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Quality Control Laboratory Jobs in Baltimore, MD

Working knowledge of Good Manufacturing Practices (GMPs), Good Laboratory Practices (GLPs), and food safety principles. * Understanding of quality control and quality assurance concepts, including ...

JOB SUMMARY The Quality Assurance Coordinator reports to the Laboratory Quality Assurance Manager ... laboratory including but not limited to document control, CAPA, internal audits, control charts ...

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Quality Control Laboratory information

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$13

$22

$30

How much do quality control laboratory jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for quality control laboratory in Baltimore, MD is $22.47, according to ZipRecruiter salary data. Most workers in this role earn between $18.85 and $23.89 per hour, depending on experience, location, and employer.

What is a quality control laboratory?

A Quality Control (QC) Laboratory job involves testing and analyzing materials, products, or samples to ensure they meet established quality standards and regulatory requirements. QC lab technicians and analysts perform various tests, document results, and identify deviations from specifications. They work in industries like pharmaceuticals, food production, manufacturing, and environmental science. Their role helps maintain product consistency, safety, and compliance with industry regulations.

What are the typical daily responsibilities of someone working in a quality control laboratory?

Professionals in a Quality Control Laboratory are responsible for conducting routine and non-routine tests on raw materials, in-process samples, and finished products to ensure they meet established quality standards. This typically involves preparing and analyzing samples using various laboratory instruments, accurately documenting results, and reporting findings to supervisors or production teams. You may also assist with troubleshooting equipment, participating in investigations if discrepancies arise, and helping maintain compliance with regulatory requirements. The role often requires collaboration with other laboratory staff and production teams to support continuous quality improvement.

What are the key skills and qualifications needed to thrive in the quality control laboratory position, and why are they important?

Excelling in a Quality Control Laboratory role requires a solid understanding of laboratory testing procedures, attention to detail, and a background in chemistry, biology, or a related science, often supported by a relevant degree. Familiarity with laboratory equipment, analytical instruments (such as HPLC or GC), and quality management systems like ISO standards is essential; certifications such as ASQ may be advantageous. Strong problem-solving abilities, communication skills, and a commitment to teamwork set top professionals apart. These competencies are crucial for ensuring product safety and regulatory compliance while maintaining high standards in testing and reporting.

How to become a quality control laboratory technician?

To become a quality control laboratory technician, candidates typically need a high school diploma or equivalent, with some roles requiring an associate degree or relevant certification in laboratory techniques or quality assurance. Skills in using laboratory equipment, attention to detail, and knowledge of safety protocols are essential; some positions may also require experience in specific industries or with certain testing methods.

Is quality control laboratory a good career?

A career in a quality control laboratory involves testing and analyzing products to ensure they meet safety and quality standards, often requiring knowledge of laboratory techniques and attention to detail. It can offer stable employment, opportunities for advancement, and the chance to work in industries like pharmaceuticals, food, or manufacturing. Certifications such as ASQ or laboratory skills can enhance job prospects and career growth.

What does a quality control laboratory do?

A quality control laboratory is responsible for testing and inspecting products, raw materials, and processes to ensure they meet safety, quality, and regulatory standards. Technicians and scientists use tools like microscopes, spectrometers, and test kits to analyze samples and verify compliance throughout manufacturing. Accurate documentation and adherence to protocols are essential in this role.

What are the most commonly searched types of Quality Control Laboratory jobs in Baltimore, MD?

The most popular types of Quality Control Laboratory jobs in Baltimore, MD are:

What are popular job titles related to Quality Control Laboratory jobs in Baltimore, MD?

For Quality Control Laboratory jobs in Baltimore, MD, the most frequently searched job titles are:

What job categories do people searching Quality Control Laboratory jobs in Baltimore, MD look for?

The top searched job categories for Quality Control Laboratory jobs in Baltimore, MD are:

Infographic showing various Quality Control Laboratory job openings in Baltimore, MD as of August 2026, with employment types broken down into 86% Full Time, and 14% Contract. Highlights an 100% In-person job distribution, with an average salary of $46,740 per year, or $22.5 per hour.

QC Data Reviewer I

Pharmaceutics International Inc

Hunt Valley, MD โ€ข On-site

Other

Re-posted 17 days ago


Job description

Job Summary:
The Quality Control Data Reviewer I is responsible for the accurate and timely review of analytical data generated in the QC laboratory. This entry-level role ensures all documentation meets regulatory, internal, and client requirements in support of pharmaceutical product development and manufacturing. The Data Reviewer I will verify compliance with Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), and related company standard operating procedures (SOPs), state, FDA, local laws and international (e.g., EU, Chinese, Japanese) as applicable to maintain data integrity across analytical activities.
Duties/Responsibilities:
  • Perform thorough review of analytical chemistry testing data for completeness, accuracy, and compliance with SOPs, test methods, and applicable regulatory standards.
    1. High-performance Liquid Chromatography (HPLC)
    2. Gas chromatography (GC)
    3. Dissolution
    4. Integrated Software Empower 3.
    5. UV-Vis Spectrophotometer
    6. Mastersizer 3000 for Particle Size Distribution (PSD)
    7. Karl Fischer (KF)
    8. pH
  • Data Review of Analytical Chemistry Testing:
    1. Raw Material (RM) including API (active pharmaceutical ingredients) and excipients
    2. In Process (IP) Testing
    3. Clinical Verification
    4. Packaging Material
    5. Components
  • Review the data to Comply with GLPs, cGMPs, and GDP (Good Documentation Practice).
  • Confirm that calculations, units, and transcriptions are correct and traceable.
  • Ensure chromatographic integrations and results are scientifically sound and compliant with established protocols.
  • Verify that all test methods and procedures are properly followed and documented.
  • Identify, document, and escalate any data discrepancies or deviations for investigation.
  • Maintain a thorough understanding of current USP, EP, and ICH guidelines related to QC testing.
  • Support audit readiness and participate in internal/external audits as needed.
  • Collaborate closely with analysts, supervisors, and QA to resolve issues and ensure timely batch release.
  • Maintain good documentation practices (GDP) and support data archival processes.
  • Continuously improve and educate analytical chemists to improve analytical data reporting, adhering to GDP and cGMP to increase efficiency, compliance, and Quality.
  • Review analytical data to ensure ALCOA+.
  • Ensure compliance of testing with laboratory procedures, test methods, and protocols. Work with laboratory personnel to correct any errors and omissions in GMP documentation and promote a cGMP culture. Ability to pay attention to detail, focus, and multitask on review of analytical laboratory data.
  • Adhere to the Safety and Health Program and associated plans.
  • Review time of use logs on cGMP instrumentation and other analytical equipment.
  • Completion of work within the assigned time frame, to perform or assist in general organizational tasks including open tasks and timelines and tracking of tasks.
  • Knowledge of QA events/deviations/Investigations.
  • Any other responsibilities are assigned by the manager or department head.
Required Skills/Abilities:
  • Demonstrates excellent personal organizational skills
  • Knowledgeable in Pharmaceutical industry regulations
  • Health and Safety Awareness
  • Must work as a team member in the QC Lab environment
Education and Experience:
  • Bachelor's degree or higher, in Chemistry, Pharmacy, Sciences, or Quality (QA/QC), or equivalent work experience
  • 0-3 years of relevant work experience in Quality Assurance/Data review of Chemistry QC in the pharmaceutical industry.
  • Experience in all areas of Pharmaceutical, e.g., CMO, CDMO, Clinical and commercial products is preferred.
  • Experience with MS Programs such as Word, Excel, PowerPoint, Access, Project, Proofreading skills, etc.
  • Knowledge of Quality Management Systems such as Master Control.
  • Knowledge of current federal, local, and international regulations regarding the Testing, production, and release of drug substances and products.
  • Basic understanding of analytical techniques (e.g., HPLC, GC) and laboratory data documentation requirements.
  • Familiarity with cGMP, GLP, and regulatory compliance standards (FDA, EMA, ICH).
  • Proficient in Microsoft Office (Word, Excel, Outlook); experience with electronic laboratory systems (e.g., Empower, LIMS, LabWare) is an advantage.
  • Strong communication, organizational, and time management skills.
  • Ability to manage multiple priorities and re-prioritize tasks as required.
  • Strong attention to detail and ability to detect data inconsistencies.
  • Excellent problem-solving skills.

Physical Requirements:
โ€ข Fluent in English
โ€ข Ability to travel between and within facilities to visit staff, operations, projects, etc.
โ€ข Ability to sit, stand, climb stairs, and climb ladders to mezzanines (when necessary).
โ€ข Ability to lift up to 40 pounds on occasion.
โ€ข Ability to use PPE (safety shoes, goggles, respirators, gloves, etc. when necessary).
All job requirements in the job description provided indicate the level of knowledge, skills, and/or abilities deemed necessary to perform the job competently. Job descriptions are an overview of the duties, responsibilities, and requirements of the position. Employees may be required to perform other job-related assignments as requested.