Sterile Manufacturing Supervisor

Sterile Filling Line Supervisor

We are seeking an experienced Sterile Filling Line Supervisor to lead clean room manufacturing operations within a fast-growing nutritional and pharmaceutical-grade production environment. This individual will play a critical role in overseeing sterile filling operations, ensuring equipment runs efficiently, production goals are achieved, and all activities comply with GMP, quality, and safety standards. The ideal candidate will possess a strong background in sterile manufacturing, pharmaceutical, nutraceutical, biotechnology, medical device, or other regulated production environments.

This is a hands-on leadership role responsible for setting up, operating, troubleshooting, and optimizing sterile filling equipment while supervising production personnel and maintaining the highest standards of product quality and regulatory compliance.

• Production & Equipment Operations
  • Set up, operate, monitor, and troubleshoot sterile filling and bottling equipment to ensure efficient and compliant production operations.
  • Perform equipment changeovers, adjustments, calibrations, and line clearances as required.
  • Ensure filling lines consistently meet production, quality, and efficiency targets.
  • Identify and resolve equipment, process, and operational issues to minimize downtime and maximize throughput.
  • Coordinate preventative maintenance activities and work closely with maintenance personnel to ensure equipment reliability.
  • Monitor production schedules and adjust staffing and resources as necessary to meet operational demands.
• Leadership & Personnel Management
  • Supervise, train, coach, and develop production personnel assigned to sterile filling and bottling operations.
  • Ensure team members follow all Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMPs), and clean room protocols.
  • Conduct performance evaluations, provide ongoing feedback, and support employee development initiatives.
  • Foster a culture of accountability, teamwork, safety, and continuous improvement.
  • Assist with staffing decisions, onboarding, and training of new employees.
• Quality & Compliance
  • Ensure all manufacturing activities comply with cGMP, FDA, OSHA, and company quality standards.
  • Review and maintain accurate batch records, production logs, and manufacturing documentation.
  • Verify completion of in-process inspections and quality checks throughout production activities.
  • Support internal audits, regulatory inspections, investigations, corrective actions, and continuous improvement initiatives.
  • Ensure strict adherence to aseptic processing, contamination control, and clean room procedures.
• Operational Excellence
  • Monitor key performance indicators including throughput, yields, downtime, waste reduction, and labor efficiency.
  • Recommend and implement process improvements that increase productivity while maintaining product quality.
  • Collaborate with Quality Assurance, Quality Control, Warehouse, Planning, and Operations teams to support overall business objectives.
  • Maintain a clean, organized, and audit-ready manufacturing environment.

• Education
  • High School Diploma or GED required.
  • Associate's or Bachelor's degree in Engineering, Manufacturing, Life Sciences, Biotechnology, Pharmaceutical Sciences, or a related field preferred.
• Experience
  • Minimum of 5 years of manufacturing experience within a pharmaceutical, nutraceutical, biotechnology, medical device, cosmetic, or other regulated production environment.
  • Minimum of 2 years of supervisory or leadership experience overseeing production personnel.
  • Proven experience operating, setting up, troubleshooting, and optimizing filling, bottling, packaging, or related manufacturing equipment.
  • Experience working within clean room and sterile manufacturing environments strongly preferred.
  • Experience with aseptic processing and contamination control practices is highly desirable.
• Technical Skills
  • Strong knowledge of GMP, cGMP, FDA, and quality system requirements.
  • Familiarity with batch records, manufacturing documentation, deviation reporting, and corrective actions.
  • Ability to diagnose and resolve mechanical, operational, and production…