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Night Shift Supervisor, Aseptic Filling

Job in Concord, Cabarrus County, North Carolina, 28027, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-09-12
Job specializations:
  • Manufacturing / Production
    Production QC/QA, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 35 - 52 USD Hourly USD 35.00 52.00 HOUR
Job Description & How to Apply Below

Position Overview

  • Support PAR (parenteral) area startup: coordinate training, develop technical proficiency, lead operational readiness, and help build a diverse/inclusive culture.
  • Lead PAR operations teams after turnover: develop inclusive culture and manufacturing technical expertise; ensure adequate staffing with trained/qualified employees; enforce safety and quality procedures. Direct supervision includes line leaders and operators.
Key Objectives / Deliverables Integrity
  • Lead with Safety first/Quality Always; encourage/execute Stop Work Authority for unsafe or product-impacting conditions.
  • Maintain safe work environment and support HSE goals.
  • Act as admin and technical leader; demonstrate procedure knowledge and quality-system compliance.
Excellence
  • Collaborate with area supervisors for consistent communication and best-practice sharing across shifts.
  • Execute shop-floor work to business plan, cGMP conformance, and operational standards.
  • Drive continuous improvement; identify and implement ideas with business value.
  • Ensure trained/compliant staffing; review/update training plans.
  • Develop area documentation (procedures, work instructions, job aides).
  • Originate/investigate deviations and quality issues; support root-cause and corrective actions.
Respect for People
  • Build diverse, empowered team; manage multiple direct reports across manufacturing lines.
  • Coach, develop, and evaluate operators; communicate cross-functionally on quality/equipment/operational concerns.
Requirements
  • High School Diploma (or equivalent); prior supervisory experience.
  • Basic MS Office/desktop skills.
  • Operations/manufacturing experience (pharma/food/clean-room or applicable).
  • Strong interpersonal, written, and oral communication; strong organizational skills; technical aptitude to train/mentor.
  • Valid driver's license.
  • Authorized to work in the U.S. full-time;
    Lilly does not sponsor visas.
  • Ability to work overtime; wear safety equipment; gown in cleanroom (Grade C, ISO
    8); 12-hour night shift (6pm-6am on a 2-2-3 schedule).
Preferred
  • 4+ years manufacturing/operations with 2+ years supervisory role.
  • cGMP and FDA (or other) guidelines; STEM degree/certification.
  • Aseptic filling/single-use assemblies/isolator technology; automated/semi-automated/manual inspection.
  • Highly automated equipment; MES and SAP/other electronic systems.
  • Continuous improvement (lean/six sigma); root-cause analysis and corrective actions.
Compensation/Benefits (if eligible)
  • Anticipated wage: $.
  • Potential company bonus; comprehensive benefits (401(k), medical/dental/vision, life insurance, vacation/time off, flexible benefits, and well-being programs).
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