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Biotech Cleanroom Jobs in Tennessee (NOW HIRING)

August Bioservices

Production Scheduler

Nashville, TN · On-site

... biotech, or sterile/aseptic manufacturing; CDMO experience strongly preferred. * Working knowledge of aseptic processing concepts (isolators/RABS, cleanroom classifications, media fills, autoclave ...

New

August Bioservices

Production Scheduler

Nashville, TN · On-site

... biotech, or sterile/aseptic manufacturing; CDMO experience strongly preferred. * Working knowledge of aseptic processing concepts (isolators/RABS, cleanroom classifications, media fills, autoclave ...

New

August Bioservices

Production Scheduler

Nashville, TN

... biotech, or sterile/aseptic manufacturing; CDMO experience strongly preferred. * Working knowledge of aseptic processing concepts (isolators/RABS, cleanroom classifications, media fills, autoclave ...

New

Augustbio

Reliability Engineer

Nashville, TN · On-site

$110 - $160/hr

... biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our ... safety, cleanroom performance, or regulatory compliance. Maintenance and condition‑based ...

August Bioservices

Reliability Engineer

Nashville, TN · On-site

$99K - $124K/yr

... biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our ... safety, cleanroom performance, or regulatory compliance. Maintenance and condition-based ...

August Bioservices

Reliability Engineer

Nashville, TN · On-site

$99K - $124K/yr

... biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our ... safety, cleanroom performance, or regulatory compliance. Maintenance and condition-based ...

August Bioservices

Reliability Engineer

Nashville, TN · On-site

$99K - $124K/yr

... biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our ... safety, cleanroom performance, or regulatory compliance. Maintenance and condition-based ...

Medium

Reliability Engineer

Nashville, TN · On-site

$110 - $170/hr

... biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our ... safety, cleanroom performance, or regulatory compliance. * Maintenance and condition-based ...

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Biotech Cleanroom information

What is a biotech cleanroom?

A Biotech Cleanroom is a specially designed, controlled environment used in biotechnology labs and manufacturing facilities to minimize contamination from dust, microbes, or other airborne particles. These rooms maintain strict temperature, humidity, and particle count standards to protect sensitive biological samples and processes. Workers in biotech cleanrooms follow rigorous gowning and hygiene protocols, and equipment is regularly sterilized. Cleanrooms are essential in producing pharmaceuticals, medical devices, and other biotech products that require high levels of purity and safety.

What are the key skills and qualifications needed to thrive as a biotech cleanroom technician?

To thrive as a Biotech Cleanroom Technician, you need knowledge of aseptic techniques, good laboratory practices (GLP), and a background in biology or biotechnology, often with an associate’s or bachelor’s degree. Familiarity with cleanroom protocols, environmental monitoring equipment, and compliance systems like GMP (Good Manufacturing Practice) is typically required. Attention to detail, reliability, and effective communication are critical soft skills for maintaining sterile environments and following strict procedures. These skills ensure product safety, regulatory compliance, and consistent quality in sensitive biotech manufacturing processes.

What are some common challenges faced when working in a biotech cleanroom environment?

One of the main challenges in a biotech cleanroom is maintaining strict adherence to contamination control protocols while performing complex tasks. Employees must follow rigorous gowning procedures, regularly sanitize equipment, and be vigilant about minimizing particle generation. The controlled environment can feel restrictive due to specialized attire and limited personal items, but it's essential for ensuring product quality and safety. Teamwork and clear communication are crucial, as tasks often require coordination with colleagues to maintain workflow efficiency and compliance with regulatory standards.

What is the difference between Biotech Cleanroom vs Laboratory Technician?

AspectBiotech CleanroomLaboratory Technician
Required CredentialsCleanroom certification, life sciences trainingAssociate degree or relevant certification, lab safety training
Work EnvironmentControlled cleanroom environment, strict contamination controlStandard laboratory setting, varied equipment
Industry UsageBiotech manufacturing, pharmaceutical productionResearch labs, clinical testing

Biotech Cleanroom specialists focus on maintaining contamination-free environments for biotech and pharmaceutical manufacturing, requiring specialized cleanroom protocols. Laboratory Technicians support research and testing in general lab settings. While both roles require scientific knowledge, cleanroom roles emphasize contamination control and certification, whereas lab technicians focus on testing and data collection.

What are popular job titles related to Biotech Cleanroom jobs in Tennessee?

For Biotech Cleanroom jobs in Tennessee, the most frequently searched job titles are:

What job categories do people searching Biotech Cleanroom jobs in Tennessee look for?

The top searched job categories for Biotech Cleanroom jobs in Tennessee are:

What cities in Tennessee are hiring for Biotech Cleanroom jobs?

Cities in Tennessee with the most Biotech Cleanroom job openings:

Biotech Cleanroom jobs near you
Infographic showing various Biotech Cleanroom job openings in Tennessee as of August 2026, with employment types broken down into 1% As Needed, 94% Full Time, 1% Part Time, and 4% Contract. Highlights an 76% Physical, 4% Hybrid, and 20% Remote job distribution.

Production Scheduler

August Bioservices

Nashville, TN • On-site

Full-time

Posted 3 days ago

New

Job description

Headquartered in Nashville, TN - one of the fastest-growing and most exciting cities in the United States - August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO). As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. To support our growth plans, August is investing significant capital in a two-phase expansion project - including building a new state-of-the-art facility adjacent to our current facility. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August!
The Production Scheduler is responsible for developing and maintaining the detailed, day-to-day production schedule across sterile manufacturing suites - including dispensing, formulation, aseptic filling, visual inspection, and packaging. This role translates the master production schedule and client demand into an executable schedule that accounts for cleanroom availability, personnel availability/competencies, equipment changeovers, campaign sequencing, and material readiness. The Scheduler works cross-functionally with Manufacturing, Quality, Supply Chain, Warehouse, Facilities/Engineering, and Client Services to maximize suite utilization while protecting product quality, batch genealogy, and client commitments.
This is a highly detail-oriented, execution-focused role suited to someone comfortable balancing competing priorities in a highly regulated, capacity-constrained aseptic manufacturing environment.
Responsbilities
  • Detailed Scheduling & Execution
    • Build and maintain rolling detailed production schedules (daily/weekly/monthly horizons) for dispensing, compounding, filling lines, visual inspection, and packaging suites.
    • Sequence batches to minimize changeover time, cleaning/sanitization cycles, and gowning transitions while respecting product segregation
    • Adjust schedules in real time in response to deviations, equipment downtime, material delays, QC hold times, or client priority changes; communicate impacts promptly.
  • Capacity & Constraint Management
    • Model suite, equipment, and labor capacity constraints (fill line speeds, autoclave loads, fill line availability, inspection throughput) to identify bottlenecks.
    • Partner with Manufacturing and Engineering on preventive maintenance and calibration scheduling to minimize disruption to production.
    • Flag capacity gaps or overbooking risks to leadership with proposed mitigation options.
  • Cross-Functional Coordination
    • Align detailed schedules with the Master Production Schedule (MPS), demand plan, and client-committed delivery dates.
    • Coordinate with Warehouse/Materials Management to confirm raw material, component (vials, stoppers, syringes), and primary packaging availability ahead of scheduled batches.
    • Work with QA to sequence batch record issuance, in-process testing, and release timelines into the schedule.
    • Support Client Services/Program Management with schedule visibility, risk communication, and root-cause input for schedule adherence metrics.
  • Systems & Data Integrity
    • Maintain accurate schedule data in ERP system
    • Ensure batch numbers, lot genealogy, and campaign sequencing are correctly reflected across scheduling and quality systems.
    • Generate schedule adherence, OTIF (on-time-in-full), and utilization reports for operations reviews.
  • Continuous Improvement & Compliance
    • Support root cause analysis for schedule misses and participate in CAPA activities related to planning/scheduling.
    • Operate within cGMP, data integrity, and site SOP requirements at all times; complete required training.
    • Participate in S&OP (Sales & Operations Planning) and tiered daily management meetings, providing schedule status and risk escalation.

Qualifications
  • Bachelor's degree in Supply Chain, Operations Management, Engineering, Life Sciences, or related field (or equivalent combination of education and experience).
  • 3+ years of production scheduling/planning experience in pharmaceutical, biotech, or sterile/aseptic manufacturing; CDMO experience strongly preferred.
  • Working knowledge of aseptic processing concepts (isolators/RABS, cleanroom classifications, media fills, autoclave cycles).
  • Experience with ERP and/or advanced planning/scheduling (APS) systems (SAP, Oracle, JDE, PlanetTogether, Kinaxis, or similar).

Knowledge, Skills, & Abilities
  • Strong Excel skills (pivot tables, lookups); experience with scheduling/Gantt tools.
  • Solid understanding of cGMP, batch record processes, and regulated manufacturing documentation.
  • Excellent organizational skills and ability to manage multiple, shifting priorities under time pressure.
  • Strong cross-functional communication skills; comfortable presenting schedule risk to operations leadership.

At August Bioservices, Our Credo is our culture. Everything we do, we do with great care. We believe in the promise of discovery and the power of science to transform lives. We assert that excellence is not a static destination, but a standard, and an every-day measuring stick of our advancement. We aspire to unlock the potential in every person, every process and every molecule - from start to finish. We are committed to doing the right thing the first time and every time, meeting or exceeding all regulatory requirements. We strive to be exceptional, preferred and indispensable partners for our customers; responsible and engaged citizens within our communities; and active, mindful stewards of our environment.
We are August Bioservices. We are pointing the way forward. If this sounds like your kind of working environment, we want you on our team!
August Bioservices is an equal opportunity employer and values diversity. All aspects of employment including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. August Bioservices does not discriminate on the basis of any status protected under federal, state, or local law.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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