Production Scheduler

August-Bioservices; Nashville (TN); On-site; USD 70,000 - 100,000; Full time

Job summary

August Bioservices, headquartered in Nashville, TN, is seeking a Production Scheduler to translate the master production schedule into executable day-to-day plans across sterile manufacturing suites, balancing cleanroom capacity, personnel readiness, and material availability.

This role collaborates closely with Manufacturing, Quality, Supply Chain, Warehouse, Facilities/Engineering, and Client Services to maximize suite utilization while protecting product quality and batch genealogy in a

Qualifications

• Bachelor's degree in a related field or equivalent experience.
• 3+ years of production scheduling in pharma/biotech/sterile manufacturing.
• Knowledge of aseptic processing concepts and scheduling systems.

Responsibilities

• Build and maintain detailed production schedules for multiple suites.
• Sequence batches to minimize changeovers and keep quality.
• Coordinate with QA, Manufacturing, and Materials to ensure availability.
• Generate schedule adherence and OTIF reports for reviews.

Skills

Production scheduling

Cross-functional communication

Excel (pivot tables)

cGMP knowledge

ERP/APS systems

Education

Bachelor's degree in related field

Tools

ERP/APS systems (SAP, Oracle, JDE, PlanetTogether, Kinaxis)

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 servicesto 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.