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Supervisor - Operations Visual Inspection

Job in Durham, Durham County, North Carolina, 27703, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-03-04
Job specializations:
  • Manufacturing / Production
    Operations Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Role Summary

Supervisor overseeing visual inspection operations for drug product lines at Lilly's Raleigh-Durham facility. Responsible for on-the-floor leadership, commissioning/qualification support for automated and semi automated inspection lines, and developing manufacturing staff. Directly involved in hiring and ensuring staffing is qualified, while maintaining safety and cGMP compliance.

Responsibilities
  • Support site leadership to build a diverse, inclusive, and capable site organization by delivering area operational procedures and quality processes for Parenteral areas
  • Hire/manage 10+ direct reports across multiple manufacturing lines
  • Maintain a safe work environment and support all health, safety, and environmental goals
  • Ensure qualified/trained staffing for operators on manufacturing lines
  • Communicate with the area Manager on quality, equipment, and operational issues and areas for improvement
  • Coach, develop, and evaluate the performance of operators/technicians
  • Originate or investigate deviations or operational quality issues
  • Collaborate with support functions to resolve unexpected events during manufacturing
  • Act as administrator and technical leader for operations, adhering to procedures and quality systems
  • Oversee shop floor execution to meet business plans and cGMP conformance
Qualifications
  • Required:

    High School Diploma or equivalent
  • Required:

    2+ years of experience in operations or directly supporting pharmaceutical manufacturing
  • Required:

    Demonstrated leadership with respect for people
  • Required:

    Skills in providing/receiving feedback and creating employee development plans
  • Required:

    Basic computer skills (desktop software)
  • Required:

    Strong understanding of FDA guidelines and cGMP requirements
  • Required:

    Excellent interpersonal, written, and oral communication skills
  • Required:

    Strong organizational skills and ability to handle multiple requests
  • Required:

    Strong technical aptitude and ability to train and mentor others
  • Required:

    Ability to work overtime as required
  • Required:

    Ability to travel
  • Required:

    Qualified candidates must be legally authorized to work in the United States
Skills
  • Leadership and people development
  • Effective communication and collaboration with cross-functional teams
  • Problem solving and root cause analysis
  • Quality systems and cGMP knowledge
  • Operational planning and staffing management
  • Training and mentoring
  • Adaptability to shift schedules and project phases
Education
  • High School Diploma or equivalent (required)
  • Bachelor’s Degree in science, engineering, or technical field (preferred)
Additional Requirements
  • Position may include short-duration assignments in Indianapolis or internationally
  • Ability to wear safety equipment (safety glasses, safety shoes, protective gloves, etc.)
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