A

August Bioservices

US-based CDMO for end-to-end drug development

GMP Cleaner

Janitorial ServicesConfirmed live in the last 24 hours
Full-timeNashville, TN, USANo salary listedIn-person

About the Job

Requirements

  • A high school diploma or equivalent.
  • Previous experience in a Good Manufacturing Practice-regulated environment or pharmaceutical manufacturing facility is a plus, not a requirement.
  • Knowledge of Good Manufacturing Practice guidelines and cleanroom practices is highly desirable.
  • Strong communication and documentation skills.
  • Ability to work as part of a team and follow strict procedures.
  • Willingness to undergo gowning and cleanroom training.

Responsibilities

  • Perform daily cleaning and disinfection of cleanrooms, including floors, walls, ceilings, and equipment, following Good Manufacturing Practice Standard Operating Procedures.
  • Clean and sanitize manufacturing equipment and utensils used in the production process, ensuring they are free from contaminants.
  • Manage and dispose of waste generated in the manufacturing facility in compliance with Good Manufacturing Practice guidelines and safety protocols.
  • Adhere to strict gowning procedures and maintain personal hygiene and cleanliness to prevent contamination within the facility.
  • Maintain accurate records of cleaning activities and environmental monitoring results, and report deviations from standard procedures.
  • Handle and store cleaning chemicals safely and in accordance with safety data sheets and Good Manufacturing Practice requirements.
  • Collaborate with the Quality Assurance team to address cleanliness-related non-conformities and participate in investigations to identify root causes.
  • Identify and suggest improvements in cleaning processes and contribute to the development of new cleaning procedures and protocols.
  • Comply with all safety rules, regulations, and best practices to maintain a safe work environment.

Desired Qualifications

  • Previous experience in a Good Manufacturing Practice-regulated environment or pharmaceutical manufacturing facility.
  • Knowledge of Good Manufacturing Practice guidelines and cleanroom practices.

About the Company

August Bioservices

US-based CDMO for end-to-end drug development

August Bioservices is a US-based CDMO that provides end-to-end drug development and manufacturing from preclinical to commercial stages. It manages all steps in a single program, including research, development, testing, laboratory services, and sterile fill/finish, while following cGMP standards. It differentiates itself with a hybrid model that combines large-CDMO scale and capabilities with a strong focus on customer service and integrated workflows. Its goal is to help clients bring safe and effective drugs to market efficiently by delivering comprehensive development and manufacturing under one roof.

Company size
51-200
Company stage
Series B
Total funding
$88.6M
Headquarters
Nashville, TN
Founded
2017

Recently Posted Jobs

Explore more opportunities at August Bioservices

See more jobs