Medasource
Location
LKC site in Pleasant Prairie, WI Duration
6 month contract to hire Key Responsibilities
Participate in qualification and validation activities related to bioburden control strategies for facilities and equipment. Execute routine sterility assurance activities Support media fill simulations and provide documentation to ensure compliance with regulatory guidelines. Analyze and interpret environmental monitoring data, identifying trends and potential risks to product quality. Collaborate with cross-functional teams to troubleshoot contamination events and recommend corrective actions. Maintain accurate records and ensure timely reporting of sterility assurance results. Qualifications
Experience in qualification or validation activities supporting contamination control measures in manufacturing facilities or equipment. Comprehensive understanding of aseptic techniques, either through hands‑on operational experience or involvement in media fill processes. Prior experience participating in media fill simulations in a regulated environment. Ability to work in a fast‑paced environment with strong attention to detail and organizational skills. Excellent written and verbal communication skills. Bachelor's degree in Microbiology, Biology, or a related field preferred, or equivalent work experience. Schedule
Night shift, 12‑hour shifts on a 4 days on, 3 days off, 3 days on, 4 days off rotation. Must be flexible to accommodate additional work in extended hours and/or off‑hour work (including potential nights & weekends). Seniority Level
Associate Employment Type
Full‑time Job Function
Quality Assurance Industry
Pharmaceutical Manufacturing Benefits
Medical insurance Vision insurance
#J-18808-Ljbffr
LKC site in Pleasant Prairie, WI Duration
6 month contract to hire Key Responsibilities
Participate in qualification and validation activities related to bioburden control strategies for facilities and equipment. Execute routine sterility assurance activities Support media fill simulations and provide documentation to ensure compliance with regulatory guidelines. Analyze and interpret environmental monitoring data, identifying trends and potential risks to product quality. Collaborate with cross-functional teams to troubleshoot contamination events and recommend corrective actions. Maintain accurate records and ensure timely reporting of sterility assurance results. Qualifications
Experience in qualification or validation activities supporting contamination control measures in manufacturing facilities or equipment. Comprehensive understanding of aseptic techniques, either through hands‑on operational experience or involvement in media fill processes. Prior experience participating in media fill simulations in a regulated environment. Ability to work in a fast‑paced environment with strong attention to detail and organizational skills. Excellent written and verbal communication skills. Bachelor's degree in Microbiology, Biology, or a related field preferred, or equivalent work experience. Schedule
Night shift, 12‑hour shifts on a 4 days on, 3 days off, 3 days on, 4 days off rotation. Must be flexible to accommodate additional work in extended hours and/or off‑hour work (including potential nights & weekends). Seniority Level
Associate Employment Type
Full‑time Job Function
Quality Assurance Industry
Pharmaceutical Manufacturing Benefits
Medical insurance Vision insurance
#J-18808-Ljbffr