As a QCEMII you will conduct environmental monitoring (EM) according to Standard Operating Procedures (SOPs) in a cleanroom facility. Use sophisticated laboratory instrumentation and computer systems to collect and record environmental monitoring data. Process and evaluate environmental monitoring samples according to SOPs. Review and trend data for documentation of procedures and reports. Initiates and writes investigations and SOPs. Receive and ship in process and final product samples. Apply knowledge of Good Documentation Practices (GDP) and Current Good Tissue Practices (cGTP) on a daily basis.
Interacts effectively with company management and internal departments
This positon requires a minimum 2 years work experience within the biotechnology or pharmaceutical industry performing EM or microbiology duties. Must be proficient in other compliance disciplines, i.e., cGTP, GLPs, GDP, GxPs
Osiris Therapeutics, Inc. is an Equal Opportunity Employer with a commitment to diversity. Applicants are considered on the basis of individual merit without regard to race, color, national or ethnic origin, gender, gender identity, sexual orientation, marital status, veteran status, pregnancy, age, religion, disability, genetic information, or any other characteristic protected by law.
Proficiency in other compliance disciplines, i.e., cGTP, GLPs, GDP, GxPs