×
Register Here to Apply for Jobs or Post Jobs. X

Production Scheduler

Job in Nashville, Davidson County, Tennessee, 37247, USA
Listing for: August-Bioservices
Full Time position
Listed on 2026-08-22
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Manufacturing & Industrial Operations
Salary/Wage Range or Industry Benchmark: 70000 - 100000 USD Yearly USD 70000.00 100000.00 YEAR
Job Description & How to Apply Below

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…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary