We are seeking a detail-oriented Environmental Monitoring Technician I to play a key role in ensuring compliance with regulatory requirements in cutting-edge cell and gene therapy facilities. This position offers the opportunity to work in state-of-the-art environments, including aseptic (Class 100) cleanrooms and laboratory settings, directly supporting critical GMP operations. What You'll Do Operate specialized equipment in classified and non-classified GMP areas Perform routine environmental monitoring and sampling Accurately document activities, results, and observations in compliance with cGMP standards Read, interpret, and follow SOPs, diagrams, and schematics Maintain meticulous records, including laboratory notebooks and quality documentation Conduct audits of SOPs and work instructions to ensure ongoing compliance Train and guide others in proper SOP execution and documentation practices Recommend and implement improvements to processes, equipment, and compliance practices Collaborate with support teams to coordinate daily operations Wear and maintain required gowning and PPE for sterile operations Minimum Qualifications Bachelor's degree in Life Sciences (Biology preferred) 1-2 years of experience in a pharmaceutical production or laboratory environment Strong attention to detail and ability to maintain accurate records Competence in following written procedures and performing mathematical calculations Proficient in English (reading, writing, and verbal communication) Preferred Skills Experience in a LEAN manufacturing environment Familiarity with cGMP regulations and FDA requirements 2+ years of relevant industry experience This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! INDBH
Astrix Inc