Maintenance & Facilities Manager

Maintenance Manager About Krystal Bio At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases with high unmet medical needs. Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented gene therapy platform, innovative manufacturing supported by our commercial scale facilities, and a unique commercialization model that focuses on the patient’s end to end experience. Krystal received U.S. FDA approval for the first and only redosable gene therapy treatment, VYJUVEK®, for the treatment of Dystrophic Epidermolysis Bullosa (DEB). Krystal continues to leverage our proprietary platform to rapidly advance a robust pipeline of investigational genetic medicines in respiratory, oncology, dermatology, and ophthalmology. Krystal is headquartered in Pittsburgh, PA which is home to our two state‑of‑the‑art CGMP manufacturing facilities with teams around the world and satellite offices in Switzerland, Germany, and Japan. We are a company built and run by people who care, are fearless in the face of a challenge, love the work they do, and practice the highest level of scientific integrity. As we grow, we are seeking team members that embody these values. Job Description Summary Krystal Biotech, Inc is seeking a highly motivated Maintenance Manager to provide technical and administrative leadership at our state-of-the-art GMP facility in Moon Township, PA. This is a hands‑on role that involves direct contributions with troubleshooting as well as oversight of maintenance programs, facility optimization and consistent reliability. Primary Responsibilities Leverage knowledge of GMP facilities and engineering processes, mechanical and utility systems and instrumentation to develop capabilities in diagnosis and troubleshooting of issues Triage and resolve issues related to maintenance process non‑conformances Lead lifecycle assessments and provide recommendations for replacements and/or upgrades as needed to ensure consistent reliability Maintain awareness of industry and regulatory trends for calibration, instrumentation and maintenance Provide input for responses to regulatory inspections or internal audits relating to instrument calibrations or maintenance programs Perform daily operations, maintenance and repairs on utility systems, manufacturing equipment and building systems in a cGMP environment with minimal supervision Ensure safe and efficient hands‑on maintenance of all manufacturing equipment and related support equipment with strict adherence to SOP's, cGMP's, and quality standards Identify any off‑nominal conditions with mechanical equipment and mechanical troubleshooting of manufacturing/utility equipment in a clean room environment Execute daily Work Orders (WOs) and Preventative Maintenance (PM) items, and coordinate associated documentation and workflow Act as a subject matter expert for the Facilities and Maintenance group in relevant equipment and system root cause investigations and fill the role of lead investigator where required Ensure a safe work environment is maintained through adherence to safety guidelines and policies Provide on‑call support during operation, project and shutdown activities, as required Experience and Skills Desired 6+ years of meaningful work experience in operations/manufacturing environment 3+ years of experience within highly regulated environments (i.e. cGMP, OSHA, EPA) Experience working with GMP systems, and in-depth technical knowledge of GMP instrumentation, highly preferred Demonstrated leadership attributes as an individual contributor (e.g., leadership of initiatives or participation on network level or continuous improvement teams) Strong background in process improvement methodologies Demonstrate a strong background in GMP Maintenance combined with excellent leadership and communication skills (written and verbal) Good interpersonal, communication and problem‑solving skills Must be knowledgeable of the regulatory and GMP requirements for process equipment, instrumentation and calibration Knowledge of Six Sigma and lean systems is a plus Ability to make informed and timely decisions that consider the facts, goals, constraints, and associated risks A team player with a can‑do, proactive attitude with a passion for continuous improvement Equal Employment Opportunity Krystal Biotech, Inc. is an Equal Employment Opportunity and affirmative action employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. Headhunters and recruitment agencies may not submit resumes/CVs through this website or directly to managers. Krystal Biotech, Inc. does not accept unsolicited headhunter and agency resumes. Krystal Biotech, Inc. will not pay fees to any third‑party agency or company that does not have a signed agreement with Krystal Biotech, Inc. #J-18808-Ljbffr