GVS
Microbiology - Internship
Skills
24 days ago
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Important information
Contract type:
Internship
Location:
United States
Work mode:
Onsite
Published on:
3 October 2026
What they need
- This position supports Production, Facilities, Engineering, and Quality by monitoring environmental systems and performing microbial analysis, water testing, and environmental testing. Responsibilities include recording and reporting test results, supporting microbial growth and promotion activities, and conducting quality inspections according to established procedures to ensure compliance with quality standards.
Must be flexible to work from 8:00 am to 3:30 pm.
Responsibilities/Essential Duties
Conduct Quality Control (QC) testing of products, facilities, and critical systems. Perform entry-level analytical method development and R&D activities, while supporting general and research projects.
Perform quality inspections according to established procedures and /or work instructions.
Maintain laboratory equipment, facility systems, etc.
Maintain inventory of supplies and equipment.
Perform accurate and compliant data and record management.
Develop and maintain laboratory procedures.
Learn relative regulations. Train, understand, and perform assays according to procedures and regulations. Must maintain all training requirements for the position, while seeking out opportunities for continuous development and growth.
Adhere to the Quality Management System and its processes to meet FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements.
Develop, write, update and review laboratory SOP’s for various microbiology procedures in compliance to USP, ISO and AAMI standards.
Support sterilization validation and dose audits for new and existing products utilizing Ethylene Oxide and gamma radiation sterilization methods by using biological indicators, LAL Endotoxin Chromogenic testing, sterility procedures and B&F following USP 71.
Check inventory for lab equipment and supplies, including sending equipment for calibration and ordering biologics and supplies for micro testing.
Assist on stability studies for anticoagulation products for real and accelerated time periods and writes protocols and reports.
Will demonstrate proficiency in Aseptic Process Environmental Monitoring, Aseptic Testing, Microbial Monitoring, Gram Staining, Subculturing, Bacterial Endotoxin Testing, Bioburden Testing, Membrane Filtration, Growth Promotion, Gram Staining and other USP and ISO testing.
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