We are a family and women-owned local company with over 50 years of experience in environmental solutions, specializing in infection prevention for complex facilities. Our responsiveness allows us to quickly meet staff and client needs. Servicon’s Culture of Caring drives our commitment to healthy environments, supported by three pillars: People, Programs, and Performance. These focus areas reinforce our values and help improve people's lives, patient care, infection prevention, and operational efficiency. 

GMP Cleaner team members are responsible for a wide variety of routine cleaning as well as auditing production and facility spaces to ensure a safe and sanitary work environment to meet or exceed all regulatory requirements. 

• Responsible for performing and maintaining a high level of clients’ Good Manufacturing Practices (cGMP) product and quality safety through the cleaning and sanitation of processing equipment, utensils, and the facility.
• Wear required and appropriate Personal Protective Equipment (PPE) in accordance with standard operating procedures (SOPs).
• Participate in required training on the use of sanitization disinfectants and equipment.
• Able to use cleaning chemicals as well as understand chemical safety and chemical handling procedures, including appropriate dilution and usage.
• Empty, clean and remove all waste receptacles from the premises to designated area, damp wipe receptacles. Waste may be recyclables, perishables and biohazard materials.
• Vacuum and sanitize floors, drains, walls, ceilings and shelves utilizing appropriate tools, including but not limited to, mops, vacuums, disinfectants, and speciality equipment.
• Perform record keeping and data tracking following Good Documentation Practices (GDP); responsible for completing the designated sanitation schedule.
• Sanitize and clean machines and machine parts using chemicals, manually, with high pressure hoses, spraying and/or scrubbing.
• Clean under tacky mats and/or change them, as needed.
• Follow all sanitation procedures to ensure compliance with the SOP and FDA requirements.
• Practice Good Documentation Practices (GDP) with cleaning times, chemicals dates and Lot # following client SOPs.
• May train new employees.
• Additional duties and responsibilities, as identified and assigned.

• Demonstrate continuous improvement thinking, searching for the next improvement opportunity. Be curious and creative.
• Experienced in a manufacturing, aerospace or pharmaceutical work environment that fostered collaboration and teamwork is preferable.
• Demonstrated willingness to ensure routine work gets done and can adjust to the unexpected with limited or no supervision. Act with urgency and deliver results.
• Demonstrate continuous focus on safety and quality for self and others.
• A solid understanding of the importance of effective recordkeeping, following procedures and communication.

Physical Requirements:

• No make-up, nail polish, and/or jewelry may be worn in the GMP process areas.
• Ability to wear a clean room (bunny suit) during the entire shift.
• Stand/walk for most of the work shift.
• 1+ year in sanitation in a GMP environment/aerospace is preferable.
• Customer service and professional
• Self-starter, motivated, team player with the ability to prioritize work.
• Able to work independently and productively as well as accept direction.
  Highly organized and excellent record-keeping abilities
• Willing to accept change and work in a team-based environment.
• Ability to handle multiple tasks in a fast-paced environment.
• Ability to read and communicate in English sufficiently to understand operating procedures, label instructions for handling chemical cleaners and solvents, and SDS sheets.
• Ability to work at different heights, climb ladders/stairs and assemble and disassemble equipment