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Job Requirements of QC Analyst I-Microbiology:
-
Employment Type:
Contractor
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Location:
Memphis, TN (Onsite)
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QC Analyst I-Microbiology
Careers Integrated Resources Inc
Memphis, TN (Onsite)
Contractor
Job Title: QC Analyst I-Microbiology
Job Location: Memphis, TN
Job Duration: 5 Months (possibility of extension)
Shift: Tuesday - Saturday, 2:00pm - 11:00pm; Sunday - Thursday, 2:00pm - 11:00pm
Job Location: Memphis, TN
Job Duration: 5 Months (possibility of extension)
Shift: Tuesday - Saturday, 2:00pm - 11:00pm; Sunday - Thursday, 2:00pm - 11:00pm
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 and 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.
- Reviews test results of other QC analysts for accuracy and precision and maintains and efficient workflow of all required testing documentation ensuring timely submission relative to product release dates.
- Perform all other related duties as assigned.
- Bachelors or higher degree in the biological sciences or related field required.
- 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.
- 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.
- Detail-oriented with strong written and verbal communication skills.
- Familiarity with laser particle counters, viable air samplers, microProduct, Endosafe® Instrumentation, PCR, BacT/ALERT systems preferred.
- Familiarity with laboratory data systems such as MODA, LIMS, etc preferred.
Interview Process:
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Virtual interview for 45 minutes.
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