Technician, Microbiology

When joining PerkinElmer, you select an experienced and trusted leader in scientific solutions, with the support of a global service network and distribution centers, providing the right solution, at the right time, to meet critical customer needs. With over an 80+ year legacy of advancing science and a mission of innovating for a healthier world, our dedicated team collaborates closely with commercial, government, academic and healthcare customers to deliver our broad portfolio of analytical solutions, and OneSource services.

Job Title

Technician, Microbiology

• Location(s)
• Altria (East Jackson St, Richmond) - Customer Site VA

Job Description

Job Description Summary

The Technician, Microbiology performs microbiological testing and environmental monitoring activities that support product quality, safety, and regulatory compliance programs. As part of an End-to-End (E2E) Laboratory Modernization Program, this role supports laboratory operations through the execution of microbiological analyses and associated quality activities. The Scientist is responsible for conducting microbial testing, preparing culture media and reagents, performing environmental monitoring activities, and evaluating microbiological data generated within the laboratory, collaborating with scientific and quality teams to support investigations, method validation activities, and continuous improvement initiatives while ensuring compliance with applicable procedures and regulatory requirements. The Technician provides hands-on sample preparation and laboratory support for these activities under direct supervision.

Job Responsibilities

• Conduct microbiological analyses and environmental monitoring activities supporting product quality and safety programs.
• Prepare culture media, reagents, and microbiological supplies in accordance with approved procedures.
• Operate and maintain laboratory equipment used for microbiological testing and sample analysis.
• Perform microbial identification and enumeration activities and evaluate microbiological data for accuracy and compliance.
• Support investigations involving atypical results, deviations, and corrective actions.
• Participate in method validation, verification, and technology transfer activities.
• Maintain laboratory records and documentation in accordance with quality requirements and good documentation practices.
• Collaborate with laboratory personnel and quality teams to ensure timely delivery of high-quality results.
• Identify opportunities for continuous improvement and operational excellence.
• Maintain training and compliance in health, safety, environmental, and operational requirements.
• Maintain a clean, organized, and well-stocked work area, including routine housekeeping and supply inventory.

Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities of this job at any time.

Critical Skills

• Deep subject matter expertise of microbiological principles, aseptic technique, and laboratory safety protocols.
• Proficiency with microbiological equipment including microscopes, autoclaves, and incubators.
• Attention to detail in colony counting, data recording, and quality documentation.
• Understanding of ISO 17025 quality management systems.
• Ability to follow written methods and procedures precisely.
• Ability to trouble shoot methodologies and input into method development

Basic Qualifications

• High school diploma or equivalent with 0–2 years of relevant laboratory or manufacturing experience.
• OR Associate degree in a science-related field.
• Demonstrated ability to work collaboratively under close to direct supervision in a regulated laboratory environment.
• Adaptable, self-motivated, and capable of following detailed instructions and completing routine tasks.

Preferred Qualifications

• Experience performing microbiological analyses and environmental monitoring activities.
• Familiarity with microbial identification and culture techniques.
• Experience working within ISO 17025, GLP, GMP, or FDA-regulated laboratories.
• Experience supporting investigations, deviations, and CAPA activities.
• Knowledge of consumer products, pharmaceuticals, or regulated products.
• Experience supporting method validation and technology transfer activities.

Working Environment

• Must be able to work in a laboratory, controlled environments requiring personal protective equipment (e.g., lab coat, safety glasses, etc.) in laboratory.
• Job pace may be fast and job completion demands may be high.
• Must be able to remain in a stationary position more than 25% of the time.
• The person needs to occasionally move between labs, corridors, adjoining rooms, and buildings onsite. Frequently operate on instruments, objects, tools or controls, which will require regularly bending, squatting, stretching and reaching in order to perform in a service function.
• Occasionally move or lift up to 25 pounds (potential for occasional lifting of up to 50 pounds).
• Specific vision abilities required by this position include without limitation, the ability to observe details at close range distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus in order to perform the essential service functions of this position.
• Occasionally operates a computer and other office machinery, such as a calculator, copy machine, and computer printer.
• Employee may be required to handle hazardous waste according to local, state, and federal regulations. Duties may include identifying, handling, generating, accumulating, storing and labeling hazardous waste.
• Potential risk to lab-based hazards including but not limited to extreme temperature, biological materials, and hazardous chemicals.
• May be required to complete Medical Clearance, Respiratory Protection Training, and Fit Testing to wear a respirator as protection against hazards present in the laboratory environment.

The annual compensation range for this full-time position is $40,000 to $55,000. The final base pay offered to the successful candidate will be determined by factors including internal equity, work location, as well as individual qualifications, such as job-related skills, experience, and relevant education or training.

PerkinElmer is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, or veteran status or any other characteristics protected by applicable law. PerkinElmer is committed to a culturally diverse workforce.