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Permanent Quality Control Laboratory Jobs (NOW HIRING)

Lonza

QC Laboratory Support Associate

Houston, TX · On-site

QC Laboratory Support Associate Location: Houston, Texas - Onsite Shift: Monday-Friday | 8:00 AM - 3:30 PM As a QC Laboratory Support Associate , you will play a vital role in supporting Quality ...

Lonza

QC Laboratory Support Associate

Houston, TX

QC Laboratory Support Associate Location: Houston, Texas - Onsite Shift: Monday-Friday | 8:00 AM - 3:30 PM As a QC Laboratory Support Associate , you will play a vital role in supporting Quality ...

Artech

Quality Control Laboratory Specialist

Bogart, GA · On-site

$30 - $34.80/hr

May be qualified and assigned to review some laboratory data or documentation. Qualifications * 0-2 years of experience in a QC Microbiology role. * Experienced in microbiology techniques: Aseptic ...

- Zoetis Belgium S.A.

QC Laboratory Technician

Buellton, CA · On-site

$20.25 - $25.75/hr

... laboratory work, including internal testing and coordinating sample submission to third-party labs. The QC Lab Technician collects, processes, and tests samples from raw materials (RAW), work-in ...

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How much do permanent quality control laboratory jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for permanent quality control laboratory in the United States is $22.61, according to ZipRecruiter salary data. Most workers in this role earn between $18.99 and $24.04 per hour, depending on experience, location, and employer.

What is a permanent quality control laboratory?

A Permanent Quality Control Laboratory is a dedicated facility within a company or organization where the quality of products, materials, or processes is consistently monitored and tested. These laboratories are equipped with specialized instruments and staffed by trained professionals who perform various tests to ensure that products meet required standards and regulations. The term 'permanent' indicates that the lab operates on a continual basis, rather than temporarily or for specific projects. Such labs play a critical role in maintaining product safety, compliance, and customer satisfaction across industries such as pharmaceuticals, food, and manufacturing.

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

To thrive as a Permanent Quality Control Laboratory professional, you need a solid background in chemistry or biology, analytical testing skills, and at least a bachelor's degree in a relevant scientific field. Familiarity with laboratory instruments such as HPLC, GC, and spectrophotometers, as well as experience with LIMS and GMP/GLP standards, is typically required. Attention to detail, critical thinking, and effective teamwork are essential soft skills for identifying issues and ensuring accurate results. These competencies are crucial for maintaining product quality, regulatory compliance, and the overall safety of laboratory operations.

What are some common challenges faced by professionals working in a permanent quality control laboratory, and how can they be addressed?

Professionals in a permanent quality control laboratory often encounter challenges such as maintaining accuracy under tight deadlines, adapting to evolving regulatory standards, and managing large volumes of samples. To address these, effective time management, staying updated with industry regulations, and utilizing laboratory information management systems (LIMS) can be helpful. Regular training and collaboration with cross-functional teams also support continuous improvement and ensure high-quality results.

What is the difference between Permanent Quality Control Laboratory vs Quality Control Technician?

AspectPermanent Quality Control LaboratoryQuality Control Technician
CredentialsTypically requires a degree in science or related field, certifications may varyOften requires a diploma or associate degree, certifications are common but less extensive
Work EnvironmentLaboratory setting with specialized equipment, controlled environmentManufacturing or production sites, performing tests and inspections
Industry UsageUsed across industries like pharmaceuticals, food, chemicalsCommonly employed in similar industries for testing and inspection

The Permanent Quality Control Laboratory focuses on detailed testing, analysis, and maintaining quality standards within a lab environment, often involving complex procedures. In contrast, the Quality Control Technician typically performs routine inspections and tests on-site during production. Both roles are essential for quality assurance but differ in scope, environment, and certification requirements.

How to become a permanent quality control laboratory technician?

To become a permanent quality control laboratory technician, candidates typically need a high school diploma or equivalent, with some roles requiring an associate degree or certification in laboratory techniques or quality assurance. Relevant skills include attention to detail, knowledge of laboratory equipment, and understanding of quality standards such as ISO or GMP. Gaining experience through internships or entry-level positions can also improve job prospects.

What cities are hiring for Permanent Quality Control Laboratory jobs?

Cities with the most Permanent Quality Control Laboratory 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 Permanent Quality Control Laboratory jobs?

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

Permanent Quality Control Laboratory jobs near you

QC Laboratory Operations Lead

WuXi AppTec

Middletown, DE • On-site

Other

Posted 24 days ago

Job description

Overview
The QC Laboratory Operations Lead is responsible for managing core Quality Control support functions at WuXi STA's drug product manufacturing facility in Middletown, DE. This role provides leadership and oversight for Stability Program Management, Sample Lifecycle Management, Metrology and Laboratory Equipment Lifecycle Management, Inventory and Consumable Control Management, and critical laboratory electronic systems, like Empower and LIMS. The position ensures laboratory operations are adequately resourced, compliant with current GMP requirements, inspection-ready, and capable of supporting manufacturing, product release, and stability commitments. The QC Laboratory Operations Lead collaborates closely with QC Analytical, QC Microbiology, Manufacturing, Quality Assurance, Validation, Engineering, and Information Technology to ensure effective laboratory operations and continuous improvement.
Responsibilities
Stability Program Management
  • Own and manage the site stability program, including study initiation, sample pulls, scheduling, storage, inventory tracking, and sample reconciliation.
  • Ensure stability studies are executed in accordance with approved protocols, regulatory requirements, and client commitments.
  • Coordinate stability chamber utilization, monitoring, qualification activities, and capacity planning.
  • Maintain stability databases and ensure accurate tracking of all stability samples throughout the study lifecycle.
  • Monitor program performance and ensure timely communication of upcoming testing requirements.
Sample Lifecycle Management
  • Lead laboratory sample management operations from receipt through storage, distribution throughout the testing groups, reconciliation, retention, and disposal.
  • Develop and/or maintain procedures governing sample custody, chain of custody documentation, and sample traceability.
  • Manage sample logistics supporting release testing, stability testing, investigations, validation activities, and client requests.
  • Ensure sample inventory systems are maintained accurately and support efficient laboratory workflows.
  • Identify and implement improvements to sample handling processes that enhance compliance and operational efficiency.
Metrology and Equipment Lifecycle Management
  • Oversee the full lifecycle management of laboratory equipment, including procurement, commissioning, qualification, calibration, preventive maintenance, repair, and retirement.
  • Manage equipment scheduling to ensure continuous laboratory readiness and minimize downtime.
  • Partner with Validation, Engineering, and vendors to support instrument qualification and maintenance activities.
  • Ensure calibration and maintenance programs are executed within established due dates.
  • Monitor equipment performance metrics and drive continuous improvement initiatives.
  • Monitor vendor performance metrics and implement contingency plans where necessary to ensure there is no disruption to throughput.
  • Maintain equipment inventory records and ensure compliance with applicable GMP requirements.
Inventory and Consumable Management
  • Establish and manage laboratory inventory programs for reagents, consumables, reference standards, columns, and critical supplies.
  • Monitor inventory levels and implement forecasting processes to ensure uninterrupted laboratory operations.
  • Coordinate purchasing activities and maintain appropriate stock levels while minimizing waste and expired materials.
  • Ensure materials are received, stored, qualified, and utilized according to approved procedures.
  • Develop key performance metrics related to inventory utilization, availability, and cost management.
  • Lead small team of dedicated contractors supporting consumable materials.
Laboratory Electronic System Oversight
  • Serve as business owner or system administrator for critical laboratory computerized systems, including LIMS, CDS, Electronic Laboratory Notebooks, and related GMP applications.
  • Coordinate system access management, user administration, configuration changes, periodic reviews, and data integrity activities.
  • Partner with IT, Quality Assurance, and system vendors to maintain system compliance and operational effectiveness.
  • Support computer system validation activities and change control processes.
  • Ensure regulatory compliance with data integrity requirements and maintain inspection readiness for all laboratory systems.
Compliance and Quality Systems
  • Ensure laboratory operational processes comply with FDA, EMA, ICH, and applicable GMP regulations.
  • Support investigations, deviations, CAPAs, change controls, and risk assessments associated with laboratory operations.
  • Participate in internal audits, client audits, and regulatory inspections.
  • Monitor compliance trends and implement preventive actions to reduce operational risk.
  • Drive continuous improvement initiatives to improve efficiency, compliance, and employee engagement.
People Management & Leadership
  • Build, develop, and lead the Laboratory Operations team.
  • Provide coaching, mentoring, training and career development opportunities for team members.
  • Establish performance expectations and conduct routine performance evaluations.
  • Manage staffing, resource allocation, and succession planning.
  • Foster a culture focused on compliance, operational excellence, accountability, and continuous improvement.

Qualifications
Required Qualifications:
  • Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, Engineering, or related scientific discipline required; advanced degree preferred.
  • Minimum 7 years of GMP pharmaceutical laboratory experience with at least 3 years in leadership or supervisory roles.
  • Demonstrated experience managing laboratory operations, stability programs, sample management, metrology, equipment programs, or laboratory systems.
  • Strong understanding of GMP regulations, data integrity principles (ALCOA+), and regulatory inspection expectations.
  • Experience with LIMS, CDS, stability management software, inventory systems, and computerized system compliance.
  • Proven ability to manage multiple priorities in a fast-paced pharmaceutical manufacturing environment.
  • Strong organizational, communication, project management, and leadership skills.

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against based on disability
This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management.

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