Temporary GMP Cleaner

Summary Third shift GMP cleaner Job Description GMP Cleaner Position. This position requires strict adherence to current Good Manufacturing Practices (cGMPs), established cleaning practices and procedures, and compliance with quality standards and regulations. The purpose of the sanitization program is to control microbial contamination and to serve as a corrective action for the loss of control for viable excursion contamination. Standard Operating Procedures (SOPs) must be followed and strictly enforced to ensure acceptable environmental monitoring results of the cleaned GMP environment. This position may require working non-standards shifts (swing) and on Saturdays or Sundays. The incumbent may be required to work weekends , holidays, and overtime if required . This is a full time Union, exempt position, overtime eligible. Essential Functions:   Must be able to perform sanitization activities Ensure to adhere to SOP and sanitization practices Reviews cleaning log and ensure to adhere to GDP Responsible for verifying that the proper sanitization disinfectant rotation is followed and that the proper sanitization disinfectant is used for each assignment Responsible for completing required GMP documentation to ensure records are properly and accurately maintained Responsible for organization and upkeep of sanitization supply areas Responsible to participate in cycle counting and inventory of sanitization supplies and gowning articles to maintain inventory properly stocked for daily sanitization. Other Responsibilities Include: Collaborate with Manufacturing, GMP Operations Manager, and Quality teams to manage schedules necessary to sanitize the GMP controlled environment and support areas to comply with GMP requirements Participate in required training making sure to meet deadlines. Understands and follows proper procedures with Environmental Health and Safety (EHS) and personal protective equipment (PPE Performs related duties as assigned, no deviation.

In: Accurate GMP documentation and sign off on work performed with an emphasis on Good Documentation Practices (GDPs) Communicating clearly and concisely, both orally and in writing, (bilingual a plus) Ability to read, write and understand documentation in English Ability to work in a team environment and independently Establish and maintaining collaborative working relationships with Management and Client. Providing excellent customer service. Knowledge of preferred but will train the right candidate. Current Good Manufacturing Practices (cGMP) Good Documentation Practices (GDP) Company policies and practices, including safety rules and regulations Education and/or Experience: High School Diploma or equivalent Prior experience on a biopharmaceutical GMP controlled environment. English usage, spelling and punctuation Business computer applications Attention to detail is required Excellent attendance record Must follow work instructions 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 Continuous standing and walking throughout workday Majority of time spent in cleanroom, fully gowned including head covering, facemask, gloves, plant shoes, safety glasses/goggles and/or face shield Perform sanitization activities with ceiling mops, wall mops, floor mops, and wipers Cushman & Wakefield also provides eligible employees with an opportunity to enroll in a variety of benefit programs, generally including health, vision, and dental insurance, flexible spending accounts, health savings accounts, retirement savings plans, life, and disability insurance programs, and paid and unpaid time away from work. In addition