Environmental Compliance Technician I 3rd shift

Kindeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector Inhalation Transdermal/Intradermal Patch Technologies. We partner with our customers to improve patient outcomes around the world. Together as One Team we will manufacture many more to work with purpose Look no further we are hiring for a motivated talented passionate Compliance Technician I to join our St. Louis Missouri team!The main responsibilities of an Environmental Compliance Technician I involve performing environmental monitoring of the Aseptic Processing Area (APA). Individuals will also perform activities outside of the cleanroom including the examination of environmental monitoring samples for the recovery of microbial growth and the entry of data into a validated database. Sampling activities for this position includes viable surface and air monitoring non-viable air monitoring and water sampling across the position will be based at the St. Louis Brentwood site and offered as aflex roleto provide support at the St. Louis Bridgeton site as position opening is for 3rd shift (10:00pm to 06:30am)ROLE RESPONSIBILITIESAcquire and maintain knowledge of company and departmental policies related to current Good Manufacturing Practices (cGMPs) Good Laboratory Practices (GLPs) safety health and practical laboratory knowledge and proficiency in microbiological methodologies laboratory procedures and the use of standard laboratory equipment to examine microbiological samples for the presence or absence of routine environmental monitoring and sampling throughout the aseptic processing facility including viable surface and air sampling non-viable air sampling facility water sampling compressed gas sampling and other required sampling activities (CS/AA/PA/Waters/Gas/NVP).Prepare label distribute and maintain environmental monitoring plates using proper aseptic handling qualified in aseptic gowning and aseptic technique and maintain compliance with gowning and verify environmental conditions including temperature humidity and differential pressure using the REES verify and correct environmental monitoring plate data in MODA to ensure accuracy completeness and GMP quality functions related to batch processing GMP documentation review and quality compliance investigations within the QTS system by documenting findings assisting with root cause investigations and implementing corrective Environmental Control (EC) identification numbers to ensure documentation and complete ad hoc sampling requests in accordance with Environmental Control procedures and applicable with smoke studies Quality Risk Assessments (QRA) protocol-driven sampling validation activities and other quality initiatives as analyze interpret and present laboratory and environmental monitoring data using sound mathematical reasoning and analytical accurate detailed and concise records with strong attention to detail in accordance with GMP documentation procedural deviations and promptly notify Quality Management while maintaining the highest standards of ethics and effectively by listening seeking clarification from supervisory staff when needed and presenting written and numerical information clearly and assignments on time develop plans to meet deadlines and communicate alternative plans when changing priorities or unforeseen circumstances effectively to frequent changes delays and unexpected events while maintaining productivity and professionally and respectfully with management and non-management employees fostering a collaborative work environment that values diversity and all safety health and security procedures and consistently meet departmental safety objectives aligned with job QUALIFICATIONSHigh School/GED and one-year general work experience and/or training; or equivalent combination of education and QUALIFICATIONSAssociate degree or bachelors degree in biology microbiology or related field and previous experience preferred.