GMP Cleaner
No salary listed
Entry
Nashville, TN, USA
In Person
Cleaning & Custodial ServicesJanitorial Services
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 is a US-based CDMO offering end-to-end drug development and manufacturing from pre-clinical to commercial. It combines large-CDMO scale with a customer-focused hybrid model to serve startups and big pharma. It provides full development programs including research, development, testing, lab services, and sterile fill/finish under one integrated process, ensuring cGMP and FDA-quality standards. Its goal is to help clients bring safe, effective drugs to market efficiently through a seamless, integrated pathway.
Company Size
51-200
Company Stage
Series B
Total Funding
$88.6M
Headquarters
Nashville, Tennessee
Founded
2017
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Simplify's Take
What believers are saying
- Vial filling qualified in July 2026, unlocking throughput from the $60 million expansion.
- Series B funding in 2025 financed an additional high-speed vial suite and automation.
- August Bioservices' 2026 event calendar signals active business development across BIO, CPHI, and Contract Pharma.
What critics are saying
- Sterile injectable capacity takes roughly 30 months to qualify, delaying revenue from expansion.
- A single FDA contamination finding can halt lines, erase customer trust, and trigger recalls.
- Specialization in sterile injectables concentrates exposure if outsourcing demand shifts or major clients leave.
What makes August Bioservices unique
- Nashville campus offers sterile injectables, development, and manufacturing on one contiguous site.
- August Bio runs fully isolated vial, syringe, and IV bag lines with in-house analytics.
- The 2026 site integrates automated inspection, labeling, packaging, and serialization for faster releases.
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Benefits
- Health Insurance
- Dental Insurance
- Vision Insurance
- Life Insurance
- Disability Insurance
- Health Savings Account/Flexible Spending Account
- Unlimited Paid Time Off
- Flexible Work Hours
- Remote Work Options
- Paid Vacation
- Paid Sick Leave
- Paid Holidays