Job Description
Job Summary:
- The Quality Control Analyst I for the QC Microbiology Department will be responsible for performing processing of routine environmental monitoring samples, product-release testing, and raw material testing.
- The position requires the utmost attention to detail, good organizational skills, computer proficiency, and a basic understanding of microbiology and laboratory instrumentation.
- In addition, effective communication skills, and the ability to function in a fast-paced, highly technical environment with minimal supervision are essential for success.
Duties and Responsibilities:
- Performs environmental monitoring, including air viable particulate, non-viable particulate and surface sampling and personnel monitoring.
- Receives raw materials, supplies for the QC laboratory, and maintains laboratory supplies, media, and reagents inventory.
- Adheres to standard operating procedures and good documentation practices to ensure data integrity and traceability.
- Participates with maintaining proper overall operation of department (physical inventories, logs, documentation, filing, etc.)
- Responsible for assisting with routine laboratory upkeep and organization.
- Utilizes GMP systems such as MODA and other laboratory computer systems.
Education and Experience:
- Bachelor’s degree in science.
- Minimum of 1-2 years relevant laboratory experience or experience in a cGMP/FDA regulated industry, or a combination of years of educated and relevant laboratory experience or experience in a cGMP/FDA regulated industry.
Knowledge and Abilities:
- Demonstrated knowledge in Microbiology and aseptic techniques required.
- Ability to work independently or as a team member.
- Ability to work in Clean Room environment with full gowning requirements.
- Ability to problem-solve and troubleshoot as necessary.
Interview Process:
- Virtual interview for 45 minutes.