Microbiology Supervisor

Global Compliance Partners (GCP) is a GxP and GMP compliance consulting firm with over a decade of experience supporting biopharma and cell & gene therapy organizations. We partner with leading drug developers and manufacturers to deliver validation, quality, and compliance solutions, from QC, QA, CSV/CQV and process validation through tech transfer and BLA support. Our consultants embed directly with client teams to move programs forward with rigor and speed. Summary: The Microbiology Supervisor is responsible for overseeing the daily operations of the microbiology laboratory, including scheduling and directing the work of analysts and technicians. This role ensures compliance with cGMP requirements, company policies, and regulatory standards by coordinating microbiological testing, environmental monitoring, and laboratory studies. The Supervisor provides technical expertise, training, and guidance to laboratory staff; monitors equipment performance and laboratory supplies; and supports investigations, audits, and cross-functional initiatives. Additionally, the Microbiology Supervisor collaborates closely with the Microbiology Manager and other departments to maintain laboratory readiness, ensure data integrity, and drive continuous improvement within the microbiology function. Essential Duties and Responsibilities: Supervise daily operations of the microbiology laboratory, including scheduling, task assignments, and coordination of analysts and technicians. Ensure completion of microbiological testing, environmental monitoring, and isolate identification in compliance with cGMP, regulatory standards, and company procedures. Train, mentor, and qualify laboratory staff in microbiological test methods, equipment operation, and proper documentation practices; assist with onboarding of temporary personnel as needed. Monitor laboratory equipment performance, troubleshoot technical issues, and elevate unresolved problems to the Microbiology Manager. Oversee inventory of reagents, media, and test materials; ensure aseptic preparation, timely ordering, and accurate documentation. Review and approve attendance records, vacation schedules, and other administrative requirements; implement corrective or disciplinary actions when necessary. Prepare, revise, and maintain standard operating procedures (SOPs), protocols, and related documentation. Coordinate specialized laboratory activities, including quarterly gamma sterilization dose audits, BI qualification, bioburden audits, and routine analyses (e.g., growth promotion, water testing, biennial biological indicators). Perform and review cGMP documentation and calculations; prepare preliminary investigations and provide support for full investigations as required. Support the Microbiology Manager during internal, customer, and regulatory audits; provide technical input and ensure laboratory readiness. Partner with cross-functional groups, including R&D, Technical Services, and the Laboratory Systems Supervisor, to support laboratory initiatives and company projects. Prepare study protocols, summary reports, and other documentation as requested by the Microbiology Manager or Associate Director, Laboratories. Promote continuous improvement within the microbiology laboratory by identifying opportunities to streamline processes, improve efficiency, and uphold quality standards. Education and/or Experience Bachelor’s degree in a scientific discipline, preferably microbiology or related field Minimum of one (1) year related work experience, required; Minimum of three (3) years’ related work experience, preferred Minimum of one (1) year experience in leadership role, required; Minimum of two (2) years’ experience in a leadership role, preferred Minimum of two (2) years’ industry experience in a GMP or GLP environment, preferred Experienced and proficient in the validation/qualification of lab microbiological techniques Previous experience with pharmaceutical cleanroom environments, preferred Working knowledge of GMPs/pharmaceutical environments is desirable #J-18808-Ljbffr