JLL empowers you to shape a brighter way . Our people at JLL are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are committed to hiring the best, most talented people and empowering them to thrive, grow meaningful careers and to find a place where they belong. Whether you’ve got deep experience in commercial real estate, skilled trades or technology, or you’re looking to apply your relevant experience to a new industry, join our team as we help shape a brighter way forward. *You must join Local SIEU within 90 days* *Day, Swing, Grave & Weekend shifts are available* What this job involves This position requires strict adherence to current Good Manufacturing Practices (cGMPs), established cleaning policies and procedures, to maintain compliance with quality standards and FDA regulations. This position will follow all applicable standard operation procedures (SOP), guidelines and policies to ensure sanitary conditions are maintained, that appropriate room and equipment sanitization records are neat and accurate, and that professional behavior is displayed within the controlled areas. The position plays a critical role in assuring sanitary conditions of the controlled areas is maintained to manufacture biopharmaceuticals. This position may be required to work weekends, holidays, and overtime if required. Your day-to-day tasks will include: Perform sanitization and cleaning per governing SOPs in GMP spaces Participate in required training on the use of sanitization disinfectants and equipment Sanitization activities will be performed with ceiling mops, wall mops, floor mops, and wipers Responsible for verifying that the proper sanitization disinfectant is followed and that the proper sanitization disinfectant is used for each cleaning assignment Understands and follows proper solvent handling procedures (EHS) and personal protective equipment (PPE) Ensure proper disposal of waste from GMP manufacturing process area waste receptacles on a daily basis Strictly follow Standard Operating Procedures and ensuring technicians adhere to SOP and cleaning practices Provide support, guidance, and training (technical and SOP compliance) to the union cleaning crew Responsible for completing, reviewing, and verifying required GMP documentation at the end of each shift to ensure adherence to GDP and records are properly and accurately maintained Responsible for organization and upkeep of sanitization supply areas Support inventory of general sanitization supplies and gowning supplies, working with the Supervisor and GMP Cleaning coordinator Performs related duties as assigned Other Responsibilities can Include: Collaborate with Supervisors, Operational Compliance, and GMP Operations Manager to manage schedules necessary to clean the GMP controlled environment and support areas to comply with GMP requirements Participate in required training on the use of sanitization disinfectants and equipment Follow cGMPs as outlined in 21 CFR Part 211 Helps control what enters the GMP process areas Provide refresher training of sanitization practices as needed. Understands and follows proper procedures with Environmental Health and Safety (EHS) and personal protective equipment (PPE) Act as a backup to the Supervisor/s Performs related duties as assigned Physical Requirements and Working Environment: No make-up, nail polish, and/or jewelry may be worn in the GMP process areas Incumbent is subject to extended periods of standing, walking, pushing and pulling, bending and crouching, climbing, and lifting of equipment and/or materials weighing up to 50 pounds Continuous mental and visual attention to manufacturing functions Majority of time spent fully gowned including head covering, facemask, gloves, plant shoes, safety glasses/goggles and/or face shield Working in the ancillary support space adjacent to the GMP areas described above to ensure cleanliness Required Qualifications High School Diploma or equivalent Prior experience of cleaning a biopharmaceutical GMP controlled environment is a plus but not required Excellent communication - reading and writing Computer experience Attention to detail is required Excellent attendance record Must follow work instructions Ability to work in a team environment and independently Establish and maintain collaborative working relationships with internal and external customers Providing excellent customer service with both internal and external customers Preferred Qualifications Accurate GMP documentation and sign off on work performed with an emphasis on Good Documentation Practices (GDPs) Current Good Manufacturing Practices (cGMP) Good Documentation Practices (GDP) This position does not provide visa sponsorship. Candidates must be authorized to work in the United States without sponsorship. Estimated compensation for this position: 37,057.00 – 46,321.60 USD per year This range is an estimate and actual compensation m