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Quality Control Lab Technology Jobs in Columbia, MD

System One

QC Analyst - Potency

Rockville, MD · On-site

$24.50 - $32.75/hr

Job Title: QC Analyst - Potency Location: Rockville, MD Type: Contract Schedule: Monday - Friday ... Maintain a clean, organized, and compliant lab environment, adhering to safety standards and ...

New

System One

QC Analyst - Potency

Rockville, MD · On-site

$24.50 - $32.75/hr

Job Title: QC Analyst - Potency Location: Rockville, MD Type: Contract Schedule: Monday - Friday ... Maintain a clean, organized, and compliant lab environment, adhering to safety standards and ...

New

Johns Hopkins Healthcare

Lab Tech I

Baltimore, MD · On-site

$19 - $25/hr

Will Consider Lab Tech I, II or Lab Tech Certified Phlebotomist*** Position Summary: • Performs ... quality checks on scanned images to ensure accuracy and clarity. • Organize and upload scanned ...

System One Holdings, LLC

QC Analyst - Potency

Rockville, MD · On-site

$24.50 - $32.75/hr

Job Title: QC Analyst - Potency Location: Rockville, MD Type: Contract Schedule: Monday - Friday ... Maintain a clean, organized, and compliant lab environment, adhering to safety standards and ...

RWD Consulting

Quality Control Manager

Falls Church, VA · On-site

$150K/yr

Information Technology Services * Healthcare Systems & Services * Program Management * Facilities ... Quality Control Manager ID: 2242 Location: Falls Church, VA Openings: 1 Status: "Projected Need ...

Mercy Medical Center

MLT Lab Tech

Baltimore, MD · On-site

$25.30/hr

Summary Join Our Team at Mercy Medical Center - Now a Medical Lab Tech! Mercy Medical Center is ... control, and preventive maintenance. Participates in Quality management processes as needed.

Cp Marine Llc

QC Manager

Arlington, VA · On-site

$110K - $120K/yr

A leader in cutting-edge research and technology in the cyber arena, CPMG focuses on using business ... The Quality Control (QC) Manager oversees all quality assurance and control activities for overseas ...

Cp Marine Llc

QC Manager

Arlington, VA · On-site

$110K - $120K/yr

A leader in cutting-edge research and technology in the cyber arena, CPMG focuses on using business ... The Quality Control (QC) Manager oversees all quality assurance and control activities for overseas ...

Goldbelt, Inc.

QC Manager

Arlington, VA · On-site

$110K - $120K/yr

A leader in cutting-edge research and technology in the cyber arena, CPMG focuses on using business ... The Quality Control (QC) Manager oversees all quality assurance and control activities for overseas ...

Solargaines

Quality Control Manager

Hunt Valley, MD · On-site

$100K - $130K/yr

Quality Control Manager Solar Gaines is seeking a Quality Control Manager who will oversee ... Use video/photograph and other technologies to report/retrieve data on all aspects of installation ...

Goldbelt, Inc.

QC Manager

Arlington, VA · On-site

$110K - $120K/yr

A leader in cutting-edge research and technology in the cyber arena, CPMG focuses on using business ... The Quality Control (QC) Manager oversees all quality assurance and control activities for overseas ...

Neko Health

Laboratory Technologist

Washington, DC · On-site

In a single, non-invasive visit under an hour, proprietary technology and direct clinical care ... Review QC data, spot trends and deviations early, and escal * Hold the lab to inspection-ready ...

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All JobsQuality Control Lab Technology JobsQuality Control Lab Technology Jobs in Columbia, MD

Quality Control Lab Technology information

See Columbia, MD salary details

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How much do quality control lab technology jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for quality control lab technology in Columbia, MD is $22.44, according to ZipRecruiter salary data. Most workers in this role earn between $18.85 and $23.85 per hour, depending on experience, location, and employer.

What is the difference between Quality Control Lab Technology vs Quality Control Analyst?

AspectQuality Control Lab TechnologyQuality Control Analyst
CredentialsAssociate's or Bachelor's in Science, certifications in lab techniquesAssociate's or Bachelor's in Science, certifications in testing methods
Work EnvironmentLaboratory setting, equipment operationLaboratory testing, data analysis
Industry UsageManufacturing, pharmaceuticals, food productionPharmaceuticals, biotech, manufacturing

Both roles work in laboratory environments within manufacturing or pharmaceutical industries. Quality Control Lab Technicians often focus on operating equipment and supporting testing processes, while Quality Control Analysts primarily perform testing and data analysis. Understanding these differences helps clarify career paths and employer expectations.

How to become a quality control lab technician?

To become a quality control lab 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 testing procedures, and familiarity with safety protocols. Gaining experience through internships or entry-level positions can also improve job prospects.

What is the role of a quality control lab technology?

A quality control lab technician is responsible for testing and analyzing products, raw materials, and processes to ensure they meet quality standards and regulatory requirements. They use laboratory instruments and techniques, such as spectroscopy or chromatography, and often follow standard operating procedures and safety protocols. Their work helps maintain product consistency, safety, and compliance in manufacturing environments.

What cities near Columbia, MD are hiring for Quality Control Lab Technology jobs?

Cities near Columbia, MD with the most Quality Control Lab Technology job openings:

Quality Control Lab Technology jobs near you

Specialist QC Microbiology

Baltimore, MD • On-site

Syngene International Limited
See more jobs at Syngene International Limitedexternal

$25.25 - $33.25/hr

Full-time

Posted 11 days ago

Job description

Job Title: Specialist - Quality Control Microbiology
Reporting to: Head of Quality Control Microbiology
Department: Quality Control
Location: Baltimore, Maryland
About Syngene
Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene' s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, and Merck KGaA. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation.
At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit.
Job Summary
The Specialist - Quality Control Microbiology (QC Microbiology), will serve as an analyst/specialist for the Microbiology side of the QC unit at a large molecule manufacturing plant. The incumbent will work within the QC Microbiology group for the site and partner cross-functionally with QC Analytical, Manufacturing, Quality Assurance, Regulatory Affairs, and Supply Chain to ensure timely analysis and inspection readiness. This role is a working Specialist role, and will include hands-on QC work, including sampling and testing, as well as working with analysts and specialists within QC Microbiology group to develop, qualify/validate, and transfer methods.
Primary Responsibilities
  • Responsible for working in Quality Control (QC) Microbiology operations, including product support for stability studies, raw material, ensuring compliance with Good Laboratory Practices (GLP) and applicable regulatory requirements.
  • Operate as the specialist in performing routine sampling and testing for all Microbiology tests, including for utility, raw material, in-process and product, and stability.
  • Coordinate with Quality Assurance (QA), and other departments to ensure development and transfer of microbiology tests and methods.
  • Ensure qualification, validation, performance, and transfer of Microbiology methods within the QC department.
  • Interact with clients and project teams to ensure seamless execution of project-related activities.
  • Collaborate with the Biologics Process Development team to plan and execute testing activities in support of drug substance development and manufacturing.
  • Ensure that laboratory incidents, out-of-specifications (OOS), deviations, out-of-trend (OOT) results, and client complaints related to QC testing are thoroughly investigated, root causes identified, and corrective and preventive actions (CAPA) implemented in a timely manner.
  • Ensure all documentation, including SOPs, IOPs, EOPs, and STPs, is periodically reviewed, updated, and maintained as per the documentation control system.
  • Ensure timely completion of QC activities as per project timelines. Update work plans periodically to accommodate changes in project scope, priorities, or timelines.
  • Adhere to ALCOA principles of data integrity for self and ensure compliance by team members.
  • Participate in functional working teams for self-assessment of compliance to SOPs and data integrity standards.
  • Support preparation and timely closure of audit action plans and escalate concerns appropriately.
  • Support investigations and closure of client and regulatory audit observations related to QC Microbiology.
  • Ensure lab safety protocols are followed at all times and resolve technical issues in the QC Microbiology lab effectively.
  • Support QC Microbiology documentation in regulatory filings, including Prior Approval Submissions, renewals, updates, and supplements, as required.
  • Support monitoring of QC microbiology trends, complaints, failures, deviations, and changes to identify opportunities for process, system, and product improvements.

Education & Qualifications
  • Education: Bachelor's degree in Chemistry, Biochemistry, Chemical Engineering, or a related scientific discipline is required;
  • Experience: 5-8 years of progressively responsible experience in Quality Control within biologics or pharmaceutical manufacturing environments, specifically for large molecule products.
  • Regulatory Knowledge: Understanding of USDA and USFDA, ICH, EU, and Health Canada regulations, as well as USP and other pharmacopeial standards relevant to biologics manufacturing.
  • Audit Experience: Experience supporting regulatory inspections and third-party audits.
  • Technical Expertise: Working knowledge of biologic techniques and validation of methods.
  • Leadership Skills: Ability to lead cross-functional teams, build relationships across departments, and foster a culture of quality, compliance, and accountability.
  • Training & Development: Experience working within quality systems, qualifications and validations and product lifecycle quality management.
  • Continuous Improvement: A track record of driving successful continuous improvement projects to enhance efficiency, reduce deviations, and increase product quality.

Additional Competencies:
  • Experience in bioanalytical and bioassay methods for monoclonal antibodies and other biologic molecules.
  • Plan and manage resources for smooth operations in the QC Microbiology lab.

Equal Opportunity Employer:
It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, colour, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

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