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Quality Control Laboratory Jobs in Baltimore, MD

Actalent

QC Technician

Baltimore, MD

$21.63/hr

Experience in quality control, preferably in a laboratory setting. * Proficiency in using lab equipment such as gram scales, moisture balance measuring, PH Meter, refractometer, and density meter.

Actalent

QC Technician

Baltimore, MD

$21.63/hr

Experience in quality control, preferably in a laboratory setting. * Proficiency in using lab equipment such as gram scales, moisture balance measuring, PH Meter, refractometer, and density meter.

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How much do quality control laboratory jobs pay per hour?

As of Sep 6, 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:

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

Specialist QC Microbiology

Syngene International Limited

Baltimore, MD • On-site

$25.25 - $33.25/hr

Full-time

Posted 6 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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