Analyst?

AspectQuality Control Laboratory ManagerQuality Control Analyst
CredentialsBachelor's degree in science, often with management certificationsBachelor's degree in science or related field
Work EnvironmentSupervises lab staff, manages operations, oversees testing processesPerforms testing and analysis of samples under supervision
Employer & Industry UsageUsed in pharmaceutical, biotech, and manufacturing industries for lab oversightCommonly employed in similar industries for sample analysis

The main difference is that the Quality Control Laboratory Manager oversees the entire lab operations and staff, ensuring compliance and quality standards, while the Quality Control Analyst focuses on conducting specific tests and analyses. The manager has more responsibilities related to supervision and process management, whereas the analyst is primarily involved in testing tasks.

What cities are hiring for Quality Control Laboratory Manager jobs?

Cities with the most Quality Control Laboratory Manager job openings:

What are the most commonly searched types of Quality Control Laboratory jobs?

The most popular types of Quality Control Laboratory jobs are:

What states have the most Quality Control Laboratory Manager jobs?

States with the most job openings for Quality Control Laboratory Manager jobs include:

What are popular job titles related to Quality Control Laboratory Manager jobs?

For Quality Control Laboratory Manager jobs, the most frequently searched job titles are:

Infographic showing various Quality Control Laboratory Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $81,324 per year, or $39.1 per hour.

Scientist - Quality Control Laboratory Informatics

Concord, NH • On-site

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 7 days ago


Job description

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work, but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

The Scientist – QC Laboratory Informatics role is responsible for supporting laboratory operations through ensuring that electronic laboratory systems function per intended purpose and use, specifically related to end user functionality and to system compliance with company and regulatory requirements. Responsibilities will initially involve interacting with global and local IT support functions to populate master data, configure systems, and assist with installing and qualifying laboratory IT systems such as LabVantage LIMS, MODA, NuGenesis ELN and SDMS, Empower, and other laboratory systems. The role will evolve into monitoring, execution and maintenance of the Laboratory IT Systems for the QC laboratory with an emphasis on continuous improvement and a focus on data integrity. This role will serve as business representative for laboratory IT systems and will be responsible for mentoring and educating peers on the use of laboratory systems and equipment, oversight for management reviews, laboratory metrics and laboratory documentation as well as supporting internal and external audits as a laboratory IT system subject matter expert.

Key Objectives/Deliverables
  • Performs and/or supports the laboratory with the validation of laboratory equipment and software systems.
  • Supports the establishment and maintenance of the validated state of software-based computerized systems in use within the laboratory.
  • Leads and/or supports site deployment and upgrades of QC laboratory IT systems such as LabVantage LIMS, Empower, MODA, NuGenesis ELN and SDMS.
  • Ensures data integrity by design within the QC laboratory.
  • Acts as QC laboratory data integrity local representative.
  • Partners and builds relationships with Global Quality Laboratory Network, Global and Site IT team members.
  • Acts as a contact SME for QC laboratory IT systems.
  • Performs non-terminal record monitoring activities.
  • Supports audit trail discrepancies if found during system audit trail review.
  • Supports continuous improvement of quality systems as they relate to the QC laboratory.
  • Applies knowledge of quality principles, cGMP, and laboratory systems towards the development and execution of local procedures, training courses, and practices.
  • Assists in improvement of quality systems by creating or revising worksheets, developing or updating laboratory execution system documentation, updating laboratory methods, and maintaining other laboratory documentation systems.
  • Supports audit and inspection activities for the laboratory.
  • Implements and complies with corporate, site, and laboratory safety standards.
Basic Qualifications
  • Bachelor’s degree in a computer science, life science, or applied science or other relevant field.
  • IT systems experience (installation and qualification of laboratory IT systems, population of master data, and configuration of systems).
  • Minimum 3 years experience in a GMP laboratory.
  • Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1
Additional Skills/ Preferences
  • Master’s degree in a computer science, life science, or applied science or other relevant field.
  • Proficiency with computer systems including Microsoft Office products, LIMS, Laboratory Execution Systems, chromatography systems, electronic laboratory notebook systems including implementation of systems.
  • Experience operating or implementing laboratory IT systems including LIMS and Automated Lab Execution systems.
  • Investigation and deviation management experience.
  • Demonstrated proficiency in computer system validation.
  • Experience with compliance requirements and regulatory expectations.
  • Excellent oral and written communication skills and demonstrated through documentation and presentation skills.
  • Demonstrated accuracy and proficiency in analytical skills.
  • Ability to work in a laboratory environment including wearing appropriate PPE and other safety related equipment or considerations.
  • Previous experience with cross-function leadership utilizing problem-solving and decision‑making skills.
Additional Information
  • Tasks may require repetitive motion and standing for long periods of time.
  • 8-hour days – Monday through Friday
  • May require support outside of regular schedule (weekend days or off-hours) in support of continuous (24/7) manufacturing operations.
  • Applicant will work in various areas within the site. Some allergens are present in the parenteral plant. Mobility requirements and exposure to allergens should be considered when applying for this position.
  • Minimal travel required.
  • Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( https://careers.lilly.com/us/en/workplace-accommodation ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
  • Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
  • Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL).

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $65,250 - $169,400

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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