Facility Cleaner

The Facility Cleaner supports the manufacture of commercial and clinical biologics by performing routine and non‑routine cleaning and sanitization of production and operational areas in a cGMP cleanroom environment. This role focuses on precise, right‑the‑first‑time execution of cleaning activities, meticulous documentation, and strict adherence to Current Good Manufacturing Practices (cGMPs) to prevent quality deviations and maintain a highly controlled, compliant facility.

Responsibilities

• Execute routine and non‑routine cleaning and sanitizing of operational and production areas according to work instructions, standard operating procedures (SOPs), and cGMP requirements.
• Thoroughly clean and sanitize stainless steel equipment and other production surfaces to prevent quality deviations and maintain aseptic conditions.
• Prepare and formulate cleaning solutions in accordance with established procedures, safety guidelines, and cGMP standards.
• Perform environmental cleaning in cleanroom and controlled areas, ensuring all assigned spaces meet required cleanliness and sterility standards.
• Accurately document all cleaning, sanitization, and sterilization activities in compliance with cGMP documentation practices.
• Complete preventive maintenance and cleaning‑related tasks on time and in accordance with established schedules.
• Use a clear method of prioritization to ensure critical cleaning activities are completed efficiently and in the correct order.
• Conduct visual inspections of equipment and areas to verify cleanliness, identify potential issues, and escalate concerns as needed.
• Participate in shift exchanges, one‑on‑one meetings, and team shift meetings to ensure effective communication and seamless handoffs between shifts.
• Follow cleanroom and gowning protocols at all times, including proper donning and doffing of gowning materials and use of required personal protective equipment (PPE).
• Adhere to all safety, quality, and compliance procedures while working in a cleanroom and biopharmaceutical manufacturing environment.

• 1–3 years of professional cleaning experience, preferably in an industrial, manufacturing, or similar controlled environment.
• Experience performing detailed cleaning and sanitization tasks beyond basic trash removal and sweeping.
• Strong attention to detail to ensure complete and accurate execution of cleaning and sterilization processes and documentation.
• Ability to follow cGMP guidelines and standard operating procedures with a focus on compliance and quality.
• Basic computer skills to enter data, complete documentation, and follow electronic work instructions.
• Ability to work effectively in a cleanroom environment under strict protocols and procedures.
• Capability to lift a minimum of 25 lbs independently and stand for approximately 80% of the shift.
• Ability to wear required PPE, including full gowning and a respirator, for extended periods.

• Prior experience working under cGMP or in a regulated manufacturing environment is preferred.
• Familiarity with cleanroom practices and cleanroom or industrial cleaning is highly beneficial.
• Experience with janitorial duties in a production, packaging, or industrial setting is an advantage.
• Comfort working around stainless steel production equipment and understanding its importance in preventing contamination.
• Strong organizational skills to manage multiple cleaning tasks and priorities during the shift.
• Good communication skills to participate effectively in shift exchanges and team meetings.

You will join a growing organization that offers long‑term career potential in a stable and expanding industry. The company provides strong opportunities for internal advancement and prefers to promote from within when the right talent is already in house. Once converted to a permanent role, employees gain access to competitive benefits and pay increases, supporting both professional development and financial growth. You will work in a professional, team‑oriented environment where your attention to detail and commitment to quality directly contribute to the success of critical biopharmaceutical products.

Work Environment

This position is based in a cleanroom and cGMP biopharmaceutical manufacturing facility with strict cleanliness, safety, and documentation standards. The role will likely transition to a 2nd shift schedule after a site‑wide shift change, but initially operates on a 5:30 a.m. to 5:30 p.m. rotating 2‑2‑3 schedule (two days on, two days off, three days on, etc.). You will work in controlled environments that require adherence to cleanroom and GMP protocols, including full gowning. Required attire includes a full gowning suit consisting of a body suit, gloves, hair and beard nets (as applicable), face covers, and safety glasses. Gowning materials may include Tyvek garments and Nitrile and/or Latex gloves. The environment prohibits the use of makeup, jewelry, nail polish, cologne, and perfume while on the production floor. You must be able to wear a respirator as needed, lift at least 25 lbs independently, and stand for approximately 80% of the shift. The facility uses stainless steel equipment and follows rigorous sanitization and documentation practices to support commercial and clinical biologics manufacturing.

Job Type & Location

This is a Contract position based out of Saint Louis, MO.

The pay range for this position is $19.50 - $22.43/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in Saint Louis,MO.

This position is anticipated to close on Apr 28, 2026.

We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.

Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.